DOI QR코드

DOI QR Code

Subcellular Responses in Nonhost Plant Infected with Pathogenic and Non-pathogenic Strains of Xanthomonas axonopodis pv. glycines

  • Jeong, Yong-Ho (School of Agricultural Biotechnology and Center for Plant Molecular Genetics & Breeding Research) ;
  • Kim, Jung-Gun (School of Agricultural Biotechnology, Seoul National Univeristy) ;
  • Chang, Sung-Pae (School of Agricultural Biotechnology and Center for Plant Molecular Genetics & Breeding Research) ;
  • Hwang, In-Gyu (School of Agricultural Biotechnology, Seoul National Univeristy) ;
  • Kim, Young-Ho (School of Agricultural Biotechnology and Center for Plant Molecular Genetics & Breeding Research)
  • Published : 2002.06.01

Abstract

Xanthomonas axonopodis pv. glycines, the causal agent of bacterial pustule of soybean, induces hypersensitive response (HR) in a non-host plant, hot pepper (Capsicum annuum). A wild-type strain (8ra) and its non-patho-genic mutant (8-13) of X. axonopodis pv. glycines were inoculated into the pepper leaf tissues and their subcellular responses to the bacterial infections were examined by electron microscopy. Intrastructural changes related to HR were found in the leaf tissues infected with 8ra from 8 h after inoculation, characterized by separation of plasmalemma from the cell wall, formation of small vacuoles and vesicles, formation of cell wall apposition, and cellular necrosis. No such responses were observed in the tissues infected with the mutant. In 8ra, the bacterial cells were attached to the cell walls, with the cell wall material dissolved into and appearing to encapsulate the bacterial cells. The bacterial cells later became entirely embedded in the cell wall material. On the other hand, in 8-13, the bacterial cells were usually not attached tightly to the plant cell wall, and no or poor encapsulation of the bacteria by the wall material occurred, although these were encircled by rather loose wall materials at the later stages.

Keywords

References

  1. Dangl, J. L. and Jones, J. D. G. 2001. Plant pathogens and inte-grated defense responses to infection. Nature 411:826-833 https://doi.org/10.1038/35081161
  2. Darvill, A. G., Albersheim, R, McMeil, M., Lau, J. M., York, W. S., Stevenson, T. T, Thomas, J., Doares, S., Gollin, D. J. and Chelf, P. et al. 1985. Structure and function of plant cell wall polysaccharides. J. CellSci. Suppl. 2:203-217
  3. de Pozo, O. and Lam, E. 1998. Caspases and programmed cell death in the hypersensitive response of plants to pathogens. Curr.Biotogy 8:1129-1132 https://doi.org/10.1016/S0960-9822(98)70469-5
  4. Fett, W. F. and Dunn, M. F. 1987. Auxin production by plant-pathogenic pseudomonads and xanthomonads. Appl. Environ. Microbiol. 53:1839-1845
  5. Flor, H. H. 1946. Genetics of reaction to mst in flax. J. Agric. Res. 73:680-685
  6. Han, S.-W., Oh, C.-S. and Heu, S.-G. 2001. The characterization of the hrp gene cluster isolated from Xanthomonas axonopo-dis pv. gIycines and X oryzae pv. oryzae. Ptant Pathol. J. 17: 362 (Abstr.)
  7. Hueck, C. J. 1998. Type protein secretion systems in bacterial pathogens of animals and plants. Microbiol. Mol. Biol. Rev. 62:379-433
  8. Hwang, I. and Lim, S. M. 1992. Use of detached soybean cotyle-dons for testing pathogenicity of Xanthomonas campestris pv. glycines. PlantDis. 76:182-183
  9. Hwang, I., Lim, S. M. and Shaw, P. D. 1992. Cloning and charac-terization ofpathogenicity genes from Xanthomonas campes-tris pv. gIycines. J. Bacteriol. 174:1923-1931
  10. Jones, S. B. and Fett, W. F. 1985. Fate of Xanthomonas campes-tris infiltrated into soybean leaves: An ultrastructural study. Phytopathology 75:733-741 https://doi.org/10.1094/Phyto-75-733
  11. Keen, N. T. 1990. Gene-for-gene complementahty in plant-patho-gen interactions. Ann. Rev. Genet. 24:447-463 https://doi.org/10.1146/annurev.ge.24.120190.002311
  12. Kim, Y. H., Riggs, R. D. and Kim, K. S. 1987. Structural changes associated with resistance of soybean to Heterodera gIycines. J.Nematol. 19:177-187
  13. Lindgren, P. B., Peet, R. C. and Panopoulos, N. J. 1986. Gene cluster of Pseudomonas syringae pv. phaseolicola controls pathogenicity of bean plants and hypersensitive on nonhost plants. J. Bacteriol. 168:512-522
  14. Mittler, R., Simon, L. and Lam, E. 1997. Pathogen-induced pro-grammed cell death in tobacco. J. CeIISci. 110:1333-1344
  15. Mur, L. A. J., Brown, I. R., Darby, R. M., Bestwick, C. S., Bi, Y.-M., Mansfield, J. W. and Drapper, J. 2000. A loss of resistance to avirulent bacterial pathogens in tobacco is associated with the attenuation of a salicylic acid-potentiated oxidative burst. Plant J. 23:609-621 https://doi.org/10.1046/j.1365-313x.2000.00825.x
  16. Noel, L., Thieme, R., Nennstiel, D. and Bonas, U. 2002. Two novel type -secreted proteins of Xanthomonas campestris pv. vesicatoria are encoded within the hrp pathogenicity island. J. BacteioI. 184:1340-1348 https://doi.org/10.1128/JB.184.5.1340-1348.2002
  17. Oh, C., Heu, S., Yoo, J. Y. and Cho, Y. 1999. An hrcU-homo1o-gous gene mutant of' Xanthomonas campestris pv. gtycines 8ra that lost pathogenicity on the host plant but was able to elicit the hypersensitive response on nonhosts. Mol. Plant MicrobeInteract. 12:633-639 https://doi.org/10.1094/MPMI.1999.12.7.633
  18. Park, B. K. and Hwang, I. 1999. Identification ofhrcC, hrpF, and miaA genes of Xanthomonas campestris pv. glycines 8ra: Roles in pathogenicity and inducing hypersensitive response on nonhost plants. Plant Pathol. J. 15:21 -27
  19. Riggs, R. D., Kim, K. S. and Gipson, I 1973. Ultrastructural changes in Peking soybeans infected with Heterodera gty-cines. Phytopathology 63:76-84 https://doi.org/10.1094/Phyto-63-76
  20. Schaad, N. W. 1998. Laboratory guide for identification ofplant pathogenic bacteha. 2nd ed. Amehcan Phytopathological Society., St Paul, Miim, USA
  21. Shin, J.-S., Chae, S.-Y. and K-im, Y. H. 2001. Ultrastructural changes during programmed cell death of tobacco leaf tissues infected with Tobacco mosaic virus. Plant pathol. J. 17:315-324
  22. 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
  23. Tu, J. C. and Hiruki, C. 1971. Electron microscopy ofcell wall thickenings in local lesions of potato vims-M infected red kid-ney bean. Phytopathology 61:862-868 https://doi.org/10.1094/Phyto-61-862

Cited by

  1. Comparative ultrastructure of nonwounded Mexican lime and Yuzu leaves infected with the citrus canker bacteriumXanthomonas citripv.citri vol.72, pp.7, 2009, https://doi.org/10.1002/jemt.20707
  2. 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