DOI QR코드

DOI QR Code

Effect of Delayed Inoculation After Wounding on the Development of Anthracnose Disease Caused by Colletotrichum acutatum on Chili Pepper Fruit

  • Kim, Sang-Gyu (Department of Agricultural Biotechnology, Seoul National University) ;
  • Kim, Yn-Hee (Department of Agricultural Biotechnology, Seoul National University) ;
  • Kim, Heung-Tae (Department of Plant Medicine, Chungbuk National University) ;
  • Kim, Young-Ho (Department of Agricultural Biotechnology, Seoul National University)
  • Published : 2008.12.01

Abstract

Detached chili pepper fruits were inoculated with the conidial suspension of Colletotrichum acutatum JC-24 simultaneously (simultaneous inoculation, SI) and at delayed time (delayed inoculation, DI) after wounding with (delayed wound inoculation, DWI) or without additional wounding (delayed non-wound inoculation, DNI) at the inoculation time. Disease severity was significantly lowered by DNI, compared to SI. By DNI, the disease reduction rates were proportional with the length of delayed time, and greater at the high temperature range (18, 23 and $28^{\circ}$) than at the low temperature ($13^{\circ}$) tested. DWI was also effective in reducing the disease severity especially at 18oC; however, its effectiveness was lower than for DNI. In light microscopy, parenchyma cells at the wounding sites were modified structurally, initially forming new cell walls crossing cytoplasm, enlarged with multiple periclinal cell divisions, and finally layered like wound periderms. In DWI, the above structural modifications occurred, showing the restriction of the fungal invasion by the cell walls in enlarged modified cells, while no definite cellular modifications were found with proliferation of fungal hyphae in SI. Sclerenchyma-like cells with thickened cell walls were proliferated around the wounding sites, which were partially dissolved by DWI, probably leading to some disease development. All of these results suggest that the decline of the anthracnose disease in pepper fruit by the delayed inoculations may be derived from the structural modifications related to the healing processes of the previous wound inflicted on the tissues.

