CN102180952A - Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine - Google Patents
Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine Download PDFInfo
- Publication number
- CN102180952A CN102180952A CN 201110120265 CN201110120265A CN102180952A CN 102180952 A CN102180952 A CN 102180952A CN 201110120265 CN201110120265 CN 201110120265 CN 201110120265 A CN201110120265 A CN 201110120265A CN 102180952 A CN102180952 A CN 102180952A
- Authority
- CN
- China
- Prior art keywords
- ala
- antigen polypeptide
- foot
- leu
- gly
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Abstract
The invention provides a foot and mouth disease virus antigen polypeptide, a foot and mouth disease virus fusion antigen polypeptide and a foot and mouth disease virus vaccine containing the antigen polypeptide and/or the fusion antigen polypeptide. The invention further provides application of the antigen polypeptide, the fusion antigen polypeptide and the vaccine in prevention and control of foot and mouth disease virus infection. The foot and mouth disease virus antigen polypeptide, the fusion antigen polypeptide and the vaccine have broad-spectrum immunogenicity, and can generate good immunogenicity on different foot and mouth disease viruses and variant strains thereof.
Description
Technical field
The present invention relates to the foot-and-mouth disease virus antigen polypeptide, fused antigen polypeptide, and the foot and mouth disease virus vaccine that contains above-mentioned antigenic peptide and/or fused antigen polypeptide.The invention still further relates to above-mentioned antigenic peptide, the preparation of fused antigen polypeptide and vaccine and application thereof.
Background technology
Foot and mouth disease be by foot and mouth disease virus caused a kind of acute, hot, the height contagious infection zoonosis.Foot and mouth disease is mainly encroached on cloven-hoofed animal, and its clinical diagnosis is characterized as oral mucosa, hoof and skin of breast generation blister.It is high but its sickness rate can reach 100% that adult animals infects after the foot and mouth disease general lethality rate, and a large amount of blisters can appear in mouth, the hoof of morbidity animal, and are spiritual depressed, and then make animal yield fall sharply.Cub then loses the sudden death of symptom ground through regular meeting after infecting foot and mouth disease, and lethality rate can reach 100% when serious.Because foot and mouth disease is propagated rapidly, is difficult to control, remedial measures is few, can only butcher with collective after therefore each outburst and destroy the livestock that catches an illness by fire with trouble without offspring, thereby cause enormous economic loss for the herding industry.
Foot and mouth disease virus is the pathogenic former of foot and mouth disease, and it belongs to picornavirus, has characteristics such as many serotypes, high variability.Known foot and mouth disease virus has O, A, C, SAT1 (South Africa I type), SAT2 (South Africa II type), SAT3 (South Africa III type) and 7 main serotypes of Asial (Asia I type) at present.Every kind of principal mode divides some hypotypes again, at present the existing kind more than 70 of the hypotype of finding.Antigenicity between foot and mouth disease virus is various is usually different; immunity alternately each other; and the degree of antigenic variation is also very big in a kind of serotype, may be to but not protection of the another kind of hypotype in the same serotype to such an extent as to can resist a kind of aftosa vaccine of hypotype effectively.
Because immunity mutually usually between the high mutation of foot and mouth disease virus and each serotype is so bring huge difficulty for the preventing and controlling of foot and mouth disease.Still press at present to provide foot and mouth disease virus is had good immunogenic vaccine, the foot and mouth disease virus that the ideal vaccine is also tackled multiple different subtype all has good immunogenicity, thereby can provide immunoprotection widely for livestock.
Summary of the invention
The present invention relates to the foot-and-mouth disease virus antigen polypeptide; the fused antigen polypeptide; and the foot and mouth disease virus vaccine that contains above-mentioned antigenic peptide and/or fused antigen polypeptide; this antigenic peptide; fused antigen polypeptide and vaccine can make host animal produce immunogenicity at multiple different pedigree foot and mouth disease viruses, thereby provide immunoprotection at multiple different pedigree foot and mouth disease viruses for host animal.
For the present invention, term " immunity " is meant, with suitable form and by suitable approach to host animal give with a certain antigen after, it is antigenic specific cell-mediated and/or based on the immunne response of antibody to induce host animal to produce at this, for example, the activation of antibody and/or production of cytokines and/or cytotoxic T cell, antigen presenting cell, helper cell, dendritic cell, and/or other cell response reaction.
For the present invention, term " immunogenicity " is meant that one or more antigen induction host animals produce at this one or more antigenic specific immunoreactive ability.
For the present invention, term " antigenic peptide " be meant by two or more amino acid by peptide bond covalently bound form have an immunogenic peptide chain structure.Peptide chain structure of the present invention can be a straight chain, the band branched structure, and/or band shape structure.
For the present invention, term " vaccine " be meant contain that one or more have immunogenic antigen and be formulated into can be to the preparation of host animal form of medication.After being incorporated into vaccine in the host animal body, this vaccine just can excite host animal to produce at this one or more antigenic immune response.
For the present invention, term " host animal " is meant the animal that can be invaded and allow foot and mouth disease virus to duplicate by foot and mouth disease virus in its body.In some embodiments, host animal is an artiodactyl.In some embodiments, host animal is livestock animals such as pig, ox, sheep.The intrusion and duplicate of foot and mouth disease virus in host animal may make host animal produce the Clinical symptoms of foot and mouth disease, also may not make host animal produce any Clinical symptoms.
The invention provides the foot-and-mouth disease virus antigen polypeptide of a class synthetic.According to an aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Cys Lys Tyr Ala Gly X1 Ser Leu X2 Asn Val Arg Gly Asp Leu X3 X4 Leu X5 Gln Lys Ala Ala Arg X6 Leu Pro Thr Ser Phe Asn Tyr X7 Ala Ile Lys (SEQ ID NO:1), wherein, X1=Gly or Ala, X2=Thr, Leu or Pro, X3=Gln or Leu, X4=Val, Glu or Ala, X5=Ala or Asp, X6=Pro or Cys, X7=Gly or Cys, and X6 and X7 must have one and can only have one to get Cys.
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly X1 Ser Leu X2 Asn Val Arg Gly Asp Leu X3 X4Leu X5 Gln Lys Ala Ala Arg X6 Leu Pro Thr Ser Phe Asn Tyr X7 Ala Ile Lys (SEQ ID NO:2), wherein, X1=Gly or Ala, X2=Thr, Leu or Pro, X3=Gln or Leu, X4=Val, Glu or Ala, X5=Ala or Asp, X6=Pro or Cys, X7=Gly or Cys, and X6 and X7 must have one and can only have one to get Cys.
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly X1 Ser Leu Thr Asn Val Arg Gly Asp Leu X2 X3Leu X4 Gln Lys Ala Ala Arg Cys Leu Pro Thr Ser Phe Asn Tyr Gly Ala Ile Lys (SEQ ID NO:3), wherein, X1=Gly or Ala, X2=Gln or Leu, X3=Val, Glu or Ala, X4=Ala or Asp.
