WO2023049983A1 - Cpmv vlps displaying sars-cov-2 epitopes - Google Patents

Cpmv vlps displaying sars-cov-2 epitopes Download PDF

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Publication number
WO2023049983A1
WO2023049983A1 PCT/CA2021/051352 CA2021051352W WO2023049983A1 WO 2023049983 A1 WO2023049983 A1 WO 2023049983A1 CA 2021051352 W CA2021051352 W CA 2021051352W WO 2023049983 A1 WO2023049983 A1 WO 2023049983A1
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coat protein
cpmv
vlp
modified
protein
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PCT/CA2021/051352
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French (fr)
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Pooja Saxena
Marc-Andre D'aoust
Pierre-Olivier Lavoie
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Medicago Inc.
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Priority to PCT/CA2021/051352 priority Critical patent/WO2023049983A1/en
Publication of WO2023049983A1 publication Critical patent/WO2023049983A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/12—Viral antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/005—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/86—Viral vectors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/525—Virus
    • A61K2039/5258—Virus-like particles
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
    • C12N2770/00011—Details
    • C12N2770/18011—Comoviridae
    • C12N2770/18023—Virus like particles [VLP]
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
    • C12N2770/00011—Details
    • C12N2770/18011—Comoviridae
    • C12N2770/18041—Use of virus, viral particle or viral elements as a vector
    • C12N2770/18042—Use of virus, viral particle or viral elements as a vector virus or viral particle as vehicle, e.g. encapsulating small organic molecule
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
    • C12N2770/00011—Details
    • C12N2770/20011—Coronaviridae
    • C12N2770/20022—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
    • C12N2770/00011—Details
    • C12N2770/20011—Coronaviridae
    • C12N2770/20034—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein

Definitions

  • CPMV VLPS DISPLAYING SARS-COV-2 EPITOPES FIELD OF INVENTION This disclosure relates to modified coat proteins.
  • the present disclosure also relates to virus-like particles (VLPs) comprising modified coat protein and methods of producing the VLPs in a host or host cells.
  • VLPs virus-like particles
  • Cowpea mosaic virus (CPMV) is an icosahedral, non-enveloped plant virus of the Comoviridae family of viruses in the order Picornavirales.
  • CPMV particles are of interest in biotechnology and nanotechnology due to their well-characterized molecular structure, high stability and their inability to infect animals or humans.
  • CPMV particles have been developed as an epitope display platform, an in vivo imaging tool, and as a substrate for chemical reactions including metal deposition, among other applications (Sainsbury et al. Methods in molecular biology 2014). CPMV and CPMV virus-like particles have also been shown to have immunostimulatory and anti-tumorigenic properties (Lizotte et al Nat. Nanotechnol. 2016; Wang et al. J. Virol.2019). [0004] The CPMV genome consists of 2 separate positive-sense single-stranded RNA, namely RNA-1 (of 6 kilobases) and RNA-2 (of 3.5 kilobases).
  • Each capsid consists of 60 copies of a protomer comprising large (L or VP37) and small (S or VP23) coat protein (CP) subunits, derived from a single CP precursor (VP60) encoded by RNA-2 and processed by a proteinase (24K) encoded by RNA-1.
  • L subunit is composed of two jellyroll ⁇ -barrel domains
  • the S subunit consists of a single jellyroll ⁇ -barrel.
  • the jellyroll ⁇ -barrel is common in many icosahedral virus structures and contains two twisted antiparallel ⁇ sheets, each of which contains four ⁇ strands. Therefore, each ⁇ -barrel of the L subunit and the S subunit consist principally of 8 antiparallel ⁇ -strands connected by loops of varying length.
  • the flat ⁇ -strands are annotated ⁇ B, ⁇ C, ⁇ D, ⁇ E, ⁇ F, ⁇ G, ⁇ H and ⁇ I.
  • three short alpha helices in the L and S subunits are designated ⁇ A, ⁇ B and ⁇ C, and two short beta strands found in close proximity to ⁇ C are referred to as ⁇ C’ and ⁇ C”.
  • ⁇ B- ⁇ C refers to the loop connecting ⁇ B with ⁇ C and ⁇ C’- ⁇ C
  • ⁇ F- ⁇ G, ⁇ E- ⁇ B are some others.
  • These loops can be used as sites for expression of foreign peptide sequences, such as epitopes from heterologous viruses.
  • Potential sites for insertion of foreign sequences have been determined by examining the three-dimensional structure of CPMV and through empirical testing, but there remain a wide range of alternatives.
  • WO1992018618A1 describes the use of modified CPMV coat proteins for the presentation of foreign peptides on the exposed surface of the coat proteins of the plant virus.
  • WO1996002649A1 discloses assembled CPMV particles containing a foreign peptide insert wherein the foreign peptide is inserted immediately preceding the proline 23 (Pro23) residue in the ⁇ B- ⁇ C loop of the small (S) capsid protein (VP23).
  • WO1998056933A1 similarly discloses raising an immune response to a peptide insert within a CPMV epitope presentation system, wherein the foreign insert is made immediately preceding a proline residue in the ⁇ B- ⁇ C loop of the small (S) capsid protein (VP23), which in CPMV is the proline 23 (Pro23).
  • WO2001027282A1 discloses insertion of a foreign peptide into sites on the VP-S of CPMV, such as the N-terminus of VP-S.
  • VLPs virus-like particles
  • CPMV VLP stability can vary based on the type of antigenic peptide sequences employed and this can impact production yields.
  • Epitope selection, in terms of peptide sequence, length, orientation and insertion site, in order to achieve high yields of fusion VLPs remains unpredictable (Sainsbury et al Methods. Mol. Biol.2014; Meshcheriakova Biochem. Soc. Trans.2017).
  • WO2010146359A1 shows the processing of VP60 in plants by the 24kDa proteinase, including a demonstration that VP60 can be modified such that the S coat protein includes a 19 amino acid FMDV sequence inserted in ⁇ B- ⁇ C loop, without impairing proteolytic processing.
  • SARS-CoV-2 spike glycoprotein of SARS-CoV-2, which mediates coronavirus entry into host cells via the angiotensin-converting enzyme 2 (ACE2) receptor.
  • S spike glycoprotein of SARS-CoV-2
  • ACE2 angiotensin-converting enzyme 2
  • Peptide vaccines rely on the use of short stretches of antigenic peptides to induce targeted immune responses against a pathogen, as opposed to use of live-attenuated or inactivated pathogen vaccines, subunit vaccines, or vaccines that administer nucleic acids encoding the pathogen’s proteins such as adenoviral vector, DNA, or mRNA vaccines.
  • Peptide vaccines have benefits over other types of vaccines, such as low cost of production, specificity to the relevant epitopes, and reduction of nonspecific immune responses leading to unwanted side effects including autoimmunity.
  • Several peptide-based vaccine candidates for COVID-19 are presently in development.
  • the present disclosure relates to modified Cowpea Mosaic Virus (CPMV) coat protein and CPMV Virus-like particle (VLP) comprising modified coat protein and method of producing the VLPs in a host or host cell.
  • the VLP may be an empty VLP, being devoid of DNA or RNA.
  • a modified Cowpea Mosaic Virus (CPMV) Virus- like particle (VLP) comprising large coat protein and small coat protein, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
  • CPMV CPMV
  • VLP Virus- like particle
  • a capsomer comprising large coat protein, small coat protein or large coat protein and small coat protein, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
  • the insertion in the betaE-alphaB loop of the large coat protein may be between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1.
  • the insertion in the betaB-betaC loop of the small coat protein may be between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1.
  • the insertion in the betaC’-betaC” loop of the small coat protein is between amino acid residue corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1.
  • the heterologous peptide insertion may comprise one or more than one linker at the N-terminus, the C-terminus or both at the N-terminus and the C-terminus.
  • the linker may comprise one or more than one aspartate or the linker may comprise the amino acid sequence glycine-serine-alanine.
  • the epitope may be coronavirus peptide S14P5 or coronavirus peptide S21P2.
  • the large coat protein may comprise in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein an aspartate residue is added to the N-terminus and the C-terminus of the coronavirus peptide S14P5.
  • the heterologous peptide insert may comprise the sequence of SEQ ID: 17.
  • the small coat protein may comprise in the betaC’-betaC” loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein a glycine-serine-alanine linker is fused to the N-terminus and the C-terminus of coronavirus peptide S14P5.
  • the heterologous peptide insert may comprise the sequence of SEQ ID: 19 or SEQ ID NO: 18.
  • the large coat protein may comprise in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S21P2, wherein an aspartate residue is added to the N-terminus and the C-terminus of coronavirus peptide S21P2.
  • CPMV Cowpea Mosaic Virus
  • the modified CPMV coat protein may be a small coat protein, i) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
  • CPMV Cowpea Mosaic Virus
  • CPMV Cowpea Mosaic Virus
  • the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein
  • the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein
  • the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
  • Virus like particle comprising the modified CPMV coat protein as described above are also provided.
  • composition comprising an effective dose of the VLP as described above and a pharmaceutically acceptable carrier, adjuvant, vehicle or excipient.
  • a vaccine comprising an effective dose of the VLP as described above for inducing an immune response against coronavirus.
  • the vaccine may be a multivalent vaccine, comprising a mixture of monovalent VLPs.
  • a method for inducing immunity to a Coronavirus infection in a subject the method comprising administering the composition or the vaccine as described above.
  • An antibody or antibody fragment prepared using the composition or the vaccine are also provided.
  • a host or host cell may comprise the VLP of the current disclosure.
  • the host may be a plant and the host cell may be a plant cell.
  • the disclosure further provided a nucleic acid comprising a nucleotide sequence encoding a Cowpea Mosaic Virus (CPMV) polyprotein, the polyprotein comprising the large coat protein and the small coat protein of CPMV, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope
  • CPMV Cowpea Mosaic Virus
  • CPMV Cowpea Mosaic Virus
  • VLP virus like particle
  • a method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) introducing a first nucleic acid comprising the nucleic acid as described above into the host or host cell; b) introducing a second nucleic acid encoding CPMV protease into the host or host cell; c) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acid, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell.
  • CPMV Cowpea Mosaic Virus
  • the ratio of introduced amounts of the first nucleic acid relative to the second nucleic acid may be 2:1.
  • a method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) providing the host or host cell, comprising a first nucleic acid comprising the nucleic acid as described above and a second nucleic acid encoding CPMV protease; b) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acids, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell.
  • CPMV Cowpea Mosaic Virus
  • FIGURE 1 shows a stain-free gel detection (top panel) and Western blot detection (bottom panel) of clarified extracts of biomasses expressing CPMV-S14P5 fusion constructs (named 8720 to 8725), harvested at 6 or 9 days post infiltration (dpi).
  • Construct 7384 encodes the native CPMV polyprotein VP60 (no insertions).
  • Construct 8720 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the ⁇ B- ⁇ C loop (“Site 1”) of the small coat protein (S14P5-1).
  • Construct 8721 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the ⁇ E- ⁇ B loop (“Site 2”) of the large coat protein (S14P5-2).
  • Construct 8722 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the ⁇ C’- ⁇ C” loop (“Site 4”) of the small coat protein (S14P5-4).
  • Construct 8723 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to an aspartate (D) linker at each terminus inserted into the ⁇ E- ⁇ B loop of the large coat protein (S14P5 (+DD)-2).
  • Construct 8724 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to a glycine-serine-alanine (GSA) linker at each terminus inserted into the ⁇ B- ⁇ C loop of the small coat protein (GSA-S14P5-GSA-1).
  • Construct 8725 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to a GSA linker at each terminus inserted into the ⁇ C’- ⁇ C” loop of the small coat protein (GSA-S14P5-GSA-4). Biomasses infiltrated with construct 8721 or 8725 and incubated 9 DPI were chosen for purification.
  • Expected MW of CPMV-L is 35 kDa for the native protein and ⁇ 37 kDa in presence of a peptide insertion.
  • the expected MW is 22 kDa for the native protein and ⁇ 24 kDa in presence of a peptide insertion.
  • FIGURE 2 shows a stain-free gel detection (top panel) and Western blot detection (bottom panel) of clarified extracts of biomasses expressing CPMV-S21P2 fusion constructs (named 8726 to 8731), harvested at 6 or 9 dpi.
  • Construct 7384 encodes the native CPMV polyprotein (no insertions).
  • Construct 8726 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the ⁇ B- ⁇ C loop (“Site 1”) of the small coat protein (S21P2-1).
  • Construct 8727 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the ⁇ E- ⁇ B loop (“Site 2”) of the large coat protein (S21P2-2).
  • Construct 8728 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the ⁇ C’- ⁇ C” loop (“Site 4”) of the small coat protein (S21P2-4).
  • Construct 8729 encodes CPMV polyprotein (CPMV VP60) with S21P2 fused to an aspartate (D) linker at each terminus inserted into the ⁇ E- ⁇ B loop of the large coat protein (S21P2 (+DD)-2).
  • Construct 8730 encodes CPMV polyprotein (CPMV VP60) with S21P2 having a GSA linker at each terminus inserted into the ⁇ B- ⁇ C loop of the small coat protein (GSA- S21P2-GSA-1).
  • Construct 8731 encodes CPMV polyprotein (CPMV VP60) with S21P2 having GSA linker at each terminus inserted into the ⁇ C’- ⁇ C” loop of the small coat protein (GSA- S21P2-GSA-4). Biomasses infiltrated with construct 8727 or 8729 and incubated 9 DPI were chosen for purification.
  • FIGURE 3 shows stain-free gel detection of fractions harvested from density gradient purification of clarified and concentrated biomasses infiltrated with constructs 8721 (panel A), 8725 (panel B), 8727 (panel C) and 8729 (panel D).
  • FIGURE 4 shows electron microscopy images at 30K and 50 K magnifications of native CPMV VP60 VLP (i.e.
  • FIGURE 5 shows the location of the epitope S14P5 and S21P2 (marked by boxes) in the SARS-CoV-2 spike (S) protein (SEQ ID NO: 21).
  • S14P5 corresponds to residues 538-555 of the S-protein
  • S21P2 corresponds to residues 794-811 of the S-protein.
  • FIGURE 6A shows a representation of acceptor plasmid 7140
  • FIGURE 6B shows a representation of construct 7384 encoding native CPMV VP60.
  • FIGURE 6C shows a representation of construct 7387 encoding native CPMV 24K protease.
  • FIGURE 6D shows a representation of acceptor plasmid 7142.
  • FIGURE 7A shows a representation of construct 8720 encoding CPMV VP60 with S14P5-1 insert.
  • FIGURE 7B shows a representation of construct 8721 encoding CPMV VP60 with S14P5-2 insert.
  • FIGURE 7C shows a representation of construct 8722 encoding CPMV VP60 with S14P5-4 insert.
  • FIGURE 7D shows a representation of construct 8723 encoding CPMV VP60 with S14P5 (+DD)-2 insert.
  • FIGURE 7E shows a representation of construct 8724 encoding CPMV VP60 with GSA-S14P5-GSA-1 insert.
  • FIGURE 7F shows a representation of construct 8725 encoding CPMV VP60 with GSA-S14P5-GSA-4 insert.
  • FIGURE 7G shows a representation of construct 8726 encoding CPMV VP60 with S21P2-1 insert.
  • FIGURE 7H shows a representation of construct 8727 encoding CPMV VP60 with S21P2-2 insert.
  • FIGURE 7I shows a representation of construct 8728 encoding CPMV VP60 with S21P2-4 insert.
  • FIGURE 7J shows a representation of construct 8729 encoding CPMV VP60 with S21P2 (+DD)-2 insert.
  • FIGURE 7K shows a representation of construct 8730 encoding CPMV VP60 with GSA-S21P2-GSA-1 insert.
  • FIGURE 7L shows a representation of construct 8731 encoding CPMV VP60 with GSA-S21P2-GSA-4 insert.
  • DETAILED DESCRIPTION [0043] The following description is of a preferred embodiment.
  • the present disclosure relates to modified viral coat protein of a plant virus.
  • the viral protein is also referred to as coat protein, viral capsid protein or capsid protein.
  • the modified viral coat protein may also be referred to as modified coat protein, modified viral capsid protein or modified capsid protein.
  • modified polyprotein comprising a small coat protein and a large coat protein are also provided.
  • the small coat protein, the large coat protein or a small coat protein and a large coat protein may be modified.
  • the modified polyprotein may comprise a modified small coat protein, a modified large coat protein or both a modified small coat protein and a modified large coat protein.
  • the modified coat protein may be modified to display a heterologous peptide or peptide insertion for example in exposed surface loops of the coat protein.
  • the heterologous peptide insertion may comprise an epitope that is derived from a coronavirus spike protein.
  • the heterologous peptide or peptide insertion may comprise an epitope and one or more than one linker or linker sequence.
  • the present disclosure further relates to virus-like particle (VLP) comprising one or more than one modified viral coat protein as described herewith.
  • the VLP may comprise or may consist of one or more than one coat protein, wherein the coat protein has been modified to display a heterologous peptide.
  • the VLP may comprise or may consist of large coat proteins and small coat proteins of the plant virus, wherein the large coat protein, the small coat protein or the large and the small coat protein have been modified to comprise a heterologous peptide or peptide insertion in exposed surface loops of the coat proteins.
  • the VLP may comprise or may consist of one or more than one coat protein, wherein the coat protein has been modified to display an epitope derived from a coronavirus spike protein. Accordingly, the VLP may comprise or may consist of one or more than one modified coat protein.
  • the one or more than one modified coat protein may be a modified small coat protein, a modified large coat protein or may be a modified small coat protein and a modified large coat protein.
  • the coat protein may be derived from an icosahedral plant virus such as, for example Comoviruses, Tombusviruses, Sobemoviruses, or Nepoviruses. In a preferred embodiment, the plant virus is a Comovirus.
  • the Comovirus is cowpea mosaic virus (CPMV).
  • CPMV cowpea mosaic virus
  • the present disclosure also relates to one or more than one modified coat protein from an icosahedral plant virus such as, for example, Comoviruses, Tombusviruses, Sobemoviruses, or Nepoviruses.
  • the modified coat protein may be derived from the large (L or VP37) coat protein or small (S or VP23) coat protein from cowpea mosaic virus (CPMV).
  • the coat protein may be modified by inserting a heterologous peptide into the coat protein and/or adding a heterologous peptide to the sequence of the coat protein.
  • the coat protein may be modified by replacing residues of the coat protein with a heterologous peptide.
  • the coat protein may have one or more than one beta-barrel structure or beta barrel domain.
  • the large coat protein may contain two covalently linked beta barrel domains and the small coat protein may contain a single beta barrel domain.
  • the beta-barrel structure or domain may comprise or may consist of eight strands of antiparallel beta-sheet connected by loops of varying length.
  • the beta strands are named ⁇ B, ⁇ C, ⁇ D, ⁇ E, ⁇ F, ⁇ G, ⁇ H and ⁇ I sheets.
  • ⁇ A, ⁇ B and ⁇ C three short alpha helices in the L and S subunits are designated ⁇ A, ⁇ B and ⁇ C, and two short beta strands found in close proximity to ⁇ C are referred to as ⁇ C’ and ⁇ C”.
  • the connecting regions or loops between these structural features are referred to using the annotations of the features flanking that loop.
  • ⁇ B- ⁇ C refers to the loop connecting ⁇ B with ⁇ C and ⁇ C’- ⁇ C
  • ⁇ F- ⁇ G, ⁇ E- ⁇ B are some others.
  • the connecting loops may be referred to as the ⁇ B- ⁇ C (beta B-beta C), ⁇ D- ⁇ E (beta D-beta E), ⁇ F- ⁇ G (beta F-beta G) and ⁇ H- ⁇ I (beta H-beta I) loops.
  • These loops can be used as sites for expression of foreign peptide sequences, such as epitopes from heterologous viruses.
  • the heterologous peptide may be inserted within an exposed portion of the coat protein.
  • the heterologous peptide may be inserted in a loop between individual strands of the beta sheet of the beta barrel structure or beta barrel domain.
  • the heterologous peptide may be inserted in the ⁇ B- ⁇ C loop of the S protein, the ⁇ C'- ⁇ C" loop of the S protein or the ⁇ E- ⁇ B loop of the L protein.
  • the present disclosure therefore relates to modified coat protein derived from Comoviruses such as CPMV, wherein the coat protein comprises a heterologous peptide insertion, in an exposed portion of the coat protein.
  • the modified coat protein may be derived from the large (L or VP37) coat protein or small (S or VP23) coat protein of CPMV.
  • the large coat protein of CPMV may comprise in the ⁇ E- ⁇ B (betaE-alphaB) loop (also referred to as site 2) a heterologous peptide insertion.
  • the large coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1.
  • the small coat protein may comprise in the ⁇ B- ⁇ C (betaB- betaC) loop (also referred to as site 1) a heterologous peptide insertion.
  • the small coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1.
  • the small coat protein may comprise in the ⁇ C’- ⁇ C” (betaC’- betaC”) loop (also referred to as site 4) a heterologous peptide insertion.
  • the small coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1.
  • the small and large coat protein may be produced as a polyprotein which is proteolytically processed in a host cell into the small and large coat protein.
  • the polyprotein includes a cleavage site naturally recognized by a proteinase from the same or a closely related plant virus.
  • the cleavage site may be from an unrelated virus or source, and a proteinase which is specific for that site may be used to cleave the polyprotein.
  • the small and/or large coat proteins may self-assemble into protein suprastructures such as for example protein rosettes, capsomeres, nanoparticles, large protein complexes, and/or virus-like particles (VLPs).
  • VLPs virus-like particles
  • the modified polyprotein may comprise: i) a modified small coat protein and a native (unmodified) large coat protein, ii) a native (unmodified) small coat protein and a modified large coat protein, or iii) a modified small coat protein and a modified large coat protein.
  • the modified polyprotein may comprise from 80% to 100% identity or similarity with amino acids of SEQ ID NO: 2, 3, 4, 5, 6 or 7.
  • modified polyprotein as described herewith included modified polyprotein with amino acid sequences that have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween, sequence identity, or sequence similarity, with the amino acid sequence of SEQ ID NO: 1, 2, 3, 4, 5, 6 or 7 and wherein modified polyprotein is expressed and processed in a host or host cell to form protein suprastructures such as for example VLP or nanoparticles.
  • Modified polyprotein ⁇ E- ⁇ B (betaE-alphaB L protein)
  • the modified polyprotein may have a heterologous peptide insertion in the ⁇ E- ⁇ B ⁇ (betaE-alphaB) loop of the large coat protein (also referred to as site “2”).
  • the modified polyprotein may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1.
  • the modified polyprotein may have 80%-100% identity or similarity with the amino acids of SEQ ID NO: 2, 4, 6 or 7.
  • modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 2, 4, 6 or 7.
  • Modified polyprotein ⁇ B- ⁇ C (betaB-betaC) S protein) [0059]
  • the modified polyprotein may have a heterologous peptide insertion in the ⁇ B- ⁇ C (betaB-betaC) loop of the small coat protein (also referred to as site “1”).
  • the modified polyprotein may comprise a heterologous peptide between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1.
  • the modified polyprotein may have 80%-100% identity or similarity with the amino acids of SEQ ID NO: 1.
  • the modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 1.
  • Modified polyprotein ⁇ C’- ⁇ C” (betaC’-betaC’’) S protein)
  • the modified polyprotein may have a heterologous peptide insertion in the ⁇ C’- ⁇ C” (betaC’-betaC”) loop of the small coat protein (also referred to as site “4”).
  • the modified polyprotein may comprise a heterologous peptide between amino acid residue corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1.
  • the modified polyprotein may have 80%- 100% identity or similarity with the amino acids of SEQ ID NO: 3 or 5.
  • modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 3 or 5.
  • percent similarity “sequence similarity”, “percent identity”, or “sequence identity”, when referring to a particular sequence, are used for example as set forth in the University of Wisconsin GCG software program, or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology, Ausubel et al., eds.1995 supplement). Methods of alignment of sequences for comparison are well-known in the art.
  • Optimal alignment of sequences for comparison can be conducted, using for example the algorithm of Smith & Waterman, (1981, Adv. Appl. Math.2:482), by the alignment algorithm of Needleman & Wunsch, (1970, J. Mol. Biol.48:443), by the search for similarity method of Pearson & Lipman, (1988, Proc. Natl. Acad. Sci. USA 85:2444), by computerized implementations of these algorithms (for example: GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.).
  • BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins of the disclosure.
  • a nucleic acid sequence or nucleotide sequence referred to in the present disclosure may be “substantially homologous”, “substantially similar” or “substantially identical” to a sequence, or a compliment of the sequence if the nucleic acid sequence or nucleotide sequence hybridise to one or more than one nucleotide sequence or a compliment of the nucleic acid sequence or nucleotide sequence as defined herein under stringent hybridisation conditions.
  • Sequences are “substantially homologous” “substantially similar” “substantially identical” when at least about 70%, or between 70 to 100%, or any amount therebetween, for example 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100%, or any amount therebetween, of the nucleotides match over a defined length of the nucleotide sequence providing that such homologous sequences exhibit one or more than one of the properties of the sequence, or the encoded product as described herein.
  • the modified polyprotein may be proteolytically processed in the host cell into small and large coat proteins, which may assemble into protein suprastructures such as for example virus-like particles (VLPs) or nanoparticles.
  • modified viral coat protein for example modified small coat proteins and modified large coat proteins.
  • the modified viral coat protein may comprise a heterologous peptide insertion.
  • the modified coat protein may be a modified small coat protein comprising a heterologous peptide insertion or may be a modified large coat protein comprising a heterologous peptide.
  • the modified large coat protein may have a heterologous peptide insertion in the ⁇ E- ⁇ B (betaE-alphaB) loop.
  • a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 8.
  • the modified large coat protein may have 80%-100% sequence identity or similarity with the amino acid sequence of SEQ ID NO: 9, 10, 11 or 51.
  • the modified large coat protein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 9, 10, 11 or 51.
  • the modified small coat protein may have a heterologous peptide insertion such as an epitope in the ⁇ B- ⁇ C (betaB-betaC) loop.
  • a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 22 and 23 of the sequence of SEQ ID NO: 12.
  • the modified small coat protein may have a heterologous peptide insertion such as an epitope in the ⁇ C'- ⁇ C’’ (betaC’-betaC”) loop.
  • a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 44 and 45 of the sequence of SEQ ID NO: 12.
  • the modified small coat protein may have 80%-100% sequence identity or similarity with the amino acid sequence of SEQ ID NO: 13, 14 or 51.
  • the modified small coat protein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 13, 14 or 51.
  • Coronavirus Epitopes [0070]
  • the heterologous peptide insertion (also referred to as heterologous peptide) may be heterologous to the plant virus coat protein. More specifically, the heterologous peptide insertion may be heterologous to the small coat protein of a plant virus and/or the heterologous peptide insertion may be heterologous to the large coat protein of a plant virus.
