Effect of passage of a Potato virus Y isolate on a line of tobacco containing the recessive resistance gene va2 on the development of isolates capable of overcoming alleles 0 and 2

European Journal of Plant Pathology

Volumn 130, Issue 2, 2011, Pages 259-269

  Lacroix, Christelle ^a,b   Glais, Laurent ^c   Verrier, Jean Louis ^b   Jacquot, Emmanuel ^a  

^a AGROCAMPUS OUEST   (France)

^b Seita   (France)

^c FNPPPT ^*  (France)

Author keywords

Adaptation; Point mutation; Potyvirus; Virulence; VPg protein

Indexed keywords

ADAPTATION; ALLELE; CLONE; CULTIVAR; DISEASE CONTROL; EMERGENCE; GENE EXPRESSION; INTEGRATED APPROACH; INTROGRESSION; MOLECULAR ANALYSIS; MUTATION; PLANT BREEDING; POTATO; SYMPTOM; TOBACCO; VIRAL DISEASE; VIRULENCE; VIRUS;

FRANCE;

NICOTIANA TABACUM; POTATO VIRUS Y; POTYVIRUS;

EID: 79955659649     PISSN: 09291873     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10658-011-9751-0     Document Type: Article

References (49)

1. Abdul-Razzak, A., Guiraud, T., Peypelut, M., Walter, J., Houvenaghel, M. C., Candresse, T., et al. (2009). Involvement of the cylindrical inclusion (CI) protein in the overcoming of an eIF4E-mediated resistance against Lettuce mosaic potyvirus. Molecular Plant Pathology, 10, 109-113.
2. Acosta-Leal, R., & Xiong, Z. G. (2008). Complementary functions of two recessive R-genes determine resistance durability of tobacco 'Virgin A Mutant' (VAM) to Potato virus Y. Virology, 379, 275-283.
3. Acosta-Leal, R., Bryan, B. K., Smith, J. T., & Rush, C. M. (2010). Breakdown of host resistance by independent evolutionary lineages of Beet necrotic yellow vein virus involves a parallel C/U mutation in its p25 gene. Phytopathology, 100, 127-133.
4. Ano, G., Blancard, D., & Cailleteau, B. (1995). Mise au point sur la résistance récessive aux souches nécrotiques du virus Y de la pomme de terre (PVY) présente chez Nicotiana tabacum. Annales du Tabac, 27, 35-42.
5. Ayme, V., Petit-Pierre, J., Souche, S., Palloix, A., & Moury, B. (2007). Molecular dissection of the Potato Virus Y VPg virulence factor reveals complex adaptations to the pvr2 resistance allelic series in pepper. Journal of General Virology, 88, 1594-1601.
6. Blancard, D., Ano, G., & Cailleteau, B. (1995). Etude du pouvoir pathogène d'isolats de PVY sur tabac: proposition d'une classification intégrant la résistance à la nécrose. Annales du Tabac, 27, 43-50.
7. Carstens, H., & Seehofer, F. (1960). How Virginia SCR is obtained and cultivated in the Federal Republic of Germany. Coresta, 3, 39-43.
8. Chain, F., Riault, G., Trottet, M., & Jacquot, E. (2007). Evaluation of the durability of the Barley yellow dwarf virus-resistant Zhong ZH and TC14 wheat lines. European Journal of Plant Pathology, 117, 35-43.
9. Chung, B. Y. W., Miller, W. A., Atkins, J. F., & Firth, A. E. (2008). An overlapping essential gene in the Potyviridae. Proceedings of the National Academy of Sciences of the United States of America, 105, 5897-5902.
10. Clark, M. F., & Adams, A. N. (1977). Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. Journal of General Virology, 34, 475-483.
11. Desbiez, C., Gal-On, A., Girard, M., Wipf-Scheibel, C., & Lecoq, H. (2003). Increase in Zucchini yellow mosaic virus symptom severity in tolerant zucchini cultivars is related to a point mutation in P3 protein and is associated with a loss of relative fitness on susceptible plants. Phytopathology, 93, 1478-1484.
12. Domingo, E. (2002). Quasispecies theory in virology. Journal of Virology, 76, 463-465.
13. Domingo, E., & Holland, J. J. (1997). RNA virus mutations and fitness for survival. Annual Review of Microbiology, 51, 151-178.
14. Drake, J. W., Charlesworth, B., Charlesworth, D., & Crow, J. F. (1998). Rates of spontaneous mutation. Genetics, 148, 1667-1686.