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Cys
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Val?Tyr?Asn?Gly?Asn?Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Cys?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Gly?Ala?Ile?Lys(SEQ?ID?NO：5)。
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Cys?Ala?Ile?Lys(SEQ?ID?NO：6)。
According to another aspect of the present invention, antigenic peptide provided by the invention contains aminoacid sequence as follows:
Val?Tyr?Asn?Gly?Asn?Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Cys?Ala?Ile?Lys(SEQ?ID?NO：7)。
Antigenic peptide of the present invention comprises above-mentioned aminoacid sequence and carries out the sequence that one or more amino acid whose replacement, interpolation and/or deletion produced at one or more amino acid sites.Amino acid is replaced and is comprised conservative the replacement and non-conservative replacement.Conservative replacement is meant the replacement between the amino acid of similar performance, the for example replacement between the polare Aminosaeren (as the replacement between glutamine and the l-asparagine), replacement between the hydrophobic amino acid (as the replacement between leucine, Isoleucine, methionine(Met) and the Xie Ansuan), and the replacement between the band amino acids with identical charges (as the replacement between arginine, Methionin and the Histidine, the perhaps replacement between L-glutamic acid and the aspartic acid) etc.Non-conservative replacement is meant the replacement between the amino acid of different nature, and the non-conservative replacement that the present invention comprised will can not change specific immunity originality and the activity of described antigenic peptide at foot and mouth disease virus.Amino acid whose replacement of the present invention, interpolation and/or deletion will be no more than 1, and 2,3,4,5,6,7,8,9 or 10 amino acid.
According to another aspect of the present invention, the invention provides the fused antigen polypeptide that a class comprises two or more antigenic peptides of the present invention.A plurality of antigenic peptides that the fused antigen polypeptide is comprised covalently or non-covalently connect each other.Covalently bound for example can be that perhaps C interconnects by ester bond, ehter bond, phosphoric acid ester bond, amido linkage, peptide bond, imide key, carbon-sulfide linkage.Non-covalent connection for example can be that perhaps hydrogen bond interconnects by interionic interaction force, hydrophobic interaction.
In an embodiment of the invention, the contained a plurality of antigenic peptides of fused antigen polypeptide connect by connection chain.For the present invention, term " connection chain " is meant, is used for covalently or non-covalently connecting the structural unit of two adjacent peptide sequences, and the introducing of this structural unit can not produce infringement to the immunogenicity of fused antigen polypeptide.Connection chain can comprise one or more amino-acid residues, and connection chain can also comprise for example C
1-C
6Alkyl, C
3-C
6Structures such as cycloalkyl, aryl or heteroaryl.Prior art has disclosed some known connection chains, and those skilled in the art can easily be selected as required.
In yet another embodiment of the present invention, connection chain used in the fused antigen polypeptide is by one or more Methionins, L-Ala, and glycine, Serine and/or proline(Pro) or its arbitrary combination are formed.For example connection chain is by 1, and 2,3,4,5,6,7,8,9,10 or more a plurality of aforementioned amino acid or its arbitrary combination are formed.In yet another embodiment of the present invention, used connection chain is the small peptide of being made up of one or more Methionins in the fused antigen polypeptide, for example short peptide sequence Lys Lys, Lys Lys Lys, Lys Lys Lys Lys, Lys Lys Lys Lys Lys, Lys Lys Lys Lys Lys Lys.In yet another embodiment of the present invention, used connection chain is to mix the small peptide of forming by one or more Methionins and L-Ala in the fused antigen polypeptide, Lys Ala Lys for example, Ala Lys Ala, Lys Ala Ala Lys, Ala Lys Lys Ala, Lys Lys Ala Lys, Ala Lys Ala Lys, Lys Lys Ala Lys Lys or Lys Ala Lys Lys Ala Lys.In yet another embodiment of the present invention, used connection chain is by one or more proline(Pro) in the fused antigen polypeptide, and/or the polypeptide of Serine and/or glycine mixing composition, Pro Ser Pro for example, Ser Pro Ser, Ser Ser Pro, Pro Pro Ser, Gly Ser Gly, Ser Gly Ser, Ser Ser Gly Ser, Gly Gly Ser Gly, Gly Ser Gly Ser, Gly Ser Gly Ser Ser, Gly Gly Gly Gly Ser.
The antigenic peptide quantity that the fused antigen polypeptide is comprised for example can be 2,3, and 4,5,6,7,8,9,10 or more a plurality of.The antigenic peptide that the fused antigen polypeptide is comprised can be identical also can be inequality.For example, the fused antigen polypeptide comprises two antigenic peptides shown in the SEQ ID NO.1, perhaps comprise two antigenic peptides shown in the SEQ ID NO.2, also or comprise the antigenic peptide shown in an antigenic peptide shown in the SEQ ID NO.1 and the SEQ ID NO.2.
The antigenic peptide that the fused antigen polypeptide comprises can be natural foot-and-mouth disease virus antigen peptide sequence, also can be the foot-and-mouth disease virus antigen polypeptide of synthetic.In an embodiment of the invention, the fused antigen polypeptide comprises one or more antigenic peptide sequences provided by the invention and one or more natural antigen peptide sequence.For example, the fused antigen polypeptide comprises one section antigenic peptide sequence provided by the invention and one section natural antigen peptide sequence.Again for example, the fused antigen polypeptide comprises at least one section antigenic peptide sequence provided by the invention and at least one section natural antigenic peptide sequence.
In yet another embodiment of the present invention, fused antigen polypeptide of the present invention comprises all or part of aminoacid sequence of foot and mouth disease virus surface glutelin VP1.A kind of natural acid sequence of the glutelin VP1 of known O type foot and mouth disease virus contains 213 amino acid, and its aminoacid sequence is as follows:
Thr?Thr?Ser?Thr?Gly?Glu?Ser?Ala?Asp?Pro?Val?Ala?Pro?Thr?Val?Glu?Ser?Tyr?Val?Gly?Gln?Thr?Gln?Val?Gln?Arg?Arg?His?His?Thr?Asp?Val?Ser?Phe?Ile?Leu?Asp?Arg?Phe?Val?Lys?Val?Thr?Pro?Lys?Asp?Ser?Ile?Asn?Val?Leu?Asp?Leu?Met?Gln?Thr?Pro?Pro?His?Thr?Leu?Val?Gly?Ala?Leu?Leu?Arg?Thr?Ala?Thr?Tyr?Tyr?Phe?Ala?Asp?Leu?Glu?Val?Ala?Val?Lys?His?Glu?Gly?Asp?Leu?Thr?Trp?Val?Pro?Asn?Gly?Ala?Pro?Glu?Ala?Ala?Leu?Asp?Asn?Thr?Thr?Asn?Pro?Thr?Ala?Tyr?His?Lys?Ala?Pro?Leu?Thr?Arg?Leu?Ala?Leu?Pro?Tyr?Thr?Ala?Pro?His?Arg?Val?Leu?Ala?Thr?Val?Tyr?Asn?Gly?Asn?Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Gly?Ala?Ile?Lys?Ala?Thr?Arg?Val?Thr?Glu?Leu?Leu?Tyr?Arg?Met?Lys?Arg?Ala?Glu?Thr?Tyr?Cys?Pro?Arg?Pro?Leu?Leu?Ala?Val?His?Pro?Ser?Ala?Ala?Arg?His?Lys?Gln?Lys?Ile?Val?Ala?Pro?Val?Lys?Gln?Ser?Leu(GenBank?No.：ADH32342.1)(SEQ?ID?NO：8)。
In yet another embodiment of the present invention, fused antigen polypeptide of the present invention comprises one or more natural antigen peptide sequences as follows:
Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Gly?Ala?Ile?Lys(SEQ?ID?NO：9)；
Val?Tyr?Asn?Gly?Asn?Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Gly?Ala?Ile?Lys(SEQ?ID?NO：10)。
In another aspect of the present invention, the invention provides the fused antigen polypeptide that a class comprises antigenic peptide of the present invention and t helper cell epi-position.Antigenic peptide that the fused antigen polypeptide is comprised and t helper cell epi-position can be respectively one or more, and for example the fused antigen polypeptide comprises 1 respectively, 2, and 3,4,5,6,7,8,9,10 or more a plurality of antigenic peptide and t helper cell epi-position.The antigenic peptide that the fused antigen polypeptide is comprised can be identical also can be inequality, the t helper cell epi-position that is comprised can be identical also can be inequality.Can connect by himself amino acids formed peptide bond between adjacent antigenic peptide and the t helper cell epi-position, between the adjacent antigenic peptide or between the adjacent t helper cell epi-position, also or other any-mode of mentioning by the aforementioned part of the present invention be connected, for example connect antigenic peptide and t helper cell epi-position by connection chain.