  • the plant virus coat protein comprises a peptide insertion that is heterologous to the plant virus coat protein i.e. is not derived from the same virus as the plant virus coat protein.
  • the heterologous peptide insertion may be heterologous to the small coat protein of CPMV and/or the heterologous peptide insertion may be heterologous to the large coat protein of CPMV.
  • the heterologous peptide insertion may comprise sequences derived from a Coronavirus protein, for example a coronavirus spike (S) protein.
  • the heterologous peptide insertion may comprise or may consist of one or more than one epitope.
  • the epitope may be a linear epitope or a sequential epitope, consisting of continuous residues of a protein sequence.
  • the epitope may be a conformational epitope.
  • the heterologous peptide insertion may comprise or may consist of an epitope derived from coronavirus S protein, for example a linear epitope derived from coronavirus S protein or a conformational epitope derived from coronavirus S protein.
  • the coronavirus S-protein may for example be derived from a Coronavirus, such as an Alphacoronavirus (Alpha-CoV), a Betacoronavirus (Beta-CoV), a Gammacoronavirus (Gamma-CoV) or a Deltacoronavirus (Delta-CoV).
  • a Coronavirus such as an Alphacoronavirus (Alpha-CoV), a Betacoronavirus (Beta-CoV), a Gammacoronavirus (Gamma-CoV) or a Deltacoronavirus (Delta-CoV).
  • the Coronavirus is a Betacoronavirus (Beta-CoV).
  • the Betacoronavirus may be a lineage A Betacoronavirus, such for example HCoV-OC43 or HCoV-HKU1, a lineage B Betacoronavirus, such for example SARS-CoV or SARS-CoV 2 or a lineage C Betacoronavirus such for example MERS-CoV.
  • the coronavirus S-protein may be derived from an Alphacoronavirus such for example Human coronavirus 229E (HCoV-229E).
  • the heterologous peptide insertion may comprise or may consist of an epitope from SARS-CoV-2 spike protein.
  • the epitopes may be determined as for example described in Li et al.2020 (Cellular & Molecular Immunology volume 17, pages1095–1097(2020)), Yi et al.2020 (Emerging Microbes & Infections, 9:1, 1988-1996 (2020)), Shrock et al. (Science 29 Sep 2020), Poh et al. 2020 (Nat Commun 11, 2806 (2020), Nelde et al. (Nature Immunology 22, pages 74– 85 (2021)) which are hereby incorporated by reference. [0075]
  • the epitope may be derived from the S1 subunit of the coronavirus S protein.
  • the epitope may be derived from the C terminal domain (CTD) that immediately follows the Receptor Binding Domain (RBD) of the coronavirus S protein.
  • CTD C terminal domain
  • RBD Receptor Binding Domain
  • the epitope may be derived from the region between amino acids 553-564, 577-588, 595-612, 625-642 or 661-684 of the S1 subunit of the SARS-CoV-2 spike protein.
  • the epitope might also be derived from a region of the S-protein that includes the fusion peptide (FP) (amino acids 788-806) or the S2’ cleavage site (amino acid R815).
  • FP fusion peptide
  • the epitope may be derived from the region between amino acids 764-829 or 788-806 of the S2 subunit of the SARS-CoV-2 spike protein.
  • the epitope may be derived from a region that connects the heptad repeat 1 (HR1) and heptad repeat 2 (HR2) on the S2 subunit of the SARS-CoV-2 spike protein.
  • the epitope may be derived from a region between amino acids 1148-1159 on the S2 subunit of the SARS-CoV-2 spike protein.
  • the epitope may be derived from a region between amino acids 884–895 or amino acids 1256–1273 on the S2 subunit of the SARS-CoV-2 spike protein.
  • the SARS-CoV-2 epitope may have the following sequences: S14P5: TESNKKFLPFQQFGRDIA (SEQ ID NO: 15) S21P2: PSKPSKRSFIEDLLFNKV (SEQ ID NO: 16) [0077] Accordingly, it is also provided a modified small coat protein and/or a modified large coat protein wherein the modified small coat protein and/or the modified large coat protein comprises an epitope comprising the sequence of SEQ ID NO: 15, the sequence of SEQ ID NO: 16 or both the sequence of SEQ ID NO: 15 and SEQ ID NO: 16. As described above, the modified coat protein may assemble into VLP, comprising or consisting of the modified coat protein.
  • the heterologous peptide insertion may be between 5 to 30 amino acids in length, or any amino acid length therebetween.
  • the heterologous peptide insertion may be 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 amino acids in length or any amount therebetween.
  • the heterologous peptide insertion is 18 amino acids in length.
  • the heterologous peptide insertion is 20 amino acids in length.
  • the heterologous peptide insertion is 24 amino acids in length.
  • the heterologous peptide insertion or the one or more than one coat protein may further be modified to improve biochemical characteristics advantageous for formulation or immunogenic effect.
  • peptides with a high proportion of hydrophobic amino acids may negatively affect solubility in aqueous solutions.
  • basic polar (His, Lys, Arg) residues may be added to a peptide insertion to improve solubility of the peptide and/or bring the pI of the peptide closer to the pH of the buffer or biological pH.
  • the heterologous peptide insertion may comprise one or more than one linker or linker sequence.
  • the heterologous peptide insertion may comprise or may consist of one or more than one linker and an epitope. The linker or linker sequence may be fused to the epitope.
  • linker or linker sequence may be fused to the N-terminal end, the C terminal end or the N-terminal end and the C terminal end of the epitope.
  • linker or “linker sequence” in the context of the disclosure concerns an amino acid sequence of from about 1 to about 10 or more amino acid residues positioned at the N-terminus, the C-terminus or the N-terminus and the C- terminus of the heterologous peptide insertion. Accordingly, the linker or linker sequence may have a length of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids.
  • the one or more than one linker may be directly adjacent to or fused directly to the terminus or termini of the epitope.
  • the one or more than one linker may be fused directly to the N-terminus, the C-terminus or the N-terminus and the C-terminus of an epitope.
  • the linker may be covalently linked to the amino acid residues in its vicinity.
  • the modified coat protein or modified polyprotein therefore may comprise a heterologous peptide comprising one or more than one linker (L) and an epitope (E) as follows: - N’-mP –L1- epitope- L2 –mP-C’ - N’-mP –L- epitope - mP-C’ - N’-mP – epitope - L- mP-C’ [0083]
  • the one or more than one linker (L, L1 or L2) may have a length of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 or more amino acid residues.
  • the one or more than one linker may be one or more than one aspartate residues (D).
  • the one or more than one linker may be glycine-serine-alanine (GSA).
  • the modified coat protein or modified polyprotein may comprise the following heterologous peptide insertions comprising an epitope and linker sequences: D-S14P5-D: DTESNKKFLPFQQFGRDIAD (SEQ ID NO: 17) D-S21P2-D: DPSKPSKRSFIEDLLFNKVD (SEQ ID NO: 18) GSA-S14P5-GSA: GSATESNKKFLPFQQFGRDIAGSA (SEQ ID NO: 19) GSA-S21P2-GSA: GSAPSKPSKRSFIEDLLFNKVGSA (SEQ ID NO: 20) [0085] As shown in Figure 1, when epitope S14P5 with an aspartate (D) linker (construct (SEQ ID NO: 17) D-S21P2-D
  • a modified large coat protein comprises in the ⁇ E- ⁇ B (betaE-alphaB) loop, a heterologous peptide insertion comprising coronavirus epitope S14P5 wherein aspartate linkers are fused to the N-terminus and the C- terminus of the epitope.
  • a modified small coat protein comprising, between amino acid residues corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1, a heterologous peptide insertion comprising coronavirus epitope S14P5, wherein glycine-serine-alanine linkers (GSA) are fused to the N-terminus and the C-terminus of the epitope.
  • modified large coat protein comprising in the ⁇ E- ⁇ B (betaE-alphaB) loop, a heterologous peptide insertion comprising coronavirus epitope S21P2 wherein aspartate (D) residues or linkers are added or fused to the N-terminus and the C-terminus of the epitope.
  • the modified polyprotein may have an amino acid sequence that has 90%-100% sequence similarity or 90%-100% sequence identity to the sequence of SEQ ID NOs: 2, 3, 4, 5, 6, 7 or 30 or any amount there between.
  • the modified polyprotein may have 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100% sequence similarity or sequence identity to the sequence of SEQ ID NOs: 2, 3, 4, 5, 6, 7 or 30.
  • the one or more than one modified coat protein may have an amino acid sequence that has 90%-100% sequence similarity or 90%-100% sequence identity to the sequence of SEQ ID NOs: 9, 10, 11, 13, 14, 51, 52 or any amount there between.
  • the one or more than on modified coat protein may have 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100% sequence similarity or sequence identity to the sequence of SEQ ID NOs: 9, 10, 11, 13, 14, 51, 52.
  • the present disclosure therefore provides a “modified coat protein”, “chimeric coat protein”, or “modified polyprotein”, “chimeric polyprotein”, “fusion protein”, “fusion polyprotein” wherein the coat protein or polyprotein has been modified to comprise a heterologous peptide insertion, wherein the heterologous peptide insertion comprises an epitope.
  • the heterologous peptide insertion may further comprise one or more than one linker sequence.
  • chimeric coat protein or “chimeric polyprotein”, also referred to as a “fusion protein” or “fusion polyprotein, it is meant a protein or polyprotein that comprises amino acid sequences originating from two or more than two biological or synthetic sources, for example but not limited to a coat protein from CPMV and a epitope that is derived from coronavirus.
  • the chimeric protein or polyprotein may include a signal peptide that is native to CPMV or the signal peptide might be non- native or heterologous to CPMV.
  • Protein Suprastructures [0092]
  • the modified coat proteins may self-assemble into protein suprastructures such for example nanoparticles or nanofilaments.
  • the nanoparticles may be for example protein rosettes, capsomeres, large protein complexes, inactivated virus, nanorods, nanospheres, and/or virus-like particles (VLPs).
  • the modified coat proteins may self-assemble into protein suprastructures such as capsomeres, rosettes or Virus-like particles (VLPs).
  • the suprastructures such for example VLPs may also be referred to as CPMV nanoparticles or CPMV-based nanoparticles.
  • VLPs of CPMV were purified using density gradients and detected upon SDS-PAGE of harvested gradient fractions.
  • Modified large coat proteins comprising S14P5 in the ⁇ E- ⁇ B (betaE-alphaB) loop (construct 8721) were processed and assembled into VLPs as can be seen in iodixanol fractions 7-10 (see Figure 3A).
  • Modified small coat proteins comprising S14P5 with GSA linkers at both termini inserted in the ⁇ C’- ⁇ C” (betaC’-betaC’’) loop (construct 8725) also formed VLPs (see Figure 3B).
  • VLP comprising or consisting of one or more than one modified coat protein
  • a VLP comprising or consisting of i) a large coat protein comprising in the ⁇ E- ⁇ B (betaE- alphaB) loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) a small coat protein comprising in the ⁇ B- ⁇ C (betaB- betaC) loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) a small coat protein comprising in the ⁇ C’- ⁇ C’’(betaC’-betaC’’) a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
  • VLP virus-like particle
  • virus-like particles or “virus-like particles” or “VLPs” refer to the spontaneous organization of coat proteins into the three-dimensional capsid structure of a particular virus for example icosahedral plant virus, for example Comoviruses such as cowpea mosaic virus (CPMV).
  • CPMV cowpea mosaic virus
  • VLPs are generally morphologically and antigenically similar to virions produced in an infection but lack genetic information sufficient to replicate and thus, are non-infectious. Since the VLPs do not contain viral nucleic acids (RNA or DNA) and the space inside the capsid is unoccupied, they may also be referred to as “empty” VLP (eVLP) or “empty” CPMV (eCPMV).
  • VLPs While lacking the genetic material, VLPs retain key immunological characteristics of viruses including particulate structures; repetitive surfaces; and capability to induce innate immunity by activating molecular-pattern pathogen-associated recognition receptors. Like infectious viruses, these VLPs are in the 20-250 nm size range. For example, the CPMV VLP may have a size of approximately 30 nm.
  • VLPs are structures that may self-assemble and comprise or consist of one or more structural proteins such as modified coat proteins, for example large and small coat proteins.
  • the VLP may comprise modified large coat protein and/or modified small protein.
  • the VLP may comprise modified large coat protein and native (unmodified) small coat protein or the VLP may comprise native (unmodified) large coat protein and modified small coat protein.
  • the VLP may comprise or consist of coat protein from cowpea mosaic virus (CPMV) and may be referred to as cowpea mosaic virus-like particle (CPMV VLP).
  • CPMV VLP cowpea mosaic virus-like particle
  • the cowpea mosaic virus-like particle may be free of RNA and therefore may be referred to as “empty” cowpea mosaic virus-like particle or eCPMV.
  • a method of producing virus like particle (VLP) comprising one or more than one modified coat protein as described herewith in a host or host cell is also provided.
  • the method comprises the introduction of i) a first nucleic acid comprising a first regulatory region active in the host or host cell operatively linked to a first nucleotide sequence encoding a modified polyprotein into the host or host cell, and ii) a second nucleic acid comprising a second regulatory region active in the host or host cell operatively linked to a second nucleotide sequence encoding a protease.
  • a first nucleic acid comprising a first regulatory region active in the host or host cell operatively linked to a first nucleotide sequence encoding a modified polyprotein
  • a second nucleic acid comprising a second regulatory region active in the host or host cell operatively linked to a second nucleotide sequence encoding a protease.
  • the host or host cell may be a plant or plant cell and the first and second nucleic acid may be inserted into the plant or plant cell by agroinfiltration.
  • the first and second nucleic acid are located on two different constructs (vectors) and the ratio between the first and second nucleic acid may be modulated as further described below.
  • modified CPMV VLPs are produced in a host or host cell, by co-expressing a nucleic acid (a first nucleic acid) encoding a modified CPMV polyprotein or CPMV coat protein precursor (VP60) comprising the small coat protein and the large coat protein of CPMV, with a second nucleic acid encoding CPMV protease (24K).
  • the CPMV protease processes the polyprotein into the small coat protein and the large coat protein, which may assemble into viral capsids or virus-like particles (VLPs).
  • VLPs virus-like particles
  • the level of protein yield and/or VLP accumulation in the host or host cell may be influenced by the ratio of the polyprotein-containing Agrobacterium, to protease-containing Agrobacterium infiltrated into the host or host.
  • the ratio of the polyprotein-containing to protease-containing Agrobacterium may range for example from about 20:1 to about 0.5:1 (polyprotein:protease), or any amount therebetween, for example from about 20:1, 18:1, 16:1, 14:1, 12:1, 10:1, 9:1, 8:1, 7:1, 6:1, 5:1, 4:1, 3:1, 2:1, 1:1, 0.5:1 (polyprotein:protease), or any amount therebetween.
  • the ratio between polyprotein to protease is 2:1.
  • the ratio of the polyprotein-containing to protease-containing Agrobacterium may range for example from about 1:2 to 1:20 (polyprotein:protease), or any amount therebetween, for example 1:2, 1:4, 1:6, 1:8, 1:10, 1:12, 1:14, 1:16, 1:18, 1:20 (polyprotein:protease), or any amount therebetween.
  • the ratio of polyprotein to protease may be varied for example by introducing different ratios of Agrobacterium containing the first nucleic acid (encoding a modified polyprotein) to Agrobacterium containing the second nucleic acid (encoding a protease) into the host or host cell.
  • polyprotein and protease are present on the same construct, and therefore are introduced into the same Agrobacterium, they may be differentially expressed within the host or host cell using suitable promoters so that the desired ratio of polyprotein to protease is obtained. Expression may be varied by modulating for example replication, transcription, translation, or a combination thereof, of the polyprotein, the protease, or both the protein and the protease. For example, different regulatory elements, including promoters, amplification elements, enhancers or a combination thereof, may be used in addition to varying the ratio of the polyprotein-containing Agrobacterium to protease-containing Agrobacterium infiltrated as described above.
  • VLPs may be purified or extracted using any suitable method for example chemical or biochemical extraction.
  • VLPs are relatively sensitive to desiccation, heat, pH, surfactants and detergents. Therefore it may be useful to use methods that maximize yields, minimize contamination of the VLP fraction with cellular proteins, maintain the integrity of the proteins, or VLPs, and, where required, the associated lipid envelope or membrane, methods of loosening the cell wall to release the proteins, or VLP. Minimizing or eliminating the use of detergents or surfactants such for example SDS or Triton TM X-100 may be beneficial for improving the yield of VLP extraction.
  • VLPs may be then assessed for structure and size by, for example, density gradient (see for example Figure 3) electron microscopy (see for example Figure 4) or by size exclusion chromatography. [00105] The size (i.e.
  • the diameter) of the above-defined VLPs may be measured for example by dynamic light scattering (DLS) or electron microscope (EM) techniques, is usually between 20 to 50 nm, or any size therebetween.
  • the size of the intact VLP structure may range from about 25 nm to about 35 nm, or any size therebetween, or from 20nm, 21nm, 22nm, 23nm, 24nm, 25nm, 26nm, 27 nm, 28nm, 29nm, 30nm, 31nm, 32nm, 33nm, 34nm, 35nm, or any size therebetween.
  • the small and/or large coat proteins may self-assemble into capsomeres.
  • capsomere refers to a morphological unit of the capsid of a virus.
  • a “capsomere” may comprise monomeric or oligomeric viral structural proteins.
  • the capsomere may comprise one or more than one modified coat protein as described herewith.
  • small coat protein may self-assemble into pentameric capsomeres.
  • Capsomeres may self-assemble into virus-like particle (VLP) or nanoparticles. Accordingly, it is further provided a capsomere or capsomere composition, the capsomere or capsomere composition may comprise or may consist of one or more than one modified coat protein.
  • the one or more than one modified coat protein may be a modified small coat protein, a modified large coat protein or may be a modified small coat protein and a modified large coat protein.
  • Genetic Constructs and regulators [00107] Further provided are genetic constructs that comprise nucleic acids comprising nucleotide sequences encoding the modified coat proteins or modified polyproteins as described herewith. [00108] The term “construct”, “vector” or “expression vector”, as used herein, refers to a recombinant nucleic acid for transferring exogenous nucleic acid sequences into host cells (e.g. plant cells) and directing expression of the exogenous nucleic acid sequences in the host cells.
  • host cells e.g. plant cells
  • “Expression cassette” refers to a nucleotide sequence comprising a nucleic acid of interest under the control of, and operably (or operatively) linked to, an appropriate promoter or other regulatory elements for transcription of the nucleic acid of interest in a host cell.
  • the expression cassette may comprise a termination (terminator) sequence that is any sequence that is active the plant host.
  • the termination sequence may be derived from the RNA-2 genome segment of a bipartite RNA virus, e.g. a comovirus, the termination sequence may be a NOS terminator, or terminator sequence may be obtained from the 3’UTR of the alfalfa plastocyanin gene.
  • regulatory region By “regulatory region” “regulatory element” or “promoter” it is meant a portion of nucleic acid typically, but not always, upstream of the protein coding region of a gene, which may be comprised of either DNA or RNA, or both DNA and RNA. When a regulatory region is active, and in operative association, or operatively linked, with a nucleotide sequence of interest, this may result in expression of the nucleotide sequence of interest.
  • a regulatory element may be capable of mediating organ specificity, or controlling developmental or temporal gene activation.
  • a “regulatory region” includes promoter elements, core promoter elements exhibiting a basal promoter activity, elements that are inducible in response to an external stimulus, elements that mediate promoter activity such as negative regulatory elements or transcriptional enhancers. “Regulatory region”, as used herein, also includes elements that are active following transcription, for example, regulatory elements that modulate gene expression such as translational and transcriptional enhancers, translational and transcriptional repressors, upstream activating sequences, and mRNA instability determinants. Several of these latter elements may be located proximal to the coding region. [00110] There are several types of regulatory regions, including those that are developmentally regulated, inducible or constitutive.
  • a regulatory region that is developmentally regulated, or controls the differential expression of a gene under its control, is activated within certain organs or tissues of an organ at specific times during the development of that organ or tissue.
  • some regulatory regions that are developmentally regulated may preferentially be active within certain organs or tissues at specific developmental stages, they may also be active in a developmentally regulated manner, or at a basal level in other organs or tissues within the plant as well.
  • tissue-specific regulatory regions for example see- specific a regulatory region, include the napin promoter, and the cruciferin promoter (Rask et al., 1998, J. Plant Physiol.152: 595-599; Bilodeau et al., 1994, Plant Cell 14: 125-130).
  • An example of a leaf-specific promoter includes the plastocyanin promoter (see US 7,125,978, which is incorporated herein by reference).
  • An inducible regulatory region is one that is capable of directly or indirectly activating transcription of one or more DNA sequences or genes in response to an inducer. In the absence of an inducer the DNA sequences or genes will not be transcribed.
  • the protein factor that binds specifically to an inducible regulatory region to activate transcription may be present in an inactive form, which is then directly or indirectly converted to the active form by the inducer. However, the protein factor may also be absent.
  • the inducer can be a chemical agent such as a protein, metabolite, growth regulator, herbicide or phenolic compound or a physiological stress imposed directly by heat, cold, salt, or toxic elements or indirectly through the action of a pathogen or disease agent such as a virus.
  • a plant cell containing an inducible regulatory region may be exposed to an inducer by externally applying the inducer to the cell or plant such as by spraying, watering, heating or similar methods.
  • Inducible regulatory elements may be derived from either plant or non-plant genes (e.g. Gatz, C. and Lenk, I.R.P., 1998, Trends Plant Sci.3, 352-358).
  • inducible promoters examples include, but not limited to, tetracycline- inducible promoter (Gatz, C.,1997, Ann. Rev. Plant Physiol. Plant Mol. Biol.48, 89- 108), steroid inducible promoter (Aoyama, T. and Chua, N.H.,1997, Plant J.2, 397- 404) and ethanol-inducible promoter (Salter, M.G., et al, 1998, Plant Journal 16, 127- 132; Caddick, M.X., et al,1998, Nature Biotech.16, 177-180) cytokinin inducible IB6 and CKI1 genes (Brandstatter, I.
  • a constitutive regulatory region directs the expression of a gene throughout the various parts of a plant and continuously throughout plant development. Examples of known constitutive regulatory elements include promoters associated with the CaMV 35S transcript.
  • Biol.29: 637-646 the Arabidopsis ubiquitin 1 and 6 genes (Holtorf et al, 1995, Plant Mol. Biol.29: 637-646), the tobacco translational initiation factor 4A gene (Mandel et al, 1995 Plant Mol. Biol.29: 995-1004), the Cassava Vein Mosaic Virus promoter, pCAS, (Verdaguer et al., 1996); the promoter of the small subunit of ribulose biphosphate carboxylase, pRbcS: (Outchkourov et al., 2003), the pUbi (for monocots and dicots ).
  • the term "constitutive" as used herein does not necessarily indicate that a nucleotide sequence under control of the constitutive regulatory region is expressed at the same level in all cell types, but that the sequence is expressed in a wide range of cell types even though variation in abundance is often observed.
  • the genetic constructs of the present disclosure may also include enhancers, either translation or transcription enhancers, as may be required. Enhancers may be located 5' or 3' to the sequence being transcribed. Enhancer regions are well known to persons skilled in the art, and may include an ATG initiation codon, adjacent sequences or the like.
  • the initiation codon if present, may be in phase with the reading frame ("in frame") of the coding sequence to provide for correct translation of the transcribed sequence.
  • the nucleic acid comprising a nucleotide sequence encoding a modified coat protein or modified polyprotein, as described herein may further comprise sequences that enhance expression of the modified coat protein or modified polyprotein in the host, portion of the host or host cell. Sequences that enhance expression may include, a 5’ UTR enhancer element, or a plant-derived expression enhancer, in operative association with the nucleic acid encoding the modified coat protein or modified polyprotein.
  • the sequence encoding the modified coat protein or modified polyprotein may also be optimized to increase expression by, for example, optimizing for human codon usage, increased GC content, or a combination thereof.
  • plant-derived expression enhancer refers to a nucleotide sequence obtained from a plant, the nucleotide sequence encoding a 5'UTR. Examples of a plant derived expression enhancer are described in International Application No. PCT/CA2019/050317 and International Application No. PCT/CA2019/050319 (Filed March 14, 2019); which are incorporated herein by reference) or in Diamos A.G. et al. (2016, Front Plt Sci.7:1-15; which is incorporated herein by reference).
  • the plant-derived expression enhancer may be selected from nbEPI42, nbSNS46, nbCSY65, nbHEL40, nbSEP44, nbMT78, nbATL75, nbDJ46, nbCHP79, nbEN42, atHSP69, atGRP62, atPK65, atRP46, nb30S72, nbGT61, nbPV55, nbPPI43, nbPM64 and nbH2A86 as described in International Application No. PCT/CA2019/050317 and PCT/CA2019/050319.
  • the plant derived expression enhancer may be used within a plant expression system comprising a regulatory region that is operatively linked with the plant-derived expression enhancer sequence and a nucleotide sequence of interest, for example a nucleotide sequence encoding modified coat proteins or modified polyprotein.
  • Stability and/or translation efficiency of an RNA may further be improved by the inclusion of a 3' untranslated region (3’UTR).
  • the one or more genetic constructs of the present description may therefore further comprise a 3’ UTR.
  • a 3’ untranslated region may contain a polyadenylation signal and any other regulatory signals capable of effecting mRNA processing, mRNA stability or gene expression.
  • the polyadenylation signal is usually characterized by effecting the addition of polyadenylic acid tracks to the 3’ end of the mRNA precursor.
  • Polyadenylation signals are commonly recognized by the presence of homology to the canonical form 5’ AATAAA-3’ although variations are not uncommon.
  • Non-limiting examples of suitable 3’ regions are the 3’ transcribed non-translated regions containing a polyadenylation signal of Agrobacterium tumor inducing (Ti) plasmid genes, such as the nopaline synthase (Nos gene) and plant genes such as the soybean storage protein genes, the small subunit of the ribulose-1, 5-bisphosphate carboxylase gene (ssRUBISCO; US 4,962,028; which is incorporated herein by reference), the promoter used in regulating plastocyanin expression, described in US 7,125,978 (which is incorporated herein by reference), 3’ UTR derived from a Arracacha virus B isolate gene (AvB) (SEQ ID NO: 40), 3’UTR derived from Beet necrotic yellow vein virus (trBNYVV) (SEQ ID NO: 41), 3’UTR derived from Southern bean mosaic virus (SBMV) (SEQ ID NO: 42), 3’UTR derived from Turnip ringspot virus (TuRSV)
  • Signal peptides or peptide sequences for directing localization of an expressed protein or polypeptide to the apoplast include, but are not limited to, a native (with respect to the protein) signal or leader sequence, or a heterologous signal sequence, for example but not limited to, a rice amylase signal peptide (McCormick 1999, Proc Natl Acad Sci USA 96:703-708), a protein disulfide isomerase signal peptide (PDI). Therefore, as described herein, the modified S protein may further comprise a heterologous amino acid signal peptide sequence.
