US20130205443A1

US20130205443A1 - Pathogen resistant citrus compositions, organisms, systems, and methods

Info

Publication number: US20130205443A1
Application number: US13/751,936
Authority: US
Inventors: T. Erik Mirkov; Javier Gonzalez-Ramos
Original assignee: Texas A&M University System
Current assignee: Texas A&M University System
Priority date: 2012-01-27
Filing date: 2013-01-28
Publication date: 2013-08-08
Also published as: ZA201405470B; US10285333B2; WO2013112997A1; US20140109472A1; BR112014018559A2; EP2806731A4; CN104244705A; EP2806731A1; MX2014009113A; CN104244705B; AR089830A1

Abstract

The present disclosure relates, according to some embodiments, to pathogen resistant citrus compositions, organisms, systems, and methods. For example, a composition may comprise a peptide (e.g., a defensin peptide) and/or a nucleic acid (e.g., a defensin nucleic acid). A pathogen resistant citrus plant may comprise, in some embodiments, a defensin peptide and/or an expressable nucleic acid encoding a defensin peptide.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application 61/591,680, filed on Jan. 27, 2012 and U.S. Provisional Patent Application 61/641,641, filed on May 2, 2012, both of which applications are incorporated herein by reference.

FIELD OF THE DISCLOSURE

The present disclosure relates, in some embodiments, to pathogen resistant citrus compositions, organisms, systems, and methods.

BACKGROUND OF THE DISCLOSURE

At present, there are no Citrus cultivars resistant to bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las). Indeed, no genetic resistance to these microbial pathogens has ever been found within the Citrus genus. Conventional cross-breeding efforts to produce resistant cultivars have been hindered by the complex reproductive biology and long life cycle of Citrus spp.

SUMMARY

Accordingly, a need has arisen for plants (e.g., citrus) with improved resistance to disease. A further need has arisen for improved methods, compositions, and systems for preparing genetically modified plants (e.g., citrus).
The present disclosure relates, according to some embodiments, to pathogen resistant citrus compositions, organisms, systems, and methods. For example, a composition may comprise a nucleic acid (e.g., a defensin nucleic acid). In some embodiments, a nucleic acid may comprise a nucleic acid sequence (a) having from about 75% to about 100% identity (e.g., about 98% identity) to a defensin sequence (e.g., SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, and/or 29) and/or (b) encoding an amino acid sequence having from about 95% to about 100% identity (e.g., 98% identity) to SEQ ID NOS: 1, 2, 7, 8, and/or 28. A nucleic acid may comprise, in some embodiments, a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 3 and SEQ ID NO: 5 and encoding a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 1. A nucleic acid may comprise, in some embodiments, a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 4 and SEQ ID NO: 6 and encoding a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 2. According to some embodiments, a nucleic acid may comprise a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 9 and SEQ ID NO: 11 and encoding a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 7. A nucleic acid may comprise a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 10 and SEQ ID NO: 12 and encoding a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 8, in some embodiments.
The present disclosure relates, in some embodiments, to defensin expression vectors operable in citrus. For example, an expression vector may comprise, in a 5′ to 3′ direction, (a) an expression control sequence; (b) an expressable nucleic acid (e.g., a nucleic acid encoding an exogenous polypeptide) operably linked to the expression control sequence; and (c) a 3′ termination sequence operably linked to the expressable nucleic acid. In some embodiments, an exogenous nucleic acid may comprise a nucleic acid sequence having at least about 75% identity (e.g., at least about 98% identity) to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 29. An expression vector may be located in a bacterial cell or a plant cell according to some embodiments. An expression vector may comprise, in some embodiments, the nucleotide sequence AACAATGG at positions −4 to 4 relative to a coding sequence (e.g., encoded by an exogenous nucleic acid sequence). According to some embodiments, an expression vector may comprise a linker (e.g., 3′ of the expression control sequence and/or 5′ of the nucleic acid (e.g., a nucleic acid encoding an exogenous polypeptide) having a length of from about 1 to about 200 nucleotides.
The present disclosure relates, in some embodiments, to a bacterial cell comprising an expression vector. For example, a bacterial cell may comprise an expression vector comprising, in a 5′ to 3′ direction, (a) an expression control sequence; (b) an expressable nucleic acid (e.g., a nucleic acid encoding an exogenous polypeptide) operably linked to the expression control sequence; and (c) a 3′ termination sequence operably linked to the expressable nucleic acid. A bacterial cell may comprise, for example, an expression vector comprising, in a 5′ to 3′ direction, (a) an expression control sequence; (b) an exogenous nucleic acid operably linked to the expression control sequence; and/or (c) a 3′ termination sequence operably linked to the exogenous nucleic acid, wherein the exogenous nucleic acid comprises a nucleic acid sequence having at least about 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12.
The present disclosure relates, in some embodiments, to a plant cell (e.g., a citrus plant cell) comprising an expression vector. For example, a plant cell (e.g., a citrus plant cell) may comprise an expression vector comprising, in a 5′ to 3′ direction, (a) an expression control sequence; (b) an expressable nucleic acid (e.g., a nucleic acid encoding an exogenous polypeptide) operably linked to the expression control sequence; and (c) a 3′ termination sequence operably linked to the expressable nucleic acid. A plant cell (e.g., a citrus plant cell) may comprise, for example, an expression vector comprising, in a 5′ to 3′ direction, (a) an expression control sequence; (b) an exogenous nucleic acid operably linked to the expression control sequence; and/or (c) a 3′ termination sequence operably linked to the exogenous nucleic acid, wherein the exogenous nucleic acid comprises a nucleic acid sequence having at least about 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 29. A plant cell (e.g., a citrus plant cell) may be located in a plant (e.g., a citrus plant) according to some embodiments. Examples of citrus plants include, without limitation, orange and grapefruit. A plant cell may comprise a defensin peptide. A defensin peptide may have, in some embodiments, an amino acid sequence having at least about 99% identity to SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7, SEQ ID NO: 8 or SEQ ID NO: 28 (e.g., encoded by and/or expressed from an expression vector nucleic acid) according to some embodiments.
In some embodiments, the present disclosure relates to a citrus plant (e.g., orange and/or grapefruit) comprising an expression vector. A citrus plant may comprise an expression vector in a single cell, a plurality of cells (e.g., mosaic), or in all cells. A mosaic plant may arise from a graft in some embodiments. For example, a citrus plant may comprise a graft of a transgenic plant having an expression vector in all cells (e.g., scion) and a plant having a different expression vector or no expression vector in its cells (e.g., rootstock). A citrus plant may comprise, in some embodiments, in a single cell, a plurality of cells (e.g., mosaic), or in all cells a first expression vector (e.g., encoding a first defensin peptide) and in a single cell, a plurality of cells (e.g., mosaic), or in all cells a second expression vector (e.g., encoding a second defensin peptide). For example, a citrus plant cell may comprise (a) a first expression vector, the first expression vector comprising, in a 5′ to 3′ direction, (i) a first expression control sequence; (ii) a first exogenous nucleic acid operably linked to the first expression control sequence; and (iii) a first 3′ termination sequence operably linked to the first exogenous nucleic acid, wherein the first exogenous nucleic acid comprises a nucleic acid sequence having at least about 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 9, and SEQ ID NO: 11; and (b) a second expression vector, the second expression vector comprising, in a 5′ to 3′ direction, (iv) a second expression control sequence; (v) a second exogenous nucleic acid operably linked to the second expression control sequence; and (vi) a second 3′ termination sequence operably linked to the second exogenous nucleic acid, wherein the second exogenous nucleic acid comprises a nucleic acid sequence having at least about 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 10, and SEQ ID NO: 12. According to some embodiments, a citrus plant may comprise in a single cell, a plurality of cells (e.g., mosaic), or in all cells an expression vector comprising a first nucleic acid sequence encoding a first defensin peptide (e.g., SoD2) and a second nucleic acid sequence encoding a second defensin peptide (e.g., SoD7). In some embodiments, a citrus plant may comprise a defensin peptide in a single cell, a plurality of cells (e.g., mosaic), or in all cells. A citrus plant may comprise in a single cell, a plurality of cells (e.g., mosaic), or in all cells a first defensin peptide (e.g., a peptide having at least about 99% identity to SEQ ID NO: 1 or SEQ ID NO: 7) and in a single cell, a plurality of cells (e.g., mosaic), or in all cells a second defensin peptide (e.g., a peptide having at least about 99% identity to SEQ ID NO: 2 or SEQ ID NO: 8).
The present disclosure relates, in some embodiments, to methods of expressing in a citrus plant an exogenous nucleic acid comprising a nucleic acid sequence encoding an expressed peptide (e.g., a defensin peptide). For example, a method may comprise contacting an expression cassette comprising an exogenous nucleic acid or an expression vector comprising an exogenous nucleic acid with the cytosol of a cell of a citrus plant under conditions that permit expression of the exogenous nucleic acid and formation of the expressed peptide. In some embodiments, an exogenous nucleic acid may comprise a nucleic acid sequence having at least 98% identity to a nucleic acid sequence selected from SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and/or SEQ ID NO: 29. In some embodiments, an expression vector and/or an expression cassette may comprise, in a 5′ to 3′ direction, an expression control sequence, the exogenous nucleic acid operably linked to the expression control sequence, and a 3′ termination sequence operably linked to the exogenous nucleic acid. An expressed peptide may comprise an amino acid sequence having at least 99% identity to an amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7, SEQ ID NO: 8, and/or SEQ ID NO: 28 according to some embodiments. Contacting an expression vector or cassette may further comprise, in some embodiments, co-cultivating the cell with an Agrobacterium cell comprising the expression vector or expression cassette to form a co-cultivated plant cell. According to some embodiments, a plant may be regenerated from a co-cultivated plant cell.
The present disclosure relates, in some embodiments, to methods for treating a citrus plant having and/or at risk of having a microbial infection (e.g., bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las)). For example, a method may comprise forming in the citrus plant at least one defensin peptide. Forming in the citrus plant at least one defensin peptide may comprise, in some embodiments, grafting the citrus plant to cutting (e.g., a scion or a rootstock) from a second citrus plant, the second citrus plant comprising an expression vector and/or an expression cassetted comprising, in a 5′ to 3′ direction, an expression control sequence, a defensin nucleic acid operably linked to the expression control sequence, and a 3′ termination sequence operably linked to the defensin nucleic acid, wherein the defensin nucleic acid comprises a nucleic acid sequence encoding an amino acid sequence having at least 99% identity to an amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7, SEQ ID NO: 8, and/or SEQ ID NO: 28 under conditions that permit expression of the defensin nucleic acid.