The non-limiting example of this type of fused antigen polypeptide for example is:
Ile Ser Ile Glu Ser Ile Gly Lys Val Ile Val Lys His Ile Glu Gly Ile Phe Leu Leu Lys Val Tyr Asn Gly Asn Cys Lys TyrAla Gly Gly Ser Leu ThrAsn Val Arg Gly Asp Leu Gln Val Leu Ala Gln Lys Ala Ala Arg Cys Leu Pro Thr Ser Phe Asn Tyr Gly Ala Ile Lys (SEQ ID NO.11) and
Ile?Ser?Ile?Glu?Ser?Ile?Gly?Lys?Val?Ile?Val?Lys?His?Ile?Glu?Gly?Ile?Phe?Leu?Leu?Lys?Val?Tyr?Asn?Gly?Asn?Cys?Lys?Tyr?Ala?Gly?Gly?Ser?Leu?Thr?Asn?Val?Arg?Gly?Asp?Leu?Gln?Val?Leu?Ala?Gln?Lys?Ala?Ala?Arg?Pro?Leu?Pro?Thr?Ser?Phe?Asn?Tyr?Cys?Ala?Ile?Lys(SEQ?ID?NO.12)。
The t helper cell epi-position of herein addressing is meant the aminoacid sequence of discerning for t helper cell on the antigen.T helper cell is meant the T cell that a class is specific, thereby its effect is auxiliary T killer cell to be made the T killer cell combine with target antigen or cell and eliminate or kill this target antigen or cell.Prior art has disclosed some known t helper cell epi-positions, and those skilled in the art can select suitable t helper cell epi-position and are used in the fused antigen polypeptide of the present invention on understanding the basis of this purpose according to the technology general knowledge of its grasp.The example of t helper cell epi-position includes but not limited to, hepatitis B virus surface and cAg t helper cell epi-position, Toxins, pertussis t helper cell epi-position, tetanus toxin t helper cell epi-position, Measles virus F albumen t helper cell epi-position, chlamydia trachomatis major outer membrane albumen t helper cell epi-position, diphtheria toxin t helper cell epi-position, plasmodium falciparum ring sporophyte t helper cell epi-position, graceful Sen Shi fluke trisaccharide phosphoric acid salt isomerase t helper cell epi-position, and intestinal bacteria TraT t helper cell epi-position.
United States Patent (USP) U.S.7,744, No. 898 (applying date is on September 8th, 2005, denomination of invention is " Peptides for Inducing Cytotoxic T Lymphocyte Responses to Hepatitis B Virus "), and United States Patent (USP) U.S.7,833, No. 532 (its applying date is on August 12nd, 2003, denomination of invention for " Immunogenic Lipopeptides Comprising T-helper and Cytotoxic T Lymphocyte (CTL) Epitopes) in introduced multiple t helper cell epi-position.For example, U.S.7,744,898 specification sheetss have listed the wherein t helper cell epi-position shown in the SEQ ID NOs.6-9.Again for example, U.S.7 has listed wherein SEQ ID NOs.1 in 833,532 specification sheetss, the described t helper cell epi-position of 14-52.U.S.7,744,898 and U.S.7,833,532 are incorporated among the application with for referencial use by reference in full at this.
In another aspect of the present invention, the invention provides the fused antigen polypeptide that a class comprises antigenic peptide of the present invention and immunostimulatory sequence.Antigenic peptide that the fused antigen polypeptide is comprised and immunostimulatory sequence can be respectively one or more, and for example the fused antigen polypeptide comprises 1 respectively, 2, and 3,4,5,6,7,8,9,10 or more a plurality of antigenic peptide and immunostimulatory sequence.The antigenic peptide that the fused antigen polypeptide is comprised can be identical also can be inequality, the immunostimulatory sequence that is comprised can be identical also can be inequality.Can connect by himself amino acids formed peptide bond between the adjacent antigenic peptide and immunostimulatory sequence, between the adjacent antigenic peptide or between the adjacent immunostimulatory sequence, also or other any-mode of mentioning by the aforementioned part of the present invention be connected, for example connect antigenic peptide and immunostimulatory sequence by connection chain.
The immunostimulatory sequence of herein addressing be meant can the enhancement antigen immunogenicity of polypeptides material, the structural domain of the invasin albumen (Inv) that belongs to from the bacterium Yersinia (people such as Brett for example, the Europe Journal of Immunology, 1993,23:1608-1614) or from the immunostimulation analogue of respective regions in other Yersinia invasin albumen.Immunostimulatory sequence commonly used is the known technology of this area, and those skilled in the art can select suitable immunostimulatory sequence and are used in the fused antigen polypeptide of the present invention according to the technology general knowledge of its grasp.
In another aspect of the present invention, the invention provides a fused antigen polypeptide that comprises antigenic peptide of the present invention, t helper cell epi-position and immunostimulatory sequence roughly the same the time.Antigenic peptide, t helper cell epi-position and the quantity of immunostimulatory sequence in the fused antigen polypeptide can be respectively one or more, for example 1, and 2,3,4,5,6,7,8,9,10 or more a plurality of.For example, the fused antigen polypeptide comprises an antigenic peptide, two or more t helper cell epi-positions, and two or more immunostimulatory sequences.Again for example, the fused antigen polypeptide comprises two or more antigenic peptides, a t helper cell epi-position, and an immunostimulatory sequence.Again for example, the fused antigen polypeptide comprises two or more antigenic peptides, two or more t helper cell epi-positions, and two or more immunostimulatory sequences.Can be connected by the any-mode that the aforementioned part of the present invention is mentioned between adjacent antigenic peptide, t helper cell epi-position and the immunostimulatory sequence, for example connect, for example connect again by the peptide bond that forms between himself amino acid by connection chain.Be to be understood that herein, the antigenic peptide that is comprised in the fused antigen polypeptide, t helper cell epi-position and immunostimulatory sequence can be arranged in any way, for example antigenic peptide directly is connected with immunostimulatory sequence with the t helper cell epi-position respectively, for example the t helper cell epi-position directly is connected with immunostimulatory sequence with antigenic peptide respectively again, and for example immunostimulatory sequence directly is connected with the t helper cell epi-position with antigenic peptide respectively again.