Keywords

References

  1. Agrios, G. N. 2005. Plant Pathology. Fifth Edition, Academic Press, San Diego, CA, USA. 922 pp
  2. Biggs, A. R. 1986. Phellogen regeneration in injured peach tree bark. Ann. Bot. 57:463-470 https://doi.org/10.1093/oxfordjournals.aob.a087128
  3. Biggs, A. R. 1989. Temporal changes in the infection court after wounding of peach bark are associated with cultivar variation in infection by Leucostoma persoonii. Phytopathology 79: 627-630 https://doi.org/10.1094/Phyto-79-627
  4. Biggs, A. R. and Britton, K. O. 1988. Presymptom histopathology of peach trees inoculated with Botryosphaeria obtusa and B. dothidea. Phytopathology 78:1109-1118 https://doi.org/10.1094/Phyto-78-1109
  5. Bostock, R. M. and Middleton, G. E. 1987. Relationship of wound periderm formation in resistance to Ceratocystis fimbriata in almond bark. Phytopathology 77:1174-1180 https://doi.org/10.1094/Phyto-77-1174
  6. Cline, M. N. and Neely, D. 1983. Wound-healing processes in geranium cuttings in relationship to basal stem rot caused by Pythium ultimum. Plant Dis. 67:636-638 https://doi.org/10.1094/PD-67-636
  7. Esau, K. 1977. Anatomy of Seed Plants. John Wiley & Sons, New York, NY, USA. 550 pp
  8. Jeon, Y. H. and Kim, Y. H. 2008. Differential structural responses of ginseng root tissues to different initial inoculum levels of Paenibacillus polymyxa GBR-1. Plant Pathol. J. 24:352-356 https://doi.org/10.5423/PPJ.2008.24.3.352
  9. Karnovsky, M. J. 1965. A formaldehyde-glutaraldehyde fixative of high osmolarity for use in electron microscopy. J. Cell Biol. 27:137A
  10. Kim, C.-H. 2004. Review of disease incidence of major crops in 2003. Res. Plant Dis. 10:1-7 https://doi.org/10.5423/RPD.2004.10.1.001
  11. Kim, J. T., Lee, K. H., Min, J. Y., Kang, B. K., Rho, C. W., Hong, S. T. and Kim, H. T. 2005. Response of Colletotrichum spp. causing red pepper anthracnose to protective and ergosterol biosynthesis-inhibiting fungicides. Res. Plant Dis. 11:185-192 https://doi.org/10.5423/RPD.2005.11.2.185
  12. Kim, J. T., Park, S.-Y., Choi, W., Lee, Y.-H. and Kim, H. T. 2008. Characterization of Colletotrichum isolates causing anthracnose of pepper in Korea. Plant Pathol. J. 24:17-23 https://doi.org/10.5423/PPJ.2008.24.1.017
  13. Kim, K.-H., Yoon, J.-B., Park, H.-G., Park, E. W. and Kim, Y. H. 2004. Structural modifications and programmed cell death of chili pepper fruit related to resistance responses to Colletotrichum gloeosporioides infection. Phytopathology 94:1295-1304 https://doi.org/10.1094/PHYTO.2004.94.12.1295
  14. Koga, H., Zeyen, R. J., Bushnell, W. R. and Ahlstrand, G. G. 1988. Hypersensitive cell death autofluorescence, and insoluble silicon accumulation in barley leaf epidermal cells under attack by Erysiphe graminis f. sp. hordei. Physiol. Mol. Plant Pathol. 32:395-409 https://doi.org/10.1016/S0885-5765(88)80033-X
  15. Latunde-Dada, A. O., O'Connell, R. J., Nash, C., Pringe, R. J., Lucas, J. A. and Bailey J. A. 1996. Infection process and identity of hemibiotrophic anthracnose fungus (Colletotrichum destructivum O'Gara) from cowpea (Vigna unguiculata). Mycol. Res. 100:1133-1141 https://doi.org/10.1016/S0953-7562(96)80226-7
  16. Lummerzheim, M., de Oliveira, D., Castresana, C., Miguens, F. C., Louzada, E., Roby, D., Van Montagu, M. and Timmerman, B. 1993. Identification of compatible and incompatible interactions between Arabidopsis thaliana and Xanthomonas campestris pv. campestris and characterization of the hypersensitive response. Mol. Plant-Microbe Interact. 6:532-544 https://doi.org/10.1094/MPMI-6-532
  17. Mayama, S. and Shishiyama, J. 1978. Localized accumulation of fluorescent and U.V.-absorbing compounds at penetration sites in barley leaves infected with Erysiphe graminis f. sp. hordei. Physiol. Plant Pathol. 13:347-354 https://doi.org/10.1016/0048-4059(78)90051-6
  18. Morris, S. C., Forbes-Smith, M. R. and Scriven, F. M. 1989. Determination of optimum conditions for suberization, wound periderm formation, cellular desiccation and pathogen resistance in wounded Solanum tuberosum tubers. Physiol. Mol. Plant Pathol. 35:177-190 https://doi.org/10.1016/0885-5765(89)90087-8
  19. Mullick, D. B. 1977. The non-specific nature of defense in bark and wood during wounding, insect and pathogen attack. Recent Adv. Phytochem. 11:395-441
  20. Myung, I.-S., Park, K. S., Hong, S.-K., Park, J.-W., Shim, H.-S., Lee, Y.-K., Lee, S.-Y., Lee, S.-D., Lee, S.-H., Choi, H.-W., Heu, S., Shin, D.-B., Ra, D.-S., Yeh, W.-H. and Cho, W. D. 2005. Review of disease incidence of major crops of the South Korea in 2004. Res. Plant Dis. 11:89-92 https://doi.org/10.5423/RPD.2005.11.2.089
  21. O'Brien, T. P. and McCully, M. E. 1981. The Study of Plant Structure. Principles and Selected Methods. Termarcarphi Pty Ltd., Melbourne, Australia
  22. O'Connell, R. J., Bailey, J. A. and Richmond, D. V. 1985. Cytology and physiology of infection of Phaseolus vulgaris by Colletotrichum lindemuthianum. Physiol. Plant Pathol. 27:75-98 https://doi.org/10.1016/0048-4059(85)90058-X
  23. Park, K. S. and Kim, C. H. 1992. Identification, distribution and etiological characteristics of anthracnose fungi of red pepper in Korea. Korean J. Plant Pathol. 8:61-69
  24. Riffle, J. W. and Peterson, G. W. 1986. Thyronectria canker of honey locust: Influence of temperature and wound age on disease development. Phytopathology 76:313-316 https://doi.org/10.1094/Phyto-76-313
  25. Rittinger, P. A., Biggs, A. R. and Peirson, D. R. 1987. Histochemistry of lignin and suberin deposition in boundary layers formed after wounding in various plant species and organs. Can. J. Bot. 65:1886-1892 https://doi.org/10.1139/b87-258
  26. Russin, J. S. and Shain, L. 1984. Initiation and development of cankers caused by virulent and cytoplasmic hypovirulent isolates of the chestnut blight fungus. Can. J. Bot. 62:2660-2664 https://doi.org/10.1139/b84-362
  27. Silva, M. C., Nicole, M., Guerra-Guimaraes, L., Bresson, E., Rijo, L., Geiger, J. P. and Rodrigues, C. J., Jr. 1998. Cytological and biochemical aspects associated with the hypersensitive reaction in coffee plants infected with orange rust-Hemileia vastatrix. In: Seventh International Congress of Plant Pathology, Vol. 2., Abstract 1-2-35. Edinburgh, Scotland
  28. Spurr, A. R. 1969. A low viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastr. Res. 26:31-43 https://doi.org/10.1016/S0022-5320(69)90033-1
  29. Thomas, P. 1982. Wound-induced suberization and periderm development in potato tubers as affected by temperature and gamma irradiation. Potato Res. 25:155-164 https://doi.org/10.1007/BF02359802
  30. Von Ropenack, E., Parr, A. and Schulze-Lefert, P. 1998. Structural analyses and dynamics of soluble and cell wall-bound phenolics in a broad spectrum resistance to the powdery mildew fungus in barley. J. Biol. Chem. 273:9013-9022 https://doi.org/10.1074/jbc.273.15.9013
  31. Wigginton, M. J. 1974. Effects of temperature, oxygen tension and relative humidity on the wound-healing process in the potato tuber. Potato Res. 17:200-214 https://doi.org/10.1007/BF02360387
  32. Yoon, J. B. 2003. Identification of genetic resources, interspecific hybridization and inheritance analysis for breeding pepper (Capsicum annuum) resistant to anthracnose. Ph.D. Thesis. Seoul National University, Seoul, Korea