BRIEF DESCRIPTION OF THE DRAWINGS

The file of this patent contains at least one drawing executed in color. Copies of this patent with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.

Some embodiments of the disclosure may be understood by referring, in part, to the present disclosure and the accompanying drawings, wherein:

FIG. 1 illustrates an Agrobacterium transformation construct comprising a nucleic acid encoding SoD2 according to specific example embodiments of the disclosure;

FIG. 2 illustrates an Agrobacterium transformation construct comprising a nucleic acid encoding SoD7 according to specific example embodiments of the disclosure;

FIG. 3 is a representation of a Southern blot showing insertion number among transgenic events in Hamlin and Rohde Red transformed with a SoD2 (07) nucleic acid comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 4 is a representation of a Southern blot showing insertion number among transgenic events in Hamlin and Rohde Red transformed with SoD2 (09) or SoD7 (10) nucleic acids, each comprising a CODA-optimized sequence for expression in Citrus, according to specific example embodiments of the disclosure;

FIG. 5 is a representation of a northern blot showing RNA transcripts among transgenic events in Marrs, transformed with SoD2 (07) or SoD7 (08) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 6 is a representation of a northern blot showing RNA transcripts among transgenic events in Hamlin and Rohde Red, transformed with SoD2 (09) or SoD7 (10) nucleic acids, each comprising a CODA-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 7 is a representation of a northern blot showing RNA transcripts among transgenic events in Hamlin and Rohde Red, transformed with SoD2 (07) or SoD7 (08) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 8 is a representation of a Southern blot confirming insertion of SoD2 or SoD7 in Hamlin plants, transformed with SoD2 (11) or SoD7 (12) nucleic acids, each comprising a DNA 2.0-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 9 is a representation of a Southern blot confirming insertion of defensins in Ruby Red (01) or Hamlin (04) transformed with SoD2 (09, 11), SoD7 (08, 12), or both SoD2 and SoD7 (13) nucleic acids, each comprising a sequence optimzed for expression in Citrus using a sequence optimization algorithm (GenScript for 08 and 13; Coda for 09, and DNA 2.0 for 11 and 12), according to a specific example embodiment of the disclosure;

FIG. 10 is a representation of a northern blot showing RNA transcripts among transgenic events in Ruby Red (01) or Hamlin (04), transformed with SoD2 (11), SoD7 (08, 12), or both SoD2 and SoD7 (13) nucleic acids, each comprising a GenScript-optimized sequence (08 and 13) or DNA 2.0-optimized sequence (11 and 12) for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 11 is a representation of a Southern blot confirming insertion of defensins in Carrizo Citrange (CC) transformed with SoD2 (07) or SoD7 (08) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 12 is a representation of a northern blot showing RNA transcripts among transgenic events in Carrizo Citrange (CC) transformed with SoD2 (07) or SoD7 (08) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 13A is a photograph of an excised leaf from a non-transgenic grapefruit tree innoculated with a citrus canker pathogen according to specific example embodiments of the disclosure;

FIG. 13B is a photograph of an excised leaf from an SoD2 transgenic grapefruit tree innoculated with a citrus canker pathogen according to specific example embodiments of the disclosure;

FIG. 14 is a photograph of chimeric grapefruit trees resulting from the graft of uninfected, non-transgenic scions on citrus greening infected, non-transgenic rootstocks (left and center) or the graft of uninfected, SoD2 transgenic scions on citrus greening infected, non-transgenic rootstock (right), according to specific example embodiments of the disclosure;

FIG. 15A illustrates the percentage of Generation 2 citrus plants infected upon the first, second, and third sampling of challenged material, according to specific example embodiments of the disclosure;

FIG. 15B is a continuation of the bar graph of FIG. 15A illustrating the percentage of Generation 2 citrus plants infected upon the first, second, and third sampling of challenged material, according to specific example embodiments of the disclosure;

FIG. 15C is a continuation of the bar graph of FIG. 15A illustrating the percentage of Generation 2 citrus plants infected upon the first, second, and third sampling of challenged material, according to specific example embodiments of the disclosure;

FIG. 16A illustrates the percentage of

Generations

2 and 3 citrus plants infected upon the first, second and third samplings of challenged material, according to specific example embodiments of the disclosure;

FIG. 16B is a continuation of the bar graph of FIG. 16A illustrating the percentage of

Generations

FIG. 16C is a continuation of the bar graph of FIG. 16A illustrating the percentage of

Generations

2 and 3 citrus plants infected upon the first, second and third samplings of challenged material, according to specific example embodiments of the disclosure; and

FIG. 17 is a representation of a Southern blot confirming insertion of defensins in Rio Red (01) transformed with both SoD2 and SoD7 (13) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure;

FIG. 18 is a representation of a northern blot showing RNA transcripts among transgenic events in Rio Red (01) or Hamlin (04), transformed with both SoD2 and SoD7 (13) nucleic acids, each comprising a GenScript-optimized sequence for expression in Citrus, according to a specific example embodiment of the disclosure; and

FIG. 19 is a Western blot illustrating binding of an anti-SoD7 according to specific example embodiments of the disclosure to samples containing SoD7.

BRIEF DESCRIPTION OF THE SEQUENCE LISTING

Some embodiments of the disclosure may be understood by referring, in part, to the present disclosure and the accompanying sequence listing, wherein:
SEQ ID NO: 1 illustrates an amino acid sequence of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 2 illustrates an amino acid sequence of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 3 illustrates a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 4 illustrates a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 5 illustrates a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure; SEQ ID NO: 6 illustrates a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 7 illustrates an amino acid sequence of a chimeric peptide comprising a PR-1b signal peptide and a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 8 illustrates an amino acid sequence of a chimeric peptide comprising a PR-1b signal peptide and a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 9 illustrates a chimeric nucleic acid sequence comprising a nucleic acd sequence encoding a PR-1b signal peptide and a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 10 illustrates a chimeric nucleic acid sequence comprising a nucleic acd sequence encoding a PR-1b signal peptide and a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 11 illustrates a chimeric nucleic acid sequence comprising a nucleic acd sequence encoding a PR-1b signal peptide and a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 12 illustrates a chimeric nucleic acid sequence comprising a nucleic acd sequence encoding a PR-1b signal peptide and a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 13 illustrates an expression cassette comprising a nucleic acid sequence encoding a PR-1b signal peptide and a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 14 illustrates an expression cassette comprising a nucleic acid sequence encoding a PR-1b signal peptide and a GenScript-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 15 illustrates an expression cassette comprising a nucleic acid sequence encoding a PR-1b signal peptide and a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 16 illustrates an expression cassette comprising a nucleic acid sequence encoding a PR-1b signal peptide and a CODA-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure;
SEQ ID NO: 17 illustrates an expression control sequence (CaMV 35S promoter) according to a specific example embodiment of the disclosure;
SEQ ID NO: 18 illustrates an untranslated region (TEV 5′UTR) according to a specific example embodiment of the disclosure;
SEQ ID NO: 19 illustrates an expression control sequence (CaMV 35S terminator) according to a specific example embodiment of the disclosure;
SEQ ID NO: 20 illustrates a nucleic acid sequence of a primer designated Zn5 according to a specific example embodiment of the disclosure;
SEQ ID NO: 21 illustrates a nucleic acid sequence of a primer designated Zn6 according to a specific example embodiment of the disclosure;
SEQ ID NO: 22 illustrates a nucleic acid sequence of a primer designated Fcp according to a specific example embodiment of the disclosure;
SEQ ID NO: 23 illustrates a nucleic acid sequence of a primer designated Rcp according to a specific example embodiment of the disclosure; SEQ ID NO: 24 illustrates a nucleic acid sequence of a primer designated GUSF according to a specific example embodiment of the disclosure;
SEQ ID NO: 25 illustrates a nucleic acid sequence of a primer designated GUSR according to a specific example embodiment of the disclosure;
SEQ ID NO: 26 illustrates an amino acid sequence of a chimeric peptide comprising a modified PR-1b signal peptide and a GenScript-optimized nucleic acid sequence having a single deletion for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 27 illustrates a chimeric nucleic acid sequence comprising a nucleic acid sequence encoding a modified PR-1b signal peptide and a GenScript-optimized nucleic acid sequence having a single deletion for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure;
SEQ ID NO: 28 illustrates a core amino acid sequence of a defensin according to a specific example embodiment of the disclosure;
SEQ ID NO: 29 illustrates a nucleic acid sequence for expression of a core defensin according to a specific example embodiment of the disclosure;
SEQ ID NO: 30 illustrates a DNA 2.0-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD2) according to a specific example embodiment of the disclosure; and
SEQ ID NO: 31 illustrates a DNA 2.0-optimized nucleic acid sequence for expression of a spinach (Spinacia oleracea) defensin (SoD7) according to a specific example embodiment of the disclosure.

DETAILED DESCRIPTION

The present disclosure relates, in some embodiments, to compositions, organisms, systems, and methods for enhancing a plant's innate ability, if any, to respond to contact (e.g., infection) with a pathogen (e.g., bacteria, yeast, fungus, virus). In some embodiments, the present disclosure relates to compositions, organisms, systems, and methods for expressing a gene product (e.g., an antimicrobial peptide) in a plant (e.g., citrus). For example, the present disclosure relates to expression control sequences (e.g., promoters), expression cassettes, expression vectors, microorganisms, and/or plants comprising one or more antimicrobial peptides and/or one or more nucleic acids encoding one or more antimicrobial peptides.

