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Induction of Disease Resistance by Acibenzolar-S-methyl, the Plant Activator against Gray Mold (Botrytis cinerea) in Tomato Seedlings

저항성 유도물질(acibenzolar-S-methyl)처리에 의한 토마토 잿빛곰팡이병 발병억제

  • Lee Jung-Sup (Dept. of Horticultural Environment, National Horticultural Research Institute, RDA) ;
  • Kang Nam-Jun (Protected Horticulture Experiment Station, National Horticultural Research Institute, RDA) ;
  • Seo Sang-Tae (Dept. of Horticultural Environment, National Horticultural Research Institute, RDA) ;
  • Han Kyoung-Suk (Dept. of Horticultural Environment, National Horticultural Research Institute, RDA) ;
  • Park Jong-Han (Dept. of Horticultural Environment, National Horticultural Research Institute, RDA) ;
  • Jang Han-Ik (Dept. of Horticultural Environment, National Horticultural Research Institute, RDA)
  • Published : 2006.04.01

Abstract

The plant defence activator, Acibenzolar-S-methyl [benzo (1,2,3) thiadiazole-7-carbothioic acid-S-methyl ester, ASM] was assayed on tomato seedlings for its ability to induce resistance against Botrytis cinerea, the causal agent of gray mold in tomato. Pre-treatment of plants with ASM reduced the severity of the disease as well as the growth of the mycelium in plants. In ASM treated plants, reduction in disease severity (up to 55%) was correlated with suppression of mycelia growth (up to 46.5%) during the time course of infection. In plants treated with ASM, activities of peroxidase were determined as markers of resistance. Applications of ASM induced Progressive and significant increase of the enzyme in locally treated tissues. Such responses were expressed earlier and with a much higher magnitude when ASM-treated seedlings were challenged with the pathogen, thus providing support to the concept that a signal produced by the pathogen is essential for triggering enhanced synthesis and accumulation of the enzymes. No such activities were observed in water-treated control plants. Therefore, the slower symptom development and reduction in mycelium growth in ASM treated plants might be due to the increase in activity of oxidative and antioxidative protection systems in plants.

병 저항성 유도물질인 acibenzolar-S-methyl[benzo(1,2,3) thiadiazole-7-carbothioic acid-S-methyl ester, ASM]을 토마토 유묘에 처리하여 잿빛곰팡이균(Botrytis cinerea)에 대한 유도저항성 여부를 조사하였다. 병원균 접종전 ASM 처리구에서는 병원균의 균사생장 뿐만 아니라 발병율도 현저히 감소하였다. 접종 3일전에 토마토 유묘에 처리한 ASM은 잿빛곰팡이병에 대한 균사생장억제(46.5%)와 함께 최고 55%의 발병 억제효과를 나타냈다. 한편, 토마토 유묘내 저항성 정도를 구명하기 위하여 ASM 처리에 의한 peroxidase의 활성을 측정하였다. ASM 처리된 조직 세포내에서는 현저하게 효소의 활성이 증가하였는데, 이러한 결과는 병원균을 미접종한 처리구 보다 접종 처리구에서 훨씬 크게 증가하였다. 그러나, 대조구인 물 처리구에서는 효소의 활성이 나타나지 않았다. 따라서, ASM 처리구내 병원균의 균사생장 및 발병억제는 조직세포내 산화적, 항산화적 보호시스템의 활성이 증가하였기 때문으로 판단된다.