In another aspect of the present invention, the peptide chain of antigenic peptide provided by the invention or fused antigen polypeptide can have ring texture.Described ring texture can ways of connecting forms by forming covalently or non-covalently between two or more amino acid of peptide chain, for example between two or more amino acid, form disulfide linkage, peptide bond, carbon bond (for example C-C or C=C), ester bond, ehter bond, azo bond, the C-S-C key, the mode of C-N-C key or C=N-C key forms.In an embodiment of the invention, antigenic peptide or fused antigen polypeptide form ring texture by form disulfide linkage between two halfcystines of himself.In an embodiment of the invention, the antigenic peptide that comprises sequence shown in the SEQ ID NO:1-7 has ring texture.In yet another embodiment of the present invention, comprising the ring texture that the antigenic peptide of sequence shown in the SEQ ID NO:1-7 has forms by forming disulfide linkage between halfcystine.
The polypeptide cyclisation can realize by the known technology of this area, for example can come that polypeptide is carried out cyclisation by natural method and handle, and handles the acquisition cyclized structure thereby perhaps come that by chemical synthesis process polypeptide is carried out cyclisation.Document " people such as Anwer; Int.J Pep.Protein Res.36:392-399 (1990) " and " people such as Rivera-Baeza; Neuropeptides30:327-333 (1996) " write up the method for polypeptide cyclisation, they incorporate the application into for referencial use by reference in full at this.
In an embodiment of the invention, the invention provides a kind of cyclisation degree greater than 85% antigenic peptide and fused antigen polypeptide.In an embodiment of the invention, the invention provides a kind of cyclisation degree and be at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% antigenic peptide and fused antigen polypeptide.In yet another embodiment of the present invention, the invention provides a kind of cyclisation degree greater than 87.5% antigenic peptide and fused antigen polypeptide." cyclisation degree " used herein is meant that the peptide chain that has ring texture in antigenic peptide or the fused antigen polypeptide accounts for the per-cent of total peptide chain number.Those skilled in the art can select suitable method to measure the cyclisation degree according to the form of the chemical bond that forms ring texture.For example, if form ring texture by disulfide linkage, its cyclisation degree can be measured by the Ellman method of standard, and this cyclisation degree is calculated as the per-cent that accounts for initial total free sulfhydryl group (SH) number by sulfydryl (SH) number of disulfide linkage Cheng Huan.The Ellman method belongs to the known technology of this area, and write up is in document people such as ", Anal.Biochem.94:75-81 (1979) " Ellman for it, and the document is incorporated the application into for referencial use by reference in full at this.Simply, the Ellman method can be measured the content of free sulfhydryl group in the polypeptide (SH), uses the Ellman method to measure polypeptide cyclisation degree and may be summarized to be following key step: prepare the halfcystine solution of a plurality of different concns and add Ellman reagent respectively and react; The absorbancy of free sulfhydryl group (SH) in the halfcystine solution of various concentration behind the assaying reaction is made absorbancy-concentration standard curve and is calculated the average light absorption value of SH; The working sample solution absorbency, and according to calculating the content that the average light absorption value of SH that obtains is calculated free SH in the sample solution before; The content of free SH is calculated into amount and then the cyclisation degree of polypeptide in the calculation sample solution again of the SH of ring in the solution per sample.
In another aspect of this invention, the invention provides a kind of nucleotide sequence of encode antigenic peptide of the present invention and fused antigen polypeptide.In an embodiment of the invention, the invention provides coding nucleotide sequence of fused antigen polypeptide shown in antigenic peptide and the SEQ ID NOs:11-12 shown in SEQ ID NOs:1-7.
The preparation of polypeptide can realize that it can prepare by chemical synthesis process by the known technology of this area, also can prepare by gene engineering method.Chemical synthesis process mainly comprises solid phase synthesis and the synthetic two kinds of methods of liquid phase.Solid-phase peptide synthesis comprises, Merrifield solid-phase synthesis for example, this method write up document " Merrifield, J.Am.Chem.Soc.85:2149-2154 " and " people such as M.Bodanszky; " Peptide Synthesis ", John Wiley ﹠amp; Sons, Second Edition, 1976 " and " J.Meienhofer, " Hormonal Proteins and Peptides ", Vo1.2, p.46, Academic Press (New York), 1983 " in.By reference these documents are incorporated among the application in full with for referencial use at this.The Merrifield solid-phase synthesis mainly may further comprise the steps, and according to the aminoacid sequence of target polypeptides, protected C-terminal amino acid is connected with resin; Connect the after scouring resin; Slough the protecting group (for example, tertbutyloxycarbonyl) on the C-terminal amino acid α amino, the connecting key of must guarantee when sloughing this protecting group not rupture this amino acid and interlaminar resin; The protected amino acid of coupling penult C-terminal on the resin of gained then is when carrying out this coupling, at second amino acid whose free carboxy be connected between first amino acid whose amino on the resin and form an amido linkage; The amino acid order of connection according to target polypeptides repeats the previous reaction process successively, all is connected on the resin up to all amino acid; At last, cut protected peptide, slough protecting group and can obtain target polypeptides from resin.
Polypeptide of the present invention also can prepare by liquid-phase synthesis process, for example can be with the preparation of the solution method of peptide synthesis of standard, this method write up document " E.Schroder and K.Kubke; " The Peptides "; Vol.1, Academic Press (New York), 1965 " in.By reference the document is incorporated among the application in full with for referencial use at this.Liquid phase synthesizing method mainly comprises, utilizes the chemistry or enzyme method substep coupling amino acid or the peptide fragment that form amido linkage.Gene engineering method is expressed the method that generates corresponding antigens polypeptide or fused antigen polypeptide for the nucleotide sequence that utilizes coding corresponding antigens polypeptide or fused antigen polypeptide in the host cell that is fit to.The detailed description of relevant this method can be with reference to " Sambrook, Fritsch ﹠amp; Maniatis, Molecular Cloning:A laboratory Manual (the 2nd edition, Cold Spring Harbor Laboratory, 1989) ".
According to another aspect of the present invention, the invention provides a kind of vaccine, it comprises foot-and-mouth disease virus antigen polypeptide of the present invention and/or fused antigen polypeptide, and pharmaceutically acceptable vehicle.In one embodiment, vaccine of the present invention comprises multiple foot-and-mouth disease virus antigen polypeptide of the present invention and/or fused antigen polypeptide.In another embodiment, vaccine of the present invention comprises 2 kinds, 4 kinds, 8 kinds, 16 kinds, 32 kinds or 64 kinds of foot-and-mouth disease virus antigen polypeptide of the present invention and/or fused antigen polypeptide.In another embodiment, vaccine of the present invention comprises at least 2 kinds, 4 kinds, 8 kinds, 16 kinds, 32 kinds or 64 kinds of foot-and-mouth disease virus antigen polypeptide of the present invention and/or fused antigen polypeptide.In another embodiment, vaccine of the present invention comprises at least 2 kinds, 4 kinds, 8 kinds, 16 kinds, 32 kinds or the 64 kinds foot-and-mouth disease virus antigen polypeptide that comprise sequence shown in SEQ ID NO:1-7.