I. Compositions

A. Antimicrobial Peptides
The present disclosure relates, according to some embodiments, to peptides and/or proteins having insecticidal activity, antimicrobial activity, and/or antiviral activity, which may include, without limitation, avidin, vegetative insecticidal proteins (e.g., Vip3A), insecticidal crystal proteins from Bacillus thuringiensis (e.g., Cry1, Cry1Ab, Cry2, Cry9), pea albumin (e.g., PA 1b), hirsutellin A, lectins (e.g., snow drop lily lectin, garlic lectin, onion lectin), amylase inhibitors (e.g., alpha amylase inhibitor), arcelins (e.g., arcelins from beans), proteinase inhibitors, lysozymes (e.g., bovine lysozyme, human lysozyme, mollusk lysozyme), defensin (e.g., SoD2 and/or SoD7), chitinase, β-1,3-glucanase, variants thereof, and/or combinations thereof. An antimicrobial peptide may comprise, for example, one or more antimicrobial-peptides belonging to the family of plant defensins. These polypeptides were originally isolated from spinach leaves (Spinacia oleracea). In some embodiments, a defensin may be small (about 5 kDa), may be basic and/or may be cysteine-rich. In some embodiments, a defensin may comprise a peptide having an amino acid sequence sharing at least about 95% identity, at least about 96% identity, at least about 97% identity, at least about 98% identity, at least about 99% identity, and/or about 100% identity with SEQ ID NO: 1 and/or SEQ ID NO: 2. In some embodiments, an antimicrobial peptide may further comprise one or more amino acids that are independently and/or collectively either neutral (e.g., do not adversely impact antibacterial functionality) and/or augment antibacterial functionality (e.g., by directing the peptide to a desired location (e.g., cellular and/or extracellular). For example, a defensin may comprise a signal peptide derived from the tobacco pathogenesis-related (PR)-1b protein that allows the transport of the peptides into the apoplast of plant cells (e.g., via the secretory pathway) and/or accumulation in the intercellular spaces of leaves, stems, flowers, fruits, seeds, and/or roots. A defensin may comprise, according to some embodiments, a peptide having an amino acid sequence sharing at least about 95% identity, at least about 96% identity, at least about 97% identity, at least about 98% identity, at least about 99% identity, and/or about 100% identity with SEQ ID NO: 7 and/or SEQ ID NO: 8.
B. Nucleic Acids
The present disclosure relates, in some embodiments, to nucleic acids (e.g., cassettes, vectors) comprising one or more sequences encoding one or more antimicrobial peptides. For example, a nucleic acid may comprise a cassette comprising a synthetic nucleic acid sequence of SoD2 and/or SoD7 genes. Synthetic SoD2 and/or SoD7 codons may specify the same amino acid sequences as native spinach, having their codons optimized for citrus codon usage. A nucleic acid comprising a SoD2 and/or SoD7 coding sequence may comprise a sequence encoding a signal peptide (e.g., PR-1b). In some embodiments, expression of a nucleic acid comprising a sequence encoding an antimicrobial peptide may be optimized by positioning an initiation codon in a favorable (e.g., optimal) 5′ context. According to some embodiments, a nucleic acid may comprise an expression control sequence (e.g., operably linked to a coding sequence). For example, a nucleic acid may comprise a coding gene sequence under the control of a dual enhanced CaMV 35S promoter with a 5′ UTR from TEV plant potyvirus (e.g., to provide a translation-enhancing activity to the defensin genes).
According to some embodiments, a nucleic acid may comprise a nucleotide sequence having at least about 75% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 80% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 29, at least about 85% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 90% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 95% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 97% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 98% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, at least about 99% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31, and/or about 100% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31. A nucleotide sequence may encode, in some embodiments, an amino acid sequence having at least about 98% identity to SEQ ID NOS: 1, 2, 7, 8, and/or 28, at least about 99% identity to SEQ ID NOS: 1, 2, 7, 8, and/or 28, and/or about 100% identity to SEQ ID NOS: 1, 2, 7, 8, and/or 28. According to some embodiments, a nucleic acid may have a first measure of sequence identity to a reference nucleic acid sequence and may encode an amino acid sequence having a second measure of sequence identity to a reference amino acid sequence. For example, a nucleic acid may have about 85% identity to SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31 and encode an amino acid sequence having about 100% identity with SEQ ID NOS: 1, 2, 7, 8, and/or 28, according to some embodiments.
A nucleic acid sequence, according to some embodiments, may hybridize to a nucleic acid having the nucleotide sequence of SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31 under stringent conditions. Stringent conditions may include, for example, (a) 4×SSC at 65° C. followed by 0.1×SSC at 65° for 60 minutes and/or (b) 50% formamide, 4×SSC at 65° C. A nucleic acid may comprise a deletion fragment (e.g., a deletion of from about 1 to about 12 bases) of a nucleic acid having a sequence of SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31 that retains antimicrobial activity against at least one microorganism capable of infecting a citrus plant. One of ordinary skill in the art having the benefit of the present disclosure may prepare one or more deletion fragments of a nucleic acid having a sequence of SEQ ID NOS: 3, 4, 5, 6, 9, 10, 11, 12, 29, 30, and/or 31 and screen the resulting fragments for antimicrobial activity against at least one microorganism capable of infecting a citrus plant.
A nucleic acid sequence having a sequence like SEQ ID NOS: 3, 4, 5, 6, 30, and/or 31 may be identified by database searches using the sequence or elements thereof as the query sequence using the Gapped BLAST algorithm (Altschul et al., 1997 Nucl. Acids Res. 25:3389-3402) with the BLOSUM62 Matrix, a gap cost of 11 and persistence cost of 1 per residue and an E value of 10. Sequence identity may be assessed by any available method according to some embodiments. For example, two sequences may be compared with either ALIGN (Global alignment) or LALIGN (Local homology alignment) in the FASTA suite of applications (Pearson and Lipman, 1988 Proc. Nat. Acad. Sci. 85:2444-2448; Pearson, 1990 Methods in Enzymology 183:63-98) with the BLOSUM50 matrix and gap penalties of −16, −4. Sequence similarity may be assessed according to ClustalW (Larkin et al., 2007, Bioinformatics 23(21): 2947-2948), BLAST, FASTA or similar algorithm.
C. Expression Cassettes and Vectors
The disclosure relates, in some embodiments, to expression vectors and/or expression cassettes for expressing a nucleic acid sequence (e.g., a coding sequence) in a cell and comprising an expression control sequence and the nucleic acid sequence operably linked to the expression control sequence. Thus, for example, an expression cassette may comprise a heterologous coding sequence, the expression of which may be desired in a plant.
1. Expression Vectors
The disclosure relates, in some embodiments, to an expression vector which may comprise, for example, a nucleic acid having an expression control sequence and a coding sequence operably linked to the expression control sequence. In some embodiments, an expression control sequence may comprise one or more promoters, one or more operators, one or more enhancers, one or more ribosome binding sites, and/or combinations thereof. An expression control sequence may comprise, for example, a nucleic acid having promoter activity. An expression control sequence, according to some embodiments, may be constitutively active or conditionally active in (a) an organ selected from root, leaf, stem, flower, seed, and/or fruit, and/or (b) active in a tissue selected from epidermis, periderm, parenchyma, collenchyma, sclerenchyma, xylem, phloem, and/or secretory structures. An expression control sequence, according to some embodiments, may be operable to drive expression of a nucleic acid sequence (e.g., a coding sequence) in a cell. Metrics for expression may include, for example, rate of appearance and/or accumulation of a gene product (e.g., RNA and/or protein) and/or total accumulation of a gene product as of one or more time points (e.g., elapsed time after a starting point and/or a stage of development). Comparative assays for gene products may be qualitative, semi-quantitative, and/or quantitative in some embodiments. Comparative assays may indirectly and/or directly assess the presence and/or amount of gene product. In some embodiments, an expression control sequence may be sensitive to one or more stimuli (e.g., one or more small molecules, one or more plant defense-inducing agents, mechanical damage, temperature, pressure). For example, activity of an expression control sequence may be enhanced or suppressed upon infection with a microorganism (e.g., a bacteria or a virus).
An expression vector may be contacted with a cell (e.g., a plant cell) under conditions that permit expression (e.g., transcription) of the coding sequence. Examples of expression vectors may include the Agrobacterium transformation constructs shown in FIG. 1 and FIG. 2. An expression control sequence may be contacted with a plant cell (e.g., an embryonic cell, a stem cell, a callous cell) under conditions that permit expression of the coding sequence in the cell and/or cells derived from the plant cell according to some embodiments. An expression vector may be contacted with a cell (e.g., a plant cell), in some embodiments, under conditions that permit inheritance of at least a portion of the expression vector in the cell's progeny. According to some embodiments, an expression vector may include one or more selectable markers. For example, an expression vector may include a marker for selection when the vector is in a bacterial host, a yeast host, and/or a plant host.
2. Expression Cassettes
According to some embodiments, the disclosure relates to an expression cassette which may comprise, for example, a nucleic acid having an expression control sequence and a coding sequence operably linked to the expression control sequence. An expression cassette may be comprised in an expression vector. A coding sequence, in some embodiments, may comprise any coding sequence expressible in at least one plant cell. For example, a coding sequence may comprise a plant sequence, a yeast sequence, a bacterial sequence, a viral sequence (e.g., plant virus), an artificial sequence, an antisense sequence thereof, a fragment thereof, a variant thereof, and/or combinations thereof. A coding sequence may comprise, in some embodiments, a sequence encoding one or more gene products with insecticidal, antibacterial, antifungal, antimicrobial, and/or antiviral activity. A coding sequence may comprise, in some embodiments, a start codon, an intron, and/or a translation termination sequence. According to some embodiments, a coding sequence may comprise one or more natural or artificial coding sequences (e.g., encoding a single protein or a chimera). According to some embodiments, an expression cassette may optionally comprise a termination sequence. A coding sequence, in some embodiments, may comprise a sequence at least partially codon optimized for expression in an organism of interest (e.g., a citrus plant).
An expression control sequence may be used, in some embodiments, to construct an expression cassette comprising, in the 5′ to 3′ direction, (a) the expression control sequence, (b) a heterologous gene or a coding sequence, or sequence complementary to a native plant gene under control of the expression control sequence, and/or (c) a 3′ termination sequence (e.g., a termination sequence comprising a polyadenylation site). Examples of expression cassettes may include, in some embodiments, the cassettes shown in SEQ ID NOS: 13-16. An expression cassette may be incorporated into a variety of autonomously replicating vectors in order to construct an expression vector. An expression cassette may be constructed, for example, by ligating an expression control sequence to a sequence to be expressed (e.g., a coding sequence).
Some techniques for construction of expression cassettes are well known to those of ordinary skill in the art. For example, a variety of strategies are available for ligating fragments of DNA, the choice of which depends on the nature of the termini of the DNA fragments. An artisan of ordinary skill having the benefit of the present disclosure, a coding sequence (e.g., having antimicrobial activity) and/or portions thereof may be provided by other means, for example chemical or enzymatic synthesis. A nucleic acid may comprise, in a 5′ to 3′ direction, an expression control sequence, a linker (optional), and a coding sequence according to some embodiments. A nucleic acid may comprise, in some embodiments, one or more restriction sites and/or junction sites between an expression control sequence, a linker, and/or a coding sequence.

