Skip to main content
Log in

Resistance to Taiwanese race 1 strains of Ralstonia solanacearum in wild tomato germplasm

  • Published:
European Journal of Plant Pathology Aims and scope Submit manuscript

Abstract

A total of 252 wild Solanum accessions and one population of 49 introgression lines of LA716 were screened for resistance to a race 1/biovar 4/phylotype I strain Pss186 of Ralstonia solanacearum. Most wild tomato accessions were highly susceptible. However, five accessions of S. pennellii, i.e. LA1943, LA716, LA1656, LA1732 and TL01845 were resistant to strain Pss186. These accessions were then challenged against two other race 1/phylotpye I strains Pss4 and Pss190, which were more aggressive. All the five S. pennellii accessions were susceptible to Pss4, but displayed high to moderate resistance to Pss190 with a percentage of wilted plants ranging from 0% to 60%. Pss190 is an aggressive strain that made a resistant tomato line Hawaii 7996 susceptible. Thus, the results found in this study provide evidence of the presence of strain-specific resistance. LA3501, which has an introgression segment on chromosome 6, was found to be resistant to Pss186 among the screened introgression lines. This confirms the importance of resistance trait loci on chromosome 6 that have been identified by other studies. This is the first report of S. pennellii being resistant to bacterial wilt. These new resistant sources will provide breeders with more resources to breed for stable resistance to bacterial wilt of tomato.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Astua-Monge, G., Minsavage, G. V., Stall, R. E., Vallejos, C. E., Davis, M. J., & Jones, J. B. (2000). Xv4-vrxv4: A new gene-for-gene interaction identified between Xanthomonas campestris pv. vesicatoria race T3 and the wild tomato relative Lycopersicon pennellii. Molecular Plant–Microbe Interactions, 13, 1346–1355.

    Article  PubMed  CAS  Google Scholar 

  • Carmeille, A., Caranta, C., Dintinger, J., Prior, P., Luisetti, J., & Besse, P. (2006a). Identification of QTLs for Ralstonia solanacearum race 3-phylotype II resistance in tomato. Theoretical and Applied Genetics, 113, 110–121.

    Article  PubMed  CAS  Google Scholar 

  • Carmeille, A., Prior, P., Kodja, H., Chiroleu, F., Luisetti, J., & Besse, P. (2006b). Evaluation of resistance to race 3, biovar 2 of Ralstonia solanacearum in tomato germplasm. Journal of Phytopathology, 154, 398–402.

    Article  Google Scholar 

  • Danesh, D., & Young, N. D. (1994). Partial resistance loci for tomato bacterial wilt show differential race specificity. Tomato Genetics Cooperative Report, 44, 12–13.

    Google Scholar 

  • Denny, T. P. (2006). Plant pathogenic Ralstonia species. In S. S. Gnanamanickam (Ed.) Plant-associated bacteria (pp. 573–644). Dordrecht: Springer.

    Chapter  Google Scholar 

  • Egashira, H., Kuwashima, A., Imanishi, S., Ishiguro, H., Fukushima, K., & Kaya, T. (2000). Screening of wild accessions resistant to gray mold (Botrytis cinerea Pers.) in Lycopersicon. Acta Physiologica Plantarum, 22, 324–326.

    Article  Google Scholar 

  • Eshed, Y., & Zamir, D. (1994). A genomic library of Lycopersicon pennellii in Lycopersicon esculentum—A tool for fine mapping of genes. Euphytica, 79, 175–179.

    Article  CAS  Google Scholar 

  • Fegan, M., & Prior, P. (2005). How complex is the Ralstonia solanacearum species complex. In C. Allen, P. Prior, & C. Hayward (Eds.) Bacterial wilt: The disease and the Ralstonia solanacearum species complex (pp. 449–462). St. Paul, MN: APS.

    Google Scholar 

  • Francis, D. M., Kabelka, E., Bell, J., Franchino, B., & Clair, D. S. (2000). Resistance to bacterial canker in tomato (Lycopersicon hirsutum LA407) and its progeny derived from crosses to L. esculentum. Plant Disease, 85, 1171–1176.

    Article  Google Scholar 

  • Fry, W. E. (1978). Quantification of general resistance of potato cultivars and fungicide effects for integrated control of potato late blight. Phytopathology, 68, 1650–1655.

    CAS  Google Scholar 

  • Gonzalez, W. G., & Summers, W. L. (1996). Host-plant resistance to Pseudomonas solanacearum in tomato germplasm. Genetic Resources and Crop Evolution, 43, 569–574.

    Article  Google Scholar 

  • Hanson, P. M., Wang, J. F., Licardo, O., Hanudin Mah, S. Y., Hartman, G. L., Lin, Y. C., et al. (1996). Variable reaction of tomato lines to bacterial wilt evaluated at several locations in Southeast Asia. Hortscience, 31, 143–146.

    Google Scholar 

  • Hayward, A. C. (2000). Ralstonia solanacearum. Encyclopedia of Microbiology, 4, 32–42.

    Google Scholar 

  • Jaunet, T. X., & Wang, J. F. (1999). Variation in genotype and aggressiveness of Ralstonia solanacearum race 1 isolated from tomato in Taiwan. Phytopathology, 89, 320–327.