For the present invention, term " pharmaceutically acceptable vehicle " is meant, any suitable pharmaceutically acceptable adjuvant that is used for pharmaceutical preparation, carrier, thinner, sanitas etc.Term " pharmaceutically acceptable " is meant that other composition in corresponding vehicle and the pharmaceutical preparation is complementary at aspects such as chemical property and physicalies, and is complementary with the administration individuality on physiology, is that the administration individuality can tolerate.Only as exemplary purpose, known adjuvant includes but not limited to, complete Freund's adjuvant for example, incomplete Freund's adjuvant, the mineral substance gel is such as aluminium hydroxide, surfactant is such as the soft phosphatide of haemolysis, Pluronic polyols, polyanion, peptide, oil-emulsion, the agent of hydrocarbon emulsus, keyhole limpet hemocyanin etc.In an embodiment of the invention, the adjuvant that uses is the Montanide ISA series adjuvant that French SEPPIC company provides, and for example Montanide ISA 28, Montanide ISA 035, Montanide ISA 025, Montanide ISA 206, Montanide ISA 575, Montanide ISA 563, Montanide ISA 50V (such as Montanide ISA 50V2), Montanide ISA 775, Montanide ISA 763A, Montanide ISA 70.Known carrier includes but not limited to, sterile liquid, water for example, oil, the perhaps mixture of water and oil, described oil can be for example peanut oil, soybean oil, mineral oil, sesame wet goods.Known thinner includes but not limited to, water, salt solution, glucose, ethanol, glycerine and analogue thereof.Known sanitas includes but not limited to, Thiomersalate and EDTA etc.
Pharmaceutically acceptable vectorial selection can realize that the vaccine formulation that those skilled in the art can prepare is as required selected suitable pharmaceutically acceptable vehicle based on prior art by the known technology of this area.For example, for preparation oral liquid (for example, suspension, tincture or solution), selected vehicle can comprise for example water, oil, alcohols, seasonings, sanitas, tinting material etc.Again for example, for preparation oral solid formulation (for example, pulvis, capsule or tablet), selected vehicle can comprise for example starch, carbohydrate, thinner, granulating agent, lubricant, tackiness agent, disintegrating agent etc.In addition, if desired, vaccine of the present invention can also be prepared into sweet tablet or enteric coating, also or controlled release preparation.
Can also be with foot-and-mouth disease virus antigen polypeptide of the present invention and/or fused antigen polypeptide and/or vaccine, be mixed with polyvalent vaccine with other foot-and-mouth disease virus antigen and/or vaccine.Other foot-and-mouth disease virus antigen and/or vaccine include but not limited to, other antigenic peptide or fused antigen polypeptide, inactivation of viruses strain, virus antigen, nucleic acid vaccine, immunologic stimulant etc.The polyvalent vaccine that obtains has the immunogenicity of wide spectrum, and it can have immunocompetence to the hoof-and-mouth disease strain and the variant thereof of multiple serotype or multiple hypotype, and the livestock after the polyvalent vaccine immunity can obtain the immunizing power to multiple hoof-and-mouth disease strain.
According to another aspect of the present invention, the invention provides the method for a kind of control and/or prevention animal foot and mouth disease, this method comprises the antigenic peptide of the present invention that the animal immune of these needs significant quantity is arranged, and/or the fused antigen polypeptide, and/or vaccine.Term " immune significant quantity " is meant the immunoreactive amount that causes at foot and mouth disease virus in the administration animal body.The immunity significant quantity is relevant with the factors such as species, kind, age, body weight and healthy state of administration animal.In one embodiment, vaccine of the present invention is used for control and/or prevention pig, ox or sheep foot and mouth disease.In another embodiment, vaccine of the present invention is used for control and/or prevention Schweineseuche.In another embodiment, vaccine of the present invention is used to control and/or prevent the O serotype of Schweineseuche.Therefore, the present invention provides a kind of application that antigenic peptide of the present invention and/or fused antigen polypeptide is used for preparing the medicine of control and/or prevention animal foot and mouth disease in yet another aspect.
Vaccine of the present invention can be prepared by the medicine compounding process of this area routine, for example, is mixed into uniform mixture as the antigenic peptide of the present invention of effective constituent and/or fused antigen polypeptide and pharmaceutically acceptable vehicle.Vaccine of the present invention can be by any known route of administration administration, for example subcutaneous, oral, intramuscular or other non-enteron aisles or enteron aisle administration.In an embodiment of the invention, vaccine of the present invention is through subcutaneous or intramuscularly administration.As is known to the person skilled in the art, the consumption of vaccine is according to the difference of factors such as age of the activity of activeconstituents, administration animal individual, body weight and change.Those skilled in the art can easily determine only vaccine consumption according to the factor of aforementioned affect consumption.
Antigenic peptide of the present invention, fused antigen polypeptide and vaccine can detect its immune efficacy by known several different methods.The test method that prior art provides the multiple assessment vaccine immunity to render a service for example, is attacked malicious protection test, serological test etc.Attack malicious protection test and adopt directly that strong virus is former to carry out the artificial challenge to the experimental animal after the vaccine inoculation, judge the immune efficacy of vaccine then according to the incidence of animal.Attack malicious protection test and be the most direct method that the check vaccine immunity is renderd a service, a plurality of countries that therefore comprise China all require to adopt and attack the immune efficacy that live vaccine is estimated in malicious protection test.Relevant concrete operation method of attacking malicious protection test can be referring to, relevant half protective number (PD in 2010 editions " Chinese veterinary drug allusion quotations "
50) chapters and sections measured.Also can adopt the serological test method to assess the immune efficacy of vaccine, for example by measuring anti-body contg that produces in the immune serum and then the immune efficacy of judging vaccine.Anti-body contg in the serum can be measured by the known method of prior art, for example western blot analysis (Werstern Blot) or enzyme linked immunosorbent assay (ELISA).Have cognation between these serological index and the vaccine potency, it can be used for vaccine immunity effectiveness is carried out entry evaluation.Those skilled in the art can select suitable test method according to factors such as concrete test conditions and test objectives.
According to another aspect of the present invention, the invention provides a kind of method that detects foot and mouth disease virus antibody, this method comprises: one or more antigenic peptides of the present invention or fused antigen polypeptide are provided; This antigenic peptide or fused antigen polypeptide are contacted with specimen, make antigenic peptide or fused antigen polypeptide and foot and mouth disease virus antibodies form antigen-antibody complex; Detect foot and mouth disease virus antibody.Described specimen can be any suitable biological sample from host animal, for example whole blood, serum, blood plasma, also or body fluid.Specimen can be through pretreated, also or untreated.
Can realize by various known technology for detection of antibodies in the foot and mouth disease virus antibody detection method of the present invention, for example western blot analysis, perhaps enzyme linked immunosorbent assay etc.United States Patent (USP) U.S.Nos.4 discloses the immuno analytical method of many detection antibody in 016,043,4,424,279,4,018,653, and these United States Patent (USP)s are incorporated the application into for referencial use by reference in full at this.For example, the present invention can use the double-antibody sandwich elisa method to detect foot and mouth disease virus antibody, this method generally includes following steps: capture agent (antigenic peptide for example of the present invention or fused antigen polypeptide) is fixed on the solid substrate, and the specimen (for example serum of host animal) that will contain target protein (for example foot and mouth disease virus antibody) then contacts with capture agent to form antigen-antibody complex; The detection antibody of detectable reporter molecule that added mark, reaction forms capture agent-target protein-detection antibody complex; Remove unreacted matters, then the signal that produces of examining report molecule and then as qualitative or quantitative analysis.
According to a further aspect of the invention, the invention provides a kind of test kit that detects foot and mouth disease virus antibody, this test kit comprises: a) antigenic peptide of the present invention or fused antigen polypeptide, and, b) described antigenic peptide or fused antigen polypeptide can be fixed stationary phase on it.Stationary phase is solid substrate normally.Test kit of the present invention can also the comprise mark detection antibody of detectable reporter molecule or other can with target protein bonded detection reagent, and/or can with the substrate of examining report molecular reaction.In addition, test kit of the present invention can also further comprise the operation instruction of test kit.