II. Microorganisms

The present disclosure relates, in some embodiments, to a microorganism comprising an antimicrobial peptide (e.g., a heterologous antimicrobial peptide) and/or a nucleic acid (e.g., a heterologous and/or expressible nucleic acid) comprising a nucleic acid sequence encoding an antimicrobial peptide. For example, a microorganism may comprise a bacteria, a yeast, and/or a virus. Examples of microorganisms may include, without limitation, Agrobacterium tumefaciens, Escherichia coli, a lepidopteran cell line, a Rice tungro bacilliform virus, a Commelina yellow mosaic virus, a Banana streak virus, a Taro bacilliform virus, and/or baculovirus. According to some embodiments, an antimicrobial peptide may be tolerated by and/or innocuous to its host microorganism. A microorganism may comprise an expression control sequence and an antimicrobial peptide coding sequence operably linked to the expression control sequence. A nucleic acid (e.g., a heterologous and/or expressible nucleic acid) comprising a nucleic acid sequence encoding an antimicrobial peptide may be present, in some embodiments, on a genomic nucleic acid and/or an extra-genomic nucleic acid.

III. Plants

The present disclosure relates, in some embodiments, to a plant cell (e.g., an embryonic cell, a stem cell, a callous cell), a tissue, and/or a plant comprising an antimicrobial peptide (e.g., a heterologous antimicrobial peptide) and/or a nucleic acid (e.g., a heterologous and/or expressible nucleic acid) comprising a nucleic acid sequence encoding an antimicrobial peptide. A plant and/or plant cell may be a dicot in some embodiments. Examples of a dicot may include, without limitation, coffee, tomato, pepper, tobacco, lima bean, Arabidopsis, rubber, orange, grapefruit, lemon, lime, tangerine, mandarin, pummelo, potato, squash, peas, and/or sugar beet. A plant cell may be included in a plant tissue, a plant organ, and/or a whole plant in some embodiments. A plant cell in a tissue, organ, and/or whole plant may be adjacent, according to some embodiments, to one or more isogenic cells and/or one or more heterogenic cells. In some embodiments, a plant may include primary transformants and/or progeny thereof. A plant comprising a nucleic acid (e.g., a heterologous and/or expressible nucleic acid) comprising a nucleic acid sequence encoding an antimicrobial peptide may further comprise an expression control sequence operably linked to the nucleic acid, in some embodiments. A nucleic acid sequence encoding an antimicrobial peptide may be expressed, according to some embodiments, in a plant in one or more up to all (e.g., substantially all) organs, tissues, and/or cell types including, without limitation, stalks, leaves, roots, seeds, flowers, fruit, meristem, parenchyma, storage parenchyma, collenchyma, sclerenchyma, epidermis, mesophyll, bundle sheath, guard cells, protoxylem, metaxylem, phloem, phloem companion, and/or combinations thereof. In some embodiments, a nucleic acid and/or its gene product (e.g., an antimicrobial peptide) may be located in and/or translocated to one or more organelles (e.g., vacuoles, chloroplasts, mitochondria, plastids).

IV. Methods

A. Transforming a Plant
The present disclosure relates, according to some embodiments, to methods for independent transformation of citrus (e.g., a native genome of a citrus plant). For example, a method may comprise independent transformation, using Agrobacterium tumefaciens (At), of the native genome of the orange (Citrus sinensis) cultivars “Rohde Red”, “Hamlin”, and/or “Marrs.” A transformation method may comprise contacting a nucleic acid comprising a SoD2 and/or SoD7 sequence (e.g., a SoD2 and/or SoD7 synthetic gene sequence) with a citrus plant according to some embodiments. A transformed plant (e.g., a transformed genome of a new orange cultivar) may independently contain, in some embodiments a sequence of a SoD2 gene and/or a SoD7 gene encoding microbial resistance not found within the native gene pool of the Citrus genus. According to some embodiments, a transformed orange cultivar plant may comprise a peptide encoded by a SoD2 gene and/or a SoD7 gene. A transformed plant comprising a sequence of a SoD2 gene and/or a SoD7 gene and/or comprising a peptide encoded by a SoD2 gene and/or a SoD7 gene may display resistance to a range (e.g., a broad range) of bacterial and/or fungal pathogens in some embodiments. For example, a transformed plant comprising a sequence of a SoD2 gene and/or a SoD7 gene and/or comprising a peptide encoded by a SoD2 gene and/or a SoD7 gene may display resistance to bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las). See EXAMPLE section below.
B. Grafting
The present disclosure relates to grafting at least a portion of a first plant (e.g., a citrus plant) with at least a portion of a second plant (e.g., a citrus plant), according to some embodiments. A first plant may be in any desired condition including, without limitation, a healthy condition, a diseased condition, an injured condition, a stressed condition (e.g., heat, cold, water, and the like), and/or combinations thereof. A first plant may have any desired genotype including, without limitation, wild type, transgenic, mutant, and/or the like with respect to a gene and/or trait of interest.
A second plant may be in any desired condition including, without limitation, a healthy condition, a diseased condition, an injured condition, a stressed condition (e.g., heat, cold, water, and the like), and/or combinations thereof. A second plant may have any desired genotype including, without limitation, wild type, transgenic, mutant, and/or the like with respect to a gene and/or trait of interest. A first and/or a second plant may comprises at least one antimicrobial peptide and/or at least one nucleic acid comprising a sequence encoding at least one antimicrobial peptide. Where both a first plant comprises at least one antimicrobial peptide and/or at least one nucleic acid comprising a sequence encoding at least one antimicrobial peptide and a second plant comprises at least one antimicrobial peptide and/or at least one nucleic acid comprising a sequence encoding at least one antimicrobial peptide, it may be desirable for the first and second plants to have the same and/or different antimicrobial peptides and/or nucleic acids encoding antimicrobial peptides. Grafting may comprise cutting a portion of a first plant to form a fresh cut site, cutting a portion of a second plant to create a second cut site, and/or contacting a first cut site with a second cut site. A cut site may comprise at least one vascular bundle. Grafting may comprise forming a graft junction and/or, optionally, sealing the graft junction (e.g., by coating the periphery of the graft junction with one or more barrier materials).
C. Treating Plant Disease
The present disclosure relates, in some embodiments, to compositions, organisms, systems, and methods for preventing, ameliorating, and/or treating a plant disease (e.g., a citrus disease) and/or at least one symptom of a plant disease. For example, a method may comprise grafting at least a portion of a plant (e.g., a citrus plant) having a plant disease and/or expressing at least one symptom of a plant disease with at least a portion of a plant (e.g., a citrus plant) comprising an antimicrobial peptide. Examples of a plant disease include, without limitation, bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las). According to some embodiments, preventing, ameliorating, and/or treating a plant disease (e.g., a citrus disease) and/or at least one symptom of a plant disease may comprise treating and/or curing one or more devastating bacterial diseases of citrus. For example, plants comprising stably integrated SoD2 and SoD7 transgenes in expressible form may display resistance to, without limitation, bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las). Such resistance has been observed as described in the Examples below.
According to some embodiments, the present disclosure relates to compositions, organisms, systems, and methods for augmenting a plant's native resistance to and/or conferring on a plant resistance to a plant disease (e.g., a citrus disease). For example, a method may comprise contacting a plant with an antimicrobial peptide and/or an expressible nucleic acid comprising a nucleic acid sequence encoding an antimicrobial peptide. An expressible nucleic acid comprising a nucleic acid sequence encoding an antimicrobial peptide may be and/or comprise an expression cassette in some embodiments. Contacting may comprise, according to some embodiments, grafting at least a portion of a target plant with a plant comprising an antimicrobial peptide and/or an expressible nucleic acid comprising a nucleic acid sequence encoding an antimicrobial peptide. In some embodiments, contacting may comprise contacting at least a portion of a target plant with a vector (e.g., via Agrobacterium-mediated transformation) comprising an antimicrobial peptide and/or an expressible nucleic acid comprising a nucleic acid sequence encoding an antimicrobial peptide. Examples of a plant disease include, without limitation, bacterial canker (Xanthomonas axonopodis pv. citri) (Xac), and/or citrus Huanglongbing (ex greening) caused by Candidatus Liberibacter asiaticus (Las).
D. Making a Citrus-Expressible Antimicrobial Peptide
In some embodiments, the present disclosure relates to compositions, organisms, systems, and methods for forming a citrus-expressible nucleic acid comprising a nucleic acid sequence encoding at least one spinach-derived antimicrobial peptide. For example, a method may comprise identifying an amino acid sequence of an antimicrobial peptide of interest, reverse translating the amino acid sequence to produce a first nucleic acid sequence; codon-optimizing the first nucleic acid sequence for expression in citrus to produce a second nucleic acid sequence, and/or synthesizing a nucleic acid having the second nucleic acid sequence. A method may comprise, in some embodiments, covalently bonding a nucleic acid having the second nucleic acid sequence with one or more nucleic acids having expression control sequences that are operable in citrus in an operable orientation and/or position relative to the nucleic acid having the second nucleic acid sequence.
As will be understood by those skilled in the art who have the benefit of the instant disclosure, other equivalent or alternative pathogen resistant citrus compositions, organisms, systems, and methods can be envisioned without departing from the description contained herein. Accordingly, the manner of carrying out the disclosure as shown and described is to be construed as illustrative only.
Persons skilled in the art may make various changes in the shape, size, number, and/or arrangement of parts without departing from the scope of the instant disclosure. For example, the position and number of expression control sequences, coding sequences, linkers, and/or terminator sequences may be varied. Each disclosed method and method step may be performed in association with any other disclosed method or method step and in any order according to some embodiments. Where the verb “may” appears, it is intended to convey an optional and/or permissive condition, but its use is not intended to suggest any lack of operability unless otherwise indicated. Persons skilled in the art may make various changes in methods of preparing and using a composition, device, and/or system of the disclosure. For example, a composition, device, and/or system may be prepared and or used as appropriate for microbial and/or plant (e.g., with regard to sanitary, infectivity, safety, toxicity, biometric, and other considerations). Where desired, some embodiments of the disclosure may be practiced to the exclusion of other embodiments. For example, some polypeptide embodiments may be practiced to the exclusion of a particular amino acid sequence (e.g., SEQ ID NO:26) and/or some nucleic acid embodiments may be practiced to the exclusion of a particular nucleic acid sequence (e.g., SEQ ID NO:27).
Also, where ranges have been provided, the disclosed endpoints may be treated as exact and/or approximations as desired or demanded by the particular embodiment. Where the endpoints are approximate, the degree of flexibility may vary in proportion to the order of magnitude of the range. For example, on one hand, a range endpoint of about 50 in the context of a range of about 5 to about 50 may include 50.5, but not 52.5 or 55 and, on the other hand, a range endpoint of about 50 in the context of a range of about 0.5 to about 50 may include 55, but not 60 or 75. In addition, it may be desirable, in some embodiments, to mix and match range endpoints. Also, in some embodiments, each figure disclosed (e.g., in one or more of the examples, tables, and/or drawings) may form the basis of a range (e.g., depicted value +/− about 10%, depicted value +/− about 50%, depicted value +/− about 100%) and/or a range endpoint. With respect to the former, a value of 50 depicted in an example, table, and/or drawing may form the basis of a range of, for example, about 45 to about 55, about 25 to about 100, and/or about 0 to about 100.
These equivalents and alternatives along with obvious changes and modifications are intended to be included within the scope of the present disclosure. Accordingly, the foregoing disclosure is intended to be illustrative, but not limiting, of the scope of the disclosure as illustrated by the appended claims.

