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The Role of Pathogenesis-Related Proteins in the Tomato-Rhizoctonia solani Interaction

DOI: 10.1155/2012/137037

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Abstract:

Rhizoctonia solani is one of the most destructive pathogens causing foot rot disease on tomato. In this study, the molecular and cellular changes of a partially resistant (Sunny 6066) and a susceptible (Rio Grande) tomato cultivar after infection with necrotrophic soil-borne fungus R. solani were compared. The expression of defense-related genes such as chitinase (LOC544149) and peroxidase (CEVI-1) in infected tomato cultivars was investigated using semiquantitative reverse transcription-polymerase chain reaction (RT-PCR). This method revealed elevated levels of expression for both genes in the partially resistant cultivar compared to the susceptible cultivar. One of the most prominent facets of basal plant defense responses is the formation of physical barriers at sites of attempted fungal penetration. These structures are produced around the sites of potential pathogen ingress to prevent pathogen progress in plant tissues. We investigated formation of lignin, as one of the most important structural barriers affecting plant resistance, using thioglycolic acid assay. A correlation was found between lignification and higher level of resistance in Sunny 6066 compared to Rio Grande cultivar. These findings suggest the involvement of chitinase, peroxidase, and lignin formation in defense responses of tomato plants against R. solani as a destructive pathogen. 1. Introduction Tomato (Lycopersicon esculentum) is one of the most important vegetables in the world which suffers from various fungal diseases [1, 2]. Foot rot disease of tomato plants was found in various greenhouses in Iran. Symptoms were characterized by soft rot of the seedling near the soil line. Rhizoctonia solani was consistently isolated from the damaged plant tissues. Rhizoctonia solani is a species complex composed of several anastomosis groups (AGs). This pathogen can survive in soil within diseased plant material as mycelia or sclerotia during unfavorable environmental conditions for several years. The pathogen is transported in infested soil or through movement of diseased plant tissues. Potential for seed borne inoculum also exists. In nature, usually R. solani has asexual reproduction and exists primarily as vegetative mycelium and/or sclerotia. The teleomorph of R. solani, Thanatephorus cucumeris, is classified in the phylum Basidiomycota. Formation of basidiospores on diseased host plants in nature is rarely observed. In favorable environmental conditions, following infection of the host plant by R. solani, sexual spores are formed on specialized structures called basidia. Four spores

