Disease resistance in Vitis

Multicellular living organisms and unmodified parts thereof and – Method of introducing a polynucleotide molecule into or... – The polynucleotide confers pathogen or pest resistance

Reexamination Certificate

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C800S278000, C800S298000, C435S419000, C435S460000, C435S430100, C435S431000

Reexamination Certificate

active

07151203

ABSTRACT:
Disclosed are methods for producing grape plants having resistance to bunch rot disease orBotrytisor both. Also disclosed are grape plants having resistance to bunch rot disease orBotrytisor both, wherein the plants express a cecropin B peptide Shiva-1.

REFERENCES:
patent: 5300629 (1994-04-01), Casteels et al.
patent: 5348743 (1994-09-01), Ryals et al.
patent: 5424395 (1995-06-01), Bascomb et al.
patent: 5548075 (1996-08-01), Reed et al.
patent: 5597945 (1997-01-01), Jaynes et al.
patent: 5597946 (1997-01-01), Jaynes et al.
patent: 5631007 (1997-05-01), Ryals et al.
patent: 5824861 (1998-10-01), Aldwinckle et al.
patent: 6232528 (2001-05-01), Scorza et al.
patent: WO 94 07356 (1994-04-01), None
GenBank Accession No. D11113.
GenBank Accession No. D11114.
GenBank Accession No. D25320.
GenBank Accession No. D25321.
GenBank Accession No. M10309.
GenBank Accession No. X16972.
Allefs et al., “Erwiniasoft rot resistance of potato cultivars transformed with a gene construct coding for antimicrobial peptide cecropin B is not altered,”American Potato Journal,72:437-445 (1995).
Arce, P. et al., “Enhanced resistance to bacterial infection byErwinia carotovorasubsp.atrosepticain transgenic potato plants expressing the attacin or the cecropin SB-37 genes,”Amer J of Potato Res,76:169-177 (1999).
Arrowood et al., “In Vitro Activities of Lytic Peptides against the Sporozoites ofCryptospordium parvum,” Antimicrobial Agents in Chemotherapy35:224-227 (1991).
de Carvalho et al., “Suppression of beta-1,3-glucanase transgene expression in homozygous plants,”The EMBO Journal,11:2595-2602 (1992).
Colby et al., “Cellular differences inagrobacteriumsusceptibility and regenerative capacity restrict the development of transgenic grapevines”,J. Amer. Soc. Hort. Sci.,116:356-361 (1991).
Finnegan et al., “Transgene inactivation: Plants fight back!,”Bio/Technology,12:883-888 (1994).
Florack, D. et al., “Expression of giant silkmoth cecropin B genes in tobacco,”Transgenic Research4:132-141 (1995).
Gray et al., “Grape”,Biotechnology of Perennial Fruit Crops,9:229-262 (1992).
Gunshefski et al., “In Vitro Antimicrobial Activity of Shiva-11 Against Ocular Pathogens,”Cornea13:237-242 (1994).
Hightower et al., “The expression of cecropin peptide in transgenic tobacco does not confer resistance topseudomonas syringaepvtabaci,” Plant Cell Reports,13:295-299 (1994).
Hill et al., “Multiplication and movement ofXylella fastidiosawithin grapevine and four other plants,”Phytopathology,85:1368-1372 (1995).
Hopkins, “Physiological and pathological characteristics of virulent and avlrulent strains of the bacterium that causes Pierce's Disease of the grapevine,”Phytopathology,75:713-717 (1985).
Huang, Y. et al., “Expression of an engineered Cecropin gene cassette in transgenic tobacco plants confers disease resistance toPseudomonas syringaepv.tabaci,” Phytopathology,87:494-499 (1997).
Jaynes, “Use of genes encoding novel lytic peptides and proteins that enhance microbial disease resistance in plants,”Acta Horticultura,336:33-39 (1993).
Jaynes et al., “ Expression of a cecropin B lytic peptide analog in transgenic tobacco confers enhanced resistance to bacterial wilt caused byPseudomonas solanacearum,” Plant Science,89:43-53 (1993).
Matzke et al., “How and why do plants inactivate homologous (Trans)genes?,”Plant Physiol.,107:679-685 (1995).
Mullins et al., “Agrobacterium-mediated genetic transformation of grapevines: transgenic plants ofVitis Rupestrisscheele and buds ofVitis viniferaL.,”Bio/Technology,8:1041-1045 (1990).
Okamoto, M. et al., “Enhanced expression of an antimicrobial peptide sarcotoxin IA by GUS fusion in transgenic tobacco plants,”Plant Cell Physiol.,39:57-63 (1998).
Osusky, M. et al., “Transgenic plants expressing cationic peptide chimeras exhibit broad-spectrum resistance to phytopathogens,”Nature Biotechnology,18:1162-1166 (2000).
Perl et al., “Establishment of anAgrobacterium-mediated transformation system for grape (Vitis viniferaL.): The role of antioxidants during grape-Agrobacteriuminteractions,”Nature Biotechnology,14:624-628 (1996).
Rodriguez et al., “Effect of a Cecropin-like Synthetic Peptide (Shiva-3) on the Sporogonic Development ofPlasmodium berghei,” Experimental Parasitology80:596-604 (1995).
Scorza et al., “Transformation of grape (Vitis viniferaL.) zygotic-derived somatic embryos and regeneration of transgenic plants,”Plant Cell Reports,14:589-592 (1995).
Scorza el al., “Producing transgenic ‘thompson seedless’ grape (Vitis viniferaL.) plants,”J. Amer. Soc. Hort. Sci.,121:616-619 (1996).
Sharma, A. et al., “Transgenic expression of cecropin B, an antibacterial peptide fromBombyx mori,confers enhanced resistance to bacterial leaf blight in rice,”FEBS Letters,484:7-11 (2000).
Walker A., “Grape expectations realized,”Nature Biotechnology14:582 (1996).
Williams et al., “Growth of ‘thompson seedless’ grapevines: II. Nitrogen distribution,”Journal of the American Society of Horticultural Science,112:330-333 (1987).

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