EXAMPLES

Some specific example embodiments of the disclosure may be illustrated by one or more of the examples provided herein.

Example 1

Plant Material

Plant materials (e.g., Citrus sinensis) were generally prepared for transformation as described by Yang et al., Plant Cell Reports (2000) 19:1203 et seq.

Example 2

Plasmid Construction and Bacterial Strains

Plasmid construction and bacterial strains were generally performed as described by Yang et al., Plant Cell Reports (2000) 19:1203 et seq.

Example 3

Agrobacterium Co-Culture and Plant Transformation

Agrobacterium co-culture and plant transformation were generally performed as described by Yang et al., Plant Cell Reports (2000) 19:1203 et seq.

Example 4

Selection and Regeneration of Transgenic Shoots

Selection and regeneration of transgenic shoots were generally performed as described by Yang et al., Plant Cell Reports (2000) 19:1203 et seq.

Example 5

Grafting of Transgenic Shoots

Grafting of transgenic shoots were generally performed as described by Yang et al., Plant
Cell Reports (2000) 19:1203 et seq.

Example 6

Southern and Northern Analysis

Southern and northern analysis were generally performed as described by Yang et al., Plant Cell Reports (2000) 19:1203 et seq.

Example 7

Expression in Citrus Trees

Table 1 illustrates specific example embodiments of nucleic acid sequences codon-optimized for citrus. Signal peptides and structural gene coding sequences shown are flanked on either side by specific restriction enzyme sites. These sequences were used to construct expression cassettes, vectors, and transformed Agrobacterium for preparation of transgenic plants.

TABLE 1

Example embodiments of specific nucleotide sequences
of antimicrobial genes. The nucleotide sequences were
optimized for codon usage in Citrus.

		Antimicrobial genes specific nucleotide
	Source of the	sequences. The 5′ nucleotides include
Anti-	Optimized	the cloning site and a preferred context
microbial	Synthetic	for the start codon. The 3′ nucleotides
Gene	Gene (code)	include the cloning site.

SoD2	GenScript (07)	SEQ ID NO: 9
	CODA (09)	SEQ ID NO: 11
SoD7	GenScript (08)	SEQ ID NO: 10
	CODA (10)	SEQ ID NO: 12
SoD2	DNA 2.0 (11)	SEQ ID NO: 30
SoD7	DNA 2.0 (12)	SEQ ID NO: 31
SoD2 + SoD7	GenScript (13)	SEQ ID NOS: 9 and 10
SoD2 + SoD7	DNA 2.0 (16)	SEQ ID NO: 30 and 31
no SP

The following cultivars were selected for transformation:

- Orange: Hamlin (“04”), Rohde Red (“05”), and Marrs (“06”) (FIGS. 3-7);
- Grapefruit: Ruby Red (“01”) (FIGS. 8-11) and Rio Red (Example 14 below);
- Carrizo Citrange (“CC”) (FIGS. 12-13);
- Flying Dragon rootstock (“13” and “16”);
- Frost Eureka and Frost Lisbon (13″ and “16”);
- Swingle rootstock (13″ and “16”); and
- C22 rootstock.
  Constructs used for each cultivar are shown in Table 2.

TABLE 2

Orange, grapefruit, lemon and citrus rootstock cultivars transformed (seedling epicotyls)
with three different synthetic sequences of each SoD2 and SoD7 genes encoding antimicrobial
peptides from spinach (Spinacia oleracea) (at least 521 events in total).

		Synthetic Gene
	Defensin	Optimized-		Transgenic	Number of
	Synthetic	Codon Sequence	Citrus Cultivars	Events Codes	Transgenic
Generation	Genes	(Sequence Code)	(Cultivar Code)	(Cultivar and Gene)	Events

2 (141	SoD2 + SP	GenScript (07)	Hamlin (04)	0407	14
events)			Rohde Red (05)	0507	12
			Marrs (06)	0607	6
			Carrizo Citrange (CC)	CC2	18
		CODA (09)	Hamlin (04)	0409	16
			Rohde Red (05)	0509	6
	SoD7 + SP	GenScript (08)	Hamlin (04)	0408	12
			Rohde Red (05)	0508	8
			Marrs (06)	0608	7
			Carrizo Citrange (CC)	CC7	29
		CODA (10)	Hamlin (04)	0410	5
			Rohde Red (05)	0510	8
3 (36	SoD2-no SP	DNA 2.0 (11)	Hamlin (04)	0411	11
events)			Ruby Red (01)	0111	6
	SoD7-no SP	DNA 2.0 (12)	Hamlin (04)	0412	13
			Ruby Red (01)	0112	6
4 (187	SoD2 + 7 + SP	GenScript (13)	Hamlin (04)	413	15
events +			Rhode Red (05)	513	14
157			Rio Red (02)	213	18
Swingle			Frost Eureka Lemon (10)	1013	30
			Frost Lisbon Lemon (11)	1113	33
			Swingle Rootstock (12)	1213	157
			Flying Dragon Rootstock (09)	913	46
			C22 (08)	813	15
			Carrizo Citrange (07)	713	16
4	SoD2 + 7	GenScript	Hamlin (04)	0413	15
		(07 + 08)	Rohde Red (05)	0513	1
			Rio Red (02)	0213	7
			Carrizo Citrange (CC)	CC2 + 7	6
5	SoD2 + 7-no SP	DNA 2.0 (16)	Hamlin (04)	416	Multiple
					GUS positive
					plants
			Frost Eureka Lemon (10)	1013	Multiple
					GUS positive
					plants
			Frost Lisbon Lemon (11)	1113	Multiple
					GUS positive
					plants
			Rhode Red (05)	516	Multiple
					GUS positive
					plants

A. Transformation of Orange

Orange plants were transformed with a single construct comprising GenScript-optimized SoD2 with signal peptide (“07”), GenScript-optimized SoD7 with signal peptide (“08”), CODA-optimized SoD2 with signal peptide (“09”), or CODA-optimized SoD2 with signal peptide (“10”). FIG. 3 is a representation of a Southern blot showing insertion number among transgenic events in Hamlin transformed with GenScript-optimized SoD2 (0407) and Rohde Red transformed with GenScript-optimized SoD2 (0507). FIG. 4 is a representation of a Southern blot showing insertion number among transgenic events in Hamlin transformed with CODA-optimized SoD2 (0409) or CODA-optimized SoD7 (0410) and Rohde Red transformed with CODA-optimized SoD2 (0509) or CODA-optimized SoD7 (0510). Additional tranformation events are shown for GenScript-optimized SoD7 (“08”) and CODA-optimized SoD2 (“09”) in Hamlin in FIG. 9.
Transgenic plants of the orange cultivars Hamlin, Rohde Red, and Marrs (n=82) produce high levels of transcripts of these antimicrobial genes (Table 2 and FIGS. 5-7). FIG. 5 is a representation of a northern blot showing RNA transcripts among transgenic events in Marrs, transformed with genes SoD2 (0607) or SoD7 (0608) GenScript-optimized for codon use in Citrus. FIG. 6 is a representation of a northern blot showing RNA transcripts among transgenic events in Hamlin transformed with CODA-optimized SoD2 (0409) or CODA-optimized SoD7 (0410) and Rohde Red transformed with CODA-optimized SoD2 (0509) or CODA-optimized SoD7 (0510). FIG. 7 is a representation of a northern blot showing RNA transcripts among transgenic events in Hamlin transformed with GenScript-optimized SoD2 (0407) or GenScript-optimized SoD7 (0408) and Rohde Red transformed with GenScript-optimized SoD2 (0507) or GenScript-optimized SoD7 (0508). For identification, Table 2 contains the transgenic event codes for cultivar and gene combination.
Orange plants (Hamlin) were also transformed with a single construct comprising DNA 2.0-optimized SoD2 without signal peptide (“11”) or DNA 2.0-optimized SoD7 without signal peptide (“12”). FIG. 8 is a representation of a Southern blot confirming insertion of SoD2 or SoD7 in these orange plants. Additional transformation events are shown for SoD7 (12) in Hamlin in FIG. 9.