    Article  PubMed  CAS  Google Scholar 

  • Jaworski, C. A., Phatak, S. C., Ghate, S. R., Gitaitis, R. D., & Widrlechner, M. P. (1987). Ga 1565-2-4 Bwt, Ga 219-1-2 Bwt, Ga 1095-1-4 Bwt, And Ga 1405-1-2 Bwt bacterial wilt-tolerant tomato. Hortscience, 22, 324–325.

    Google Scholar 

  • Kado, C. I., & Heskett, M. G. (1970). Selective media for isolation of Agrobacterium, Corynebacterium, Erwinia, Pseudomonas, and Xanthomonas. Phytopathology, 60, 969–976.

    Article  PubMed  CAS  Google Scholar 

  • Kelman, A. (1954). The relationship of pathogenicity in Pseudomonas solanacearum to colony appearance on a tetrazolium medium. Phytopathology, 44, 693–695.

    Google Scholar 

  • Krausz, J. P., & Thurston, H. D. (1975). Breakdown of resistance to Pseudomonas solanacearum in tomato. Phytopathology, 65, 1272–1274.

    Google Scholar 

  • Mangin, B., Thoquet, P., Olivier, J., & Grimsley, N. H. (1999). Temporal and multiple quantitative trait loci analyses of resistance to bacterial wilt in tomato permit the resolution of linked loci. Genetics, 151, 1165–1172.

    PubMed  CAS  Google Scholar 

  • Pico, B., Sifres, A., Elia, M., Diez, M. J., & Nuez, F. (2000). Searching for new resistance sources to tomato yellow leaf curl virus within a highly variable wild Lycopersicon genetic pool. Acta Physiologica Plantarum, 22, 344–350.

    Article  Google Scholar 

  • Pim, L., Gerard, P., & Hans, B. (1993). Screening wild Lycopersicon species for resistance to powdery mildew (Oidium lycoperiscum). Euphytica, 72, 43–49.

    Google Scholar 

  • Prior, P., Bart, S., Leclercq, S., Darrasse, A., & Anais, G. (1996). Resistance to bacterial wilt in tomato as discerned by spread of Pseudomonas (Burholderia) solanacearum in the stem tissues. Plant Pathology, 45, 720–726.

    Article  Google Scholar 

  • Rosello, S., Soler, S., Diez, M. J., Rambla, J. L., Richarte, C., & Nuez, F. (1999). New sources for high resistance of tomato to the tomato spotted wilt virus from Lycopersicon peruvianum. Plant Breeding, 118, 425–429.

    Article  Google Scholar 

  • Scott, J. W., Wang, J. F., & Hanson, P. (2005). Breeding tomatoes for resistance to bacterial wilt, a global view. Acta Horticullture, 695, 161–168.

    Google Scholar 

  • Shaner, G., & Finney, R. E. (1977). Effect of nitrogen-fertilization on expression of slow-mildewing resistance in knox wheat. Phytopathology, 67, 1051–1056.

    Article  CAS  Google Scholar 

  • Thoquet, P., Olivier, J., Sperisen, C., Rogowsky, P., Prior, P., Anais, G., et al. (1996). Polygenic resistance of tomato plants to bacterial wilt in the French West Indies. Molecular Plant–Microbe Interactions, 9, 837–842.

    CAS  Google Scholar 

  • Tsai, J. W., Hsu, S. T., & Chen, L. C. (1985). Bacteriocin-producing strains of Pseudomonas solanacearum and their effect on development of bacterial wilt of tomato. Plant Protection Bulletin, 27, 267–278.

    Google Scholar 

  • Wang, J. F., Hanson, P. M., & Barnes, J. A. (1997). Worldwide evaluation of an international set of resistance sources to bacterial wilt in tomato. Genomics, 7, 524–530.

    Google Scholar 

  • Wang, J. F., Olivier, J., Thoquet, P., Mangin, B., Sauviac, L., & Grimsley, N. H. (2000). Resistance of tomato line Hawaii7996 to Ralstonia solanacearum Pss4 in Taiwan is controlled mainly by a major strain-specific locus. Molecular Plant-Microbe Interactions, 13, 6–13.

    Article  PubMed  CAS  Google Scholar 

  • Wicker, E., Grassart, L., Coranson-Beaudu, R., Mian, D., Guilbaud, C., Fegan, M., et al. (2007). Ralstonia solanacearum strains from Martinique (French West Indies) exhibiting a new pathogenic potential. Applied and Environmental Microbiology, 73, 6790–6801.

    Article  PubMed  CAS  Google Scholar 

  • Winstead, N. N., & Kelman, A. (1952). Inoculation techniques for evaluating resistance to Pseudomonas solanacearum. Phytopathology, 42, 628–634.

    Google Scholar 

Download references

Acknowledgements

This paper is based on a Ph.D. dissertation by Truong Thi Hong Hai, who received a scholarship from the German government through project GTZ81070160. We thank C.-F. Hsu and H.-H. Liau for their technical assistance, and D. R. Ledesma for helpful statistical analysis.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jaw-Fen Wang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hong Hai, T.T., Esch, E. & Wang, JF. Resistance to Taiwanese race 1 strains of Ralstonia solanacearum in wild tomato germplasm. Eur J Plant Pathol 122, 471–479 (2008). https://doi.org/10.1007/s10658-008-9314-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10658-008-9314-1

Keywords

Navigation