15. Escriu, F., Fraile, A., & Garcia-Arenal, F. (2007). Constraints to genetic exchange support gene coadaptation in a tripartite RNA virus. Plos Pathogens, 3, 67-74.
16. Fabre, F., Bruchou, C., Palloix, A., & Moury, B. (2009). Key determinants of resistance durability to plant viruses: Insights from a model linking within- and between-host dynamics. Virus Research, 141, 140-149.
17. Fargette, D., Pinel, A., Traore, O., Ghesquiere, A., & Konate, G. (2002). Emergence of resistance-breaking isolates of Rice yellow mottle virus during serial inoculations. European Journal of Plant Pathology, 108, 585-591.
18. Fazio, G. M. D., Barradas, M. M., Chagas, C. M., & Vicente, M. (1977). Efficiency of a method of mechanical inoculation of citrus exocortis virus (CEV) into Petunia hybrida Vilm (Solanaceae). Summa Phytopathologica, 3, 281-288.
19. Fudal, I., Ross, S., Brun, H., Besnard, A. L., Ermel, M., Kuhn, M. L., et al. (2009). Repeat-induced point mutation (RIP) as an alternative mechanism of evolution toward virulence in Leptosphaeria maculans. Molecular Plant-Microbe Interactions, 22, 932-941.
20. Gao, Z. H., Johansen, E., Eyers, S., Thomas, C. L., Noel Ellis, T. H., Maule, A. J. (2004). The Potyvirus recessive resistance gene, sbm1, identifies a novel role for translation initiation factor eIF4E in cell-to-cell trafficking. Plant Journal, 40, 376-385.
21. Garcia-Arenal, F., & McDonald, B. A. (2003). An analysis of the durability of resistance to plant viruses. Phytopathology, 93, 941-952.
22. Garcia-Arenal, F., Fraile, A., & Malpica, J. M. (2003). Variation and evolution of plant virus populations. International Microbiology, 6, 225-232.
23. Gebre-Selassie, K., Marchoux, G., Delecolle, B., & Pochard, E. (1985). Variabilité naturelle des souches du virus Y de la pomme de terre dans les cultures de piment du sud-est de la france. Caractérisation et classification en pathotypes. Agronomie, 5, 621-630.
24. Harrison, B. D. (2002). Virus variation in relation to resistance-breaking in plants. Euphytica, 124, 181-192.
25. HovmØller, M. S., & Justesen, A. F. (2007). Rates of evolution of avirulence phenotypes and DNA markers in a northwest European population of Puccinia striiformis f. sp tritici. Molecular Ecology, 16, 4637-4647.
26. Janzac, B., Montarry, J., Palloix, A., Navaud, O., & Moury, B. (2010). A point mutation in the polymerase of Potato virus Y confers virulence towards the Pvr4 resistance of pepper and a high competitiveness cost in susceptible cultivar. Molecular Plant Microbe Interactions, 23, 823-830.
27. Jenner, C. E., Wang, X. W., Ponz, F., & Walsh, J. A. (2002). A fitness cost for Turnip mosaic virus to overcome host resistance. Virus Research, 86, 1-6.
28. Johansen, I. E., Lund, O. S., Hjulsager, C. K., & Laursen, J. (2001). Recessive resistance in Pisum sativum and Potyvirus pathotype resolved in a gene-for-cistron correspondence between host and virus. Journal of Virology, 75, 6609-6614.
29. Koelle, G. (1958). Versuche zur vererbung der kankheitsresistenz bei tabak; 2 mitt. eine rippenbräune-resistente Virgin A Mutante nach anwendung künstlicher mutations aulösung durch röntgenstrahlen. Tabak-Forschung, 24, 83-84.
30. Kyle, M. M., & Palloix, A. (1997). Proposed revision of nomenclature for Potyvirus resistance genes in Capsicum. Euphytica, 97, 183-188.
31. Lellis, A. D., Kasschau, K. D., Whitham, S. A., & Carrington, J. C. (2002). Loss-of-susceptibility mutants of Arabidopsis thaliana reveal an essential role for eIF(iso)4E during Potyvirus infection. Current Biology, 12, 1046-1051.