B. Transformation of Grapefruit

Ruby Red (“01”) plants were transformed with a single construct comprising DNA 2.0-optimized SoD2 without signal peptide (“11”) or DNA 2.0-optimized SoD7 without signal peptide (“12”). FIG. 9 is a representation of a Southern blot (membrane was exposed to probes for both SoD2 and SoD7) confirming insertion of SoD2 or SoD7 in these grapefruit plants. FIG. 10 is a representation of a northern blot (membrane was exposed to probes for both SoD2 and SoD7) showing RNA transcripts among transgenic events in Ruby Red transformed with SoD2 (0111) or SoD7 (0112). For identification, Table 2 contains the transgenic event codes for cultivar and gene combination.

C. Transformation of Carrizo Citrange and C22

Carrizo Citrange and C22 rootstocks have been transformed with a construct comprising uidA and either SoD2 or SoD7 or SoD2+SoD7. FIG. 11 is a representation of a Southern blot confirming insertion of SoD2 (lanes marked “07”) and SoD7 (lanes marked “08”) in these Carrizo Citrange plants. FIG. 12 is a representation of a northern blot showing RNA transcripts isolated from these Carrizo Citrange plants (marked “CC”) transformed with SoD2 (GenScript-optimized sequence with signal peptide) and SoD7 (GenScript-optimized sequence with signal peptide). For identification, Table 2 contains the transgenic event codes for cultivar and gene combination. A number of C22 transformation events have been confirmed in each by positive GUS staining.
Swingle and Flying Dragon (citrus rootstock) plants were transformed with various constructs including a single construct comprising GenScript-optimized SoD2 and SoD7 with signal peptide. Successful tranformation of C22, Flying Dragon, and Swingle plants has been at least confirmed by positive GUS staining.

D. Transformation of Lemon

Frost Lisbon and Frost Eureka (lemon) plants were transformed with various constructs including a single construct comprising GenScript-optimized SoD2 and SoD7 with signal peptide. Successful tranformation of C22, Flying Dragon, and Swingle plants has been at least confirmed by positive GUS staining.

Example 8

Canker Disease Resistance Assay

Canker disease resistance was assessed using a detached leaf assay generally as described by Francis M I et al., 2010, Eur J Plant Pathol 127:571-578. Briefly, detached immature leaves (˜75% expanded) were triple rinsed in sterile water to remove debris, sanitized by brief immersion in 70% ethanol followed by 0.5% sodium hypochloride, and again triple rinsed in sterile water. Sanitized leaves (3-4 per replicate×3 replicates) were infiltrated on their abaxial surface with an aqueous suspension of an Xcc strain isolated in Dade County Florida. Innoculated leaves were pressed on the surface of soft water agar plates, parafilm sealed, and incubated in an environmentally-controlled growth chamber.
FIG. 13A shows the result of inoculating a non-transgenic ‘Rio Red’ leaf with the citrus canker pathogen, as described above, and FIG. 13B shows the result of inoculating a transgenic leaf from a plant of ‘Rio Red’ expressing SoD2 with the citrus canker pathogen, as described above. A large reduction in the size and number of lesion on the transgenic can be seen.

Example 9

Citrus Greening (HLB) Disease Resistance Assay by Grafting

FIG. 14 shows the result of graft inoculating non-transgenic ‘Rio Red’ (two trees on the left) or transgenic ‘Rio Red’ expressing SoD2 one tree on the right) with the citrus greening pathogen. A non-transgenic rootstock (Cleopatra mandarin) infected with HLB is used. Onto this rootstock several buds of transgenic ‘Rio Red’ are grafted and this is replicated. The same protocol is followed for non-transgenic buds of ‘Rio Red’. After 8 weeks, vigorous growth can be seen from the transgenic graft, where there is no growth on the controls.

Example 10

Citrus Greening (HLB) Disease Resistance Assay by Psyllid Inoculation

Resistance to bacterial infection and growth was assessed by two metrics. First, resistance was evaluated by the percentage of infection, namely the number of exposed plants that were infected. Second, a PCR-based method was used to amplify bacterial sequences. In this method, the relative degree of infection influences the number of PCR cycles required to produce detectable signal. For example a heavily infested plant might only require a few cycles while a plant with a low bacterial titer may require more cycles. In general, a plant that requires 30 or more cycles to observe detectable signal is regarded to be uninfected. Since some infections of citrus progress slowly, samples were collected for testing at 5 to 11 months after the time of first exposure and thereafter over a period of 6-9 months. The frequency of sample collection may vary from about every 45 days to about every 120 days. Ten to 15 replicates of each transgenic event plus non-transgenic controls are placed haphazardly in an insect proof green house that contains thousands' of psyllids carrying the citrus greening pathogen. The first PCR testing is done about five months after continuous exposure to psyllids. DNA extraction and PCR to detect the pathogen is essentially as described by Trey M S et al., 2006, Proc. Fla. State Hort. Soc. 119:89-93.

Example 11

Propagation and Resistance of Generation 1

Red Grapefruit (2 varieties) and Sweet Orange (3 varieties) were transformed with Agrobacterium comprising an expression vector having an artificial defensin gene construct that included a 2-amino acid insertion in the signal peptide and a single amino acid deletion in the coding sequence (SEQ ID NOS: 26 and 27). A total of 6 transformation events were further tested based on having high levels of SoD2 RNA expressed. Plants were cultivated as described herein and bacterial resistance was assessed as described. A first set of samples were collected after 11 months in the field (DO). Subsequent samples were collected the indicated number of days (42-471) after the first sampling (e.g., D42=11 months+42 days). Results are shown in Table 3.

TABLE 3

Generation 1 Infection Data

Plant Line	N		0	42	90	127	271	384	471

GR 311 Hamlin	1	0%	0%	0%	0%	100%	100%	100%
Non Transgenic
	1	0%	0%	100%	100%	100%	100%	100%
Hamlin
GR 420 Grapefruit	1	0%	0%	0%	0%	0%	100%	100%
GR 824 Grapefruit	2	0%	0%	50%	50%	100%	100%	100%
GR 867 Grapefruit	1	0%	0%	0%	0%	100%	100%	100%
GR 882 Grapefruit	2	0%	0%	0%	50%	50%	50%	50%
GR 890 Grapefruit	1	0%	0%	0%	0%	0%	100%	100%
Non Transgenic
	7	0%	0%	0%	14%	0%	57%	57%
Grapefruit
Non Transgenic
	6	0%	0%	0%	0%	50%	50%	50%
Grapefruit Border
Total	22	0%	0%	9%	18%	41%	68%	68%

Example 12

Propagation and Resistance of Generation 2

Sweet Orange (2 varieties) were transformed with Agrobacterium comprising one of the following defensin gene constructs:

- (a) GenScript-optimized SoD2 with tobacco PR-1b signal peptide (SEQ ID NO: 9),
- (b) CODA-optimized SoD2 with tobacco PR-1b signal peptide (SEQ ID NO: 11),
- (c) GenScript-optimized SoD7 with tobacco PR-1b signal peptide (SEQ ID NO: 10), or
- (d) CODA-optimized SoD7 with tobacco PR-1b signal peptide (SEQ ID NO: 12).
  A total of 71 transformation events were observed. Plants were cultivated as described herein and bacterial resistance was assessed as described. A first set of samples were collected after 5 months in the psyllid house (Day 0). Subsequent samples were collected the indicated number of days after the first sampling (e.g., Day 73=5 months+73 days). Results are shown in FIG. 15, FIG. 16, Table 4, and Table 5.