  • the S protein may comprise the signal peptide from Protein disulphide isomerase (PDI SP; nucleotides 32-103 of Accession No. Z11499).
  • PDI SP Protein disulphide isomerase
  • the present disclosure therefore provides for a modified coat protein or modified polyprotein comprising a native, or a non-native signal peptide, and nucleic acids encoding such protein.
  • the one or more than one modified genetic constructs of the present description may be expressed in any suitable host or host cell that is transformed by the nucleic acids, or nucleotide sequence, or constructs, or vectors of the present disclosure.
  • the host or host cell may be from any source including plants, fungi, bacteria, insect and animals for example mammals.
  • the host or host cell may be selected from a plant or plant cell, fungi or a fungal cell, bacteria or bacterial cell, an insect or an insect cell, and animal or an animal cell.
  • the mammal or animal may not be a human.
  • the host or host cell is a plant, portion of a plant or plant cell.
  • plant may comprise an entire plant, tissue, cells, or any fraction thereof, intracellular plant components, extracellular plant components, liquid or solid extracts of plants, or a combination thereof, that are capable of providing the transcriptional, translational, and post-translational machinery for expression of one or more than one nucleic acids described herein, and/or from which an expressed protein or VLP may be extracted and purified.
  • Plants may include, but are not limited to, herbaceous plants. The herbaceous plants may be annuals, biennials or perennials plants.
  • Plants may further include, but are not limited to agricultural crops including for example canola, lettuce (Lactuca sativa), Brassica spp., maize, Nicotiana spp., (tobacco) for example, Nicotiana benthamiana, Nicotiana rustica, Nicotiana, tabacum, Nicotiana alata, Arabidopsis thaliana, alfalfa, potato, sweet potato (Ipomoea batatus), ginseng, pea, oat, rice, soybean, wheat, barley, sunflower, cotton, corn, rye (Secale cereale), sorghum (Sorghum bicolor, Sorghum vulgare), safflower (Carthamus tinctorius).
  • agricultural crops including for example canola, lettuce (Lactuca sativa), Brassica spp., maize, Nicotiana spp., (tobacco) for example, Nicotiana benthamiana, Nicotiana rustica, Nicotiana, tabacum, Nicotiana al
  • plant portion refers to any part of the plant including but not limited to leaves, stem, root, flowers, fruits, a plant cell obtained from leaves, stem, root, flowers, fruits, a plant extract obtained from leaves, stem, root, flowers, fruits, or a combination thereof.
  • the plant portion refers to the areal portion of a plant such as for example leaves, stem, flowers and fruits.
  • plant extract refers to a plant-derived product that is obtained following treating a plant, a portion of a plant, a plant cell, or a combination thereof, physically (for example by freezing followed by extraction in a suitable buffer), mechanically (for example by grinding or homogenizing the plant or portion of the plant followed by extraction in a suitable buffer), enzymatically (for example using cell wall degrading enzymes), chemically (for example using one or more chelators or buffers), or a combination thereof.
  • a plant extract may be further processed to remove undesired plant components for example cell wall debris.
  • a plant extract may be obtained to assist in the recovery of one or more components from the plant, portion of the plant or plant cell, for example a protein (including protein complexes, polyproteins, protein suprastructures and/or VLPs), a nucleic acid, a lipid, a carbohydrate, or a combination thereof from the plant, portion of the plant, or plant cell. If the plant extract comprises proteins, then it may be referred to as a protein extract.
  • a protein extract may be a crude plant extract, a partially purified plant or protein extract, or a purified product, that comprises one or more proteins, protein complexes such for example protein trimers, protein suprastructures, and/or VLPs, from the plant tissue.
  • a protein extract, or a plant extract may be partially purified using techniques known to one of skill in the art, for example, the extract may be subjected to salt or pH precipitation, centrifugation, density gradient centrifugation, filtration, chromatography, for example, size exclusion chromatography, ion exchange chromatography, affinity chromatography, or a combination thereof.
  • a protein extract may also be purified, using techniques that are known to one of skill in the art.
  • the constructs of the present disclosure can be introduced into plant cells using Ti plasmids, Ri plasmids, plant virus vectors, direct DNA transformation, micro-injection, electroporation, etc.
  • transient expression methods may be used to express the constructs of the present disclosure (see Liu and Lomonossoff, 2002, Journal of Virological Methods, 105:343-348; which is incorporated herein by reference).
  • a vacuum-based transient expression method as described by Kapila et al., 1997, which is incorporated herein by reference may be used.
  • Agro-inoculation, Agroinfiltration, or syringe infiltration a mixture of Agrobacteria comprising the desired nucleic acid enter the intercellular spaces of a tissue, for example the leaves, aerial portion of the plant (including stem, leaves and flower), other portion of the plant (stem, root, flower), or the whole plant. After crossing the epidermis, the Agrobacteria infect and transfer t- DNA copies into the cells.
  • the constructs of this disclosure may be further manipulated to include plant selectable markers.
  • Useful selectable markers include enzymes that provide for resistance to chemicals such as an antibiotic for example, gentamycin, hygromycin, kanamycin, or herbicides such as phosphinothrycin, glyphosate, chlorosulfuron, and the like.
  • transgenic plants, plant cells or seeds containing the gene construct of the present disclosure that may be used as a platform plant suitable for transient protein expression described herein. Methods of regenerating whole plants from plant cells are also known in the art (for example see Guerineau and Mullineaux (1993, Plant transformation and expression vectors. In: Plant Molecular Biology Labfax (Croy RRD ed) Oxford, BIOS Scientific Publishers, pp 121-148).
  • transformed plant cells are cultured in an appropriate medium, which may contain selective agents such as antibiotics, where selectable markers are used to facilitate identification of transformed plant cells.
  • an appropriate medium which may contain selective agents such as antibiotics, where selectable markers are used to facilitate identification of transformed plant cells.
  • shoot formation can be encouraged by employing the appropriate plant hormones in accordance with known methods and the shoots transferred to rooting medium for regeneration of plants.
  • the plants may then be used to establish repetitive generations, either from seeds or using vegetative propagation techniques.
  • Transgenic plants can also be generated without using tissue culture. Methods for stable transformation, and regeneration of these organisms are established in the art and known to one of skill in the art. Available techniques are reviewed in Vasil et al. (Cell Culture and Somatic Cell Genetics of Plants, Vol.
  • the nucleic acid construct may be introduced into the Agrobacterium in a single transfection event so that the nucleic acids are pooled, and the bacterial cells transfected.
  • the constructs may be introduced serially, in series or sequentially.
  • a first construct is introduced into the Agrobacterium as described, the cells are grown under selective conditions (e.g. in the presence of an antibiotic) where only the singly-transformed bacteria can grow.
  • a second nucleic acid construct is introduced into the Agrobacterium as described, and the cells are grown under double-selective conditions, where only the doubly-transformed bacteria can grow.
  • the double-transformed bacteria may then be used to transform a plant, portion of the plant or plant cell as described herein, or may be subjected to a further transformation step to accommodate a third nucleic acid construct.
  • the nucleic acid construct may be introduced into the plant by co-infiltrating a mixture of Agrobacterium cells with the plant, plant portion, or plant cell, each Agrobacterium cell may comprise one or more constructs to be introduced within the plant.
  • concentration of the various Agrobacteria populations comprising the desired constructs may be modulated.
  • the modified viral surface protein or VLP comprising modified viral surface protein as described herewith may be used to elicit an immune response in a subject.
  • An “immune response” generally refers to a response of the adaptive immune system of a subject.
  • the adaptive immune system generally comprises a humoral response, and a cell-mediated response.
  • a humoral response is the aspect of immunity that is mediated by secreted antibodies, produced in the cells of the B- lymphocyte lineage (B cell). Secreted antibodies bind to antigens on the surfaces of invading microbes (such as viruses or bacteria), which flags them for destruction.
  • Humoral immunity is used generally to refer to antibody production and the processes that accompany it, as well as the effector functions of antibodies, including Th2 cell activation and cytokine production, memory cell generation, opsonin promotion of phagocytosis, pathogen elimination and the like.
  • modulate or “modulation” or the like refer to an increase or decrease in a particular response or parameter, as determined by any of several assays generally known or used, some of which are exemplified herein.
  • a cell-mediated response is an immune response that involves the activation of macrophages, natural killer cells (NK), antigen-specific cytotoxic T- lymphocytes, and the release of various cytokines in response to an antigen.
  • Cell- mediated immunity is used generally to refer to some Th cell activation, Tc cell activation and T-cell mediated responses. Cell-mediated immunity may be of particular importance in responding to viral infections.
  • the induction of antigen specific CD8 positive T lymphocytes may be measured using an ELISPOT assay; stimulation of CD4 positive T- lymphocytes may be measured using a proliferation assay.
  • Anti-Coronavirus antibody titers may be quantified using an ELISA assay; isotypes of antigen-specific or cross- reactive antibodies may also be measured using anti-isotype antibodies (e.g. anti -IgG, IgA, IgE or IgM). Methods and techniques for performing such assays are well-known in the art.
  • Cytokine presence or levels may also be quantified.
  • a T-helper cell response (Th1/Th2) will be characterized by the measurement of IFN- ⁇ and IL-4 secreting cells using by ELISA (e.g. BD Biosciences OptEIA kits).
  • ELISA e.g. BD Biosciences OptEIA kits.
  • Peripheral blood mononuclear cells (PBMC) or splenocytes obtained from a subject may be cultured, and the supernatant analyzed.
  • T- lymphocytes may also be quantified by fluorescence-activated cell sorting (FACS), using marker specific fluorescent labels and methods as are known in the art.
  • FACS fluorescence-activated cell sorting
  • epitope refers to a part of an antigen to which an antibody specifically binds.
  • the epitope may be a linear epitope or the epitope may be a conformational epitope.
  • Linear epitopes refer to parts or sequences that are unstructured/linear.
  • Conformational epitopes refer to structured parts of an antigen to which an antibody specifically binds.
  • a method of producing an antibody or antibody fragment comprises administering the antigenic sequence, modified viral structural protein, a trimer or trimeric modified viral structural protein or VLP comprising the modified viral structural protein as described herewith to a subject, or a host animal, thereby producing the antibody or the antibody fragment.
  • Antibodies or the antibody fragments produced by the method are also provided.
  • the present disclosure therefore also provides the use of a viral structural protein or VLP comprising the modified viral structural protein, as described herein, for inducing immunity to a Coronavirus infection in a subject.
  • an antibody or antibody fragment prepared by administering one or more than one modified coat protein or VLP comprising one or more than one modified coat protein, to a subject or a host animal.
  • composition comprising an effective dose of one or more than one modified coat protein or VLP comprising one or more than one modified coat protein, as described herein, and a pharmaceutically acceptable carrier, adjuvant, vehicle, or excipient, for inducing an immune response in a subject.
  • a vaccine for inducing an immune response again Coronavirus in a subject, wherein the vaccine comprises an effective dose of one or more than one modified coat protein or VLP comprising one or more than one modified coat protein.
  • Adjuvant systems to enhance a subject’s immune response to a vaccine antigen are well known and may be used in conjunction with the vaccine or pharmaceutical composition as described herewith. There are many types of adjuvants that may be used.
  • adjuvants for human use are aluminum hydroxide, aluminum phosphate and calcium phosphate.
  • adjuvants based on oil emulsions oil in water or water in oil emulsions such as Freund's incomplete adjuvant (FIA), MontanideTM, Adjuvant 65, and LipovantTM), products from bacterial (or their synthetic derivatives), endotoxins, fatty acids, paraffinic, or vegetable oils, cholesterols, and aliphatic amines or natural organic compounds such for example squalene and saponin-based adjuvants.
  • Non-limiting adjuvants that might be used include for example oil-in water emulsions of squalene oil (for example MF-59 or AS-03), adjuvant composed of the synthetic TLR4 agonist glucopyranosyl lipid A (GLA) integrated into stable emulsion (SE) (GLA-SE) or CpG 1018 a toll-like receptor (TLR9) agonist adjuvant.
  • GLA synthetic TLR4 agonist glucopyranosyl lipid A
  • SE stable emulsion
  • TLR9 toll-like receptor
  • Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions.
  • Suitable excipients are, for example, water, saline, dextrose, mannitol, lactose, lecithin, albumin, sodium glutamate, cysteine hydrochloride, and the like.
  • the injectable pharmaceutical compositions may contain minor amounts of nontoxic auxiliary substances, such as wetting agents, pH buffering agents, and the like.
  • Physiologically compatible buffers include, but are not limited to, Hanks's solution, Ringer's solution, or physiological saline buffer.
  • composition or vaccine may be administered to a subject once (single dose). Furthermore, the vaccine or composition may be administered to a subject multiple times (multi-dose). Therefore, the composition, formulation, or vaccine may be administered to a subject in a single dose to illicit an immune response or the composition, formulation, or vaccine may be administered multiple time (multi dosages). For example, a dose of the composition or vaccine may be administered 2, 3, 4 or 5 times. Accordingly, the composition or vaccine may be administered to a subject in an initial dose and one or more than one doses may subsequently be administered to the subject. Administration of the doses may be separated in time from each other.
  • one or more than one subsequent dose may be administered 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months or 6 months or any time in between from the administration of the initial dose.
  • the composition or vaccine may be administered annually.
  • the composition or vaccine may be administered as a seasonal vaccine.
  • modified coat protein constructs were produced using techniques well known within the art. For example, modified coat protein displaying epitope S14P4 (constructs 8720-8725) and modified coat protein displaying epitope S21P2 (constructs 8726-8731) were cloned as described below. Constructs encoding native coat protein and 24K protease [00145] A sequence encoding VP60 was cloned into 2X35S(+C)/nbMT78/AvB/NOS expression system using the following PCR-based method.
  • a fragment containing the VP60 coding sequence was amplified using primers IF(nbMT78)-CPMV(SB).c (SEQ ID NO: X26) and IF(AVb)-CPMV(SB).r (SEQ ID NO: 27), using VP60 gene sequence (SEQ ID NO: 28) as template.
  • the PCR product was cloned into 2X35S(+C)/nbMT78/AvB/NOS expression systems using In- Fusion cloning system (Clontech, Mountain View, CA).
  • Construct number 7140 ( Figure 6A) was digested with AatII and StuI restriction enzymes and the linearized plasmid was used for the In-Fusion assembly reaction.
  • Construct number 7140 is an acceptor plasmid intended for “In Fusion” cloning of genes of interest in a 2X35S(+C)/nbMT78/AvB/NOS-based expression cassette.
  • This acceptor plasmid also incorporates a gene construct for the co-expression of the TBSV P19 suppressor of silencing under the alfalfa Plastocyanin gene promoter and terminator.
  • the backbone is a pCAMBIA binary plasmid and the sequence from left to right t-DNA borders is presented in SEQ ID NO: 31.
  • the resulting construct was given number 7384 (SEQ ID NO: 32).
  • the amino acid sequence of VP60 is presented in SEQ ID NO: 1.
  • FIG. 6B A representation of plasmid 7384 is presented in Figure 6B.
  • Construct 7387 was cloned using the same methodology and a summary of primers, templates, accepting vectors and products is provided in Table 2.
  • a sequence encoding VP60 was cloned into 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm expression system using the following PCR-based method.
  • a fragment containing the VP60 coding sequence was amplified using primers IF(nbMT78)-CPMV(SB).c (SEQ ID NO: 26) and IF(AVb)- CPMV(SB).r (SEQ ID NO: 27), using VP60 gene sequence (SEQ ID NO: 29) as template.
  • the PCR product was cloned into 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm expression systems using In-Fusion cloning system (Clontech, Mountain View, CA). Construct number 7142 ( Figure 6D) was digested with AatII and StuI restriction enzymes and the linearized plasmid was used for the In-Fusion assembly reaction.
  • Construct number 7142 is an acceptor plasmid intended for “In Fusion” cloning of genes of interest in a 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm-based expression cassette.
  • This acceptor plasmid also incorporates a gene construct for the co-expression of the TBSV P19 suppressor of silencing under the alfalfa Plastocyanin gene promoter and terminator.
  • the backbone is a pCAMBIA binary plasmid and the sequence from left to right t-DNA borders is presented in SEQ ID NO: 49.
  • the resulting construct was given number 8720 (SEQ ID NO: 50).
  • the amino acid sequence of VP60 is presented in SEQ ID NO: 30.
  • a representation of plasmid 8720 is presented in Figure 7A. Constructs 8721 to 8731 were cloned using the same methodology and a summary of primers, templates, accepting vectors and products is provided in Table 2. d i ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I Example 2: Methods Agrobacterium tumefaciens Transfection [00147] Agrobacterium tumefaciens strain AGL1 was transfected by electroporation with the modified coat protein expression vectors using the methods described by D’Aoust et al., 2008 (Plant Biotech. J.6:930-40).
  • Transfected Agrobacterium were grown in YEB medium supplemented with 10 mM 2-(N- morpholino)ethanesulfonic acid (MES), 20 ⁇ M acetosyringone, 50 ⁇ g/ml kanamycin and 25 ⁇ g/ml of carbenicillin pH 5.6 to an OD 600 between 0.6 and 1.6.
  • Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6).
  • infiltration medium 10 mM MgCl2 and 10 mM MES pH 5.6.
  • Agrobacteria transfected with each expression vector were grown in a YEB medium supplemented with 10 mM 2-(N-morpholino)ethanesulfonic acid (MES), 20 ⁇ M acetosyringone, 50 ⁇ g/ml kanamycin and 25 ⁇ g/ml of carbenicillin pH 5.6 until they reached an OD 600 between 0.6 and 1.6.
  • MES 2-(N-morpholino)ethanesulfonic acid
  • Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6) and stored overnight at 4° C. On the day of infiltration, culture batches were diluted in 2.5 culture volumes and allowed to warm before use. Whole plants of N. benthamiana were placed upside down in the bacterial suspension in an air-tight stainless steel tank under a vacuum of 20-40 Torr for 2-min. Plants were returned to the greenhouse for a 6 or 9 day incubation period until harvest.
  • infiltration medium 10 mM MgCl2 and 10 mM MES pH 5.6
  • Biomasses expressing constructs 8720 – 8725 in addition to construct 7387 (proteinase 24K) were harvested at 6- and 9-days post infiltration (dpi) and screened to detect accumulation of CPMV coat proteins. Detection of bands for CPMV-L at 35 kDa and CPMV-S at 22 kDa upon SDS-PAGE of clarified biomasses, using protein staining and by using an anti-CPMV antibody, are taken as a confirmation for the expression of these proteins in planta.
  • CPMV coat proteins were confirmed from construct 8720, 8721, 87228723 and 8725, and an increase in MW was observed corresponding to the expected size of the inserted peptide in each case ( Figure 1). Accumulation was found to be higher at 9 dpi, compared to 6 dpi. Biomasses expressing two of these constructs: 8721 and 8725, harvested at 9 dpi, were selected for purification and characterization of VLPs. [00151] Biomasses expressing constructs 8726 – 8731 in addition to construct 7387 (proteinase 24K) were harvested at 6- and 9-days post infiltration (dpi) and screened to detect accumulation of CPMV coat proteins.
  • VLPs Purification of VLPs
  • biomasses were processed using routine purification protocols. Clarified extracts were concentrated using PEG precipitation methods and separated on a 18- 24% iodixanol density gradient. Fractions were collected from the bottom of gradients and analyzed by SDS-PAGE. Properly assembled VLPs of CPMV are expected to migrate to 18-22% iodixanol layers. Results showed detection of CPMV coat proteins in these specific iodixanol layers in case of CPMV-S14P5 constructs 8721 and 8725, and in case of CPMV-S21P2 construct 8729 ( Figure 3).
  • SEQ ID NO: 1 Native CPMV polyprotein (large and small coat protein) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDDNWN

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Abstract

The present disclosure relates to the production of modified coat proteins in a host or host cell. More specifically, the present disclosure relates to producing virus-like particle (VLP) production in host or host cells, wherein the VLPs comprise the modified coat protein. The modified coat protein may comprise a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. Further provided are nucleic acid sequences encoding the modified coat proteins and methods of producing VLPs that comprise the modified coat protein.

