References
- Agrama, H. A. and Scott, J. W. 2006. Quantitative trait loci for tomato yellow leaf curl virus and tomato mottle virus resistance in tomato. J. Am. Soc. Hort. Sci. 131: 267-272.
- Balatero, C. H., Hautea, D. M., Narciso, J. O. and Hanson, P. M. 2005. QTL mapping for bacterial wilt resistance in Hawaii 7996 using AFLP, RGA, and SSR markers. In : Bacterial Wilt Disease and the Ralstonia solanacearum Species Complex, ed. by C. Allen, P. Prior and A. C. Hayward, pp. 301-307. APS press, St. Paul, USA.
- Dannon, E., and Wydra, K.. 2004. Interaction between silicon amendment, bacterial wilt development and phenotype of Ralstonia solanacearum in tomato genotypes. Physiol. Mol. Plant Pathol. 64: 233-243. https://doi.org/10.1016/j.pmpp.2004.09.006
- Denesh, D., Aarons, S., McGill, G. E. and Young, N. D. 1994. Genetic dissection of oligogenic resistance to bacterial wilt in tomato. Mol. Plant-Microbe Interact. 7: 464-471. https://doi.org/10.1094/MPMI-7-0464
- Graham, T., Sequeira, L. and Huang, T. 1977. Bacterial lipopolysaccharides as inducers of disease resistance in tobacco. Appl. Environ. Microbiol. 34: 424-432.
- Grimault, V., Gelie, B., Lamattre, M., Prior, P. and Schimidt, J. 1994. Comparative histology of resistant and susceptible tomato cultivars infected by Pseudomonas solanacearum. Physiol. Mol. Pathol. 44: 105-123 https://doi.org/10.1016/S0885-5765(05)80105-5
- Grimault, V., Prior, P. and Anais, G.. 2008. A monogenic dominant resistance of tomato to bacterial wilt in Hawaii 7996 is associated with plant colonization by Pseudomonas solanacearum. J. Phytopathol. 143: 349-352. https://doi.org/10.1111/j.1439-0434.1995.tb00274.x
- Hayward, A. C. 1991. Biology and epidemiology of bacterial wilt caused by Pseudomonas solanacearum. Ann. Rev. Phytopathol. 29: 65-87. https://doi.org/10.1146/annurev.py.29.090191.000433
- Hayward, A. C. 1994. Systematics and phylogeny of Pseudomonas solanacearum and related bacteria. In: Bacterial wilt: the disease and its causative agent Pseudomonas solanacearum. ed. By A. C. Hayward and G. L. Hartman, pp. 127-135. CAB International, Oxford, UK.
- Jeong, Y., Cheong, H., Choi, O., Kim, J., K., Kang, Y., Kim, J., Lee, S., Koh, S., Moon, J. S. and Hwang, I. 2011. An HrpBdependent but type III-independent extracellular aspartic protease is a virulence factor of Ralstonia solanacearum. Mol. Plant Pathol. 12: 373-380. https://doi.org/10.1111/j.1364-3703.2010.00679.x
- Jeong, Y., Kim, J., Kang, Y., Lee, S. and Hwang, I. 2007. Genetic diversity and distribution of Korean isolates of Ralstonia solanacearum. Plant Dis. 91: 1277-1287. https://doi.org/10.1094/PDIS-91-10-1277
- Kelman, A. 1954. The relationship of pathogenicity in Pseudomonas solanacearum to colony appearance on a tetrazolium medium. Phytopathology 44: 693-695.
- Lopes, C. A., Carvalho, S. I. C. and Boiteux, L. S. 2005. Search for resistance to bacterial wilt in a Brazilian Capsicum germplasm collection. In : Bacterial Wilt Disease and the Ralstonia solanacearum Species Complex, ed. by C. Allen, P. Prior and A. C. Hayward, pp. 247-251. APS press, St. Paul, USA.
- Marco, Y., Trigalet, A., Vasse, J., Oliver, J., Feng, D. X. and Deslandes, L. 2005. Host resistance to Ralstonia solanacearum. In : Bacterial Wilt Disease and the Ralstonia solanacearum Species Complex, ed. by C. Allen, P. Prior and A. C. Hayward, pp. 275-283. APS press, St. Paul, USA.