Keywords

References

  1. Alscher, R. G, Donahue, J. L. and Cramer, C. L. 1997. Reactive oxygen species and antioxidants: relationships in green cells. Physiol. Plant. 100: 224-1712 https://doi.org/10.1111/j.1399-3054.1997.tb04778.x
  2. Anfoka, G H. 2000. Benzo-(l,2,3)-thiadiazole-7-carbothioic acid S-methyl ester induces systemic resistance in tomato (Lycopersicon esculentum Mill.cv. Volledung) to cucumber mosaic virus. Crop Protection 19: 401-405 https://doi.org/10.1016/S0261-2194(00)00031-4
  3. Benhamou, N. 1996. Elicitor-induced plant defence pathways. Trends Plant Sci. 1: 233-240 https://doi.org/10.1016/1360-1385(96)86901-9
  4. Benhamou, N. and Belanger, R. 1998. Benzothiazole-mediated induced resistance to Fusarium oxysporum f. sp. radicislycopersici in tomato. Plant Physiol, 118: 1203-1212 https://doi.org/10.1104/pp.118.4.1203
  5. Bestwick, C. S., Brown, T. R. and Mansfield, J. W. 1998. Localized changes in peroxidase activity accompany hydrogen peroxide generation during the development of a nonhost hypersensitive reaction in lettuce. Plant Physiol. 118: 1067-1078 https://doi.org/10.1104/pp.118.3.1067
  6. Brisson, L. F., Tengaken, R. and Lamb, C. J. 1994. Function of oxidative cross-linking of cell wall structural proteins in plant disease resistance. Plant Cell 6: 1703-1712 https://doi.org/10.1105/tpc.6.12.1703
  7. Cohen, Y., Niederman, T., Mosinger, E. and Fluhr, R. 1994. 13Aminobutyric acid inducestheaccumulation of pathogenesisrelated proteins in tomato (Lycopersicon esculentum L.) plants and resistance to late blight infection caused by Phytophthora irfestans, Plant Physiol. 104: 59-66 https://doi.org/10.1104/pp.104.1.59
  8. Cole, D. L. 1999. The efficacy of acibenzolar-S-methyl, an inducer of systemic acquired resistance against bacterial and fungal diseases of tobacco. Crop Protection 18: 267-273 https://doi.org/10.1016/S0261-2194(99)00026-5
  9. Conrath, U., Thulke, O., Katz, V. and Schwindling, S. 2001. A. Kohler. Priming as a mechanism in induced systemic resistance of plants. Eur. J Plant Pathol. 107: 113-119 https://doi.org/10.1023/A:1008768516313
  10. Gleason, M. L., Gitaitia, R. D. and Ricker, M, K. 1993. Recent progress in understanding and controlling bacterial canker of tomato in eastern North America. Plant Dis. 77: 1069-1076 https://doi.org/10.1094/PD-77-1069
  11. Godard, J. P., Ziadi, S., Monot, C., Le Corre, D. and Silue, D. 1999. Benzothiadiazole (BTH) induces resistance in cauliflower (Brassica oleracea var botrytis) to downy mildew of crucifers caused by Peronospora parasitica. Crop Protection 18: 397-405 https://doi.org/10.1016/S0261-2194(99)00040-X
  12. Kampranis, S. C., Damiavova, R., Atallah, M., Toby, G, Kondi, G, Tsichlis, P. N. and Makris, A. M. 2000. A novel plant glutathione S-transferase/peroxidase suppresses bax lethality in yeast. J Biol. Chern. 275: 29207-29216 https://doi.org/10.1074/jbc.M002359200
  13. Kurama, E. E., Fenille, R. C., Rosa, V. E., Rosa, D. D. Jr. and Ulian, E. C. 2002. Mining the enzyme involved in the detoxification of reactive oxygen species (ROS) in sugarcane. Mol. Plant PathoI, 3: 251-259 https://doi.org/10.1046/j.1364-3703.2002.00119.x
  14. Kuzniak, E. and Sklodoska, M. 2001. Ascorbate, gletathione and related enzymes in chloroplasts of tomato leaves infected by Botrytis cinerea. Plant Sci. 160: 723-731 https://doi.org/10.1016/S0168-9452(00)00457-X
  15. Lamb, C. J. and Dixon, R. A. 1997. The oxidative burst in plant disease resistance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 251-275 https://doi.org/10.1146/annurev.arplant.48.1.251
  16. Levine, A., Tenhaken, R., Dixon, R. and Lamb, C. 1994. $H_2O_2$ from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79: 583-593 https://doi.org/10.1016/0092-8674(94)90544-4
  17. Maehly, A. C. and Chane, B. 1954. Methods of Biochemical Analysis, Vol. 1, lnterscienc Publishers, New York,' pp. 357424
  18. Mehdy, M. C., Sharma, Y. K., Sathasivan, K. and Bays, N. W. 1996. The role of activated oxygen species in plant disease resistance. Physiol. Plant. 98: 365-374 https://doi.org/10.1034/j.1399-3054.1996.980219.x
  19. Nicholson, R. I. and Hammerschmidt, R. 1992. Phenolic compounds and their role in disease resistance. Annu. Rev. Plant Pathol. 30: 369-389
  20. Oostendor, M. P, Kunz, w., Dietrich, B. and Staub, T. 2001. Induced disease resistance in plants by chemicals. Eur. J Plant Pathol. 107: 19-28 https://doi.org/10.1023/A:1008760518772
  21. Reaende, M. L. V., Nojosa, G B. A., Cavalcanti, L. S., Aguilar, M. A. G, Silva, L. H. C. P., Perez, J. O., Andrade, G C. G, Carvalho, G. A. and Castro, R. M. 2002. Induction of resistance in cocoa against Crinipellis perniciosa and Verticillium dahlia by acibenzolar-S-methyl (ASM). Plant Pathol. 51: 621-628 https://doi.org/10.1046/j.1365-3059.2002.00754.x
  22. Ryals, J. A., Neuenschwander, U. H., Willits, M. G, Molina, A., Steiner, H. Y. and Hunt, M. D. 1996. Systemic acquired resistance. Plant Cell 8: 1809-1819 https://doi.org/10.1105/tpc.8.10.1809
  23. Scarponi, L., Buonaurio, R. and Martivetti, L. 2001. Persistence and trandlocation of a benzothiadiazole derivative in tomato plants in relation to systemic acquired resistance against Pseudomonas syringae pv. tomato. Pest. Manage. Sci. 57: 262-268 https://doi.org/10.1002/ps.285
  24. van den Bulk, R. W., Jansen, J., Lindhaut, W. H. and Lsffier, H. J. M. 1991. Screening of tamato somaclones for resistance to bacterial canker (Clavibacter michiganensis subsp. michiganensis). Plant Breeding 107: 190-196 https://doi.org/10.1111/j.1439-0523.1991.tb01206.x
  25. Wojtaszek, P. 1997. The oxidative burst: a plant early response against infection. Biochem. J 322: 681-692 https://doi.org/10.1042/bj3220681