Description

CPMV VLPS DISPLAYING SARS-COV-2 EPITOPES FIELD OF INVENTION [0001] This disclosure relates to modified coat proteins. The present disclosure also relates to virus-like particles (VLPs) comprising modified coat protein and methods of producing the VLPs in a host or host cells. BACKGROUND OF THE INVENTION [0002] Cowpea mosaic virus (CPMV) is an icosahedral, non-enveloped plant virus of the Comoviridae family of viruses in the order Picornavirales. CPMV particles are of interest in biotechnology and nanotechnology due to their well-characterized molecular structure, high stability and their inability to infect animals or humans. [0003] CPMV particles have been developed as an epitope display platform, an in vivo imaging tool, and as a substrate for chemical reactions including metal deposition, among other applications (Sainsbury et al. Methods in molecular biology 2014). CPMV and CPMV virus-like particles have also been shown to have immunostimulatory and anti-tumorigenic properties (Lizotte et al Nat. Nanotechnol. 2016; Wang et al. J. Virol.2019). [0004] The CPMV genome consists of 2 separate positive-sense single-stranded RNA, namely RNA-1 (of 6 kilobases) and RNA-2 (of 3.5 kilobases). Each of the two RNAs are encapsidated into separate particles and both RNA-1 and RNA-2 are required for production of infectious viral particles of CPMV. CPMV capsids are approximately 30 nm in diameter and display pseudo T = 3 icosahedral symmetry. Each capsid consists of 60 copies of a protomer comprising large (L or VP37) and small (S or VP23) coat protein (CP) subunits, derived from a single CP precursor (VP60) encoded by RNA-2 and processed by a proteinase (24K) encoded by RNA-1. The L subunit is composed of two jellyroll β-barrel domains, and the S subunit consists of a single jellyroll β-barrel. The jellyroll β-barrel is common in many icosahedral virus structures and contains two twisted antiparallel β sheets, each of which contains four β strands. Therefore, each β-barrel of the L subunit and the S subunit consist principally of 8 antiparallel β-strands connected by loops of varying length. The flat β-strands are annotated βB, βC, βD, βE, βF, βG, βH and βI. In addition, three short alpha helices in the L and S subunits are designated αA, αB and αC, and two short beta strands found in close proximity to βC are referred to as βC’ and βC”. The connecting regions or loops between these structural features are referred to using the annotations of the features flanking that loop. For example: βB- βC refers to the loop connecting βB with βC and βC’-βC”, βF-βG, βE-αB are some others. These loops can be used as sites for expression of foreign peptide sequences, such as epitopes from heterologous viruses. [0005] Potential sites for insertion of foreign sequences have been determined by examining the three-dimensional structure of CPMV and through empirical testing, but there remain a wide range of alternatives. In most cases, foreign sequences have been inserted into the βB-βC loop, which is well-exposed on the surface of the virus and therefore, a logical site for epitope display. Because foreign peptides can be expressed from multiple loops on either the S or L protein or from both coat proteins on the same virion, it is possible to express multiple copies of a peptide, on a single CPMV particle. However, it is unclear how to best determine optimal sites within the connecting loops for expression of foreign epitopes for a given CPMV-fusion peptide composition (Brennan et al. Mol. Biotech.2001; Lin, et al. Fold. Des.1996). [0006] WO1992018618A1 describes the use of modified CPMV coat proteins for the presentation of foreign peptides on the exposed surface of the coat proteins of the plant virus. [0007] WO1996002649A1 discloses assembled CPMV particles containing a foreign peptide insert wherein the foreign peptide is inserted immediately preceding the proline 23 (Pro23) residue in the βB-βC loop of the small (S) capsid protein (VP23). WO1998056933A1 similarly discloses raising an immune response to a peptide insert within a CPMV epitope presentation system, wherein the foreign insert is made immediately preceding a proline residue in the βB- βC loop of the small (S) capsid protein (VP23), which in CPMV is the proline 23 (Pro23). WO2001027282A1 discloses insertion of a foreign peptide into sites on the VP-S of CPMV, such as the N-terminus of VP-S. [0008] Until recently, a limitation of the CPMV nanoparticle was that there was no straightforward method for making the CPMV capsid from individual subunits or protomer building blocks and that it was impossible to reproducibly generate a population of empty virus-like particles devoid of the infectious RNA genome. This posed a disadvantage for immunogenic compositions such as vaccines, since CPMV preparations containing an RNA genome retain infectivity unless specific inactivation steps are taken, and the space within the capsid occupied by RNA limits the capacity to load the particles with heterologous material. To address these issues, transient expression has been developed to co-express VP60 and the 24K protease necessary for processing of VP60. This results in formation of virus-like particles (VLPs), that are devoid of RNA but retain the capacity for engineered peptide display on CPMV coat proteins. Such VLPs may be engineered for antigen presentation and vaccine development among other biotechnology applications. However, CPMV VLP stability can vary based on the type of antigenic peptide sequences employed and this can impact production yields. Epitope selection, in terms of peptide sequence, length, orientation and insertion site, in order to achieve high yields of fusion VLPs remains unpredictable (Sainsbury et al Methods. Mol. Biol.2014; Meshcheriakova Biochem. Soc. Trans.2017). [0009] WO2010146359A1 shows the processing of VP60 in plants by the 24kDa proteinase, including a demonstration that VP60 can be modified such that the S coat protein includes a 19 amino acid FMDV sequence inserted in βB-βC loop, without impairing proteolytic processing. [0010] To control the spread of COVID-19, several efforts are underway to develop vaccines for inducing immunity against the causative coronavirus SARS-CoV-2. Most of these efforts target the spike (S) glycoprotein of SARS-CoV-2, which mediates coronavirus entry into host cells via the angiotensin-converting enzyme 2 (ACE2) receptor. Among the approaches being pursued worldwide for COVID-19 vaccine development are peptide-based vaccines. Peptide vaccines rely on the use of short stretches of antigenic peptides to induce targeted immune responses against a pathogen, as opposed to use of live-attenuated or inactivated pathogen vaccines, subunit vaccines, or vaccines that administer nucleic acids encoding the pathogen’s proteins such as adenoviral vector, DNA, or mRNA vaccines. Peptide vaccines have benefits over other types of vaccines, such as low cost of production, specificity to the relevant epitopes, and reduction of nonspecific immune responses leading to unwanted side effects including autoimmunity. [0011] Several peptide-based vaccine candidates for COVID-19 are presently in development. Poh et al.2020 (Nat Commun 11, 2806 (2020) report the immunodominance of two B-cell linear epitopes of the spike protein (S), named S14P5 and S21P2, identified by analysis of neutralizing antibodies in sera samples from 25 convalescent patients using ELISA experiments. In addition, using depletion assays, the authors demonstrate that antibodies targeting S14P5 and S21P2 accounted for a significant fraction of the anti-S neutralizing response in these patients. S14P5 is in proximity to the ACE2 binding region of the Spike prefusion trimer and it is hypothesized that antibodies binding to S14P5 neutralize the virus by sterically hindering binding to ACE2. In case of S21P2, overlap of the peptide with the SARS- CoV-2 fusion peptide suggests that antibodies against this region may block virus function. SUMMARY OF THE INVENTION [0012] The present disclosure relates to modified Cowpea Mosaic Virus (CPMV) coat protein and CPMV Virus-like particle (VLP) comprising modified coat protein and method of producing the VLPs in a host or host cell. The VLP may be an empty VLP, being devoid of DNA or RNA. [0013] In one aspect it is provided a modified Cowpea Mosaic Virus (CPMV) Virus- like particle (VLP) comprising large coat protein and small coat protein, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0014] In another aspect it is provided a capsomer comprising large coat protein, small coat protein or large coat protein and small coat protein, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0015] The insertion in the betaE-alphaB loop of the large coat protein may be between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1. The insertion in the betaB-betaC loop of the small coat protein may be between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1. The insertion in the betaC’-betaC” loop of the small coat protein is between amino acid residue corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1. [0016] The heterologous peptide insertion may comprise one or more than one linker at the N-terminus, the C-terminus or both at the N-terminus and the C-terminus. The linker may comprise one or more than one aspartate or the linker may comprise the amino acid sequence glycine-serine-alanine. [0017] The epitope may be coronavirus peptide S14P5 or coronavirus peptide S21P2. [0018] In one aspect the large coat protein may comprise in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein an aspartate residue is added to the N-terminus and the C-terminus of the coronavirus peptide S14P5. For example the heterologous peptide insert may comprise the sequence of SEQ ID: 17. [0019] In another aspect the small coat protein may comprise in the betaC’-betaC” loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein a glycine-serine-alanine linker is fused to the N-terminus and the C-terminus of coronavirus peptide S14P5. [0020] In yet another aspect the heterologous peptide insert may comprise the sequence of SEQ ID: 19 or SEQ ID NO: 18. [0021] In a further aspect the large coat protein may comprise in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S21P2, wherein an aspartate residue is added to the N-terminus and the C-terminus of coronavirus peptide S21P2. [0022] In another aspect it is provided a modified Cowpea Mosaic Virus (CPMV) coat protein, wherein the modified CPMV coat protein may be a small coat protein, i) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0023] In a further aspect it is provided a modified Cowpea Mosaic Virus (CPMV) coat protein, wherein the coat protein may be a large coat protein comprising in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0024] It is further provided a modified Cowpea Mosaic Virus (CPMV) polyprotein comprising a large and a small coat protein, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, and ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0025] Virus like particle comprising the modified CPMV coat protein as described above are also provided. [0026] It is also provided composition comprising an effective dose of the VLP as described above and a pharmaceutically acceptable carrier, adjuvant, vehicle or excipient. [0027] In addition it is provided a vaccine comprising an effective dose of the VLP as described above for inducing an immune response against coronavirus. The vaccine may be a multivalent vaccine, comprising a mixture of monovalent VLPs. [0028] It is further provided a method for inducing immunity to a Coronavirus infection in a subject, the method comprising administering the composition or the vaccine as described above. An antibody or antibody fragment prepared using the composition or the vaccine are also provided. [0029] In a further aspect a host or host cell is provided, the host or host cell may comprise the VLP of the current disclosure. The host may be a plant and the host cell may be a plant cell. [0030] The disclosure further provided a nucleic acid comprising a nucleotide sequence encoding a Cowpea Mosaic Virus (CPMV) polyprotein, the polyprotein comprising the large coat protein and the small coat protein of CPMV, i) wherein the large coat protein may comprise in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein may comprise in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein may comprise in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0031] It is also provided a method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) introducing a first nucleic acid comprising the nucleic acid as described above into the host or host cell; b) introducing a second nucleic acid encoding CPMV protease into the host or host cell; c) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acid, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell. [0032] The ratio of introduced amounts of the first nucleic acid relative to the second nucleic acid may be 2:1. [0033] In a further aspect it is provided a method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) providing the host or host cell, comprising a first nucleic acid comprising the nucleic acid as described above and a second nucleic acid encoding CPMV protease; b) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acids, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell. [0034] The modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) may be purified from the host or host cell. The host may be a plant and the host cell may be a plant cell. [0035] This summary of the invention does not necessarily describe all features of the invention. BRIEF DESCRIPTION OF THE DRAWINGS [0036] These and other features of the invention will become more apparent from the following description in which reference is made to the appended drawings wherein: FIGURE 1 shows a stain-free gel detection (top panel) and Western blot detection (bottom panel) of clarified extracts of biomasses expressing CPMV-S14P5 fusion constructs (named 8720 to 8725), harvested at 6 or 9 days post infiltration (dpi). Construct 7384 encodes the native CPMV polyprotein VP60 (no insertions). Construct 8720 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the βB-βC loop (“Site 1”) of the small coat protein (S14P5-1). Construct 8721 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the βE-αB loop (“Site 2”) of the large coat protein (S14P5-2). Construct 8722 encodes CPMV polyprotein (CPMV VP60) with S14P5 inserted into the βC’-βC” loop (“Site 4”) of the small coat protein (S14P5-4). Construct 8723 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to an aspartate (D) linker at each terminus inserted into the βE-αB loop of the large coat protein (S14P5 (+DD)-2). Construct 8724 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to a glycine-serine-alanine (GSA) linker at each terminus inserted into the βB-βC loop of the small coat protein (GSA-S14P5-GSA-1). Construct 8725 encodes CPMV polyprotein (CPMV VP60) with S14P5 fused to a GSA linker at each terminus inserted into the βC’-βC” loop of the small coat protein (GSA-S14P5-GSA-4). Biomasses infiltrated with construct 8721 or 8725 and incubated 9 DPI were chosen for purification. Expected MW of CPMV-L is 35 kDa for the native protein and ~37 kDa in presence of a peptide insertion. For CPMV-S, the expected MW is 22 kDa for the native protein and ~24 kDa in presence of a peptide insertion. [0037] FIGURE 2 shows a stain-free gel detection (top panel) and Western blot detection (bottom panel) of clarified extracts of biomasses expressing CPMV-S21P2 fusion constructs (named 8726 to 8731), harvested at 6 or 9 dpi. Construct 7384 encodes the native CPMV polyprotein (no insertions). Construct 8726 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the βB-βC loop (“Site 1”) of the small coat protein (S21P2-1). Construct 8727 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the βE-αB loop (“Site 2”) of the large coat protein (S21P2-2). Construct 8728 encodes CPMV polyprotein (CPMV VP60) with S21P2 inserted into the βC’-βC” loop (“Site 4”) of the small coat protein (S21P2-4). Construct 8729 encodes CPMV polyprotein (CPMV VP60) with S21P2 fused to an aspartate (D) linker at each terminus inserted into the βE-αB loop of the large coat protein (S21P2 (+DD)-2). Construct 8730 encodes CPMV polyprotein (CPMV VP60) with S21P2 having a GSA linker at each terminus inserted into the βB-βC loop of the small coat protein (GSA- S21P2-GSA-1). Construct 8731 encodes CPMV polyprotein (CPMV VP60) with S21P2 having GSA linker at each terminus inserted into the βC’- βC” loop of the small coat protein (GSA- S21P2-GSA-4). Biomasses infiltrated with construct 8727 or 8729 and incubated 9 DPI were chosen for purification. Expected MW of CPMV-L is 35 kDa for the native protein and ~37 kDa in presence of a peptide insertion. For CPMV-S, the expected MW is 22 kDa for the native protein and ~24 kDa in presence of a peptide insertion. [0038] FIGURE 3 shows stain-free gel detection of fractions harvested from density gradient purification of clarified and concentrated biomasses infiltrated with constructs 8721 (panel A), 8725 (panel B), 8727 (panel C) and 8729 (panel D). Bands for CPMV-L (35-37 kDa) and CPMV-S (22-24 kDa) were detected in biomasses analyzed for constructs 8721, 8725 and 8729. Additional bands at ~25 kDa and ~15 kDa represent proteolytically-clipped forms of CPMV-L and -S proteins. Fractions F7-F10 for construct 8721 (panel A), F7-F10 for construct 8725 (panel B) and F9-F12 for construct 8729 (panel D) were selected for further characterization by electron microscopy. [0039] FIGURE 4 shows electron microscopy images at 30K and 50 K magnifications of native CPMV VP60 VLP (i.e. no insertion; construct 7384) in the upper panel and CPMV VP60-S21P2+DD-2 VLPs (i.e.60 insertions per VLP, construct 8729) in the lower panel. No obvious differences in VLP morphology are observed between the two species. [0040] FIGURE 5 shows the location of the epitope S14P5 and S21P2 (marked by boxes) in the SARS-CoV-2 spike (S) protein (SEQ ID NO: 21). S14P5 corresponds to residues 538-555 of the S-protein, while S21P2 corresponds to residues 794-811 of the S-protein. [0041] FIGURE 6A shows a representation of acceptor plasmid 7140 FIGURE 6B shows a representation of construct 7384 encoding native CPMV VP60. FIGURE 6C shows a representation of construct 7387 encoding native CPMV 24K protease. FIGURE 6D shows a representation of acceptor plasmid 7142. [0042] FIGURE 7A shows a representation of construct 8720 encoding CPMV VP60 with S14P5-1 insert. FIGURE 7B shows a representation of construct 8721 encoding CPMV VP60 with S14P5-2 insert. FIGURE 7C shows a representation of construct 8722 encoding CPMV VP60 with S14P5-4 insert. FIGURE 7D shows a representation of construct 8723 encoding CPMV VP60 with S14P5 (+DD)-2 insert. FIGURE 7E shows a representation of construct 8724 encoding CPMV VP60 with GSA-S14P5-GSA-1 insert. FIGURE 7F shows a representation of construct 8725 encoding CPMV VP60 with GSA-S14P5-GSA-4 insert. FIGURE 7G shows a representation of construct 8726 encoding CPMV VP60 with S21P2-1 insert. FIGURE 7H shows a representation of construct 8727 encoding CPMV VP60 with S21P2-2 insert. FIGURE 7I shows a representation of construct 8728 encoding CPMV VP60 with S21P2-4 insert. FIGURE 7J shows a representation of construct 8729 encoding CPMV VP60 with S21P2 (+DD)-2 insert. FIGURE 7K shows a representation of construct 8730 encoding CPMV VP60 with GSA-S21P2-GSA-1 insert. FIGURE 7L shows a representation of construct 8731 encoding CPMV VP60 with GSA-S21P2-GSA-4 insert. DETAILED DESCRIPTION [0043] The following description is of a preferred embodiment. [0044] The present disclosure relates to modified viral coat protein of a plant virus. The viral protein is also referred to as coat protein, viral capsid protein or capsid protein. Accordingly, the modified viral coat protein may also be referred to as modified coat protein, modified viral capsid protein or modified capsid protein. Furthermore, modified polyprotein comprising a small coat protein and a large coat protein are also provided. In the modified polyprotein, the small coat protein, the large coat protein or a small coat protein and a large coat protein may be modified. Accordingly, the modified polyprotein may comprise a modified small coat protein, a modified large coat protein or both a modified small coat protein and a modified large coat protein. [0045] The modified coat protein may be modified to display a heterologous peptide or peptide insertion for example in exposed surface loops of the coat protein. The heterologous peptide insertion may comprise an epitope that is derived from a coronavirus spike protein. Furthermore, the heterologous peptide or peptide insertion may comprise an epitope and one or more than one linker or linker sequence. [0046] The present disclosure further relates to virus-like particle (VLP) comprising one or more than one modified viral coat protein as described herewith. The VLP may comprise or may consist of one or more than one coat protein, wherein the coat protein has been modified to display a heterologous peptide. Furthermore, the VLP may comprise or may consist of large coat proteins and small coat proteins of the plant virus, wherein the large coat protein, the small coat protein or the large and the small coat protein have been modified to comprise a heterologous peptide or peptide insertion in exposed surface loops of the coat proteins. Therefore, the VLP may comprise or may consist of one or more than one coat protein, wherein the coat protein has been modified to display an epitope derived from a coronavirus spike protein. Accordingly, the VLP may comprise or may consist of one or more than one modified coat protein. The one or more than one modified coat protein may be a modified small coat protein, a modified large coat protein or may be a modified small coat protein and a modified large coat protein. [0047] The coat protein may be derived from an icosahedral plant virus such as, for example Comoviruses, Tombusviruses, Sobemoviruses, or Nepoviruses. In a preferred embodiment, the plant virus is a Comovirus. In a more preferred embodiment, the Comovirus is cowpea mosaic virus (CPMV). [0048] The present disclosure also relates to one or more than one modified coat protein from an icosahedral plant virus such as, for example, Comoviruses, Tombusviruses, Sobemoviruses, or Nepoviruses. For example, the modified coat protein may be derived from the large (L or VP37) coat protein or small (S or VP23) coat protein from cowpea mosaic virus (CPMV). The coat protein may be modified by inserting a heterologous peptide into the coat protein and/or adding a heterologous peptide to the sequence of the coat protein. Furthermore, the coat protein may be modified by replacing residues of the coat protein with a heterologous peptide. [0049] The coat protein may have one or more than one beta-barrel structure or beta barrel domain. For example, the large coat protein may contain two covalently linked beta barrel domains and the small coat protein may contain a single beta barrel domain. The beta-barrel structure or domain may comprise or may consist of eight strands of antiparallel beta-sheet connected by loops of varying length. The beta strands are named βB, βC, βD, βE, βF, βG, βH and βI sheets. In addition, three short alpha helices in the L and S subunits are designated αA, αB and αC, and two short beta strands found in close proximity to βC are referred to as βC’ and βC”. The connecting regions or loops between these structural features are referred to using the annotations of the features flanking that loop. For example: βB-βC refers to the loop connecting βB with βC and βC’-βC”, βF-βG, βE-αB are some others. Accordingly, the connecting loops may be referred to as the βB-βC (beta B-beta C), βD-βE (beta D-beta E), βF-βG (beta F-beta G) and βH-βI (beta H-beta I) loops. These loops can be used as sites for expression of foreign peptide sequences, such as epitopes from heterologous viruses. [0050] The heterologous peptide may be inserted within an exposed portion of the coat protein. For example, the heterologous peptide may be inserted in a loop between individual strands of the beta sheet of the beta barrel structure or beta barrel domain. For example, the heterologous peptide may be inserted in the βB-βC loop of the S protein, the βC'-βC" loop of the S protein or the βE-αB loop of the L protein. [0051] The present disclosure therefore relates to modified coat protein derived from Comoviruses such as CPMV, wherein the coat protein comprises a heterologous peptide insertion, in an exposed portion of the coat protein. For example, the modified coat protein may be derived from the large (L or VP37) coat protein or small (S or VP23) coat protein of CPMV. [0052] In one example, the large coat protein of CPMV may comprise in the βE-αB (betaE-alphaB) loop (also referred to as site 2) a heterologous peptide insertion. For example, the large coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1. [0053] In another example, the small coat protein may comprise in the βB-βC (betaB- betaC) loop (also referred to as site 1) a heterologous peptide insertion. For example, the small coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1. [0054] Furthermore the small coat protein may comprise in the βC’-βC” (betaC’- betaC”) loop (also referred to as site 4) a heterologous peptide insertion. For example, the small coat protein of CPMV may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1. [0055] The small and large coat protein may be produced as a polyprotein which is proteolytically processed in a host cell into the small and large coat protein. Typically, the polyprotein includes a cleavage site naturally recognized by a proteinase from the same or a closely related plant virus. However, the cleavage site may be from an unrelated virus or source, and a proteinase which is specific for that site may be used to cleave the polyprotein. The small and/or large coat proteins may self-assemble into protein suprastructures such as for example protein rosettes, capsomeres, nanoparticles, large protein complexes, and/or virus-like particles (VLPs). [0056] Accordingly, it is also described herewith is a modified polyprotein. The modified polyprotein may comprise: i) a modified small coat protein and a native (unmodified) large coat protein, ii) a native (unmodified) small coat protein and a modified large coat protein, or iii) a modified small coat protein and a modified large coat protein. [0057] The modified polyprotein may comprise from 80% to 100% identity or similarity with amino acids of SEQ ID NO: 2, 3, 4, 5, 6 or 7. Accordingly, modified polyprotein as described herewith included modified polyprotein with amino acid sequences that have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween, sequence identity, or sequence similarity, with the amino acid sequence of SEQ ID NO: 1, 2, 3, 4, 5, 6 or 7 and wherein modified polyprotein is expressed and processed in a host or host cell to form protein suprastructures such as for example VLP or nanoparticles. Modified polyprotein βE-αB (betaE-alphaB L protein) [0058] For example, the modified polyprotein may have a heterologous peptide insertion in the βE-αB ^(betaE-alphaB) loop of the large coat protein (also referred to as site “2”). For example, the modified polyprotein may comprise a heterologous peptide insertion between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1. In one example the modified polyprotein may have 80%-100% identity or similarity with the amino acids of SEQ ID NO: 2, 4, 6 or 7. Furthermore the modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 2, 4, 6 or 7. Modified polyprotein βB- βC (betaB-betaC) S protein) [0059] In another example, the modified polyprotein may have a heterologous peptide insertion in the βB- βC (betaB-betaC) loop of the small coat protein (also referred to as site “1”). For example, the modified polyprotein may comprise a heterologous peptide between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1. In one example the modified polyprotein may have 80%-100% identity or similarity with the amino acids of SEQ ID NO: 1. Furthermore the modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 1. Modified polyprotein βC’- βC” (betaC’-betaC’’) S protein) [0060] In another example, the modified polyprotein may have a heterologous peptide insertion in the βC’- βC” (betaC’-betaC”) loop of the small coat protein (also referred to as site “4”). For example, the modified polyprotein may comprise a heterologous peptide between amino acid residue corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1. In one example the modified polyprotein may have 80%- 100% identity or similarity with the amino acids of SEQ ID NO: 3 or 5. Furthermore the modified polyprotein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 3 or 5. [0061] The terms “percent similarity”, “sequence similarity”, “percent identity”, or “sequence identity”, when referring to a particular sequence, are used for example as set forth in the University of Wisconsin GCG software program, or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology, Ausubel et al., eds.1995 supplement). Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, using for example the algorithm of Smith & Waterman, (1981, Adv. Appl. Math.2:482), by the alignment algorithm of Needleman & Wunsch, (1970, J. Mol. Biol.48:443), by the search for similarity method of Pearson & Lipman, (1988, Proc. Natl. Acad. Sci. USA 85:2444), by computerized implementations of these algorithms (for example: GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.). [0062] An example of an algorithm suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al., (1977, Nuc. Acids Res.25:3389-3402) and Altschul et al., (1990, J. Mol. Biol.215:403-410), respectively. BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins of the disclosure. [0063] A nucleic acid sequence or nucleotide sequence referred to in the present disclosure, may be “substantially homologous”, “substantially similar” or “substantially identical” to a sequence, or a compliment of the sequence if the nucleic acid sequence or nucleotide sequence hybridise to one or more than one nucleotide sequence or a compliment of the nucleic acid sequence or nucleotide sequence as defined herein under stringent hybridisation conditions. Sequences are “substantially homologous” “substantially similar” “substantially identical” when at least about 70%, or between 70 to 100%, or any amount therebetween, for example 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100%, or any amount therebetween, of the nucleotides match over a defined length of the nucleotide sequence providing that such homologous sequences exhibit one or more than one of the properties of the sequence, or the encoded product as described herein. [0064] The modified polyprotein may be proteolytically processed in the host cell into small and large coat proteins, which may assemble into protein suprastructures such as for example virus-like particles (VLPs) or nanoparticles. [0065] Also provided are modified viral coat protein for example modified small coat proteins and modified large coat proteins. The modified viral coat protein may comprise a heterologous peptide insertion. For example, the modified coat protein may be a modified small coat protein comprising a heterologous peptide insertion or may be a modified large coat protein comprising a heterologous peptide. betaE-alphaB loop [0066] For example, the modified large coat protein may have a heterologous peptide insertion in the βE-αB (betaE-alphaB) loop. For example a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 8. In one example the modified large coat protein may have 80%-100% sequence identity or similarity with the amino acid sequence of SEQ ID NO: 9, 10, 11 or 51. Furthermore the modified large coat protein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 9, 10, 11 or 51. [0067] In another example, the modified small coat protein may have a heterologous peptide insertion such as an epitope in the βB- βC (betaB-betaC) loop. For example a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 22 and 23 of the sequence of SEQ ID NO: 12. [0068] In another example the modified small coat protein may have a heterologous peptide insertion such as an epitope in the βC'- βC’’ (betaC’-betaC”) loop. For example a heterologous peptide insertion may be inserted between amino acid residues corresponding to amino acid 44 and 45 of the sequence of SEQ ID NO: 12. [0069] In one example the modified small coat protein may have 80%-100% sequence identity or similarity with the amino acid sequence of SEQ ID NO: 13, 14 or 51. Furthermore the modified small coat protein may have about 80, 85, 87, 90, 91, 92, 9394, 95, 96, 97, 98, 99, 100% or any amount therebetween sequence identity, or sequence similarity, with the sequence of SEQ ID NO: 13, 14 or 51. Coronavirus Epitopes [0070] The heterologous peptide insertion (also referred to as heterologous peptide) may be heterologous to the plant virus coat protein. More specifically, the heterologous peptide insertion may be heterologous to the small coat protein of a plant virus and/or the heterologous peptide insertion may be heterologous to the large coat protein of a plant virus. Accordingly, the plant virus coat protein comprises a peptide insertion that is heterologous to the plant virus coat protein i.e. is not derived from the same virus as the plant virus coat protein. For example, the heterologous peptide insertion may be heterologous to the small coat protein of CPMV and/or the heterologous peptide insertion may be heterologous to the large coat protein of CPMV. [0071] In one example, the heterologous peptide insertion may comprise sequences derived from a Coronavirus protein, for example a coronavirus spike (S) protein. [0072] The heterologous peptide insertion may comprise or may consist of one or more than one epitope. For example the epitope may be a linear epitope or a sequential epitope, consisting of continuous residues of a protein sequence. In another example the epitope may be a conformational epitope. The heterologous peptide insertion may comprise or may consist of an epitope derived from coronavirus S protein, for example a linear epitope derived from coronavirus S protein or a conformational epitope derived from coronavirus S protein. [0073] The coronavirus S-protein may for example be derived from a Coronavirus, such as an Alphacoronavirus (Alpha-CoV), a Betacoronavirus (Beta-CoV), a Gammacoronavirus (Gamma-CoV) or a Deltacoronavirus (Delta-CoV). In a preferred embodiment, the Coronavirus is a Betacoronavirus (Beta-CoV). The Betacoronavirus may be a lineage A Betacoronavirus, such for example HCoV-OC43 or HCoV-HKU1, a lineage B Betacoronavirus, such for example SARS-CoV or SARS-CoV 2 or a lineage C Betacoronavirus such for example MERS-CoV. Furthermore, the coronavirus S-protein may be derived from an Alphacoronavirus such for example Human coronavirus 229E (HCoV-229E). [0074] For example the heterologous peptide insertion may comprise or may consist of an epitope from SARS-CoV-2 spike protein. The epitopes may be determined as for example described in Li et al.2020 (Cellular & Molecular Immunology volume 17, pages1095–1097(2020)), Yi et al.2020 (Emerging Microbes & Infections, 9:1, 1988-1996 (2020)), Shrock et al. (Science 29 Sep 2020), Poh et al. 2020 (Nat Commun 11, 2806 (2020), Nelde et al. (Nature Immunology 22, pages 74– 85 (2021)) which are hereby incorporated by reference. [0075] For example, the epitope may be derived from the S1 subunit of the coronavirus S protein. For example, the epitope may be derived from the C terminal domain (CTD) that immediately follows the Receptor Binding Domain (RBD) of the coronavirus S protein. For example, the epitope may be derived from the region between amino acids 553-564, 577-588, 595-612, 625-642 or 661-684 of the S1 subunit of the SARS-CoV-2 spike protein. The epitope might also be derived from a region of the S-protein that includes the fusion peptide (FP) (amino acids 788-806) or the S2’ cleavage site (amino acid R815). For example, the epitope may be derived from the region between amino acids 764-829 or 788-806 of the S2 subunit of the SARS-CoV-2 spike protein. In addition, the epitope may be derived from a region that connects the heptad repeat 1 (HR1) and heptad repeat 2 (HR2) on the S2 subunit of the SARS-CoV-2 spike protein. For example, the epitope may be derived from a region between amino acids 1148-1159 on the S2 subunit of the SARS-CoV-2 spike protein. Furthermore, the epitope may be derived from a region between amino acids 884–895 or amino acids 1256–1273 on the S2 subunit of the SARS-CoV-2 spike protein. [0076] For example, the SARS-CoV-2 epitope may have the following sequences: S14P5: TESNKKFLPFQQFGRDIA (SEQ ID NO: 15) S21P2: PSKPSKRSFIEDLLFNKV (SEQ ID NO: 16) [0077] Accordingly, it is also provided a modified small coat protein and/or a modified large coat protein wherein the modified small coat protein and/or the modified large coat protein comprises an epitope comprising the sequence of SEQ ID NO: 15, the sequence of SEQ ID NO: 16 or both the sequence of SEQ ID NO: 15 and SEQ ID NO: 16. As described above, the modified coat protein may assemble into VLP, comprising or consisting of the modified coat protein. [0002] The heterologous peptide insertion may be between 5 to 30 amino acids in length, or any amino acid length therebetween. For example the heterologous peptide insertion may be 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 amino acids in length or any amount therebetween. In a non- limiting example, the heterologous peptide insertion is 18 amino acids in length. In another non-limiting example, the heterologous peptide insertion is 20 amino acids in length. In another non-limiting example, the heterologous peptide insertion is 24 amino acids in length. Linker [0078] The heterologous peptide insertion or the one or more than one coat protein may further be modified to improve biochemical characteristics advantageous for formulation or immunogenic effect. For example, peptides with a high proportion of hydrophobic amino acids may negatively affect solubility in aqueous solutions. Accordingly, uncharged (Asn, Cys, Gly, Gln, Pro, Ser, Thr), acidic polar (Asp, Glu), or basic polar (His, Lys, Arg) residues may be added to a peptide insertion to improve solubility of the peptide and/or bring the pI of the peptide closer to the pH of the buffer or biological pH. [0079] Flexible linkers, rigid linkers, and/or in vivo cleavable linkers may also be added to link domains (for example the termini of the coat protein with the termini of the heterologous peptide insertion) together. The addition of linker or linker sequences may improve biological activity, increase expression yields, and/or increase desirable pharmacokinetic profiles. [0080] Therefore, the heterologous peptide insertion may comprise one or more than one linker or linker sequence. For example, the heterologous peptide insertion may comprise or may consist of one or more than one linker and an epitope. The linker or linker sequence may be fused to the epitope. For example the linker or linker sequence may be fused to the N-terminal end, the C terminal end or the N-terminal end and the C terminal end of the epitope. [0081] The term “linker” or “linker sequence” in the context of the disclosure concerns an amino acid sequence of from about 1 to about 10 or more amino acid residues positioned at the N-terminus, the C-terminus or the N-terminus and the C- terminus of the heterologous peptide insertion. Accordingly, the linker or linker sequence may have a length of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids. The one or more than one linker may be directly adjacent to or fused directly to the terminus or termini of the epitope. More specifically, the one or more than one linker may be fused directly to the N-terminus, the C-terminus or the N-terminus and the C-terminus of an epitope. For example the linker may be covalently linked to the amino acid residues in its vicinity. [0082] The modified coat protein or modified polyprotein (collectively referred to as mP) therefore may comprise a heterologous peptide comprising one or more than one linker (L) and an epitope (E) as follows: - N’-mP –L1- epitope- L2 –mP-C’ - N’-mP –L- epitope - mP-C’ - N’-mP – epitope - L- mP-C’ [0083] The one or more than one linker (L, L1 or L2) may have a length of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 or more amino acid residues. In an example, the one or more than one linker may be one or more than one aspartate residues (D). In another example the one or more than one linker may be glycine-serine-alanine (GSA). [0084] In a non-limiting example, the modified coat protein or modified polyprotein may comprise the following heterologous peptide insertions comprising an epitope and linker sequences: D-S14P5-D: DTESNKKFLPFQQFGRDIAD (SEQ ID NO: 17) D-S21P2-D: DPSKPSKRSFIEDLLFNKVD (SEQ ID NO: 18) GSA-S14P5-GSA: GSATESNKKFLPFQQFGRDIAGSA (SEQ ID NO: 19) GSA-S21P2-GSA: GSAPSKPSKRSFIEDLLFNKVGSA (SEQ ID NO: 20) [0085] As shown in Figure 1, when epitope S14P5 with an aspartate (D) linker (construct 8723) or without an aspartate (D) linker (construct 8721) were inserted in the βE-αB (betaE-alphaB) loop of the large coat protein, formation of the large coat protein with the S14P5 insertion was observed (as shown in the shift of molecular weight of the modified large coat protein). Similarly, when epitope S14P5 with a GSA linker (construct 8725) at each terminus or without a GSA linker (construct 8722) were inserted in the βC’- βC” (betaC’-betaC’’) loop (between residues D418 and D419) of the small coat protein, formation of the small coat protein with the S14P5 insertion was observed (as shown in the shift of molecular weight of the modified small coat protein). In contrast, when epitope S14P5 was inserted in the βB- βC (betaB-betaC) loop of the small coat protein (construct 8720), production of the small coat protein was only observed at 9 days post infection. When epitope S14P5 with a GSA linker at each terminus was inserted in the βB- βC (betaB-betaC) loop of the small coat protein (construct 8724), no polyprotein or processed coat proteins were detected. [0086] As shown in Figure 2, when epitope S21P2 with an aspartate (D) linker at both termini (construct 8729) was inserted in the βE-αB (betaE-alphaB) loop of the large coat protein, formation of the large coat protein with the S21P2 insertion was observed (as shown in the shift of molecular weight of the modified large coat protein). When epitope S21P2 was inserted in the βE-αB (betaE-alphaB) loop of the large coat protein without aspartate (D) linker sequences, weak bands representing the small coat protein were observed and there were no visible bands representing the large coat protein. Furthermore, when epitope S21P2 (without linker sequences or with GSA linker sequences at both termini) was inserted into the small coat protein (either the βB- βC (betaB-betaC) loop or the βC’- βC” (betaC’-betaC’’) loop of the small protein), no expression of either the small or the large coat protein was observed (see lanes of constructs 8726, 8728, 8730 and 8731 in Figure 2). [0087] In one example it is provided, a modified large coat protein comprises in the βE-αB (betaE-alphaB) loop, a heterologous peptide insertion comprising coronavirus epitope S14P5 wherein aspartate linkers are fused to the N-terminus and the C- terminus of the epitope. It is further provided a modified small coat protein comprising, between amino acid residues corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1, a heterologous peptide insertion comprising coronavirus epitope S14P5, wherein glycine-serine-alanine linkers (GSA) are fused to the N-terminus and the C-terminus of the epitope. It is also provided a modified large coat protein comprising in the βE-αB (betaE-alphaB) loop, a heterologous peptide insertion comprising coronavirus epitope S21P2 wherein aspartate (D) residues or linkers are added or fused to the N-terminus and the C-terminus of the epitope. [0088] Accordingly, the modified polyprotein may have an amino acid sequence that has 90%-100% sequence similarity or 90%-100% sequence identity to the sequence of SEQ ID NOs: 2, 3, 4, 5, 6, 7 or 30 or any amount there between. For example, the modified polyprotein may have 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100% sequence similarity or sequence identity to the sequence of SEQ ID NOs: 2, 3, 4, 5, 6, 7 or 30. [0089] Furthermore, the one or more than one modified coat protein may have an amino acid sequence that has 90%-100% sequence similarity or 90%-100% sequence identity to the sequence of SEQ ID NOs: 9, 10, 11, 13, 14, 51, 52 or any amount there between. For example the one or more than on modified coat protein may have 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100% sequence similarity or sequence identity to the sequence of SEQ ID NOs: 9, 10, 11, 13, 14, 51, 52. [0090] The present disclosure therefore provides a “modified coat protein”, “chimeric coat protein”, or “modified polyprotein”, “chimeric polyprotein”, “fusion protein”, “fusion polyprotein” wherein the coat protein or polyprotein has been modified to comprise a heterologous peptide insertion, wherein the heterologous peptide insertion comprises an epitope. The heterologous peptide insertion may further comprise one or more than one linker sequence. [0091] By “chimeric coat protein”, or “chimeric polyprotein”, also referred to as a “fusion protein” or “fusion polyprotein, it is meant a protein or polyprotein that comprises amino acid sequences originating from two or more than two biological or synthetic sources, for example but not limited to a coat protein from CPMV and a epitope that is derived from coronavirus. The chimeric protein or polyprotein may include a signal peptide that is native to CPMV or the signal peptide might be non- native or heterologous to CPMV. Protein Suprastructures [0092] The modified coat proteins may self-assemble into protein suprastructures such for example nanoparticles or nanofilaments. The nanoparticles may be for example protein rosettes, capsomeres, large protein complexes, inactivated virus, nanorods, nanospheres, and/or virus-like particles (VLPs). [0093] For example, the modified coat proteins may self-assemble into protein suprastructures such as capsomeres, rosettes or Virus-like particles (VLPs). The suprastructures such for example VLPs may also be referred to as CPMV nanoparticles or CPMV-based nanoparticles. [0094] As shown in Figure 3, VLPs of CPMV were purified using density gradients and detected upon SDS-PAGE of harvested gradient fractions. Modified large coat proteins comprising S14P5 in the βE-αB (betaE-alphaB) loop (construct 8721) were processed and assembled into VLPs as can be seen in iodixanol fractions 7-10 (see Figure 3A). Modified small coat proteins comprising S14P5 with GSA linkers at both termini inserted in the βC’- βC” (betaC’-betaC’’) loop (construct 8725) also formed VLPs (see Figure 3B). While no VLP formation was detected for modified large coat protein with S21P2 inserted into the βE-αB (betaE-alphaB) loop (Construct 8727, see Figure 3C), modified large coat proteins comprising S21P2 with aspartate (D) linker at both termini inserted in the βE-αB (betaE-alphaB) loop (construct 8729) were correctly processed and assembled into VLPs (see Figure 3D). [0095] Representative electron microscopy images of the VLPs are shown in Figure 4, which shows that VLPs that comprise an insertion (CPMV VP60-S21P2+DD-2, lower panel) have the same morphology as native CPMV VLPs with no insertion (upper panel). [0096] Therefore, another aspect the present disclosure relates to VLP comprising or consisting of one or more than one modified coat protein, for example a VLP comprising or consisting of i) a large coat protein comprising in the βE- ^B (betaE- alphaB) loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) a small coat protein comprising in the βB- βC (betaB- betaC) loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) a small coat protein comprising in the βC’- βC’’(betaC’-betaC’’) a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein. [0097] Virus-like particle" (VLP), or "virus-like particles" or "VLPs" refer to the spontaneous organization of coat proteins into the three-dimensional capsid structure of a particular virus for example icosahedral plant virus, for example Comoviruses such as cowpea mosaic virus (CPMV). VLPs are generally morphologically and antigenically similar to virions produced in an infection but lack genetic information sufficient to replicate and thus, are non-infectious. Since the VLPs do not contain viral nucleic acids (RNA or DNA) and the space inside the capsid is unoccupied, they may also be referred to as “empty” VLP (eVLP) or “empty” CPMV (eCPMV). While lacking the genetic material, VLPs retain key immunological characteristics of viruses including particulate structures; repetitive surfaces; and capability to induce innate immunity by activating molecular-pattern pathogen-associated recognition receptors. Like infectious viruses, these VLPs are in the 20-250 nm size range. For example, the CPMV VLP may have a size of approximately 30 nm. [0098] Accordingly, VLPs are structures that may self-assemble and comprise or consist of one or more structural proteins such as modified coat proteins, for example large and small coat proteins. For example, the VLP may comprise modified large coat protein and/or modified small protein. Furthermore, the VLP may comprise modified large coat protein and native (unmodified) small coat protein or the VLP may comprise native (unmodified) large coat protein and modified small coat protein. [0099] In one aspect, the VLP may comprise or consist of coat protein from cowpea mosaic virus (CPMV) and may be referred to as cowpea mosaic virus-like particle (CPMV VLP). The cowpea mosaic virus-like particle may be free of RNA and therefore may be referred to as “empty” cowpea mosaic virus-like particle or eCPMV. [00100] A method of producing virus like particle (VLP) comprising one or more than one modified coat protein as described herewith in a host or host cell is also provided. The method comprises the introduction of i) a first nucleic acid comprising a first regulatory region active in the host or host cell operatively linked to a first nucleotide sequence encoding a modified polyprotein into the host or host cell, and ii) a second nucleic acid comprising a second regulatory region active in the host or host cell operatively linked to a second nucleotide sequence encoding a protease. Followed by incubating the host or host cell under conditions that permit the expression of the nucleic acids, to produce the modified polyprotein and the protease, the modified polyprotein being processed by the protease into small coat protein and large coat protein, which assemble into VLP. For example, the host or host cell may be a plant or plant cell and the first and second nucleic acid may be inserted into the plant or plant cell by agroinfiltration. In one embodiment, the first and second nucleic acid are located on two different constructs (vectors) and the ratio between the first and second nucleic acid may be modulated as further described below. [00101] For example modified CPMV VLPs are produced in a host or host cell, by co- expressing a nucleic acid (a first nucleic acid) encoding a modified CPMV polyprotein or CPMV coat protein precursor (VP60) comprising the small coat protein and the large coat protein of CPMV, with a second nucleic acid encoding CPMV protease (24K). The CPMV protease processes the polyprotein into the small coat protein and the large coat protein, which may assemble into viral capsids or virus-like particles (VLPs). [00102] The level of protein yield and/or VLP accumulation in the host or host cell may be influenced by the ratio of the polyprotein-containing Agrobacterium, to protease-containing Agrobacterium infiltrated into the host or host. The ratio of the polyprotein-containing to protease-containing Agrobacterium may range for example from about 20:1 to about 0.5:1 (polyprotein:protease), or any amount therebetween, for example from about 20:1, 18:1, 16:1, 14:1, 12:1, 10:1, 9:1, 8:1, 7:1, 6:1, 5:1, 4:1, 3:1, 2:1, 1:1, 0.5:1 (polyprotein:protease), or any amount therebetween. In a preferred embodiment the ratio between polyprotein to protease is 2:1. In another embodiment, the ratio of the polyprotein-containing to protease-containing Agrobacterium may range for example from about 1:2 to 1:20 (polyprotein:protease), or any amount therebetween, for example 1:2, 1:4, 1:6, 1:8, 1:10, 1:12, 1:14, 1:16, 1:18, 1:20 (polyprotein:protease), or any amount therebetween. [00103] The ratio of polyprotein to protease may be varied for example by introducing different ratios of Agrobacterium containing the first nucleic acid (encoding a modified polyprotein) to Agrobacterium containing the second nucleic acid (encoding a protease) into the host or host cell. Alternatively, if the polyprotein and protease are present on the same construct, and therefore are introduced into the same Agrobacterium, they may be differentially expressed within the host or host cell using suitable promoters so that the desired ratio of polyprotein to protease is obtained. Expression may be varied by modulating for example replication, transcription, translation, or a combination thereof, of the polyprotein, the protease, or both the protein and the protease. For example, different regulatory elements, including promoters, amplification elements, enhancers or a combination thereof, may be used in addition to varying the ratio of the polyprotein-containing Agrobacterium to protease-containing Agrobacterium infiltrated as described above. Different regulatory elements, amplification elements and enhancers effect expressions of a protein at different levels e.g. some regulatory elements, amplification elements and enhancers will result in higher expression of a protein than others. By using regulatory elements, amplification elements and enhancers with variant expression strength for the polyprotein, the protease, or both the protein and the protease, the expression of the polyprotein, the protease, or both the protein and the protease may be modulated. For example the expression may be modulated by expressing the polyprotein and/or protease with the help of an expression enhancer for example a plant-derived expression enhancer as described below. [00104] The VLPs may be purified or extracted using any suitable method for example chemical or biochemical extraction. VLPs are relatively sensitive to desiccation, heat, pH, surfactants and detergents. Therefore it may be useful to use methods that maximize yields, minimize contamination of the VLP fraction with cellular proteins, maintain the integrity of the proteins, or VLPs, and, where required, the associated lipid envelope or membrane, methods of loosening the cell wall to release the proteins, or VLP. Minimizing or eliminating the use of detergents or surfactants such for example SDS or TritonTM X-100 may be beneficial for improving the yield of VLP extraction. VLPs may be then assessed for structure and size by, for example, density gradient (see for example Figure 3) electron microscopy (see for example Figure 4) or by size exclusion chromatography. [00105] The size (i.e. the diameter) of the above-defined VLPs, may be measured for example by dynamic light scattering (DLS) or electron microscope (EM) techniques, is usually between 20 to 50 nm, or any size therebetween. For example, the size of the intact VLP structure may range from about 25 nm to about 35 nm, or any size therebetween, or from 20nm, 21nm, 22nm, 23nm, 24nm, 25nm, 26nm, 27 nm, 28nm, 29nm, 30nm, 31nm, 32nm, 33nm, 34nm, 35nm, or any size therebetween. [00106] Furthermore, the small and/or large coat proteins may self-assemble into capsomeres. The term “capsomere” refers to a morphological unit of the capsid of a virus. A “capsomere” may comprise monomeric or oligomeric viral structural proteins. For example the capsomere may comprise one or more than one modified coat protein as described herewith. Without wishing to be bound by theory it is believed that small coat protein may self-assemble into pentameric capsomeres. Capsomeres may self-assemble into virus-like particle (VLP) or nanoparticles. Accordingly, it is further provided a capsomere or capsomere composition, the capsomere or capsomere composition may comprise or may consist of one or more than one modified coat protein. The