References

[1]  A. Fakhro, D. R. Andrade-Linares, S. von Bargen et al., “Impact of Piriformospora indica on tomato growth and on interaction with fungal and viral pathogens,” Mycorrhiza, vol. 20, no. 3, pp. 191–200, 2010.
[2]  B. Pharand, O. Carisse, and N. Benhamou, “Cytological aspects of compost-mediated induced resistance against Fusarium crown and root rot in tomato,” Phytopathology, vol. 92, no. 4, pp. 424–438, 2002.
[3]  J. Webster and R. W. S. Weber, Inrtoduction to Fungi, Cambridge University Press, 3rd edition, 2007.
[4]  D. E. Carling, “Grouping in Rhizoctonia solani by hyphal anastomosis,” in Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease Control, B. Sneh, S. Jabaji-Hare, S. Neate, and G. Dijst, Eds., pp. 37–47, Kluwer Academic, Dordrecht, The Netherlands, 1996.
[5]  D. E. Carling, R. E. Baird, R. D. Gitaitis, K. A. Brainard, and S. Kuninaga, “Characterization of AG-13, a newly reported anastomosis group of Rhizoctonia solani,” Phytopathology, vol. 92, no. 8, pp. 893–899, 2002.
[6]  S. Kuninaga, R. Yokosawa, and A. Ogoshi, “Some properties of anastomosis group 6 and BI in Rhizoctonia solani Kuhn,” Annals of the Phytopathological Society of Japan, vol. 45, no. 2, pp. 207–214, 1979.
[7]  B. Sneh, L. Burpee, and A. Ogoshi, Identification of Rhizoctonia Species, The American Phytopathological Society Press, St. Paul, Minn, USA, 1991.
[8]  T. Misawa and S. Kuninaga, “The first report of tomato foot rot caused by Rhizoctonia solani AG-3 PT and AG-2-Nt and its host range and molecular characterization,” Journal of General Plant Pathology, vol. 76, no. 5, pp. 310–319, 2010.
[9]  E. E. Kuramae, A. L. Buzeto, M. B. Ciampi, and N. L. Souza, “Identification of Rhizoctonia solani AG 1-IB in lettuce, AG 4 HG-I in tomato and melon, and AG 4 HG-III in broccoli and spinach, in Brazil,” European Journal of Plant Pathology, vol. 109, no. 4, pp. 391–395, 2003.
[10]  L. C. Van Loon, M. Rep, and C. M. J. Pieterse, “Significance of inducible defense-related proteins in infected plants,” Annual Review of Phytopathology, vol. 44, pp. 135–162, 2006.
[11]  N. Benhamou, M. H. A. J. Joosten, and P. J. G. M. De Wit, “Subcellular localization of chitinase and of its potential substrate in tomato root tissues infected by Fusarium oxysporum f. sp. Radicis-lycopersici,” Plant Physiology, vol. 92, no. 4, pp. 1108–1120, 1990.
[12]  N. Danhash, C. A. M. Wagemakers, J. A. L. van Kan, and P. J. G. M. de Wit, “Molecular characterization of four chitinase cDNAs obtained from Cladosporium fulvum-infected tomato,” Plant Molecular Biology, vol. 22, no. 6, pp. 1017–1029, 1993.
[13]  J. P. Wubben, C. B. Lawrence, and P. J. G. M. De Wit, “Differential induction of chitinase and 1,3-β-glucanase gene expression in tomato by Cladosporium fulvum and its race-specific elicitors,” Physiological and Molecular Plant Pathology, vol. 48, no. 2, pp. 105–116, 1996.
[14]  P. Taheri and S. Tarighi, “Cytomolecular aspects of rice sheath blight caused by Rhizoctonia solani,” European Journal of Plant Pathology, vol. 129, no. 4, pp. 511–528, 2011.
[15]  S. Lurie, E. Fallik, A. Handros, and R. Shapira, “The possible involvement of peroxidase in resistance to Botrytis cinerea in heat treated tomato fruit,” Physiological and Molecular Plant Pathology, vol. 50, no. 3, pp. 141–149, 1997.
[16]  C. M. Rick and J. I. Yoder, “Classical and molecular genetics of tomato: highlights and perspectives,” Annual Review of Genetics, vol. 22, pp. 281–300, 1988.
[17]  A. Yildiz and M. Timur D?ken, “Anastomosis group determination of Rhizoctonia solani Kühn (Telemorph: Thanatephorus cucumeris) isolates from tomatoes grown in Aydin, Turkey and their disease reaction on various tomato cultivars,” Journal of Phytopathology, vol. 150, no. 10, pp. 526–528, 2002.
[18]  K. Schmidt, B. Heberle, J. Kurrasch, R. Nehls, and D. J. Stahl, “Suppression of phenylalanine ammonia lyase expression in sugar beet by the fungal pathogen Cercospora beticola is mediated at the core promoter of the gene,” Plant Molecular Biology, vol. 55, no. 6, pp. 835–852, 2004.
[19]  M. A. Doster and R. M. Bostock, “Effects of low temperature on resistance of almond trees to Phytophthora pruning wound cankers in relation to lignin and suberin formation in wounded bark tissues,” Phytopathology, vol. 78, no. 4, pp. 478–483, 1988.
[20]  M. M. Campbell and B. E. Ellis, “Fungal elicitor-mediated responses in pine cell cultures—I. Induction of phenylpropanoid metabolism,” Planta, vol. 186, no. 3, pp. 409–417, 1992.
[21]  P. Taheri and S. Tarighi, “Riboflavin induces resistance in rice against Rhizoctonia solani via jasmonate-mediated priming of phenylpropanoid pathway,” Journal of Plant Physiology, vol. 167, no. 3, pp. 201–208, 2010.
[22]  S. Sareena, K. Poovannan, K. K. Kumar et al., “Biochemical responses in transgenic rice plants expressing a defence gene deployed against the sheath blight pathogen, Rhizoctonia solani,” Current Science, vol. 91, no. 11, pp. 1529–1532, 2006.
[23]  B. Mauch-Mani and A. J. Slusarenko, “Production of salicylic acid precursors is a major function of phenylalanine ammonia-lyase in the resistance of arabidopsis to Peronospora parasitica,” Plant Cell, vol. 8, no. 2, pp. 203–212, 1996.
[24]  P. Taheri and S. Tarighi, “A survey on basal resistance and riboflavin-induced defense responses of sugar beet against Rhizoctonia solani,” Journal of Plant Physiology, vol. 168, no. 3, pp. 1114–1122, 2011.
[25]  S. C. Chen, A. R. Liu, F. H. Wang, and G. J. Ahammed, “Combined overexpression of chitinase and defensin genesin transgenic tomato enhances resistance to Botrytis cinerea,” African Journal of Biotechnology, vol. 8, no. 20, pp. 5182–5188, 2009.
[26]  G. Sridevi, C. Parameswari, N. Sabapathi, V. Raghupathy, and K. Veluthambi, “Combined expression of chitinase and β-1,3-glucanase genes in indica rice (Oryza sativa L.) enhances resistance against Rhizoctonia solani,” Plant Science, vol. 175, no. 3, pp. 283–290, 2008.

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