TABLE 4

Generation 2 Infection Data

1^stSampling

2^ndSampling

3^rdSampling

Partial 4^thSampling

Code

Scion¹

Genotype²

Rootstock³

Gene⁴

Day 0

Mean Ct

Day 73

Mean Ct

Day 170

Mean Ct

Day 317

Mean Ct

0407-01	H	SO	Cm	SoD2 (G)	13%	23.02	33%	26.09	33%	23.28
0407-02	H	SO	Cm	SoD2 (G)	0%		27%	28.78	47%	26.55
0407-03	H	SO	Cm	SoD2 (G)	0%		7%	24.84	33%	29.32
0407-04	H	SO	Cm	SoD2 (G)	20%	25.56	27%	27.18	40%	25.28
0407-06	H	SO	Cm	SoD2 (G)	7%	31.07	7%	26.16	13%	22.52	67%	28.81
0407-07	H	SO	Cm	SoD2 (G)	20%	27.37	13%	25.96	27%	25.85	80%	27.26
0407-09	H	SO	Cm	SoD2 (G)	13%	26.05	27%	26.83	33%	22.90
0407-10	H	SO	Cm	SoD2 (G)	7%	23.57	27%	26.04	47%	25.32
0407-11	H	SO	Cm	SoD2 (G)	7%	26.75	33%	26.21	67%	24.87
0407-12	H	SO	Cm	SoD2 (G)	7%	31.66	13%	24.51	33%	23.39
0407-13	H	SO	Cm	SoD2 (G)	13%	23.52	27%	27.89	40%	23.54
0408-01	H	SO	Cm	SoD7 (G)	13%	24.88	27%	25.55	53%	26.15
0408-07A	H	SO	Cm	SoD7 (G)	7%	23.40	20%	28.48	27%	22.64	80%	27.08
Hamlin	H	SO	Cm	Control	0%		20%	28.83	40%	24.59	87%	25.92
NT
Control
0409-02	H	SO	Cm	SoD2 (C)	7%	27.34	0%		20%	24.04	80%	26.23
0409-03	H	SO	Cm	SoD2 (C)	7%	22.28	7%	28.79	27%	22.12	93%	25.52
0409-06	H	SO	Cm	SoD2 (C)	0%		20%	26.52	40%	24.01
0409-07	H	SO	Cm	SoD2 (C)	0%		20%	26.31	40%	23.17
0410-01	H	SO	Cm	SoD7 (C)	0%		40%	22.96	73%	24.78
0507-01	RR	SO	Cm	SoD2 (G)	0%		47%	26.35	60%	23.60
0507-02	RR	SO	Cm	SoD2 (G)	13%	28.26	40%	22.18	47%	25.14
0507-03	RR	SO	Cm	SoD2 (G)	13%	24.61	47%	26.64	60%	23.59
0507-04	RR	SO	Cm	SoD2 (G)	13%	26.21	27%	25.25	40%	24.63
0507-07	RR	SO	Cm	SoD2 (G)	0%		13%	27.42	27%	22.61	67%	29.19
0507-08	RR	SO	Cm	SoD2 (G)	7%	25.97	40%	26.37	40%	24.03
0507-10	RR	SO	Cm	SoD2 (G)	7%	26.04	27%	25.71	40%	25.29
0507-11	RR	SO	Cm	SoD2 (G)	0%		40%	26.51	53%	22.26
0507-12	RR	SO	Cm	SoD2 (G)	0%		20%	17.61	13%	22.56	77%	27.17
0507-15	RR	SO	Cm	SoD2 (G)	13%	24.49	53%	25.65	73%	23.10
0508-02	RR	SO	Cm	SoD7 (G)	13%	29.40	47%	26.25	73%	23.90
0508-03	RR	SO	Cm	SoD7 (G)	7%	31.44	33%	24.53	60%	25.43
0508-04	RR	SO	Cm	SoD7 (G)	13%	25.65	20%	28.00	60%	25.74
0508-06	RR	SO	Cm	SoD7 (G)	0%		7%	27.72	27%	24.33	79%	25.56
0508-07	RR	SO	Cm	SoD7 (G)	27%	26.86	67%	25.30	100%	24.76	100%	21.87
0508-08	RR	SO	Cm	SoD7 (G)	7%	24.35	27%	24.55	53%	23.07
0508-09	RR	SO	Cm	SoD7 (G)	20%	25.55	33%	24.69	60%	24.40
0508-10	RR	SO	Cm	SoD7 (G)	7%	25.96	33%	25.94	47%	23.30
Rohde	RR	SO	Cm	Control	13%	27.03	27%	25.64	67%	25.46	100%	22.32
Red NT
Control
0509-02	RR	SO	Cm	SoD2 (C)	13%	24.36	53%	23.07	60%	23.77
0509-03	RR	SO	Cm	SoD2 (C)	13%	25.28	27%	26.60	53%	26.02
0509-07	RR	SO	Cm	SoD2 (C)	7%	30.19	20%	24.85	47%	25.71
0509-10	RR	SO	Cm	SoD2 (C)	20%	27.29	20%	24.93	67%	26.26
0510-02	RR	SO	Cm	SoD7 (C)	7%	30.66	27%	23.36	47%	24.42
0510-03	RR	SO	Cm	SoD7 (C)	7%	22.01	20%	24.70	53%	25.39
0510-05	RR	SO	Cm	SoD7 (C)	7%	31.54	7%	31.03	7%	31.22	17%	35.78
0510-06	RR	SO	Cm	SoD7 (C)	0%		33%	26.56	80%	24.48	93%	23.67
0510-08	RR	SO	Cm	SoD7 (C)	7%	23.07	47%	25.29	60%	22.32
0510-09	RR	SO	Cm	SoD7 (C)	0%		33%	24.63	47%	24.02
0510-10	RR	SO	Cm	SoD7 (C)	0%		20%	27.68	60%	25.16
Extra NT
Controls
Hamlin	H	SO	Cm	Control	0%		40%	27.29	47%	23.25
Hamlin	H	SO	Cm	Control	7%	24.49	13%	24.87	33%	25.58
Hamlin	H	SO	Cm	Control	0%		33%	24.44	33%	25.82
Rohde	RR	SO	Cm	Control	7%	24.61	33%	26.27	27%	22.98
Red
Rohde	RR	SO	Cm	Control	0%		40%	27.07	33%	24.49
Red
Rohde	RR	SO	Cm	Control	7%	24.36	33%	29.01	47%	26.50
Red

¹H = Hamlin; RR = Rohde Red
²SO = Sweet Orange
³Cm = Cleopatra mandarin
⁴(G) = GenScript-optimized sequence; (C) = CODA-optimized sequence

Example 13

Propagation and Resistance of Generation 3

One Sweet Orange variety and one grapefruit variety were transformed with Agrobacterium comprising one of the following defensin gene constructs:

- (a) GenScript-optimized SoD2 with no signal peptide (SEQ ID NO: 3), or
- (b) GenScript-optimized SoD7 with no signal peptide (SEQ ID NO: 4).
  A total of 36 transformation events were observed. Plants were cultivated as described herein and bacterial resistance was assessed as described. A first set of samples were collected after 5 months in the psyllid house (Day 0). Subsequent samples were collected the indicated number of days after the first sampling (e.g., Day 103=5 months+103 days). Results are shown in FIG. 16 and Table 5.

TABLE 5

Generations 2 and 3 Infection Data

2^ndSampling

3^rdSampling

					1^stSampling			Ct of		Avg	Ct of
Code	Scion¹	Genotype²	Rootstock³	Gene⁴	Day 0	Day 103	Avg Ct	Positive	Day 215	Ct	Positive

41103	H	SO	Cm	SoD2 (-P)	10%	10%	37.98	24.78	10%	36.83	19.62
41108	H	SO	Cm	SoD2 (-P)	0%	0%	40.00		0%	38.93
41107	H	SO	Cm	SoD2 (-P)	10%	14%	37.24	23.44	14%	35.28	21.02
41110	H	SO	Cm	SoD2 (-P)	0%	10%	38.18	26.35	20%	35.24	23.33
40918	H	SO	Cm	SoD2 (C)	0%	0%	39.74		10%	36.97	21.53
40915	H	SO	Cm	SoD2 (C)	0%	11%	38.07	25.22	22%	34.31	24.44
41004	H	SO	Cm	SoD7 (C)	0%	10%	38.37	23.72	20%	35.24	25.54
40814	H	SO	Cm	SoD7 (G)	0%	20%	36.62	26.39	10%	36.85	24.35
40817	H	SO	Cm	SoD7 (G)	10%	10%	37.97	22.93	30%	34.17	23.40
11206	RR	Gf	Cm	SoD7 (-P)	0%	30%	35.18	23.93	40%	32.27	24.69
11204	RR	Gf	Cm	SoD7 (-P)	0%	10%	37.63	24.56	30%	33.49	22.16
40813	H	SO	Cm	SoD7 (G)	10%	11%	37.73	22.63	44%	31.96	22.62
11201	RR	Gf	Cm	SoD7 (-P)	0%	30%	35.87	26.76	30%	33.71	23.06
41109	H	SO	Cm	SoD2 (-P)	0%	10%	38.46	24.64	10%	37.25	22.14
11208	RR	Gf	Cm	SoD7 (-P)	0%	0%	39.82		0%	38.42
11108	RR	Gf	Cm	SoD2 (-P)	0%	0%	38.60		13%	36.15	21.66
11103	RR	Gf	Cm	SoD2 (-P)	0%	20%	36.98	26.00	20%	33.73	19.99
60811	M	SO	Cm	SoD7 (G)	0%	0%	39.66		0%	39.03
Marrs WT	M	SO	Cm	Control	0%	10%	38.81	28.14	20%	35.57	24.93
40820	H	SO	Cm	SoD7 (G)	10%	20%	36.99	25.96	30%	34.94	23.65
41101	H	SO	Cm	SoD2 (-P)	0%	10%	37.65	23.09	20%	34.53	21.92
Ruby Red WT	RR	Gf	Cm	Control	0%	0%	39.39		30%	34.88	26.93
11105	RR	Gf	Cm	SoD2 (-P)	0%	10%	38.64	26.38	20%	36.32	24.70
40810 A	H	SO	Cm	SoD7 (G)	0%	25%	35.46	24.94	50%	30.83	23.08
11203	RR	Gf	Cm	SoD7 (-P)	0%	20%	37.84	29.19	20%	35.55	21.51
40914	H	SO	Cm	SoD2 (C)	0%	0%	39.66		30%	35.22	26.78
40812	H	SO	Cm	SoD7 (G)	0%	10%	37.99	27.44	20%	35.67	21.75
41102	H	SO	Cm	SoD2 (-P)	10%	40%	35.03	27.58	60%	29.83	23.83
Hamlin WT	H	SO	Cm	Control	0%	40%	33.76	24.41	50%	29.52	22.14
60813	M	SO	Cm	SoD7 (G)	0%	0%	40.00		13%	37.06	24.02
60804	M	SO	Cm	SoD7 (G)	10%	0%	39.80		0%	37.74
60703	M	SO	Cm	SoD2 (G)	0%	33%	36.35	30.88	33%	36.07	25.07
60802	M	SO	Cm	SoD7 (G)	0%	0%	39.18		10%	37.87	31.23
60702	M	SO	Cm	SoD2 (G)	0%	10%	38.30	27.16	20%	35.46	24.11
41211	H	SO	Cm	SoD7 (-P)	10%	20%	36.47	24.33	30%	34.02	21.20
41203	H	SO	Cm	SoD7 (-P)	0%	0%	39.93		0%	38.17
60812	M	SO	Cm	SoD7 (G)	0%	0%	40.00		10%	36.79	23.40
60810	M	SO	Cm	SoD7 (G)	10%	20%	37.25	26.25	70%	27.87	23.44
60707	M	SO	Cm	SoD2 (G)	0%	10%	38.51	25.13	40%	33.77	25.40
60701	M	SO	Cm	SoD2 (G)	0%	20%	37.45	28.07	50%	30.37	23.85
41210	H	SO	Cm	SoD7 (-P)	0%	0%	39.60		20%	34.62	22.91
41202	H	SO	Cm	SoD7 (-P)	10%	17%	35.89	23.81	50%	30.85	22.69
60706	M	SO	Cm	SoD2 (G)	0%	10%	37.64	25.23	50%	30.82	23.24
41209	H	SO	Cm	SoD7 (-P)	0%	40%	33.36	24.97	70%	27.11	22.03
41113	H	SO	Cm	SoD2 (-P)	20%	60%	31.02	25.03	80%	25.36	21.70
41215	H	SO	Cm	SoD7 (-P)	20%	40%	33.73	24.32	70%	25.95	21.94
60808	M	SO	Cm	SoD7 (G)	0%	0%	39.35		22%	36.32	22.11
41208	H	SO	Cm	SoD7 (-P)	0%	0%	39.62		11%	37.30	22.04
41112	H	SO	Cm	SoD2 (-P)	20%	20%	35.94	25.32	40%	31.22	22.22
41214	H	SO	Cm	SoD7 (-P)	0%	20%	36.57	24.47	50%	29.72	21.99
60705	M	SO	Cm	SoD2 (G)	0%	10%	37.96	23.82	10%	36.57	21.02
41204	H	SO	Cm	SoD7 (-P)	0%	0%	40.00		10%	36.50	22.28
41111	H	SO	Cm	SoD2 (-P)	10%	13%	37.98	23.82	25%	35.18	24.46
Hamlin WT	H	SO	Cm	Control	0%	25%	35.56	26.41	55%	29.82	22.51
Marrs WT	M	SO	Cm	Control	0%	0%	39.16		33%	33.11	22.73