one or more than one modified coat protein may be a modified small coat protein, a modified large coat protein or may be a modified small coat protein and a modified large coat protein. Genetic Constructs and regulators [00107] Further provided are genetic constructs that comprise nucleic acids comprising nucleotide sequences encoding the modified coat proteins or modified polyproteins as described herewith. [00108] The term “construct”, “vector” or “expression vector”, as used herein, refers to a recombinant nucleic acid for transferring exogenous nucleic acid sequences into host cells (e.g. plant cells) and directing expression of the exogenous nucleic acid sequences in the host cells. “Expression cassette” refers to a nucleotide sequence comprising a nucleic acid of interest under the control of, and operably (or operatively) linked to, an appropriate promoter or other regulatory elements for transcription of the nucleic acid of interest in a host cell. As one of skill in the art would appreciate, the expression cassette may comprise a termination (terminator) sequence that is any sequence that is active the plant host. For example, the termination sequence may be derived from the RNA-2 genome segment of a bipartite RNA virus, e.g. a comovirus, the termination sequence may be a NOS terminator, or terminator sequence may be obtained from the 3’UTR of the alfalfa plastocyanin gene. [00109] By “regulatory region” “regulatory element” or “promoter” it is meant a portion of nucleic acid typically, but not always, upstream of the protein coding region of a gene, which may be comprised of either DNA or RNA, or both DNA and RNA. When a regulatory region is active, and in operative association, or operatively linked, with a nucleotide sequence of interest, this may result in expression of the nucleotide sequence of interest. A regulatory element may be capable of mediating organ specificity, or controlling developmental or temporal gene activation. A “regulatory region” includes promoter elements, core promoter elements exhibiting a basal promoter activity, elements that are inducible in response to an external stimulus, elements that mediate promoter activity such as negative regulatory elements or transcriptional enhancers. “Regulatory region”, as used herein, also includes elements that are active following transcription, for example, regulatory elements that modulate gene expression such as translational and transcriptional enhancers, translational and transcriptional repressors, upstream activating sequences, and mRNA instability determinants. Several of these latter elements may be located proximal to the coding region. [00110] There are several types of regulatory regions, including those that are developmentally regulated, inducible or constitutive. A regulatory region that is developmentally regulated, or controls the differential expression of a gene under its control, is activated within certain organs or tissues of an organ at specific times during the development of that organ or tissue. However, some regulatory regions that are developmentally regulated may preferentially be active within certain organs or tissues at specific developmental stages, they may also be active in a developmentally regulated manner, or at a basal level in other organs or tissues within the plant as well. Examples of tissue-specific regulatory regions, for example see- specific a regulatory region, include the napin promoter, and the cruciferin promoter (Rask et al., 1998, J. Plant Physiol.152: 595-599; Bilodeau et al., 1994, Plant Cell 14: 125-130). An example of a leaf-specific promoter includes the plastocyanin promoter (see US 7,125,978, which is incorporated herein by reference). [00111] An inducible regulatory region is one that is capable of directly or indirectly activating transcription of one or more DNA sequences or genes in response to an inducer. In the absence of an inducer the DNA sequences or genes will not be transcribed. Typically, the protein factor that binds specifically to an inducible regulatory region to activate transcription may be present in an inactive form, which is then directly or indirectly converted to the active form by the inducer. However, the protein factor may also be absent. The inducer can be a chemical agent such as a protein, metabolite, growth regulator, herbicide or phenolic compound or a physiological stress imposed directly by heat, cold, salt, or toxic elements or indirectly through the action of a pathogen or disease agent such as a virus. A plant cell containing an inducible regulatory region may be exposed to an inducer by externally applying the inducer to the cell or plant such as by spraying, watering, heating or similar methods. Inducible regulatory elements may be derived from either plant or non-plant genes (e.g. Gatz, C. and Lenk, I.R.P., 1998, Trends Plant Sci.3, 352-358). Examples of potential inducible promoters include, but not limited to, tetracycline- inducible promoter (Gatz, C.,1997, Ann. Rev. Plant Physiol. Plant Mol. Biol.48, 89- 108), steroid inducible promoter (Aoyama, T. and Chua, N.H.,1997, Plant J.2, 397- 404) and ethanol-inducible promoter (Salter, M.G., et al, 1998, Plant Journal 16, 127- 132; Caddick, M.X., et al,1998, Nature Biotech.16, 177-180) cytokinin inducible IB6 and CKI1 genes (Brandstatter, I. and Kieber, J.J.,1998, Plant Cell 10, 1009-1019; Kakimoto, T., 1996, Science 274, 982-985) and the auxin inducible element, DR5 (Ulmasov, T., et al., 1997, Plant Cell 9, 1963-1971). [00112] A constitutive regulatory region directs the expression of a gene throughout the various parts of a plant and continuously throughout plant development. Examples of known constitutive regulatory elements include promoters associated with the CaMV 35S transcript. (p35S; Odell et al., 1985, Nature, 313: 810-812; which is incorporated herein by reference), the rice actin 1 (Zhang et al, 1991, Plant Cell, 3: 1155-1165), actin 2 (An et al., 1996, Plant J., 10: 107-121), or tms 2 (U.S. 5,428,147), and triosephosphate isomerase 1 (Xu et. al., 1994, Plant Physiol.106: 459-467) genes, the maize ubiquitin 1 gene (Cornejo et al, 1993, Plant Mol. Biol.29: 637-646), the Arabidopsis ubiquitin 1 and 6 genes (Holtorf et al, 1995, Plant Mol. Biol.29: 637-646), the tobacco translational initiation factor 4A gene (Mandel et al, 1995 Plant Mol. Biol.29: 995-1004), the Cassava Vein Mosaic Virus promoter, pCAS, (Verdaguer et al., 1996); the promoter of the small subunit of ribulose biphosphate carboxylase, pRbcS: (Outchkourov et al., 2003), the pUbi (for monocots and dicots ). [00113] The term "constitutive" as used herein does not necessarily indicate that a nucleotide sequence under control of the constitutive regulatory region is expressed at the same level in all cell types, but that the sequence is expressed in a wide range of cell types even though variation in abundance is often observed. [00114] Accordingly, the genetic constructs of the present disclosure may also include enhancers, either translation or transcription enhancers, as may be required. Enhancers may be located 5' or 3' to the sequence being transcribed. Enhancer regions are well known to persons skilled in the art, and may include an ATG initiation codon, adjacent sequences or the like. The initiation codon, if present, may be in phase with the reading frame ("in frame") of the coding sequence to provide for correct translation of the transcribed sequence. Accordingly, the nucleic acid comprising a nucleotide sequence encoding a modified coat protein or modified polyprotein, as described herein may further comprise sequences that enhance expression of the modified coat protein or modified polyprotein in the host, portion of the host or host cell. Sequences that enhance expression may include, a 5’ UTR enhancer element, or a plant-derived expression enhancer, in operative association with the nucleic acid encoding the modified coat protein or modified polyprotein. The sequence encoding the modified coat protein or modified polyprotein may also be optimized to increase expression by, for example, optimizing for human codon usage, increased GC content, or a combination thereof. [00115] The term “plant-derived expression enhancer”, as used herein, refers to a nucleotide sequence obtained from a plant, the nucleotide sequence encoding a 5'UTR. Examples of a plant derived expression enhancer are described in International Application No. PCT/CA2019/050317 and International Application No. PCT/CA2019/050319 (Filed March 14, 2019); which are incorporated herein by reference) or in Diamos A.G. et al. (2016, Front Plt Sci.7:1-15; which is incorporated herein by reference). The plant-derived expression enhancer may be selected from nbEPI42, nbSNS46, nbCSY65, nbHEL40, nbSEP44, nbMT78, nbATL75, nbDJ46, nbCHP79, nbEN42, atHSP69, atGRP62, atPK65, atRP46, nb30S72, nbGT61, nbPV55, nbPPI43, nbPM64 and nbH2A86 as described in International Application No. PCT/CA2019/050317 and PCT/CA2019/050319. The plant derived expression enhancer may be used within a plant expression system comprising a regulatory region that is operatively linked with the plant-derived expression enhancer sequence and a nucleotide sequence of interest, for example a nucleotide sequence encoding modified coat proteins or modified polyprotein. [00116] Stability and/or translation efficiency of an RNA may further be improved by the inclusion of a 3' untranslated region (3’UTR). The one or more genetic constructs of the present description may therefore further comprise a 3’ UTR. [00117] A 3’ untranslated region may contain a polyadenylation signal and any other regulatory signals capable of effecting mRNA processing, mRNA stability or gene expression. The polyadenylation signal is usually characterized by effecting the addition of polyadenylic acid tracks to the 3’ end of the mRNA precursor. Polyadenylation signals are commonly recognized by the presence of homology to the canonical form 5’ AATAAA-3’ although variations are not uncommon. Non-limiting examples of suitable 3’ regions are the 3’ transcribed non-translated regions containing a polyadenylation signal of Agrobacterium tumor inducing (Ti) plasmid genes, such as the nopaline synthase (Nos gene) and plant genes such as the soybean storage protein genes, the small subunit of the ribulose-1, 5-bisphosphate carboxylase gene (ssRUBISCO; US 4,962,028; which is incorporated herein by reference), the promoter used in regulating plastocyanin expression, described in US 7,125,978 (which is incorporated herein by reference), 3’ UTR derived from a Arracacha virus B isolate gene (AvB) (SEQ ID NO: 40), 3’UTR derived from Beet necrotic yellow vein virus (trBNYVV) (SEQ ID NO: 41), 3’UTR derived from Southern bean mosaic virus (SBMV) (SEQ ID NO: 42), 3’UTR derived from Turnip ringspot virus (TuRSV) (SEQ ID NO: 43), 3’ UTR derived from Cowpea Mosaic Virus (CPMV) (SEQ ID NO: 44), 3’UTR derived from Broad bean true mosaic virus (BBTMV) (SEQ ID NO: 45) or 3’UTR derived from Ourmia melon virus (trOUMV) (SEQ ID NO: 46). The 3’UTR might be used in conjunction with 5’UTR derived from heterologous sequences to modulate expression levels. [00118] Signal peptides or peptide sequences for directing localization of an expressed protein or polypeptide to the apoplast include, but are not limited to, a native (with respect to the protein) signal or leader sequence, or a heterologous signal sequence, for example but not limited to, a rice amylase signal peptide (McCormick 1999, Proc Natl Acad Sci USA 96:703-708), a protein disulfide isomerase signal peptide (PDI). Therefore, as described herein, the modified S protein may further comprise a heterologous amino acid signal peptide sequence. For example, the S protein may comprise the signal peptide from Protein disulphide isomerase (PDI SP; nucleotides 32-103 of Accession No. Z11499). [00119] The present disclosure therefore provides for a modified coat protein or modified polyprotein comprising a native, or a non-native signal peptide, and nucleic acids encoding such protein. [00120] The one or more than one modified genetic constructs of the present description may be expressed in any suitable host or host cell that is transformed by the nucleic acids, or nucleotide sequence, or constructs, or vectors of the present disclosure. The host or host cell may be from any source including plants, fungi, bacteria, insect and animals for example mammals. Therefore, the host or host cell may be selected from a plant or plant cell, fungi or a fungal cell, bacteria or bacterial cell, an insect or an insect cell, and animal or an animal cell. The mammal or animal may not be a human. In a preferred embodiment the host or host cell is a plant, portion of a plant or plant cell. [00121] The term “plant”, “portion of a plant”, “plant portion’, “plant matter”, “plant biomass”, “plant material”, plant extract”, or “plant leaves”, as used herein, may comprise an entire plant, tissue, cells, or any fraction thereof, intracellular plant components, extracellular plant components, liquid or solid extracts of plants, or a combination thereof, that are capable of providing the transcriptional, translational, and post-translational machinery for expression of one or more than one nucleic acids described herein, and/or from which an expressed protein or VLP may be extracted and purified. Plants may include, but are not limited to, herbaceous plants. The herbaceous plants may be annuals, biennials or perennials plants. Plants may further include, but are not limited to agricultural crops including for example canola, lettuce (Lactuca sativa), Brassica spp., maize, Nicotiana spp., (tobacco) for example, Nicotiana benthamiana, Nicotiana rustica, Nicotiana, tabacum, Nicotiana alata, Arabidopsis thaliana, alfalfa, potato, sweet potato (Ipomoea batatus), ginseng, pea, oat, rice, soybean, wheat, barley, sunflower, cotton, corn, rye (Secale cereale), sorghum (Sorghum bicolor, Sorghum vulgare), safflower (Carthamus tinctorius). [00122] The term “plant portion”, as used herein, refers to any part of the plant including but not limited to leaves, stem, root, flowers, fruits, a plant cell obtained from leaves, stem, root, flowers, fruits, a plant extract obtained from leaves, stem, root, flowers, fruits, or a combination thereof. In one embodiment the plant portion refers to the areal portion of a plant such as for example leaves, stem, flowers and fruits. The term “plant extract”, as used herein, refers to a plant-derived product that is obtained following treating a plant, a portion of a plant, a plant cell, or a combination thereof, physically (for example by freezing followed by extraction in a suitable buffer), mechanically (for example by grinding or homogenizing the plant or portion of the plant followed by extraction in a suitable buffer), enzymatically (for example using cell wall degrading enzymes), chemically (for example using one or more chelators or buffers), or a combination thereof. A plant extract may be further processed to remove undesired plant components for example cell wall debris. A plant extract may be obtained to assist in the recovery of one or more components from the plant, portion of the plant or plant cell, for example a protein (including protein complexes, polyproteins, protein suprastructures and/or VLPs), a nucleic acid, a lipid, a carbohydrate, or a combination thereof from the plant, portion of the plant, or plant cell. If the plant extract comprises proteins, then it may be referred to as a protein extract. A protein extract may be a crude plant extract, a partially purified plant or protein extract, or a purified product, that comprises one or more proteins, protein complexes such for example protein trimers, protein suprastructures, and/or VLPs, from the plant tissue. If desired a protein extract, or a plant extract, may be partially purified using techniques known to one of skill in the art, for example, the extract may be subjected to salt or pH precipitation, centrifugation, density gradient centrifugation, filtration, chromatography, for example, size exclusion chromatography, ion exchange chromatography, affinity chromatography, or a combination thereof. A protein extract may also be purified, using techniques that are known to one of skill in the art. [00123] The constructs of the present disclosure can be introduced into plant cells using Ti plasmids, Ri plasmids, plant virus vectors, direct DNA transformation, micro-injection, electroporation, etc. For reviews of such techniques, see for example Weissbach and Weissbach, Methods for Plant Molecular Biology, Academy Press, New York VIII, pp.421-463 (1988); Geierson and Corey, Plant Molecular Biology, 2d Ed. (1988); and Miki and Iyer, Fundamentals of Gene Transfer in Plants. In Plant Metabolism, 2d Ed. DT. Dennis, DH Turpin, DD Lefebvre, DB Layzell (eds), Addison Wesly, Langmans Ltd. London, pp.561-579 (1997). Other methods include direct DNA uptake, the use of liposomes, electroporation, for example using protoplasts, micro-injection, microprojectiles or whiskers, and vacuum infiltration. See, for example, Bilang, et al. (Gene 100: 247-250 (1991), Scheid et al. (Mol. Gen. Genet. 228: 104-112, 1991), Guerche et al. (Plant Science 52: 111-116, 1987), Neuhause et al. (Theor. Appl Genet.75: 30-36, 1987), Klein et al., Nature 327: 70-73 (1987); Howell et al. (Science 208: 1265, 1980), Horsch et al. (Science 227: 1229-1231, 1985), DeBlock et al., Plant Physiology 91: 694-701, 1989), Methods for Plant Molecular Biology (Weissbach and Weissbach, eds., Academic Press Inc., 1988), Methods in Plant Molecular Biology (Schuler and Zielinski, eds., Academic Press Inc., 1989), Liu and Lomonossoff (J Virol Meth, 105:343-348, 2002,), U.S. Pat. Nos. 4,945,050; 5,036,006; and 5,100,792, U.S. patent application Ser. Nos.08/438,666, filed May 10, 1995, and 07/951,715, filed Sep.25, 1992, (all of which are hereby incorporated by reference). [00124] As described below, transient expression methods may be used to express the constructs of the present disclosure (see Liu and Lomonossoff, 2002, Journal of Virological Methods, 105:343-348; which is incorporated herein by reference). Alternatively, a vacuum-based transient expression method, as described by Kapila et al., 1997, which is incorporated herein by reference) may be used. These methods may include, for example, but are not limited to, a method of Agro- inoculation or Agroinfiltration, syringe infiltration, however, other transient methods may also be used as noted above. With Agro-inoculation, Agroinfiltration, or syringe infiltration, a mixture of Agrobacteria comprising the desired nucleic acid enter the intercellular spaces of a tissue, for example the leaves, aerial portion of the plant (including stem, leaves and flower), other portion of the plant (stem, root, flower), or the whole plant. After crossing the epidermis, the Agrobacteria infect and transfer t- DNA copies into the cells. The t-DNA is episomally transcribed and the mRNA translated, leading to the production of the protein of interest in infected cells, however, the passage of t-DNA inside the nucleus is transient. [00125] To aid in identification of transformed plant cells, the constructs of this disclosure may be further manipulated to include plant selectable markers. Useful selectable markers include enzymes that provide for resistance to chemicals such as an antibiotic for example, gentamycin, hygromycin, kanamycin, or herbicides such as phosphinothrycin, glyphosate, chlorosulfuron, and the like. Similarly, enzymes providing for production of a compound identifiable by colour change such as GUS (beta-glucuronidase), or luminescence, such as luciferase or GFP, may be used. [00126] Also considered part of this disclosure are transgenic plants, plant cells or seeds containing the gene construct of the present disclosure that may be used as a platform plant suitable for transient protein expression described herein. Methods of regenerating whole plants from plant cells are also known in the art (for example see Guerineau and Mullineaux (1993, Plant transformation and expression vectors. In: Plant Molecular Biology Labfax (Croy RRD ed) Oxford, BIOS Scientific Publishers, pp 121-148). In general, transformed plant cells are cultured in an appropriate medium, which may contain selective agents such as antibiotics, where selectable markers are used to facilitate identification of transformed plant cells. Once callus forms, shoot formation can be encouraged by employing the appropriate plant hormones in accordance with known methods and the shoots transferred to rooting medium for regeneration of plants. The plants may then be used to establish repetitive generations, either from seeds or using vegetative propagation techniques. Transgenic plants can also be generated without using tissue culture. Methods for stable transformation, and regeneration of these organisms are established in the art and known to one of skill in the art. Available techniques are reviewed in Vasil et al. (Cell Culture and Somatic Cell Genetics of Plants, Vol. I, Il and III, Laboratory Procedures and Their Applications, Academic Press, 1984), and Weissbach and Weissbach (Methods for Plant Molecular Biology, Academic Press, 1989). The method of obtaining transformed and regenerated plants is not critical to the present disclosure. [00127] When plants, plant portions or plant cells are to be transformed or co- transformed concomitantly or simultaneously by two or more nucleic acid constructs, the nucleic acid construct may be introduced into the Agrobacterium in a single transfection event so that the nucleic acids are pooled, and the bacterial cells transfected. Alternatively, the constructs may be introduced serially, in series or sequentially. In this case, a first construct is introduced into the Agrobacterium as described, the cells are grown under selective conditions (e.g. in the presence of an antibiotic) where only the singly-transformed bacteria can grow. Following this first selection step, a second nucleic acid construct is introduced into the Agrobacterium as described, and the cells are grown under double-selective conditions, where only the doubly-transformed bacteria can grow. The double-transformed bacteria may then be used to transform a plant, portion of the plant or plant cell as described herein, or may be subjected to a further transformation step to accommodate a third nucleic acid construct. [00128] Alternatively, if plants, plant portions, or plant cells are to be transformed or co-transformed by two or more nucleic acid constructs, the nucleic acid construct may be introduced into the plant by co-infiltrating a mixture of Agrobacterium cells with the plant, plant portion, or plant cell, each Agrobacterium cell may comprise one or more constructs to be introduced within the plant. In order to vary the relative expression levels within the plant, plant portion or plant cell, of a nucleotide sequence of interest within a construct, during the step of infiltration, the concentration of the various Agrobacteria populations comprising the desired constructs may be modulated. [00129] The modified viral surface protein or VLP comprising modified viral surface protein as described herewith, may be used to elicit an immune response in a subject. [00130] An “immune response” generally refers to a response of the adaptive immune system of a subject. The adaptive immune system generally comprises a humoral response, and a cell-mediated response. A humoral response is the aspect of immunity that is mediated by secreted antibodies, produced in the cells of the B- lymphocyte lineage (B cell). Secreted antibodies bind to antigens on the surfaces of invading microbes (such as viruses or bacteria), which flags them for destruction. Humoral immunity is used generally to refer to antibody production and the processes that accompany it, as well as the effector functions of antibodies, including Th2 cell activation and cytokine production, memory cell generation, opsonin promotion of phagocytosis, pathogen elimination and the like. The terms “modulate” or “modulation” or the like refer to an increase or decrease in a particular response or parameter, as determined by any of several assays generally known or used, some of which are exemplified herein. [00131] A cell-mediated response is an immune response that involves the activation of macrophages, natural killer cells (NK), antigen-specific cytotoxic T- lymphocytes, and the release of various cytokines in response to an antigen. Cell- mediated immunity is used generally to refer to some Th cell activation, Tc cell activation and T-cell mediated responses. Cell-mediated immunity may be of particular importance in responding to viral infections. [00132] For example, the induction of antigen specific CD8 positive T lymphocytes may be measured using an ELISPOT assay; stimulation of CD4 positive T- lymphocytes may be measured using a proliferation assay. Anti-Coronavirus antibody titers may be quantified using an ELISA assay; isotypes of antigen-specific or cross- reactive antibodies may also be measured using anti-isotype antibodies (e.g. anti -IgG, IgA, IgE or IgM). Methods and techniques for performing such assays are well-known in the art. [00133] Cytokine presence or levels may also be quantified. For example, a T-helper cell response (Th1/Th2) will be characterized by the measurement of IFN- ^ and IL-4 secreting cells using by ELISA (e.g. BD Biosciences OptEIA kits). Peripheral blood mononuclear cells (PBMC) or splenocytes obtained from a subject may be cultured, and the supernatant analyzed. T- lymphocytes may also be quantified by fluorescence-activated cell sorting (FACS), using marker specific fluorescent labels and methods as are known in the art. [00134] The term “epitope” or “epitopes”, as used herein, refers to a part of an antigen to which an antibody specifically binds. The epitope may be a linear epitope or the epitope may be a conformational epitope. Linear epitopes refer to parts or sequences that are unstructured/linear. Conformational epitopes refer to structured parts of an antigen to which an antibody specifically binds. [00135] A method of producing an antibody or antibody fragment is provided, the method comprises administering the antigenic sequence, modified viral structural protein, a trimer or trimeric modified viral structural protein or VLP comprising the modified viral structural protein as described herewith to a subject, or a host animal, thereby producing the antibody or the antibody fragment. Antibodies or the antibody fragments produced by the method are also provided. [00136] The present disclosure therefore also provides the use of a viral structural protein or VLP comprising the modified viral structural protein, as described herein, for inducing immunity to a Coronavirus infection in a subject. Also disclosed herein is an antibody or antibody fragment, prepared by administering one or more than one modified coat protein or VLP comprising one or more than one modified coat protein, to a subject or a host animal. [00137] Further provided is a composition comprising an effective dose of one or more than one modified coat protein or VLP comprising one or more than one modified coat protein, as described herein, and a pharmaceutically acceptable carrier, adjuvant, vehicle, or excipient, for inducing an immune response in a subject. Also provided is a vaccine for inducing an immune response again Coronavirus in a subject, wherein the vaccine comprises an effective dose of one or more than one modified coat protein or VLP comprising one or more than one modified coat protein. [00138] Adjuvant systems to enhance a subject’s immune response to a vaccine antigen are well known and may be used in conjunction with the vaccine or pharmaceutical composition as described herewith. There are many types of adjuvants that may be used. The most common adjuvants for human use are aluminum hydroxide, aluminum phosphate and calcium phosphate. There are also a number of adjuvants based on oil emulsions (oil in water or water in oil emulsions such as Freund's incomplete adjuvant (FIA), Montanide™, Adjuvant 65, and Lipovant™), products from bacterial (or their synthetic derivatives), endotoxins, fatty acids, paraffinic, or vegetable oils, cholesterols, and aliphatic amines or natural organic compounds such for example squalene and saponin-based adjuvants. Non-limiting adjuvants that might be used include for example oil-in water emulsions of squalene oil (for example MF-59 or AS-03), adjuvant composed of the synthetic TLR4 agonist glucopyranosyl lipid A (GLA) integrated into stable emulsion (SE) (GLA-SE) or CpG 1018 a toll-like receptor (TLR9) agonist adjuvant. [00139] The formulation, vaccine or pharmaceutical composition may be administered to a subject orally, intradermally, intranasally, intramuscularly, intraperitoneally, intravenously, or subcutaneously. [00140] Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions. Suitable excipients are, for example, water, saline, dextrose, mannitol, lactose, lecithin, albumin, sodium glutamate, cysteine hydrochloride, and the like. In addition, if desired, the injectable pharmaceutical compositions may contain minor amounts of nontoxic auxiliary substances, such as wetting agents, pH buffering agents, and the like. Physiologically compatible buffers include, but are not limited to, Hanks's solution, Ringer's solution, or physiological saline buffer. If desired, absorption enhancing preparations (for example, liposomes), may be utilized. [00141] The composition or vaccine may be administered to a subject once (single dose). Furthermore, the vaccine or composition may be administered to a subject multiple times (multi-dose). Therefore, the composition, formulation, or vaccine may be administered to a subject in a single dose to illicit an immune response or the composition, formulation, or vaccine may be administered multiple time (multi dosages). For example, a dose of the composition or vaccine may be administered 2, 3, 4 or 5 times. Accordingly, the composition or vaccine may be administered to a subject in an initial dose and one or more than one doses may subsequently be administered to the subject. Administration of the doses may be separated in time from each other. For example, after the administration of an initial dose, one or more than one subsequent dose may be administered 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months or 6 months or any time in between from the administration of the initial dose. Furthermore, the composition or vaccine may be administered annually. For example, the composition or vaccine may be administered as a seasonal vaccine. [00142] The disclosure further provides the following sequences. Table 1. SEQ ID NO: and Description of Sequences