32. Lacroix, C., Glais, L., Kerlan, C., Verrier, J. L. & Jacquot, E. (2010). Biological characterization of French Potato virus Y (PVY) isolates collected from PVY-susceptible or -resistant tobacco plants possessing the recessive resistance gene va. Plant Pathology, doi: 10. 1111/j. 365-3059. 2010. 02342. x.
33. Masuta, C., Nishimura, M., Morishita, H., & Hataya, T. (1999). A single amino acid change in viral genome-associated protein of potato virus Y correlates with resistance breaking in 'Virgin A Mutant' tobacco. Phytopathology, 89, 118-123.
34. Moury, B., Morel, C., Johansen, E., Guilbaud, L., Souche, S., Ayme, V., et al. (2004). Mutations in potato virus Y genome-linked protein determine virulence toward recessive resistances in Capsicum annuum and Lycopersicon hirsutum. Molecular Plant-Microbe Interactions, 17, 322-329.
35. Nicolas, O., Dunnington, S. W., Gotow, L. F., Pirone, T. P., & Hellmann, G. M. (1997). Variations in the VPg protein allow a Potyvirus to overcome va gene resistance in tobacco. Virology, 237, 452-459.
36. Pelham, J., Fletcher, J. T., & Hawkins, J. H. (1970). The establishment of a new strain of Tobacco mosaic virus resulting from the use of resistant varieties of tomato-D. Annals of Applied Biology, 65, 292-297.
37. Piccirillo, P., & Piro, F. (1986). PVY strains on Burley tobacco in southern Italy. (Paper presented at the Coresta Symposium, Taosmina).
38. Pinel-Galzi, A., Rakotomalala, M., Sangu, E., Sorho, F., Kanyeka, Z., Traore, O., et al. (2007). Theme and variations in the evolutionary pathways to virulence of an RNA plant virus species. Plos Pathogens, 3, 1761-1770.
39. Robaglia, C., & Caranta, C. (2006). Translation initiation factors: a weak link in plant RNA virus infection. Trends in Plant Science, 11, 40-45.
40. Roudet-Tavert, G., Michon, T., Walter, J., Delaunay, T., Redondo, E., & Le Gall, O. (2007). Central domain of a Potyvirus VPg is involved in the interaction with the host translation initiation factor eIF4E and the viral protein HcPro. Journal of General Virology, 88, 1029-1033.
41. Ruffel, S., Dussault, M. H., Palloix, A., Moury, B., Bendahmane, A., Robaglia, C., et al. (2002). A natural recessive resistance gene against Potato virus Y in pepper corresponds to the eukaryotic initiation factor 4E (eIF4E). Plant Journal, 32, 1067-1075.
42. Shaner, G., Stromberg, E. L., Lacy, G. H., Barker, K. R., & Pirone, T. P. (1992). Nomenclature and concepts of pathogenicity and virulence. Annual Review of Phytopathology, 30, 47-66.
43. Shukla, D., Ward, C., & Burnt, A. (Eds.). (1994). The Potyviridae. Cambridge: Cambridge University Press.
44. Singh, R. P., Valkonen, J. P. T., Gray, S. M., Boonham, N., Jones, R. A. C., Kerlan, C., et al. (2008). Discussion paper: the naming of Potato virus Y strains infecting potato. Archives of Virology, 153, 1-13.
45. N isolates in infected Nicotiana tabacum cv. Xanthi. Journal of General Virology, 86, 2101-2105.
46. Valkonen, J. (2007). Viruses: economical losses and biotechnological potential. In D. Vreugdenhil, J. Bradshaw, C. Gebhardt, F. Govers, M. Taylor, D. Mackerron, & H. Ross (Eds.), Potato biology and biotechnology: Advances and perspectives (pp. 619-41). Elsevier.
47. Nstrains based on seven years of field survey on a worldwide basis. (Paper presented at the 12th European Association for Potato Research Virology Section Meeting, Rennes, France).
48. Verrier, J. L., Marchand, V., Cailleteau, B., & Delon, R. (2001). Chemical change and cigarette smoke mutagenicity increase associated with CMV-DTL and PVY-N infection in Burley tobacco. (Paper presented at the CORESTA Meeting Agro-Phyto Groups, Cape Town, South Africa).
49. Yamamoto, Y. (1992). Studies on breeding of tobacco varieties resistant to veinal necrosis by Potato virus Y strain T. Bulletin Leaf Tobbacco Research Laboratory, 2, 1-85.