The invention provides foot-and-mouth disease virus antigen polypeptide, fused antigen polypeptide and the vaccine of the synthetic of a class novelty, it can be used for immune host animal makes it produce widely immunizing power at foot and mouth disease virus.Compare with existing foot and mouth disease virus vaccine, antigenic peptide of the present invention, fused antigen polypeptide and vaccine have stronger immunogenicity and immune persistence.It is qualified that the median protective dose of Ministry of Agriculture's regulation foot and mouth disease virus vaccine is greater than 3; the median protective dose of existing foot and mouth disease virus vaccine is all about 6 or lower; and the median protective dose of vaccine of the present invention can be up to more than 12, far above the regulation and the existing foot and mouth disease virus vaccine of the Ministry of Agriculture.Antigenic peptide of the present invention, fused antigen polypeptide and vaccine have the immunity of wide spectrum, and for example the different subtype at O type foot and mouth disease virus has extensive applicability.In addition, because antigenic peptide of the present invention, fused antigen polypeptide and vaccine use peptide sequence not use inactivation of viruses or weak viral disease poison as immunogen, so there is not the side effect that makes the immune animal infective virus in it, therefore antigenic peptide of the present invention, fused antigen polypeptide and vaccine also have higher security.
Embodiment
Following specific embodiment is further to explain to of the present invention, no matter it all should not be construed as under which kind of situation the present invention is constituted any restriction.
The solid phase synthesis of embodiment 1. polypeptide
Plant and instrument: PSI 300B full-automatic polypeptide synthetic instrument, with Rink Amide mbha resin as solid phase carrier; The positive tangential flow ultrafiltration system of Pall Centrasette uses Omega series membranes bag.
Raw material and reagent: the amino acid of 9-fluorenylmethyloxycarbonyl (Fmoc) protection is as starting raw material, other reagent of using in the solid phase synthesis specifically see embodiment with the lower section.All raw materials used in synthetic and reagent can obtain after simple preparation according to known technology by buying pattern acquisition or those skilled in the art on the market.
By the antigenic peptide (being designated as antigenic peptide A) shown in the synthetic SEQ ID NO.11 of Merrifield solid-phase synthesis.
1, polypeptide is synthetic
The synthetic order of Merrifield solid phase synthesis is to begin to hold to N from the C end.In the good PSI 300B full-automatic polypeptide synthetic instrument of debugging, constantly add the amino acid of Fmoc protection successively and carry out following reactions steps successively according to the amino-acid sequence of target polypeptides:
(1) Rink Amide MBHA aminoresin is placed N-Methyl pyrrolidone (NMP) solution that contains 15～30% (v/v) hexahydropyridine, reaction is 25-60 minute under 20-28 ℃ of condition, to remove the Fmoc group on the aminoresin;
(2) reacted aminoresin dries up with nitrogen, and washs 6 times with nmp solution;
(3) add I-hydroxybenzotriazole (HOBT), N in the aminoresin after washing, the amino acid of N-DIC (DIC) and first Fmoc radical protection reacted 1-3 hour under 20-28 ℃ of condition then;
(4) add the nmp solution that contains 1.5-4% (m/v) acetyl imidazole (AIM) to reacted system, under 20-28 ℃ of condition, reacted 20-40 minute then;
(5) reacted aminoresin dries up with nitrogen, and washs aminoresin 6 times with nmp solution;
(6) repeating step (1)-(5), termination reaction again after all amino acid on the target polypeptides all are connected to aminoresin, it is standby to reclaim reacted aminoresin then.
2, the cracking of polypeptide
It according to the volume ratio of trifluoroacetic acid/phenol/triethyl silicane/water 90/5/4/1 ratio preparation polypeptide lysate.Then aminoresin is mixed with lysate, and ventilate and agitation condition under room temperature successive reaction 1-4 hour.Reaction finishes the back and reclaims reaction product, promptly gets the polypeptide crude product.
3, the purifying of polypeptide
The Rotary Evaporators evaporation polypeptide crude product 30 to 120 minutes that uses the band cold-trap is to remove the trifluoroacetic acid in the crude product.Use the t-butyl methyl ether precipitation then and collect polypeptide, and use t-butyl methyl ether to clean for several times.At last polypeptide is filtered with sand core funnel and drain, promptly obtain pure target polypeptides.
4, the evaluation of polypeptide
The polypeptide that obtains is measured with substance assistant laser desorpted time-of-flight mass spectrometry (TOFMS) (MALDL-TOF), and its molecular weight is 4395+78AMU.
5, the cyclisation of polypeptide
With 10%DMSO polypeptide is configured to the solution that concentration is 2mg/ml, and at room temperature stirs with magnetic stirring apparatus.With 1% ammonia soln or 1% acetum polypeptide solution is adjusted to the about 6.0-8.0 of pH value then.Measured pH value 1 time every 24 hours, and according to circumstances regulate pH and make it maintain about 6.0-8.0 all the time.Continuous cyclization stopped reaction after 192 hours, and collecting reaction product promptly get the cyclisation polypeptide.Measure the cyclisation degree of antigenic peptide A greater than 87.5% with the Ellman method of standard.
6, the repurity of polypeptide
Use strongly basic anion exchange resin that the cyclisation polypeptide is carried out desalting treatment.Use positive tangential flow ultrafiltration system of Pall Centrasette and Omega series membranes to wrap under the 20-28 ℃ of condition cyclisation polypeptide is carried out ultrafiltration.High performance liquid phase records the purity of antigenic peptide A greater than 80%.
7, the degerming of polypeptide
Again in clean work station, using the aperture is that the sterilizing filter of 0.2 μ m carries out filtration sterilization to the cyclisation polypeptide, can obtain aseptic antigenic peptide A after the purified processing of polypeptide.
The preparation of embodiment 2. antigenic peptide vaccines
1, water preparation
The water for injection that uses sterilising treatment to cross is diluted to 50 μ g/ml with the antigenic peptide A that embodiment 1 obtains, and is the filter filtration of 0.2 μ m with the aperture.
2, oil phase preparation
Sterilization is standby after 30 minutes down at 120 ℃ for oil phase adjuvant Montanide ISA 50 V2.
3, emulsification
Earlier oil phase is added in the emulsion tank, stir with 80～100r/min then, slowly add water simultaneously, add oil phase/water ratio be 1/1, add the back and stirred 2 minutes, stirred 6 minutes with 8500r/min again, make its emulsification form water-in-oil emulsion, promptly get foot and mouth disease virus vaccine of the present invention, be designated as vaccine A.
The potency test of embodiment 3. polypeptide vaccines
The vaccine A for preparing among test sample: the embodiment 2.
Experimental animal: the healthy feeder pig of foot and mouth disease feminine gender, the about 40kg/ head of body weight is about 4 monthly ages.
The test seed culture of viruses: O/ZK/93 hoof-and-mouth disease strain (O type), this strain is provided by Lanzhou Veterinary Inst., Chinese Acedemy of Agaricultural Sciences.