Figure imgf000044_0001
Figure imgf000045_0001
[00143] The present invention will be further illustrated in the following examples. Examples Example 1: Preparation of Coat Protein Constructs [00144] The present invention will be further illustrated in the following examples. The modified coat protein constructs were produced using techniques well known within the art. For example, modified coat protein displaying epitope S14P4 (constructs 8720-8725) and modified coat protein displaying epitope S21P2 (constructs 8726-8731) were cloned as described below. Constructs encoding native coat protein and 24K protease [00145] A sequence encoding VP60 was cloned into 2X35S(+C)/nbMT78/AvB/NOS expression system using the following PCR-based method. A fragment containing the VP60 coding sequence was amplified using primers IF(nbMT78)-CPMV(SB).c (SEQ ID NO: X26) and IF(AVb)-CPMV(SB).r (SEQ ID NO: 27), using VP60 gene sequence (SEQ ID NO: 28) as template. The PCR product was cloned into 2X35S(+C)/nbMT78/AvB/NOS expression systems using In- Fusion cloning system (Clontech, Mountain View, CA). Construct number 7140 (Figure 6A) was digested with AatII and StuI restriction enzymes and the linearized plasmid was used for the In-Fusion assembly reaction. Construct number 7140 is an acceptor plasmid intended for “In Fusion” cloning of genes of interest in a 2X35S(+C)/nbMT78/AvB/NOS-based expression cassette. This acceptor plasmid also incorporates a gene construct for the co-expression of the TBSV P19 suppressor of silencing under the alfalfa Plastocyanin gene promoter and terminator. The backbone is a pCAMBIA binary plasmid and the sequence from left to right t-DNA borders is presented in SEQ ID NO: 31. The resulting construct was given number 7384 (SEQ ID NO: 32). The amino acid sequence of VP60 is presented in SEQ ID NO: 1. A representation of plasmid 7384 is presented in Figure 6B. Construct 7387 was cloned using the same methodology and a summary of primers, templates, accepting vectors and products is provided in Table 2. Constructs encoding modified coat protein displaying epitope S14P4 (constructs 8720-8725) or epitope S21P2 (constructs 8726-8731) [00146] A sequence encoding VP60 was cloned into 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm expression system using the following PCR-based method. A fragment containing the VP60 coding sequence was amplified using primers IF(nbMT78)-CPMV(SB).c (SEQ ID NO: 26) and IF(AVb)- CPMV(SB).r (SEQ ID NO: 27), using VP60 gene sequence (SEQ ID NO: 29) as template. The PCR product was cloned into 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm expression systems using In-Fusion cloning system (Clontech, Mountain View, CA). Construct number 7142 (Figure 6D) was digested with AatII and StuI restriction enzymes and the linearized plasmid was used for the In-Fusion assembly reaction. Construct number 7142 is an acceptor plasmid intended for “In Fusion” cloning of genes of interest in a 2X35S(+C)/nbMT78/AvB/NOS/RB7 MARm-based expression cassette. This acceptor plasmid also incorporates a gene construct for the co-expression of the TBSV P19 suppressor of silencing under the alfalfa Plastocyanin gene promoter and terminator. The backbone is a pCAMBIA binary plasmid and the sequence from left to right t-DNA borders is presented in SEQ ID NO: 49. The resulting construct was given number 8720 (SEQ ID NO: 50). The amino acid sequence of VP60 is presented in SEQ ID NO: 30. A representation of plasmid 8720 is presented in Figure 7A. Constructs 8721 to 8731 were cloned using the same methodology and a summary of primers, templates, accepting vectors and products is provided in Table 2. d i ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I ) I
Figure imgf000047_0001
Example 2: Methods Agrobacterium tumefaciens Transfection [00147] Agrobacterium tumefaciens strain AGL1 was transfected by electroporation with the modified coat protein expression vectors using the methods described by D’Aoust et al., 2008 (Plant Biotech. J.6:930-40). Transfected Agrobacterium were grown in YEB medium supplemented with 10 mM 2-(N- morpholino)ethanesulfonic acid (MES), 20 μM acetosyringone, 50 μg/ml kanamycin and 25 μg/ml of carbenicillin pH 5.6 to an OD600 between 0.6 and 1.6. Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6). Preparation of Plant Biomass, Inoculum and Agroinfiltration [00148] N. benthamiana plants were grown from seeds in flats filled with a commercial peat moss substrate. The plants were allowed to grow in the greenhouse under a 16/8 photoperiod and a temperature regime of 25°C day/20°C night. Three weeks after seeding, individual plantlets were picked out, transplanted in pots and left to grow in the greenhouse for three additional weeks under the same environmental conditions. [00149] Agrobacteria transfected with each expression vector were grown in a YEB medium supplemented with 10 mM 2-(N-morpholino)ethanesulfonic acid (MES), 20 μM acetosyringone, 50 μg/ml kanamycin and 25 μg/ml of carbenicillin pH 5.6 until they reached an OD600 between 0.6 and 1.6. Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6) and stored overnight at 4° C. On the day of infiltration, culture batches were diluted in 2.5 culture volumes and allowed to warm before use. Whole plants of N. benthamiana were placed upside down in the bacterial suspension in an air-tight stainless steel tank under a vacuum of 20-40 Torr for 2-min. Plants were returned to the greenhouse for a 6 or 9 day incubation period until harvest. Leaf Harvest and Total Protein and VLP Extraction [00150] Biomasses expressing constructs 8720 – 8725 in addition to construct 7387 (proteinase 24K) were harvested at 6- and 9-days post infiltration (dpi) and screened to detect accumulation of CPMV coat proteins. Detection of bands for CPMV-L at 35 kDa and CPMV-S at 22 kDa upon SDS-PAGE of clarified biomasses, using protein staining and by using an anti-CPMV antibody, are taken as a confirmation for the expression of these proteins in planta. Expression of the CPMV coat proteins was confirmed from construct 8720, 8721, 87228723 and 8725, and an increase in MW was observed corresponding to the expected size of the inserted peptide in each case (Figure 1). Accumulation was found to be higher at 9 dpi, compared to 6 dpi. Biomasses expressing two of these constructs: 8721 and 8725, harvested at 9 dpi, were selected for purification and characterization of VLPs. [00151] Biomasses expressing constructs 8726 – 8731 in addition to construct 7387 (proteinase 24K) were harvested at 6- and 9-days post infiltration (dpi) and screened to detect accumulation of CPMV coat proteins. Detection of bands for CPMV-L at 35 kDa and CPMV-S at 22 kDa upon SDS-PAGE of clarified biomasses, using protein staining and by using an anti-CPMV antibody, are taken as a confirmation for the expression of these proteins in planta. Expression of the CPMV coat proteins was confirmed from constructs 8727 and 8729, and an increase in MW was observed corresponding to the expected size of the inserted peptide in both cases (Figure 2). Accumulation was found to be higher at 9 dpi, compared to 6 dpi. Biomasses expressing the two constructs: 8727 and 8729, harvested at 9 dpi, were selected for purification and characterization of VLPs. Purification of VLPs [00152] For each of the two conditions selected for CPMV-S14P5 and CPMV- S21P2, biomasses were processed using routine purification protocols. Clarified extracts were concentrated using PEG precipitation methods and separated on a 18- 24% iodixanol density gradient. Fractions were collected from the bottom of gradients and analyzed by SDS-PAGE. Properly assembled VLPs of CPMV are expected to migrate to 18-22% iodixanol layers. Results showed detection of CPMV coat proteins in these specific iodixanol layers in case of CPMV-S14P5 constructs 8721 and 8725, and in case of CPMV-S21P2 construct 8729 (Figure 3). The best four fractions from each gradient were pooled for characterization of modified VLPs. Characterization of VLPs [00153] Pooled fractions from gradients for biomasses 8721, 8725 and 8729 were subjected to ultrafiltration for removal of iodixanol from the formulations. The samples were subsequently characterized for their identity (by anti-CPMV Western blotting), concentration (by BCA assay), purity (by gel densitometry), integrity (by electron microscopy) and their thermal stability (by differential scanning fluorimetry). Results of characterization showed close correlation with characteristics of native CPMV VLPs, used as a control. Example 3: Sequences [00154] The following sequences were used in the examples described above. SEQ ID NO: 1 Native CPMV polyprotein (large and small coat protein) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRTAAWKSGTIHVQLNVRGAGVK RADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFSFDIIGPNSGFEFAESPWA NQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMPPFPLSTETPPLLKFRFRD IERSKRSVMVGHTATAA SEQ ID NO: 2 Modified CPMV polyprotein (S14P5 βE-αB (betaE-alphaB) L protein) MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGTESNKKFLPFQQFGRD IAKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICV SGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEV RRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIA FGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCP YLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEA SDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 3 Modified CPMV polyprotein (S14P5 βC’- βC” (betaC’-betaC’’) S protein) MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDTESNKKFLPFQQFGRDIADNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 4 Modified CPMV polyprotein (D-S14P5-D βE-αB (betaE-alphaB) L protein) MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGDTESNKKFLPFQQFGR DIADKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVI CVSGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTS EVRRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFL IAFGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADG CPYLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCA EASDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRT AAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLN FSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNIL MPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 5 Modified CPMV polyprotein (GSA-S14P5-GSA βC’- βC” (betaC’-betaC’’) S protein) MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDGSATESNKKFLPFQQFGRDIAGSADNWNTHIYNPPIMN VLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGS AMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVA GNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 6 Modified CPMV polyprotein (S21P2 βE-αB (betaE-alphaB) L protein) 2 MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGPSKPSKRSFIEDLLFN KVKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICV SGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEV RRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIA FGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCP YLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEA SDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 7 Modified CPMV polyprotein (D-S14P5 -D βE-αB (betaE-alphaB) L protein) 2 MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGDPSKPSKRSFIEDLLF NKVDKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVI CVSGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTS EVRRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFL IAFGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADG CPYLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCA EASDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRT AAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLN FSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNIL MPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 8 Native large coat protein MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQ SEQ ID NO: 9 Modified L protein (S14P5 betaE-alphaB L protein) 2 MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGTESNKKFLPFQQFGRD IAKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICV SGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEV RRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIA FGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCP YLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQ SEQ ID NO: 10 Modified L protein (D-S14P5-D betaE-alphaB L protein) 2 MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGDTESNKKFLPFQQFGR DIADKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVI CVSGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTS EVRRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFL IAFGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADG CPYLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQ SEQ ID NO: 11 Modified L protein (S21P2 betaE-alphaB L protein) 2 MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGPSKPSKRSFIEDLLFN KVKYSTDVYTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICV SGWTLSPTTDVIAKLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEV RRMPLSIGGGAGATQAFLANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIA FGNLSDAFGFYESFPHRIVQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCP YLYAIIHDSTTGTISGDFNLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQ SEQ ID NO: 12 Native small coat protein GPVCAEASDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIM NVLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPG SAMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRV AGNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 13 Modified S protein (S14P5 betaC’-betaC’’ S protein) GPVCAEASDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDTESNKKFLPFQQF GRDIADNWNTHIYNPPIMNVLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQ SMNPESYDARTFVISQPGSAMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNP RQIQQFEVNMRFDPNFRVAGNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTA TAA SEQ ID NO: 14 Modified S protein (GSA-S14P5-GSA betaC’-betaC’’ S protein) GPVCAEASDVYSPCMIASTPPAPFSDVTAVTFDLINGKITPVGDGSATESNKKFLPF QQFGRDIAGSADNWNTHIYNPPIMNVLRTAAWKSGTIHVQLNVRGAGVKRADWDGQV FVYLRQSMNPESYDARTFVISQPGSAMLNFSFDIIGPNSGFEFAESPWANQTTWYLE CVATNPRQIQQFEVNMRFDPNFRVAGNILMPPFPLSTETPPLLKFRFRDIERSKRSV MVGHTATAA SEQ ID NO: 15 S14P5 TESNKKFLPFQQFGRDIA SEQ ID NO: 16 S21P2 PSKPSKRSFIEDLLFNKV SEQ ID NO: 17 D-S14P5-D DTESNKKFLPFQQFGRDIAD SEQ ID NO: 18 D-S21P2-D DPSKPSKRSFIEDLLFNKVD SEQ ID NO: 19 GSA-S14P5-GSA GSATESNKKFLPFQQFGRDIAGSA SEQ ID NO: 20 GSA-S21P2-GSA GSAPSKPSKRSFIEDLLFNKVGSA SEQ ID NO: 21 Spike protein with S14P5 and S21P2 annotated (Figure 5) SEQ ID NO: 22 IF(nbMT78)-CPMV(24k).c primer TCCCAACAACATAAGAAAACAATGTCCCTGGACCAGAGCTCCGTTGCTA SEQ ID NO: 23 IF(AVb)-CPMV(24k).r primer ACGACACGACTAAGGCCTCTACTGGGCCTGGGCGATAGGTTCTAATGGC SEQ ID NO: 24 24k Protease DNA ATGTCCCTGGACCAGAGCTCCGTTGCTATAATGTCAAAATGCCGGGCGAATCTGGTG TTTGGAGGGACCAATTTGCAGATCGTGATGGTACCCGGCAGACGGTTTTTGGCTTGC AAACACTTCTTCACTCATATTAAAACCAAGCTGCGCGTGGAGATAGTCATGGACGGC CGGCGATACTACCACCAATTCGATCCCGCTAATATCTACGACATCCCTGATTCTGAG CTGGTGTTATATTCCCATCCCTCACTTGAGGACGTGTCACACAGCTGCTGGGATTTG TTTTGTTGGGACCCAGATAAGGAGCTACCCTCAGTGTTTGGTGCCGATTTCCTCTCT TGTAAGTACAACAAGTTTGGCGGCTTTTACGAGGCTCAATATGCTGATATTAAAGTG AGGACAAAGAAAGAGTGCCTGACGATACAGTCCGGCAACTATGTTAACAAGGTGAGC AGATATCTGGAATACGAGGCCCCCACCATTCCTGAGGACTGTGGGAGTCTCGTAATA GCGCACATTGGCGGGAAGCACAAGATAGTAGGTGTGCACGTGGCTGGCATCCAAGGA AAGATTGGCTGCGCCAGTCTTCTGCCGCCATTAGAACCTATCGCCCAGGCCCAGTAG SEQ ID NO: 25 24k Protease AA MSLDQSSVAIMSKCRANLVFGGTNLQIVMVPGRRFLACKHFFTHIKTKLRVEIVMDG RRYYHQFDPANIYDIPDSELVLYSHPSLEDVSHSCWDLFCWDPDKELPSVFGADFLS CKYNKFGGFYEAQYADIKVRTKKECLTIQSGNYVNKVSRYLEYEAPTIPEDCGSLVI AHIGGKHKIVGVHVAGIQGKIGCASLLPPLEPIAQAQ SEQ ID NO: 26 IF(nbMT78)-CPMV(SB).c primer TCCCAACAACATAAGAAAACAATGGAGCAGAATCTGTTCGCACTCAGC SEQ ID NO: 27 IF(AVb)-CPMV(SB).r primer ACGACACGACTAAGGCCTTTAGGCGGCTGTGGCGGTATGTCCCACCATA SEQ ID NO: 28 WT VP60 DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGC GACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGAC GATAATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCC GCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAG CGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAA TCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTT TCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCA AACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAG TTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATG CCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGAT ATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 29 VP60 (S14P5-1) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGACCGAGTCC AACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGCGACATAGCTCCATTCAGCGAC GTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGACGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 30 VP60 (S14P5-1) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPATES NKKFLPFQQFGRDIAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 31 Cloning vector 7140 from left to right T-DNA TGGCAGGATATATTGTGGTGTAAACAAATTGACGCTTAGACAACTTAATAACACATT GCGGACGTTTTTAATGTACTGAATTAACGCCGAATCCCGGGCTGGTATATTTATATG TTGTCAAATAACTCAAAAACCATAAAAGTTTAAGTTAGCAAGTGTGTACATTTTTAC TTGAACAAAAATATTCACCTACTACTGTTATAAATCATTATTAAACATTAGAGTAAA GAAATATGGATGATAAGAACAAGAGTAGTGATATTTTGACAACAATTTTGTTGCAAC ATTTGAGAAAATTTTGTTGTTCTCTCTTTTCATTGGTCAAAAACAATAGAGAGAGAA AAAGGAAGAGGGAGAATAAAAACATAATGTGAGTATGAGAGAGAAAGTTGTACAAAA GTTGTACCAAAATAGTTGTACAAATATCATTGAGGAATTTGACAAAAGCTACACAAA TAAGGGTTAATTGCTGTAAATAAATAAGGATGACGCATTAGAGAGATGTACCATTAG AGAATTTTTGGCAAGTCATTAAAAAGAAAGAATAAATTATTTTTAAAATTAAAAGTT GAGTCATTTGATTAAACATGTGATTATTTAATGAATTGATGAAAGAGTTGGATTAAA GTTGTATTAGTAATTAGAATTTGGTGTCAAATTTAATTTGACATTTGATCTTTTCCT ATATATTGCCCCATAGAGTCAGTTAACTCATTTTTATATTTCATAGATCAAATAAGA GAAATAACGGTATATTAATCCCTCCAAAAAAAAAAAACGGTATATTTACTAAAAAAT CTAAGCCACGTAGGAGGATAACAGGATCCCCGTAGGAGGATAACATCCAATCCAACC AATCACAACAATCCTGATGAGATAACCCACTTTAAGCCCACGCATCTGTGGCACATC TACATTATCTAAATCACACATTCTTCCACACATCTGAGCCACACAAAAACCAATCCA CATCTTTATCACCCATTCTATAAAAAATCACACTTTGTGAGTCTACACTTTGATTCC CTTCAAACACATACAAAGAGAAGAGACTAATTAATTAATTAATCATCTTGAGAGAAA ATGGAACGAGCTATACAAGGAAACGACGCTAGGGAACAAGCTAACAGTGAACGTTGG GATGGAGGATCAGGAGGTACCACTTCTCCCTTCAAACTTCCTGACGAAAGTCCGAGT TGGACTGAGTGGCGGCTACATAACGATGAGACGAATTCGAATCAAGATAATCCCCTT GGTTTCAAGGAAAGCTGGGGTTTCGGGAAAGTTGTATTTAAGAGATATCTCAGATAC GACAGGACGGAAGCTTCACTGCACAGAGTCCTTGGATCTTGGACGGGAGATTCGGTT AACTATGCAGCATCTCGATTTTTCGGTTTCGACCAGATCGGATGTACCTATAGTATT CGGTTTCGAGGAGTTAGTATCACCGTTTCTGGAGGGTCGCGAACTCTTCAGCATCTC TGTGAGATGGCAATTCGGTCTAAGCAAGAACTGCTACAGCTTGCCCCAATCGAAGTG GAAAGTAATGTATCAAGAGGATGCCCTGAAGGTACTCAAACCTTCGAAAAAGAAAGC GAGTAAGTTAAAATGCTTCTTCGTCTCCTATTTATAATATGGTTTGTTATTGTTAAT TTTGTTCTTGTAGAAGAGCTTAATTAATCGTTGTTGTTATGAAATACTATTTGTATG AGATGAACTGGTGTAATGTAATTCATTTACATAAGTGGAGTCAGAATCAGAATGTTT CCTCCATAACTAACTAGACATGAAGACCTGCCGCGTACAATTGTCTTATATTTGAAC AACTAAAATTGAACATCTTTTGCCACAACTTTATAAGTGGTTAATATAGCTCAAATA TATGGTCAAGTTCAATAGATTAATAATGGAAATATCAGTTATCGAAATTCATTAACA ATCAACTTAACGTTATTAACTACTAATTTTATATCATCCCCTTTGATAAATGATAGT ACACCAATTAGGAAGGAGCATGCTCGCCTAGGAGATTGTCGTTTCCCGCCTTCAGTT TGCAAGCTGCTCTAGCCGTGTAGCCAATACGCAAACCGCCTCTCCCCGCGCGTTGGG AATTACTAGCGCGTGTCGACAAGCTTGCATGCCGGTCAACATGGTGGAGCACGACAC ACTTGTCTACTCCAAAAATATCAAAGATACAGTCTCAGAAGACCAAAGGGCAATTGA GACTTTTCAACAAAGGGTAATATCCGGAAACCTCCTCGGATTCCATTGCCCAGCTAT CTGTCACTTTATTGTGAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAATGCCATCA TTGCGATAAAGGAAAGGCCATCGTTGAAGATGCCTCTGCCGACAGTGGTCCCAAAGA TGGACCCCCACCCACGAGGAGCATCGTGGAAAAAGAAGACGTTCCAACCACGTCTTC AAAGCAAGTGGATTGATGTGATAACATGGTGGAGCACGACACACTTGTCTACTCCAA AAATATCAAAGATACAGTCTCAGAAGACCAAAGGGCAATTGAGACTTTTCAACAAAG GGTAATATCCGGAAACCTCCTCGGATTCCATTGCCCAGCTATCTGTCACTTTATTGT GAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAATGCCATCATTGCGATAAAGGAAA GGCCATCGTTGAAGATGCCTCTGCCGACAGTGGTCCCAAAGATGGACCCCCACCCAC GAGGAGCATCGTGGAAAAAGAAGACGTTCCAACCACGTCTTCAAAGCAAGTGGATTG ATGTGATATCTCCACTGACGTAAGGGATGACGCACAATCCCACTATCCTTCGCAAGA CCCTTCCTCTATATAAGGAAGTTCATTTCATTTGGAGAGGCACACAATTTGCTTTAG TGATTAAACTTTCTTTTACAACAAATTAAAGGTCTATTATCTCCCAACAACATAAGA CGTCACGTACTCCTCAGCCAAAACGACACCCCCATCTGTCTATCCACTGGCCCCTGG ATCTGCTGCCCAAACTAACTCCATGGTGACCCTGGGATGCCTGGTCAAGGGCTATTT CCCTGAGCCAGTGACAGTGACCTGGAACTCTGGATCCCTGTCCAGCGGTGTGCACAC CTTCCCAGCTGTCCTGCAGTCTGACCTCTACACTCTGAGCAGCTCAGTGACTGTCCC CTCCAGCACCTGGCCCAGCGAGACCGTCACCTGCAACGTTGCCCACCCGGCCAGCAG CACCAAGGTGGACAAGAAAATTGTGCCCAGGGATTGTGGTTGTAAGCCTTGCATATG TACAGTCCCAGAAGTATCATCTGTCTTCATCTTCCCCCCAAAGCCCAAGGATGTGCT CACCATTACTCTGACTCCTAAGGTCACGTGTGTTGTGGTAGACATCAGCAAGGATGA TCCCGAGGTCCAGTTCAGCTGGTTTGTAGATGATGTGGAGGTGCACACAGCTCAGAC GCAACCCCGGGAGGAGCAGTTCAACAGCACTTTCCGCTCAGTCAGTGAACTTCCCAT CATGCACCAGGACTGGCTCAATGGCAAGGAGACGTCCAGATTTTGGCGATCTATTCA ACTGTCGCCAGTTCATTGGTACTGGTAGTCTCCCTGGGGGCAATCAGTTTCTGGATG TGCTCTAATGGGTCTCTACAGTGTAGAATATGTATTTAAAGGCCTTAGTCGTGTCGT TTTTCAAATAATATAATCCTTTTAGGGTTTTAGTTAGTTTAAATTTTCTGTTGCTCC TGTTTAGCAGGTCGTGCCTTCAGCAAGCACACAAAAACAGAGTGTTTATTTTAAGTT GTTTGTTTAGTGATTCAAAAAAAAAATCGTTCAAACATTTGGCAATAAAGTTTCTTA AGATTGAATCCTGTTGCCGGTCTTGCGATGATTATCATATAATTTCTGTTGAATTAC GTTAAGCATGTAATAATTAACATGTAATGCATGACGTTATTTATGAGATGGGTTTTT ATGATTAGAGTCCCGCAATTATACATTTAATACGCGATAGAAAACAAAATATAGCGC GCAAACTAGGATAAATTATCGCGCGCGGTGTCATCTATGTTACTAGATCTCTAGAGT CTCAAGCTTGGCGCGCCCACGTGACTAGTGGCACTGGCCGTCGTTTTACAACGTCGT GACTGGGAAAACCCTGGCGTTACCCAACTTAATCGCCTTGCAGCACATCCCCCTTTC GCCAGCTGGCGTAATAGCGAAGAGGCCCGCACCGATCGCCCTTCCCAACAGTTGCGC AGCCTGAATGGCGAATGCTAGAGCAGCTTGAGCTTGGATCAGATTGTCGTTTCCCGC CTTCAGTTTAAACTATCAGTGTTTGACAGGATATATTGGCGGGTAAACCTAAGAGAA AAGAGCGTTTA SEQ ID NO: 32 Construct 7384 from 2X35S prom to NOS term GTCAACATGGTGGAGCACGACACACTTGTCTACTCCAAAAATATCAAAGATACAGTC TCAGAAGACCAAAGGGCAATTGAGACTTTTCAACAAAGGGTAATATCCGGAAACCTC CTCGGATTCCATTGCCCAGCTATCTGTCACTTTATTGTGAAGATAGTGGAAAAGGAA GGTGGCTCCTACAAATGCCATCATTGCGATAAAGGAAAGGCCATCGTTGAAGATGCC TCTGCCGACAGTGGTCCCAAAGATGGACCCCCACCCACGAGGAGCATCGTGGAAAAA GAAGACGTTCCAACCACGTCTTCAAAGCAAGTGGATTGATGTGATAACATGGTGGAG CACGACACACTTGTCTACTCCAAAAATATCAAAGATACAGTCTCAGAAGACCAAAGG GCAATTGAGACTTTTCAACAAAGGGTAATATCCGGAAACCTCCTCGGATTCCATTGC CCAGCTATCTGTCACTTTATTGTGAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAA TGCCATCATTGCGATAAAGGAAAGGCCATCGTTGAAGATGCCTCTGCCGACAGTGGT CCCAAAGATGGACCCCCACCCACGAGGAGCATCGTGGAAAAAGAAGACGTTCCAACC ACGTCTTCAAAGCAAGTGGATTGATGTGATATCTCCACTGACGTAAGGGATGACGCA CAATCCCACTATCCTTCGCAAGACCCTTCCTCTATATAAGGAAGTTCATTTCATTTG GAGAGGCACACAATTTGCTTTAGTGATTAAACTTTCTTTTACAACAAATTAAAGGTC TATTATCTCCCAACAACATAAGAAAACAATGGAGCAGAATCTGTTCGCACTCAGCCT AGACGATACAAGCTCCGTTCGGGGAAGTTTGTTGGATACCAAATTTGCACAAACTCG GGTGCTACTCTCTAAGGCCATGGCGGGCGGGGACGTCCTCCTCGACGAGTACCTTTA TGACGTGGTCAATGGGCAGGATTTCCGGGCTACAGTGGCTTTCCTAAGGACACACGT GATCACCGGCAAGATCAAGGTGACAGCGACAACAAATATTTCCGACAACAGTGGCTG CTGCCTGATGCTGGCTATTAACTCAGGCGTCCGCGGAAAGTACAGCACTGATGTTTA CACAATTTGTAGTCAGGACTCCATGACTTGGAACCCCGGCTGCAAAAAGAATTTTAG TTTTACCTTCAATCCGAATCCCTGTGGAGACAGTTGGAGTGCTGAGATGATTAGTAG GTCCCGCGTGAGAATGACCGTCATATGTGTGTCAGGCTGGACCTTGTCACCCACTAC TGATGTCATCGCAAAGCTGGATTGGTCAATAGTGAACGAGAAGTGTGAACCTACAAT CTACCACTTGGCGGATTGTCAAAATTGGCTGCCACTGAATCGCTGGATGGGCAAATT AACATTTCCCCAGGGAGTGACTAGCGAGGTCAGGAGAATGCCCCTGTCAATAGGAGG AGGTGCCGGGGCTACCCAGGCCTTTCTCGCCAATATGCCAAACAGCTGGATAAGTAT GTGGAGATATTTCAGGGGGGAGCTGCATTTCGAGGTTACAAAGATGTCCAGCCCTTA CATTAAGGCGACCGTTACCTTTTTGATTGCTTTCGGCAACCTAAGCGACGCTTTTGG TTTTTATGAATCTTTCCCCCATAGAATTGTGCAATTCGCTGAGGTTGAGGAGAAATG CACCCTAGTCTTTAGCCAGCAAGAGTTTGTGACAGCATGGTCTACCCAGGTCAACCC CCGCACCACACTGGAAGCCGACGGCTGTCCGTATTTGTATGCAATCATACATGATTC TACGACAGGCACGATAAGCGGCGACTTCAACCTGGGAGTCAAATTAGTGGGAATCAA AGATTTTTGCGGCATCGGGTCTAACCCCGGTATTGACGGGTCACGCCTGCTGGGAGC CATAGCTCAGGGCCCAGTATGCGCAGAAGCCAGCGACGTCTACTCTCCCTGCATGAT CGCATCAACCCCCCCTGCGCCATTCAGCGACGTTACTGCCGTGACCTTTGATCTGAT CAATGGAAAGATCACACCCGTTGGAGACGATAATTGGAATACTCACATCTACAACCC TCCAATAATGAATGTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCA GCTTAATGTTAGGGGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGT ATATCTGAGACAGAGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTC CCAGCCTGGCTCAGCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGG CTTCGAATTCGCTGAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGT AGCCACCAACCCAAGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAA CTTTCGCGTCGCAGGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCC ACCTCTGTTGAAATTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGT GGGACATACCGCCACAGCCGCCTAAAGGCCTTAGTCGTGTCGTTTTTCAAATAATAT AATCCTTTTAGGGTTTTAGTTAGTTTAAATTTTCTGTTGCTCCTGTTTAGCAGGTCG TGCCTTCAGCAAGCACACAAAAACAGAGTGTTTATTTTAAGTTGTTTGTTTAGTGAT TCAAAAAAAAAATCGTTCAAACATTTGGCAATAAAGTTTCTTAAGATTGAATCCTGT TGCCGGTCTTGCGATGATTATCATATAATTTCTGTTGAATTACGTTAAGCATGTAAT AATTAACATGTAATGCATGACGTTATTTATGAGATGGGTTTTTATGATTAGAGTCCC GCAATTATACATTTAATACGCGATAGAAAACAAAATATAGCGCGCAAACTAGGATAA ATTATCGCGCGCGGTGTCATCTATGTTACTAGAT SEQ ID NO: 33 VP60 (S14P5-2) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGCGAC ATAGCTAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACTTGG AACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGAGAC AGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGTGTG TCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCAATA GTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGGCTG CCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAGGTC AGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTCGCC AATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCATTTC GAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATTGCT TTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATTGTG CAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTTGTG ACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGTCCG TATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTCAAC CTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCCGGT ATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAAGCC AGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGCGAC GTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGACGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 34 VP60 (S14P5-4) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGC GACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGAC ACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGCGACATAGCTGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 