¹H = Hamlin; RR = Ruby Red; M = Marrs
²SO = Sweet Orange; Gf = Grapefruit
³Cm = Cleopatra mandarin
⁴(G) = GenScript-optimized sequence; (C) = CODA-optimized sequence; (-P) = DNA 2.0-optimized sequence with no signal peptide

Example 14

Propagation and Resistance of Generation 4

A first line of Sweet Orange (2 varieties), one grapefruit, and two rootstocks were prepared to co-express (i) GenScript SoD2 with tobacco PR-1b signal peptide (SEQ ID NO: 9) and (ii) GenScript SoD7 with tobacco PR-1b signal peptide (SEQ ID NO: 10). More specifically, plants were transformed with a double defensin construct comprising, in a 5′ to 3′ direction SoD2, uidA, and SoD7 (13). A total of 29 transformation events were observed with another 28 GUS-positive candidates in tissue culture or just out of tissue culture. Plants confirmed to co-express SoD2 and SoD7 will be cultivated and evaluated in infection assays to determine the degree to which coexpression prevents, ameliorates, and/or treats infection.
FIG. 9 is a representation of a Southern blot (membrane was exposed to probes for both SoD2 and SoD7) showing insertion number among transgenic events in Hamlin transformed with a double defensin construct comprising SoD2 and SoD7 (0413). FIG. 10 also shows insertion number among transgenic events in Hamlin transformed with a double defensin construct comprising SoD2 and SoD7 (0413).
Rio Red plants (02) were transformed with a double defensin construct (13). FIG. 17 is a representation of a Southern blot confirming insertion of both SoD2 and SoD7 in these Rio Red plants. DNA was cut with a single restriction enzyme that cut within SoD2, uidA, and SoD7 and blotted with both SoD2 and SoD7 probes simultaneously. FIG. 18 is a representation of a northern blot showing RNA transcripts isolated from Rio Red plants (marked “02”) transformed with SoD2 (GenScript-optimized sequence with signal peptide) and SoD7 (GenScript-optimized sequence with signal peptide). RNA transcripts isolated from Hamlin plants (marked “04”) are also shown.

Example 15

Propagation and Resistance of Generation 5

Evaluation of coexpression of SoD2 and SoD7 is underway. A line of Sweet Orange (1 variety) was prepared to co-express (i) DNA 2.0 SoD2 with no signal peptide (SEQ ID NO: 30) and (ii) DNA 2.0 SoD7 with no signal peptide (SEQ ID NO: 31). Transformation and expression may be confirmed by Southern and northern blotting analysis. Plants may be cultivated as described herein and bacterial resistance evaluated as described. Plants confirmed to co-express SoD2 and SoD7 may be cultivated and evaluated in infection assays to determine the degree to which coexpression prevents, ameliorates, and/or treats infection.

Example 16

Expression of Defensin Constructs in Various Plants

Stable expression of defensin constructs comprising nucleic acid sequences condon-optimized for citrus has been confirmed in the following:


Cultivar	Gene Code	# Events

Rio Red Grapefruit	13	18
Ruby Red Grapefruit	11 and 12	12
Hamlin Sweet Orange	07, 08, 09, 10, 11,	over 86
	12, 13, and 16
Marrs Sweet Orange	07 and 08	13
Rohde Red Valencia	07, 08, 09, 10, 13	over 48
Orange
Frost Eureka Lemon	13 and 16	over 30
Frost Lisbon Lemon	13 and 16	over 33
C22 and Carrizo	07, 08, 13	42
Citrange Rootstocks
Flying dragon and	13	Multiple GUS+
Swingle Rootstocks

For all constructs, individual transformation events have been found spanning a range of expression levels from no expression (e.g., since Southern results demonstrate the gene is present, often in multiple copies, it may be that the transgene has been silenced) to low expression to high expression.

Example 17

Antibodies to SoD2 and SoD7

Antibodies were raised to SoD2 and SoD7. Full length SoD7 peptide was synthesized by GenScript. Aliquots of synthetic SoD7 (200 ug each time) were injected into each of 2 different rabbits every three weeks for a total of 4 injections. Sera was collected 2 weeks after the third 2 weeks after the fourth injections. IgG was purified using a Protein A column. SoD7 specific IgG was purified by passing the IgG preparation over a column of synthetic SoD7 conjugated to agarose beads and then eluting with a low pH buffer Eluate was screened for binding to a dilution series from 1 ng to 100 ng synthetic SoD7. FIG. 19 is a Western blot illustrating binding of the purified SoD7-specific IgG antibodies to about 20 ng of SoD7 peptide in either trangenic plants ( lanes 3, 4, and 6-9), non-trangenic plants spiked with synthetic SoD7 peptide (lane 5), or pure synthetic SoD7 (lane 10).

Claims

What is claimed is:

1. A nucleic acid comprising a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 30 and SEQ ID NO: 5 and encoding a peptide having an amino acid sequence having at least 99% identity to SEQ ID NO: 1.

2. A nucleic acid comprising a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 31 and SEQ ID NO: 6 and encoding a peptide having an amino acid sequence having at least 99% identity to SEQ ID NO: 2.

3. A nucleic acid comprising a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 9 and SEQ ID NO: 11 and encoding a peptide having an amino acid sequence having at least 99% identity to SEQ ID NO: 7.

4. A nucleic acid comprising a nucleic acid sequence having about 98% identity to a sequence selected from the group consisting of SEQ ID NO: 10 and SEQ ID NO: 12 and encoding a peptide having an amino acid sequence having at least 99% identity to SEQ ID NO: 8.

5. An expression vector comprising, in a 5′ to 3′ direction:

an expression control sequence;

an exogenous nucleic acid operably linked to the expression control sequence; and

a 3′ termination sequence operably linked to the exogenous nucleic acid, wherein the exogenous nucleic acid comprises a nucleic acid sequence having at least 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO:30, and SEQ ID NO:31.

6. An expression vector according to claim 5, wherein the expression vector is located in a bacterial cell.

7. An expression vector according to claim 5, wherein the expression vector is located in a plant cell.

8. An expression vector according to claim 5, wherein the nucleotide sequence of positions −4 to +4 is AACAATGG.

9. An expression vector according to claim 5 further comprising a linker 3′ of the expression control sequence, 5′ of the exogenous nucleic acid, and having a length of from about 1 to about 200 nucleotides.

10. A bacterial cell comprising an expression vector, the expression vector comprising, in a 5′ to 3′ direction:

an expression control sequence;

11. A citrus plant cell comprising an expression vector, the expression vector comprising, in a 5′ to 3′ direction:

an expression control sequence;

12. A citrus plant cell according to claim 11, wherein the citrus plant cell is located in a citrus plant.

13. A citrus plant cell according to claim 11, wherein the plant is selected from the group consisting of orange and grapefruit.

14. A citrus plant cell according to claim 11 further comprising a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7 or SEQ ID NO: 8.

15. A citrus plant comprising an expression vector, the expression vector comprising, in a 5′ to 3′ direction:

an expression control sequence;

16. A citrus plant according to claim 15, wherein the plant is selected from the group consisting of orange and grapefruit.

17. A citrus plant according to claim 15 further comprising a peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7 or SEQ ID NO: 8.

18. A citrus plant cell comprising

(a) a first expression vector, the first expression vector comprising, in a 5′ to 3′ direction:

a first expression control sequence;

a first exogenous nucleic acid operably linked to the first expression control sequence; and

a first 3′ termination sequence operably linked to the first exogenous nucleic acid, wherein the first exogenous nucleic acid comprises a nucleic acid sequence having at least 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 9, SEQ ID NO: 11 and SEQ ID NO: 30; and

(b) a second expression vector, the second expression vector comprising, in a 5′ to 3′ direction:

a second expression control sequence;

a second exogenous nucleic acid operably linked to the second expression control sequence; and

a second 3′ termination sequence operably linked to the second exogenous nucleic acid, wherein the second exogenous nucleic acid comprises a nucleic acid sequence having at least 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 10, SEQ ID NO: 12, and SEQ ID NO: 31.

19. A citrus plant according to claim 18, wherein the plant is selected from the group consisting of orange and grapefruit.

20. A citrus plant according to claim 18 further comprising:

a first peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 1 or SEQ ID NO: 7; and

a second peptide having an amino acid sequence having at least about 99% identity to SEQ ID NO: 2 or SEQ ID NO: 8.

21. A method of expressing in a citrus plant an exogenous nucleic acid comprising a nucleic acid sequence encoding an expressed peptide, the method comprising:

contacting an expression cassette comprising the exogenous nucleic acid or an expression vector comprising the exogenous nucleic acid with the cytosol of a cell of the citrus plant under conditions that permit expression of the exogenous nucleic acid and formation of the expressed peptide,

wherein the exogenous nucleic acid comprises a nucleic acid sequence having at least 98% identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO:30, and SEQ ID NO:31,

the expression cassette or expression vector comprises, in a 5′ to 3′ direction, an expression control sequence, the exogenous nucleic acid operably linked to the expression control sequence, and a 3′ termination sequence operably linked to the exogenous nucleic acid, and

the expressed peptide comprises an amino acid sequence having at least 99% identity to an amino acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 7, and SEQ ID NO: 8.

22. A method according to claim 21, wherein the contacting further comprises co-cultivating the cell with a Agrobacterium cell comprising the expression vector or expression cassette to form a co-cultivated cell.

23. A method according to claim 21 further comprising regenerating a plant from the co-cultivated cell.