1, test method
Half protective number (PD according to 2010 editions " Chinese veterinary drug allusion quotation " record
50) measuring method measures the half protective number of vaccine A.Vaccine A is divided into 1 part (1ml vaccine A), 1/3 part (1/3ml vaccine A), 3 dosage groups of 1/9 part (1/9ml vaccine A).Each dosage group respectively by 5 pigs of intramuscular inoculation behind the basal part of the ear once.After the vaccine inoculation 28 days, together with 2 of contrast pigs, intramuscular injection 1000 median infective dose (ID behind every pig basal part of the ear
50The O/ZK/93 hoof-and-mouth disease strain of)/2ml was observed 10 days continuously.Write down the incidence of each treated animal, the animal morbidity promptly is judged to not to be protected.Calculate the percentage of each dosage group immune animal protection.Bubble or ulcer appear in all at least one hoof of contrast pig.The last PD that calculates vaccine A again according to the Reed-Muench method
50
The Reed-Muench method of calculation are prior arts of this area, existing document " Reed; L.J.and Muench; H. (1938). " A Simple Method of Estimating Fifty Percent Endpoints " .The American Journal of Hygiene 27:493-497 " in this is described in detail, the document is incorporated the application into for referencial use by reference at this.
2, test-results
The PD of table 1. vaccine A
50Measurement result
Calculate the PD of vaccine A according to the Reed-Muench method
50Be 12.5.
3, discussion of results
As can be seen from Table 1, vaccine of the present invention for the median protective dose of pig up to more than 12.Median protective dose (the PD of Ministry of Agriculture's regulation aftosa vaccine
50) be greater than 3 qualified, and at present the median protective dose of existing similar foot and mouth disease virus vaccine also all about 6.This shows that the median protective dose of vaccine of the present invention is much larger than the standard of the Ministry of Agriculture, but also far above existing similar vaccine.
Claims (19)
1. foot-and-mouth disease virus antigen polypeptide that comprises aminoacid sequence as follows: Cys Lys Tyr Ala Gly X1 Ser Leu X2 Asn Val Arg Gly Asp Leu X3 X4 Leu X5 Gln Lys Ala Ala Arg X6 Leu Pro Thr Ser Phe Asn Tyr X7 Ala Ile Lys, wherein, X1=Gly or Ala, X2=Thr, Leu or Pro, X3=Gln or Leu, X4=Val, Glu or Ala, X5=Ala or Asp, X6=Pro or Cys, X7=Gly or Cys, and X6 and X7 must have one and can only have one to get Cys.
2. foot-and-mouth disease virus antigen polypeptide as claimed in claim 1, it is characterized in that, comprise aminoacid sequence as follows: Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly X1 Ser Leu X2 Asn Val Arg Gly Asp Leu X3 X4 Leu X5 Gln Lys Ala Ala Arg X6 Leu Pro Thr Ser Phe Asn Tyr X7 Ala Ile Lys, wherein, X1=Gly or Ala, X2=Thr, Leu or Pro, X3=Gln or Leu, X4=Val, Glu or Ala, X5=Ala or Asp, X6=Pro or Cys, X7=Gly or Cys, and X6 and X7 must have one and can only have one to get Cys.
3. foot-and-mouth disease virus antigen polypeptide as claimed in claim 1, it is characterized in that, comprise aminoacid sequence as follows: Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly X1 Ser Leu Thr Asn Val Arg Gly Asp Leu X2 X3Leu X4 Gln Lys Ala Ala Arg Cys Leu Pro Thr Ser Phe Asn Tyr Gly Ala Ile Lys, wherein, X1=Gly or Ala, X2=Gln or Leu, X3=Val, Glu or Ala, X4=Ala or Asp.
4. foot-and-mouth disease virus antigen polypeptide as claimed in claim 1, it is characterized in that, comprise aminoacid sequence as follows: Cys Lys Tyr Ala Gly Gly Ser Leu Thr Asn Val Arg Gly Asp Leu Gln Val Leu Ala Gln Lys Ala Ala Arg Cys Leu Pro Thr SerPheAsn Tyr GlyAla Ile Lys.
5. foot-and-mouth disease virus antigen polypeptide as claimed in claim 4, it is characterized in that, comprise aminoacid sequence as follows: Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly Gly Ser Leu Thr Asn Val Arg Gly Asp Leu Gln Val Leu Ala Gln Lys Ala Ala Arg Cys Leu Pro Thr Ser Phe Asn Tyr Gly Ala Ile Lys.
6. foot-and-mouth disease virus antigen polypeptide as claimed in claim 1, it is characterized in that, comprise aminoacid sequence as follows: Cys Lys Tyr Ala Gly Gly Ser Leu Thr Asn Val Arg Gly Asp Leu Gln Val Leu Ala Gln Lys Ala Ala Arg Pro Leu Pro Thr Ser Phe Asn Tyr Cys Ala Ile Lys.
7. foot-and-mouth disease virus antigen polypeptide as claimed in claim 6, it is characterized in that, comprise aminoacid sequence as follows: Val Tyr Asn Gly Asn Cys Lys Tyr Ala Gly Gly Ser Leu Thr Asn Val Arg Gly Asp Leu Gln Val Leu Ala Gln Lys Ala Ala Arg Pro Leu Pro Thr Ser Phe Asn Tyr Cys Ala Ile Lys.
8. as each described foot-and-mouth disease virus antigen polypeptide among the claim 1-7, it is characterized in that described antigenic peptide has ring texture.
9. foot-and-mouth disease virus antigen polypeptide as claimed in claim 8 is characterized in that, the cyclisation degree of described antigenic peptide is at least 85%.
10. a foot and mouth disease virus fused antigen polypeptide is characterized in that, comprises at least two and is selected from each described antigenic peptide among the claim 1-7.
11. foot and mouth disease virus fused antigen polypeptide, it is characterized in that, comprising at least one is selected among the claim 1-7 each described antigenic peptide and is selected from one or more peptide sequences of following group: t helper cell epi-position, immunostimulatory sequence and natural port fever aphthous virus antigen polypeptide.
12., it is characterized in that described fused antigen polypeptide has ring texture as claim 10 or 11 described foot and mouth disease virus fused antigen polypeptide.
13. foot and mouth disease virus fused antigen polypeptide as claimed in claim 12 is characterized in that the cyclisation degree of described fused antigen polypeptide is at least 85%.
14. a nucleotide sequence is characterized in that, each described foot and mouth disease virus fused antigen polypeptide among each described foot-and-mouth disease virus antigen polypeptide or the coding claim 10-11 among the coding claim 1-7.
15. a foot and mouth disease virus vaccine is characterized in that, comprises one or more and is selected from each described antigenic peptide or fused antigen polypeptide and pharmaceutically acceptable vehicle among the claim 1-13.
16. as each described antigenic peptide among the claim 1-9 or as the application of each described fused antigen polypeptide among the claim 10-13 in the medicine of preparation prevention and/or control foot and mouth disease virus.
17. application as claimed in claim 16 is characterized in that, described antigenic peptide or fused antigen polypeptide are used to prepare the medicine of prevention and/or control pig, ox or sheep foot and mouth disease.
18. a method that detects foot and mouth disease virus antibody, this method comprises: a) provide a kind of as each described antigenic peptide among the claim 1-9 or as each described fused antigen polypeptide among the claim 10-13; B) thus described antigenic peptide or fused antigen polypeptide contacted with specimen form antigen-antibody complex; C) the foot and mouth disease virus antibody in the test sample.