- Min, J. S., Park, J. H., Han, K. S, Kim, D. H, Lee, J. S and Kim, H. H. 2009. Screening of tmato cultivars resistant to bacterial wilts. Res. Plant Dis. 15: 198-201. https://doi.org/10.5423/RPD.2009.15.3.198
- Nonomurai, T., Matsuda, Y., Tsuda,, M., Uranaka, K. and Toyoda, H. 2001. Susceptibility of commercial tomato cultivars to bacterial wilt in hydroponic system. Gen. Plant Pathol. 67: 224-227. https://doi.org/10.1007/PL00013016
- Park, E. J., Lee, S. D., Chung, E. J., Lee, M. H., Um, H. Y., Murugaiyan, S., Moon, B. J. and Lee, S-W. 2007. MicroTom- A model plant system to study bacterial wilt by Ralstonia solanacearum. Plant Pathology J. 23: 239-244. https://doi.org/10.5423/PPJ.2007.23.4.239
- Pflieger, S., Lefebvre, V., Caranta, C., Blattes, A., Goffinet, B., and Palloix A. 1999. Disease resistance gene analogs as candidates for QTLs involved in pepper-pathogen interactions. Genome 42: 1100-1110. https://doi.org/10.1139/g99-067
- Roberts, P. D., Denny, T. P. and Schell, M. A. 1988. Cloning of the egl genes of Pseudomonas solanacearum and analysis of its role in phytopathogenicity. J. Bacteriol. 170: 1445-1451.
- Saile, E., McGarvey, J. A., Schell, M. A. and Denny, T. P. 1997. Role of extracellular polysaccharide and endoglucanase in root invasion and colonization of tomato plants by Ralstonia solanacearum. Phytopathology 87: 1264-1271. https://doi.org/10.1094/PHYTO.1997.87.12.1264
- Sakata, Y., Kubo, N., Morishita, M., Kitadani, E., Sugiyama, M., and Hirai, M. 2006. QTL analysis of powdery mildew resistance in cucumber (Cucumis sativus L.). Theor Appl Genet 112: 243-250. https://doi.org/10.1007/s00122-005-0121-1
- Schaad, N. W., Jones, J. B. and Chun, W. 2001. Laboratory Guide for Identification of Plant Pathogenic Bacteria, 3rd ed. APS Press, St. Paul, USA.
- Schell, M. A. 2000. Control of virulence and pathogenicity genes of Ralstonia solanacearum by an elaborate sensory network. Ann. Rev. Phytopathol. 38: 263-292. https://doi.org/10.1146/annurev.phyto.38.1.263
- Takabatake, R., Seo, S., Mitsuhara, I., Tsuda, S. and Ohashi, Y. 2006. Accumulation of the two transcripts of the N gene, conferring resistance to Tobacco Mosaic Virus, is probably important for N gene-dependent hypersensitive cell death. Plant Cell Physiol. 47: 254-261. https://doi.org/10.1093/pcp/pci243
- Thoquet, P., Oliver, J., Sperisen, C., Rogowsky, P., Laterrot, H. and Grimsley, N. 1996. Quantitative trait loci determining resistance to bacterial wilt in tomato cultivar Hawaii 7996. Mol. Plant-Microbe Interact. 9: 826-836. https://doi.org/10.1094/MPMI-9-0826
- Vasse, J., Frey, P. and Trigalet, A. 1995. Microscopic studies of intercellular infection and protoxylem invasions of tomato roots by Pseudomonas solanacearum. Mol. Plant-Microbe Interact. 8: 241-251. https://doi.org/10.1094/MPMI-8-0241
- Wallis, F. M. and Truter, S. J. 1978. Histopathology of tomato plants infected with Pseudomonas solanacearum, with emphasis on ultrastructure. Physiol. Plant Pathol. 13: 307-317. https://doi.org/10.1016/0048-4059(78)90047-4
- Wang, J. F., Hanson, P. and Barnes, J. A. 1998. World wide evolution of an international set of resistance source to bacterial wilt in tomato. In: Bacterial Wilt Disease: Molecular and Ecological Aspects. ed. by P. Prior, C. Allen and J. Elphinstone, pp 269-275. INRA Springer.
- Yao, J. and Allen, C. 2006. Chemotaxis is required for virulence and competitive fitness of the bacterial wilt pathogen Ralstonia solanacearum. J. Bacteriol. 188:3697-3708. https://doi.org/10.1128/JB.188.10.3697-3708.2006
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