35 VP60 (S14P5 (+DD)-2) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAGATACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGC GACATAGCTGACAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATG ACTTGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGT GGAGACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATA TGTGTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGG TCAATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAAT TGGCTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGC GAGGTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTT CTCGCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTG CATTTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTG ATTGCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGA ATTGTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAG TTTGTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGC TGTCCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGAC TTCAACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAAC CCCGGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCA GAAGCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTC AGCGACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGA GACGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACC GCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTG AAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCC GAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAAC TTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGG GCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAA CAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTG ATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGG GATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 36 VP60 (GSA-S14P5-GSA-1) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGGGCTCAGCT ACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGCGACATAGCTGGC TCAGCTCCATTCAGCGACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATC ACACCCGTTGGAGACGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAAT GTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGG GGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAG AGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCA GCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCT GAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCA AGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCA GGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAA TTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCC ACAGCCGCCTAA SEQ ID NO: 37 VP60 (GSA-S14P5-GSA-1) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAGSA TESNKKFLPFQQFGRDIAGSAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMN VLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGS AMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVA GNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 38 VP60 (GSA-S14P5-GSA-4) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGC GACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGAC GGCTCAGCTACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATTCGGTCGCGAC ATAGCTGGCTCAGCTGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAAT GTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGG GGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAG AGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCA GCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCT GAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCA AGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCA GGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAA TTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCC ACAGCCGCCTAA SEQ ID NO: 39 VP60 (S21P2-1) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCGTCAAAA CCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTCAATAAGGTCCCATTCAGCGAC GTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGACGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 40 VP60 (S21P2-1) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPSK PSKRSFIEDLLFNKVPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 41 VP60 (S21P2-2) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGACCGTCAAAACCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTCAAT AAGGTCAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACTTGG AACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGAGAC AGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGTGTG TCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCAATA GTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGGCTG CCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAGGTC AGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTCGCC AATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCATTTC GAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATTGCT TTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATTGTG CAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTTGTG ACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGTCCG TATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTCAAC CTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCCGGT ATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAAGCC AGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGCGAC GTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGACGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 42 VP60 (S21P2-4) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGC GACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGAC CCGTCAAAACCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTCAATAAGGTCGAT AATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACCGCCGCT TGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTGAAGCGG GCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCCGAATCA TATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAACTTTTCT TTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGGGCAAAC CAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAACAGTTT GAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTGATGCCT CCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGGGATATA GAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 43 VP60 (S21P2-4) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDPSKPSKRSFIEDLLFNKVDNWNTHIYNPPIMNVLRTAA WKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGSAMLNFS FDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVAGNILMP PFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 44 VP60 (S21P2 (+DD)-2) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAGATCCGTCAAAACCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTC AATAAGGTCGACAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATG ACTTGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGT GGAGACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATA TGTGTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGG TCAATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAAT TGGCTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGC GAGGTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTT CTCGCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTG CATTTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTG ATTGCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGA ATTGTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAG TTTGTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGC TGTCCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGAC TTCAACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAAC CCCGGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCA GAAGCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTC AGCGACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGA GACGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAATGTTCTCAGGACC GCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGGGGCGCCGGGGTG AAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAGAGCATGAACCCC GAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCAGCTATGTTGAAC TTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCTGAGTCACCGTGG GCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCAAGACAGATCCAA CAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCAGGCAATATTTTG ATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAATTCCGTTTCAGG GATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCCACAGCCGCCTAA SEQ ID NO: 45 VP60 (GSA-S21P2-GSA-1) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGGGCTCAGCT CCGTCAAAACCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTCAATAAGGTCGGC TCAGCTCCATTCAGCGACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATC ACACCCGTTGGAGACGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAAT GTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGG GGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAG AGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCA GCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCT GAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCA AGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCA GGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAA TTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCC ACAGCCGCCTAA SEQ ID NO: 46 VP60 (GSA-S21P2-GSA-1) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAGSA PSKPSKRSFIEDLLFNKVGSAPFSDVTAVTFDLINGKITPVGDDNWNTHIYNPPIMN VLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGS AMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVA GNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 47 VP60 (GSA-S21P2-GSA-4) DNA ATGGAGCAGAATCTGTTCGCACTCAGCCTAGACGATACAAGCTCCGTTCGGGGAAGT TTGTTGGATACCAAATTTGCACAAACTCGGGTGCTACTCTCTAAGGCCATGGCGGGC GGGGACGTCCTCCTCGACGAGTACCTTTATGACGTGGTCAATGGGCAGGATTTCCGG GCTACAGTGGCTTTCCTAAGGACACACGTGATCACCGGCAAGATCAAGGTGACAGCG ACAACAAATATTTCCGACAACAGTGGCTGCTGCCTGATGCTGGCTATTAACTCAGGC GTCCGCGGAAAGTACAGCACTGATGTTTACACAATTTGTAGTCAGGACTCCATGACT TGGAACCCCGGCTGCAAAAAGAATTTTAGTTTTACCTTCAATCCGAATCCCTGTGGA GACAGTTGGAGTGCTGAGATGATTAGTAGGTCCCGCGTGAGAATGACCGTCATATGT GTGTCAGGCTGGACCTTGTCACCCACTACTGATGTCATCGCAAAGCTGGATTGGTCA ATAGTGAACGAGAAGTGTGAACCTACAATCTACCACTTGGCGGATTGTCAAAATTGG CTGCCACTGAATCGCTGGATGGGCAAATTAACATTTCCCCAGGGAGTGACTAGCGAG GTCAGGAGAATGCCCCTGTCAATAGGAGGAGGTGCCGGGGCTACCCAGGCCTTTCTC GCCAATATGCCAAACAGCTGGATAAGTATGTGGAGATATTTCAGGGGGGAGCTGCAT TTCGAGGTTACAAAGATGTCCAGCCCTTACATTAAGGCGACCGTTACCTTTTTGATT GCTTTCGGCAACCTAAGCGACGCTTTTGGTTTTTATGAATCTTTCCCCCATAGAATT GTGCAATTCGCTGAGGTTGAGGAGAAATGCACCCTAGTCTTTAGCCAGCAAGAGTTT GTGACAGCATGGTCTACCCAGGTCAACCCCCGCACCACACTGGAAGCCGACGGCTGT CCGTATTTGTATGCAATCATACATGATTCTACGACAGGCACGATAAGCGGCGACTTC AACCTGGGAGTCAAATTAGTGGGAATCAAAGATTTTTGCGGCATCGGGTCTAACCCC GGTATTGACGGGTCACGCCTGCTGGGAGCCATAGCTCAGGGCCCAGTATGCGCAGAA GCCAGCGACGTCTACTCTCCCTGCATGATCGCATCAACCCCCCCTGCGCCATTCAGC GACGTTACTGCCGTGACCTTTGATCTGATCAATGGAAAGATCACACCCGTTGGAGAC GGCTCAGCTCCGTCAAAACCTTCCAAGCGTTCTTTCATCGAGGACCTTTTGTTCAAT AAGGTCGGCTCAGCTGATAATTGGAATACTCACATCTACAACCCTCCAATAATGAAT GTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCTTAATGTTAGG GGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGTATATCTGAGACAG AGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTCCCAGCCTGGCTCA GCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGGCTTCGAATTCGCT GAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGTAGCCACCAACCCA AGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAACTTTCGCGTCGCA GGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCCACCTCTGTTGAAA TTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGGACATACCGCC ACAGCCGCCTAA SEQ ID NO: 48 VP60 (GSA-S21P2-GSA-4) AA MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFR ATVAFLRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGKYSTDVYTICSQDSMT WNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIAKLDWS IVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRI VQFAEVEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDF NLGVKLVGIKDFCGIGSNPGIDGSRLLGAIAQGPVCAEASDVYSPCMIASTPPAPFS DVTAVTFDLINGKITPVGDGSAPSKPSKRSFIEDLLFNKVGSADNWNTHIYNPPIMN VLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQSMNPESYDARTFVISQPGS AMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNPRQIQQFEVNMRFDPNFRVA GNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTATAA SEQ ID NO: 49 Cloning vector 7142 from left to right T-DNA TGGCAGGATATATTGTGGTGTAAACAAATTGACGCTTAGACAACTTAATAACACATT GCGGACGTTTTTAATGTACTGAATTAACGCCGAATCCCGGGCTGGTATATTTATATG TTGTCAAATAACTCAAAAACCATAAAAGTTTAAGTTAGCAAGTGTGTACATTTTTAC TTGAACAAAAATATTCACCTACTACTGTTATAAATCATTATTAAACATTAGAGTAAA GAAATATGGATGATAAGAACAAGAGTAGTGATATTTTGACAACAATTTTGTTGCAAC ATTTGAGAAAATTTTGTTGTTCTCTCTTTTCATTGGTCAAAAACAATAGAGAGAGAA AAAGGAAGAGGGAGAATAAAAACATAATGTGAGTATGAGAGAGAAAGTTGTACAAAA GTTGTACCAAAATAGTTGTACAAATATCATTGAGGAATTTGACAAAAGCTACACAAA TAAGGGTTAATTGCTGTAAATAAATAAGGATGACGCATTAGAGAGATGTACCATTAG AGAATTTTTGGCAAGTCATTAAAAAGAAAGAATAAATTATTTTTAAAATTAAAAGTT GAGTCATTTGATTAAACATGTGATTATTTAATGAATTGATGAAAGAGTTGGATTAAA GTTGTATTAGTAATTAGAATTTGGTGTCAAATTTAATTTGACATTTGATCTTTTCCT ATATATTGCCCCATAGAGTCAGTTAACTCATTTTTATATTTCATAGATCAAATAAGA GAAATAACGGTATATTAATCCCTCCAAAAAAAAAAAACGGTATATTTACTAAAAAAT CTAAGCCACGTAGGAGGATAACAGGATCCCCGTAGGAGGATAACATCCAATCCAACC AATCACAACAATCCTGATGAGATAACCCACTTTAAGCCCACGCATCTGTGGCACATC TACATTATCTAAATCACACATTCTTCCACACATCTGAGCCACACAAAAACCAATCCA CATCTTTATCACCCATTCTATAAAAAATCACACTTTGTGAGTCTACACTTTGATTCC CTTCAAACACATACAAAGAGAAGAGACTAATTAATTAATTAATCATCTTGAGAGAAA ATGGAACGAGCTATACAAGGAAACGACGCTAGGGAACAAGCTAACAGTGAACGTTGG GATGGAGGATCAGGAGGTACCACTTCTCCCTTCAAACTTCCTGACGAAAGTCCGAGT TGGACTGAGTGGCGGCTACATAACGATGAGACGAATTCGAATCAAGATAATCCCCTT GGTTTCAAGGAAAGCTGGGGTTTCGGGAAAGTTGTATTTAAGAGATATCTCAGATAC GACAGGACGGAAGCTTCACTGCACAGAGTCCTTGGATCTTGGACGGGAGATTCGGTT AACTATGCAGCATCTCGATTTTTCGGTTTCGACCAGATCGGATGTACCTATAGTATT CGGTTTCGAGGAGTTAGTATCACCGTTTCTGGAGGGTCGCGAACTCTTCAGCATCTC TGTGAGATGGCAATTCGGTCTAAGCAAGAACTGCTACAGCTTGCCCCAATCGAAGTG GAAAGTAATGTATCAAGAGGATGCCCTGAAGGTACTCAAACCTTCGAAAAAGAAAGC GAGTAAGTTAAAATGCTTCTTCGTCTCCTATTTATAATATGGTTTGTTATTGTTAAT TTTGTTCTTGTAGAAGAGCTTAATTAATCGTTGTTGTTATGAAATACTATTTGTATG AGATGAACTGGTGTAATGTAATTCATTTACATAAGTGGAGTCAGAATCAGAATGTTT CCTCCATAACTAACTAGACATGAAGACCTGCCGCGTACAATTGTCTTATATTTGAAC AACTAAAATTGAACATCTTTTGCCACAACTTTATAAGTGGTTAATATAGCTCAAATA TATGGTCAAGTTCAATAGATTAATAATGGAAATATCAGTTATCGAAATTCATTAACA ATCAACTTAACGTTATTAACTACTAATTTTATATCATCCCCTTTGATAAATGATAGT ACACCAATTAGGAAGGAGCATGCTCGCCTAGGAGATTGTCGTTTCCCGCCTTCAGTT TGCAAGCTGCTCTAGCCGTGTAGCCAATACGCAAACCGCCTCTCCCCGCGCGTTGGG AATTACTAGCGCGTGTCGACAAGCTTGCATGCCGGTCAACATGGTGGAGCACGACAC ACTTGTCTACTCCAAAAATATCAAAGATACAGTCTCAGAAGACCAAAGGGCAATTGA GACTTTTCAACAAAGGGTAATATCCGGAAACCTCCTCGGATTCCATTGCCCAGCTAT CTGTCACTTTATTGTGAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAATGCCATCA TTGCGATAAAGGAAAGGCCATCGTTGAAGATGCCTCTGCCGACAGTGGTCCCAAAGA TGGACCCCCACCCACGAGGAGCATCGTGGAAAAAGAAGACGTTCCAACCACGTCTTC AAAGCAAGTGGATTGATGTGATAACATGGTGGAGCACGACACACTTGTCTACTCCAA AAATATCAAAGATACAGTCTCAGAAGACCAAAGGGCAATTGAGACTTTTCAACAAAG GGTAATATCCGGAAACCTCCTCGGATTCCATTGCCCAGCTATCTGTCACTTTATTGT GAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAATGCCATCATTGCGATAAAGGAAA GGCCATCGTTGAAGATGCCTCTGCCGACAGTGGTCCCAAAGATGGACCCCCACCCAC GAGGAGCATCGTGGAAAAAGAAGACGTTCCAACCACGTCTTCAAAGCAAGTGGATTG ATGTGATATCTCCACTGACGTAAGGGATGACGCACAATCCCACTATCCTTCGCAAGA CCCTTCCTCTATATAAGGAAGTTCATTTCATTTGGAGAGGCACACAATTTGCTTTAG TGATTAAACTTTCTTTTACAACAAATTAAAGGTCTATTATCTCCCAACAACATAAGA CGTCACGTACTCCTCAGCCAAAACGACACCCCCATCTGTCTATCCACTGGCCCCTGG ATCTGCTGCCCAAACTAACTCCATGGTGACCCTGGGATGCCTGGTCAAGGGCTATTT CCCTGAGCCAGTGACAGTGACCTGGAACTCTGGATCCCTGTCCAGCGGTGTGCACAC CTTCCCAGCTGTCCTGCAGTCTGACCTCTACACTCTGAGCAGCTCAGTGACTGTCCC CTCCAGCACCTGGCCCAGCGAGACCGTCACCTGCAACGTTGCCCACCCGGCCAGCAG CACCAAGGTGGACAAGAAAATTGTGCCCAGGGATTGTGGTTGTAAGCCTTGCATATG TACAGTCCCAGAAGTATCATCTGTCTTCATCTTCCCCCCAAAGCCCAAGGATGTGCT CACCATTACTCTGACTCCTAAGGTCACGTGTGTTGTGGTAGACATCAGCAAGGATGA TCCCGAGGTCCAGTTCAGCTGGTTTGTAGATGATGTGGAGGTGCACACAGCTCAGAC GCAACCCCGGGAGGAGCAGTTCAACAGCACTTTCCGCTCAGTCAGTGAACTTCCCAT CATGCACCAGGACTGGCTCAATGGCAAGGAGACGTCCAGATTTTGGCGATCTATTCA ACTGTCGCCAGTTCATTGGTACTGGTAGTCTCCCTGGGGGCAATCAGTTTCTGGATG TGCTCTAATGGGTCTCTACAGTGTAGAATATGTATTTAAAGGCCTTAGTCGTGTCGT TTTTCAAATAATATAATCCTTTTAGGGTTTTAGTTAGTTTAAATTTTCTGTTGCTCC TGTTTAGCAGGTCGTGCCTTCAGCAAGCACACAAAAACAGAGTGTTTATTTTAAGTT GTTTGTTTAGTGATTCAAAAAAAAAATCGTTCAAACATTTGGCAATAAAGTTTCTTA AGATTGAATCCTGTTGCCGGTCTTGCGATGATTATCATATAATTTCTGTTGAATTAC GTTAAGCATGTAATAATTAACATGTAATGCATGACGTTATTTATGAGATGGGTTTTT ATGATTAGAGTCCCGCAATTATACATTTAATACGCGATAGAAAACAAAATATAGCGC GCAAACTAGGATAAATTATCGCGCGCGGTGTCATCTATGTTACTAGATCTCTAGGTA AAAATCCCAATTATATTTGGTCTAATTTAGTTTGGTATTGAGTAAAACAAATTCGAA CCAAACCAAAATATAAATATATAGTTTTTATATATATGCCTTTAAGACTTTTTATAG AATTTTCTTTAAAAAATATCAAGAAATATTTGCGACTCTTCTGGCATGTAATATTTC GTTAAATATGAAGTGCTCCATTTTTATTAACTTTAAATAATTGGTTGTACGATCACT TTCTTATCAAGTGTTACTAAAATGCGTCAATCTCTTTGTTCTTCCATATTCATATGT CAAAATCTATCAAAATTCTTATATATCTTTTTCGAATTTGAAGTGAAATTTCGATAA TTTAAAATTAAATAGAACATATCATTATTTAGGTATCATATTGATTTTTATACTTAA TTACTAAATTTGGTTAACTTTGAAAGTGTACATCAACGAAAAATTAGTCAAACGACT AAAATAAATAAATATCATGTGTTATTAAGAAAATTCTCCTATAAGAATATTTTAATA GATCATATGTTTGTAAAAAAAATTAATTTTTACTAACACATATATTTACTTATCAAA AATTTGACAAAGTAAGATTAAAATAATATTCATCTAACAAAAAAAAAACCAGAAAAT GCTGAAAACCCGGCAAAACCGAACCAATCCAAACCGATATAGTTGGTTTGGTTTGAT TTTGATATAAACCGAACCAACTCGGTCCATTTGCACCCCTAATCATAATAGCTTTAA TATTTCAAGATATTATTAAGTTAACGTTGTCAATATCCTGGAAATTTTGCAAAATGA ATCAAGCCTATATGGCTGTAATATGAATTTAAAAGCAGCTCGATGTGGTGGTAATAT GTAATTTACTTGATTCTAAAAAAATATCCCAAGTATTAATAATTTCTGCTAGGAAGA AGGTTAGCTACGATTTACAGCAAAGCCAGAATACAAAGAACCATAAAGTGATTGAAG CTCGAAATATACGAAGGAACAAATATTTTTAAAAAAATACGCAATGACTTGGAACAA AAGAAAGTGATATATTTTTTGTTCTTAAACAAGCATCCCCTCTAAAGAATGGCAGTT TTCCTTTGCATGTAACTATTATGCTCCCTTCGTTACAAAAATTTTGGACTACTATTG GGAACTTCTTCTGAAAATTCTAGAGTCTCAAGCTTGGCGCGCCCACGTGACTAGTGG CACTGGCCGTCGTTTTACAACGTCGTGACTGGGAAAACCCTGGCGTTACCCAACTTA ATCGCCTTGCAGCACATCCCCCTTTCGCCAGCTGGCGTAATAGCGAAGAGGCCCGCA CCGATCGCCCTTCCCAACAGTTGCGCAGCCTGAATGGCGAATGCTAGAGCAGCTTGA GCTTGGATCAGATTGTCGTTTCCCGCCTTCAGTTTAAACTATCAGTGTTTGACAGGA TATATTGGCGGGTAAACCTAAGAGAAAAGAGCGTTTA SEQ ID NO: 50 Construct 8720 from 2X35S prom to NOS term GTCAACATGGTGGAGCACGACACACTTGTCTACTCCAAAAATATCAAAGATACAGTC TCAGAAGACCAAAGGGCAATTGAGACTTTTCAACAAAGGGTAATATCCGGAAACCTC CTCGGATTCCATTGCCCAGCTATCTGTCACTTTATTGTGAAGATAGTGGAAAAGGAA GGTGGCTCCTACAAATGCCATCATTGCGATAAAGGAAAGGCCATCGTTGAAGATGCC TCTGCCGACAGTGGTCCCAAAGATGGACCCCCACCCACGAGGAGCATCGTGGAAAAA GAAGACGTTCCAACCACGTCTTCAAAGCAAGTGGATTGATGTGATAACATGGTGGAG CACGACACACTTGTCTACTCCAAAAATATCAAAGATACAGTCTCAGAAGACCAAAGG GCAATTGAGACTTTTCAACAAAGGGTAATATCCGGAAACCTCCTCGGATTCCATTGC CCAGCTATCTGTCACTTTATTGTGAAGATAGTGGAAAAGGAAGGTGGCTCCTACAAA TGCCATCATTGCGATAAAGGAAAGGCCATCGTTGAAGATGCCTCTGCCGACAGTGGT CCCAAAGATGGACCCCCACCCACGAGGAGCATCGTGGAAAAAGAAGACGTTCCAACC ACGTCTTCAAAGCAAGTGGATTGATGTGATATCTCCACTGACGTAAGGGATGACGCA CAATCCCACTATCCTTCGCAAGACCCTTCCTCTATATAAGGAAGTTCATTTCATTTG GAGAGGCACACAATTTGCTTTAGTGATTAAACTTTCTTTTACAACAAATTAAAGGTC TATTATCTCCCAACAACATAAGAAAACAATGGAGCAGAATCTGTTCGCACTCAGCCT AGACGATACAAGCTCCGTTCGGGGAAGTTTGTTGGATACCAAATTTGCACAAACTCG GGTGCTACTCTCTAAGGCCATGGCGGGCGGGGACGTCCTCCTCGACGAGTACCTTTA TGACGTGGTCAATGGGCAGGATTTCCGGGCTACAGTGGCTTTCCTAAGGACACACGT GATCACCGGCAAGATCAAGGTGACAGCGACAACAAATATTTCCGACAACAGTGGCTG CTGCCTGATGCTGGCTATTAACTCAGGCGTCCGCGGAAAGTACAGCACTGATGTTTA CACAATTTGTAGTCAGGACTCCATGACTTGGAACCCCGGCTGCAAAAAGAATTTTAG TTTTACCTTCAATCCGAATCCCTGTGGAGACAGTTGGAGTGCTGAGATGATTAGTAG GTCCCGCGTGAGAATGACCGTCATATGTGTGTCAGGCTGGACCTTGTCACCCACTAC TGATGTCATCGCAAAGCTGGATTGGTCAATAGTGAACGAGAAGTGTGAACCTACAAT CTACCACTTGGCGGATTGTCAAAATTGGCTGCCACTGAATCGCTGGATGGGCAAATT AACATTTCCCCAGGGAGTGACTAGCGAGGTCAGGAGAATGCCCCTGTCAATAGGAGG AGGTGCCGGGGCTACCCAGGCCTTTCTCGCCAATATGCCAAACAGCTGGATAAGTAT GTGGAGATATTTCAGGGGGGAGCTGCATTTCGAGGTTACAAAGATGTCCAGCCCTTA CATTAAGGCGACCGTTACCTTTTTGATTGCTTTCGGCAACCTAAGCGACGCTTTTGG TTTTTATGAATCTTTCCCCCATAGAATTGTGCAATTCGCTGAGGTTGAGGAGAAATG CACCCTAGTCTTTAGCCAGCAAGAGTTTGTGACAGCATGGTCTACCCAGGTCAACCC CCGCACCACACTGGAAGCCGACGGCTGTCCGTATTTGTATGCAATCATACATGATTC TACGACAGGCACGATAAGCGGCGACTTCAACCTGGGAGTCAAATTAGTGGGAATCAA AGATTTTTGCGGCATCGGGTCTAACCCCGGTATTGACGGGTCACGCCTGCTGGGAGC CATAGCTCAGGGCCCAGTATGCGCAGAAGCCAGCGACGTCTACTCTCCCTGCATGAT CGCATCAACCCCCCCTGCGACCGAGTCCAACAAGAAATTCCTGCCCTTCCAGCAATT CGGTCGCGACATAGCTCCATTCAGCGACGTTACTGCCGTGACCTTTGATCTGATCAA TGGAAAGATCACACCCGTTGGAGACGATAATTGGAATACTCACATCTACAACCCTCC AATAATGAATGTTCTCAGGACCGCCGCTTGGAAGAGTGGCACCATCCATGTGCAGCT TAATGTTAGGGGCGCCGGGGTGAAGCGGGCGGACTGGGACGGACAGGTGTTCGTATA TCTGAGACAGAGCATGAACCCCGAATCATATGATGCCAGAACATTTGTGATCTCCCA GCCTGGCTCAGCTATGTTGAACTTTTCTTTCGACATAATCGGGCCAAATTCAGGCTT CGAATTCGCTGAGTCACCGTGGGCAAACCAGACTACCTGGTATCTGGAATGCGTAGC CACCAACCCAAGACAGATCCAACAGTTTGAGGTTAACATGCGCTTTGACCCTAACTT TCGCGTCGCAGGCAATATTTTGATGCCTCCATTCCCTTTGAGCACCGAGACGCCACC TCTGTTGAAATTCCGTTTCAGGGATATAGAAAGGAGCAAGCGGTCTGTTATGGTGGG ACATACCGCCACAGCCGCCTAAAGGCCTTAGTCGTGTCGTTTTTCAAATAATATAAT CCTTTTAGGGTTTTAGTTAGTTTAAATTTTCTGTTGCTCCTGTTTAGCAGGTCGTGC CTTCAGCAAGCACACAAAAACAGAGTGTTTATTTTAAGTTGTTTGTTTAGTGATTCA AAAAAAAAATCGTTCAAACATTTGGCAATAAAGTTTCTTAAGATTGAATCCTGTTGC CGGTCTTGCGATGATTATCATATAATTTCTGTTGAATTACGTTAAGCATGTAATAAT TAACATGTAATGCATGACGTTATTTATGAGATGGGTTTTTATGATTAGAGTCCCGCA ATTATACATTTAATACGCGATAGAAAACAAAATATAGCGCGCAAACTAGGATAAATT ATCGCGCGCGGTGTCATCTATGTTACTAGAT SEQ ID NO: 51 Modified S protein (S14P5-1 betaB-betaC S protein) GPVCAEASDVYSPCMIASTPPATESNKKFLPFQQFGRDIAPFSDVTAVTFDLINGKI TPVGDDNWNTHIYNPPIMNVLRTAAWKSGTIHVQLNVRGAGVKRADWDGQVFVYLRQ SMNPESYDARTFVISQPGSAMLNFSFDIIGPNSGFEFAESPWANQTTWYLECVATNP RQIQQFEVNMRFDPNFRVAGNILMPPFPLSTETPPLLKFRFRDIERSKRSVMVGHTA TAA SEQ ID NO: 52 Modified L protein (D-S21P2-D betaE-alphaB L protein) MEQNLFALSLDDTSSVRGSLLDTKFAQTRVLLSKAMAGGDVLLDEYLYDVVNGQDFRATVAF LRTHVITGKIKVTATTNISDNSGCCLMLAINSGVRGDPSKPSKRSFIEDLLFNKVDKYSTDV YTICSQDSMTWNPGCKKNFSFTFNPNPCGDSWSAEMISRSRVRMTVICVSGWTLSPTTDVIA KLDWSIVNEKCEPTIYHLADCQNWLPLNRWMGKLTFPQGVTSEVRRMPLSIGGGAGATQAFL ANMPNSWISMWRYFRGELHFEVTKMSSPYIKATVTFLIAFGNLSDAFGFYESFPHRIVQFAE VEEKCTLVFSQQEFVTAWSTQVNPRTTLEADGCPYLYAIIHDSTTGTISGDFNLGVKLVGIK DFCGIGSNPGIDGSRLLGAIAQ [00155] All citations are hereby incorporated by reference. [00156] The present invention has been described with regard to one or more embodiments. However, it will be apparent to persons skilled in the art that a number of variations and modifications can be made without departing from the scope of the invention as defined in the claims.

Claims

WHAT IS CLAIMED IS: 1. A modified Cowpea Mosaic Virus (CPMV) Virus-like particle (VLP) comprising large coat protein and small coat protein, i) wherein the large coat protein comprises in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein comprises in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein comprises in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
2. The VLP of claim 1, wherein the heterologous peptide insertion comprises one or more than one linker at the N-terminus, the C-terminus or both at the N-terminus and the C-terminus.
3. The VLP of claim 2, wherein the linker comprises one or more than one aspartate.
4. The VLP of claim 2, wherein the linker comprises the amino acid sequence glycine-serine-alanine.
5. The VLP of claim 1, wherein the VLP is an empty VLP, being devoid of DNA or RNA.
6. The VLP of claim 1, wherein the insertion in the betaE-alphaB loop of the large coat protein is between amino acid residues corresponding to amino acid 98 and 99 of the sequence of SEQ ID NO: 1.
7. The VLP of claim 1, wherein the insertion in the betaB-betaC loop of the small coat protein is between amino acid residues corresponding to amino acid 396 and 397 of the sequence of SEQ ID NO: 1.
8. The VLP of claim 1, wherein the insertion in the betaC’-betaC” loop of the small coat protein is between amino acid residue corresponding to amino acid 418 and 419 of the sequence of SEQ ID NO: 1.
9. The VLP of claim 1, wherein the epitope is coronavirus peptide S14P5.
10. The VLP of claim 1, wherein the epitope is coronavirus peptide S21P2.
11. The VLP of claim 1, wherein the large coat protein comprises in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein an aspartate residue is added to the N-terminus and the C-terminus of the coronavirus peptide S14P5.
12. The VLP of claim 11, wherein the heterologous peptide insert comprises the sequence of SEQ ID NO: 17.
13. The VLP of claim 1, wherein the small coat protein comprises in the betaC’- betaC” loop, a heterologous peptide insertion consisting of coronavirus peptide S14P5, wherein a glycine-serine-alanine linker is fused to the N-terminus and the C-terminus of coronavirus peptide S14P5.
14. The VLP of claim 13, wherein the heterologous peptide insert comprises the sequence of SEQ ID NO: 19.
15. The VLP of claim 1, wherein the large coat protein comprises in the betaE-alphaB loop, a heterologous peptide insertion consisting of coronavirus peptide S21P2, wherein an aspartate residue is added to the N-terminus and the C-terminus of coronavirus peptide S21P2.
16. The VLP of claim 15, wherein the heterologous peptide insert comprises the sequence of SEQ ID NO: 18.
17. A modified Cowpea Mosaic Virus (CPMV) coat protein, wherein the modified CPMV coat protein is a small coat protein, i) wherein the small coat protein comprises in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein comprises in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
18. A modified Cowpea Mosaic Virus (CPMV) coat protein, wherein the coat protein is a large coat protein comprising in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
19. A Virus like particle comprising the modified CPMV coat protein of claim 17 or 18.
20. A modified Cowpea Mosaic Virus (CPMV) polyprotein comprising the modified CPMV coat protein of claim 18 and the modified CPMV coat protein of claim 17.
21. A composition comprising an effective dose of the VLP of any one of claims 1-16 and 19 and a pharmaceutically acceptable carrier, adjuvant, vehicle or excipient.
22. A vaccine comprising an effective dose of the VLP of any one of claims 1-16 and 19 for inducing an immune response against coronavirus.
23. The vaccine of claim 21, wherein the vaccine is a multivalent vaccine, comprising a mixture of monovalent VLPs.
24. A method for inducing immunity to a Coronavirus infection in a subject, the method comprising administering the composition of claim 21 or the vaccine of claim 22 or 23 to the subject.
25. An antibody or antibody fragment prepared using the composition of claim 21 or the vaccine of claim 22 or 23.
26. A host or host cell comprising the VLP of any one of claims 1-16 and 19.
27. The host or host cell of claim 26, wherein the host is a plant and the host cell is a plant cell.
28. A nucleic acid comprising a nucleotide sequence encoding a Cowpea Mosaic Virus (CPMV) polyprotein, the polyprotein comprising the large coat protein and the small coat protein of CPMV, i) wherein the large coat protein comprises in the betaE-alphaB loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or ii) wherein the small coat protein comprises in the betaB-betaC loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein, or iii) wherein the small coat protein comprises in the betaC’-betaC” loop a heterologous peptide insertion comprising an epitope derived from a coronavirus spike protein.
29. A method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) introducing a first nucleic acid comprising the nucleic acid of claim 28 into the host or host cell; b) introducing a second nucleic acid encoding CPMV protease into the host or host cell; c) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acid, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell.
30. The method of claim 29, wherein the ratio of introduced amounts of the first nucleic acid relative to the second nucleic acid is 2:1.
31. A method of producing a modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) in a host or host cell comprising: a) providing the host or host cell, comprising a first nucleic acid comprising the nucleic acid of claim 28 and a second nucleic acid encoding CPMV protease; b) incubating the host or host cell under conditions that permit the expression of the first and second nucleic acids, to produce the CPMV polyprotein and the CPMV protease, the CPMV polyprotein being processed into large coat protein and the small coat protein by the CPMV protease, thereby producing the VLP; d) harvesting the host or host cell.
32. The method of any one of claims 29 to 31, wherein the host is a plant and the host cell is a plant cell.
33. The method of claims 29 or 31, wherein the modified Cowpea Mosaic Virus (CPMV) virus like particle (VLP) is purified from the host or host cell.
PCT/CA2021/051352 2021-09-28 2021-09-28 Cpmv vlps displaying sars-cov-2 epitopes WO2023049983A1 (en)

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Citations (2)

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