Cited by

  1. Sensitivity of Colletotrichum acutatum Isolates to Selected Fungicides vol.63, pp.4, 2015, https://doi.org/10.11118/actaun201563041111
  2. Identification of new resistant sources for bacterial blight in pomegranate vol.146, pp.3, 2016, https://doi.org/10.1007/s10658-016-0947-1
  3. Defense-Related Responses in Fruit of the Nonhost Chili Pepper against Xanthomonas axonopodis pv. glycines Infection vol.32, pp.4, 2016, https://doi.org/10.5423/PPJ.OA.12.2015.0256
  4. Biocontrol Efficacies of Bacillus Species Against Cylindrocarpon destructans Causing Ginseng Root Rot vol.27, pp.4, 2011, https://doi.org/10.5423/PPJ.2011.27.4.333
  5. Wound response in orange as a resistance mechanism against Penicillium digitatum (pathogen) and P. expansum (non-host pathogen) vol.78, 2013, https://doi.org/10.1016/j.postharvbio.2012.12.013
  6. Increasing maturity reduces wound response and lignification processes against Penicillium expansum (pathogen) and Penicillium digitatum (non-host pathogen) infection in apples vol.88, 2014, https://doi.org/10.1016/j.postharvbio.2013.09.009
  7. Biocontrol Characteristics of Bacillus Species in Suppressing Stem Rot of Grafted Cactus Caused by Bipolaris cactivora vol.29, pp.1, 2013, https://doi.org/10.5423/PPJ.OA.07.2012.0116