19. a test kit that detects foot and mouth disease virus antibody, this test kit comprises: a) as each described antigenic peptide among the claim 1-9 or as each described fused antigen polypeptide among the claim 10-13; B) described antigenic peptide or fused antigen polypeptide can be fixed stationary phase on it.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2011101202651A CN102180952B (en) | 2011-05-10 | 2011-05-10 | Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2011101202651A CN102180952B (en) | 2011-05-10 | 2011-05-10 | Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102180952A true CN102180952A (en) | 2011-09-14 |
| CN102180952B CN102180952B (en) | 2012-01-25 |
Family
ID=44567262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2011101202651A Ceased CN102180952B (en) | 2011-05-10 | 2011-05-10 | Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102180952B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102416174A (en) * | 2011-11-23 | 2012-04-18 | 江苏省农业科学院 | O-type foot-and-mouth disease recombined phage vaccine of pig and construction method thereof |
| CN102775478A (en) * | 2012-08-10 | 2012-11-14 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus antigen peptide and vaccine |
| CN104961809A (en) * | 2015-07-10 | 2015-10-07 | 中牧实业股份有限公司 | Foot and mouth disease O-type structure protein VP1 antibody enzyme-linked immune detection reagent kit |
| CN104987368A (en) * | 2013-08-13 | 2015-10-21 | 中牧实业股份有限公司 | Foot-and-mouth disease virus structure protein antibody ELISA kit |
| CN105418738A (en) * | 2015-07-03 | 2016-03-23 | 申联生物医药（上海）有限公司 | A-type antigen polypeptide, fusion antigen polypeptide and vaccine of foot and mouth disease virus |
| CN109187993A (en) * | 2018-09-13 | 2019-01-11 | 中国农业科学院兰州兽医研究所 | A kind of foot and mouth disease A-type virus sIgA antibody ELISA detection kit and its application |
| WO2023240458A1 (en) * | 2022-06-14 | 2023-12-21 | 中国医学科学院病原生物学研究所 | Polypeptide inhibitor of foot-and-mouth disease virus and use thereof |
-
2011
- 2011-05-10 CN CN2011101202651A patent/CN102180952B/en not_active Ceased
Non-Patent Citations (3)
| Title |
|---|
| 《华中农学报》 20090531 张昱 口蹄疫病毒结构蛋白VP1上B细胞表位的筛选鉴定 , 2 * |
| 20100529 Le,V.P. Development of the one-step RT-PCR for VP1 amplification-based , 2 * |
| 20110119 Abdul-Hamid,N.F. Phylogeography of foot-and-mouth disease virus types O and A in , 2 * |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102416174A (en) * | 2011-11-23 | 2012-04-18 | 江苏省农业科学院 | O-type foot-and-mouth disease recombined phage vaccine of pig and construction method thereof |
| CN102775478A (en) * | 2012-08-10 | 2012-11-14 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus antigen peptide and vaccine |
| CN103087156A (en) * | 2012-08-10 | 2013-05-08 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus (FMDV) antigen polypeptide and vaccine |
| CN102775478B (en) * | 2012-08-10 | 2013-06-19 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus antigen peptide and vaccine |
| CN103087156B (en) * | 2012-08-10 | 2013-10-09 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus (FMDV) antigen polypeptide and vaccine |
| CN104987368A (en) * | 2013-08-13 | 2015-10-21 | 中牧实业股份有限公司 | Foot-and-mouth disease virus structure protein antibody ELISA kit |
| CN104987368B (en) * | 2013-08-13 | 2018-09-04 | 中牧实业股份有限公司 | Foot-and-mouth disease antibody ELISA immunity detection reagent |
| CN105418738A (en) * | 2015-07-03 | 2016-03-23 | 申联生物医药（上海）有限公司 | A-type antigen polypeptide, fusion antigen polypeptide and vaccine of foot and mouth disease virus |
| CN105418738B (en) * | 2015-07-03 | 2019-04-19 | 申联生物医药（上海）有限公司 | Foot and mouth disease virus A type antigen polypeptide, fused antigen polypeptide and vaccine |
| CN104961809A (en) * | 2015-07-10 | 2015-10-07 | 中牧实业股份有限公司 | Foot and mouth disease O-type structure protein VP1 antibody enzyme-linked immune detection reagent kit |
| CN104961809B (en) * | 2015-07-10 | 2018-06-26 | 中牧实业股份有限公司 | The O-shaped Structural protein VP1 antibody ELISA immunity detection reagent of ox aftosa |
| CN109187993A (en) * | 2018-09-13 | 2019-01-11 | 中国农业科学院兰州兽医研究所 | A kind of foot and mouth disease A-type virus sIgA antibody ELISA detection kit and its application |
| CN109187993B (en) * | 2018-09-13 | 2020-06-16 | 中国农业科学院兰州兽医研究所 | Foot-and-mouth disease type A virus sIgA antibody ELISA detection kit and application thereof |
| WO2023240458A1 (en) * | 2022-06-14 | 2023-12-21 | 中国医学科学院病原生物学研究所 | Polypeptide inhibitor of foot-and-mouth disease virus and use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102180952B (en) | 2012-01-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102180952B (en) | Foot and mouth disease virus antigen polypeptide, fusion antigen polypeptide and vaccine | |
| TWI232108B (en) | Synthetic peptide vaccines for foot-and-mouth disease | |
| CN105418738B (en) | Foot and mouth disease virus A type antigen polypeptide, fused antigen polypeptide and vaccine | |
| CN104244973B (en) | For the urgent vaccine based on synthetic peptide of aftosa (FMD) | |
| AU570929B2 (en) | Broad spectrum influenza antisera | |
| KR20170102905A (en) | New multivalent nanoparticle-based vaccine | |
| CN117957016A (en) | SARS-COV-2 and influenza combined vaccine | |
| JPH05500517A (en) | Prevention and treatment of acquired immunodeficiency syndrome | |
| JP2002518523A (en) | Peptide compositions for prevention and treatment of HIV infection and immune diseases | |
| NO831098L (en) | PEPTIDES WITH THE SPECIFICITY OF ORAL AND CLOVE DISEASES ANTIGEN | |
| CN116802307A (en) | African Swine Fever (ASF) virus vaccine | |
| CN111448208A (en) | I L-31 peptide immunogen and dosage form thereof for treating and/or preventing atopic dermatitis | |
| JPH08504090A (en) | Anti-feline immunodeficiency virus (FIV) vaccine | |
| WO2012078116A1 (en) | Immunogenic chikungunya virus peptides | |
| CN103087156B (en) | Foot and mouth disease virus (FMDV) antigen polypeptide and vaccine | |
| CN101107360A (en) | HCV F protein and uses thereof | |
| TW202208400A (en) | Use of conserved peptide epitopes from sars-cov-2 for the development of a broad covid-19 vaccine | |
| JPS59501866A (en) | Polypeptides useful for vaccination against enteric viruses | |
| CN101845083B (en) | Synthetic peptide vaccine for treating porcine reproductive and respiratory syndrome and preparation method thereof | |
| AU2004226032A1 (en) | Polypeptide | |
| WO2022043449A1 (en) | Vaccines based on an antigen protein fused to a nanostructuring scaffold | |
| DK2571519T3 (en) | Marker vaccine against classical swine fever | |
| CN104162152A (en) | Swine foot and mouth disease O-type synthetic peptide vaccine and preparation method thereof | |
| CN107827958B (en) | Canine parvovirus synthetic peptide vaccine and preparation method and application thereof | |
| EP3600403A1 (en) | Herpes simplex virus type-1(hsv-1) vaccine strain vc2 generating an anti-ehv-1 immune response |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C35 | Partial or whole invalidation of patent or utility model | ||
| IW01 | Full invalidation of patent right |
Decision date of declaring invalidation: 20140819 Decision number of declaring invalidation: 23482 Granted publication date: 20120125 |