The Fate of Peripheral Vesicles in Zoospores of Phytophthora cinnamomi During Infection of Plants

  • Frank Gubler
  • Adrienne R. Hardham

Abstract

Motile zoospores play a major role in the infection of plant roots by the dieback fungus, Phytophthora cinnamomi [22]. Under moist conditions, the fungus releases vast numbers of zoospores into the soil. The zoospores can be transported passively over considerable distances by underground water, thereby facilitating the spread of the pathogen. Once in the vicinity of a root, the zoospores exhibit positive Chemotaxis to the root exudate and as a result rapidly accumulate along the zone of cell elongation just behind the root tip. Contact with root surface components triggers the encystment of the zoospores. Fucosyl residues on the root surface have been implicated in this recognition step [10] but so far no fucosyl-containing molecules which can trigger encystment have been isolated from the root surface. Encystment entails the rapid loss of motility and shedding of flagella, exocytosis of peripheral vesicles, change in cell shape and, after 5–10 min, formation of a microfibrillar cell wall. This is followed, about 20 min later, by germination and subsequent invasion of the root tissue.

Keywords

Root Surface Immunogold Label Silver Enhancement Phytophthora Cinnamomi Cyst Surface 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    Bartnicki-Garcia S, Hemmes DE (1976) Some aspects of the form and function of Oomycete spores. In: Weber DJ, Hess WM (eds) The fungal spore: form and structure. John Wiley, New York, pp 593Google Scholar
  2. 2.
    Beakes GW (1987) Oomycete phylogeny: ultrastructural perspectives. In: Rayner ADM, Brasier CM, Moore D (eds) Evolutionary biology of the fungi. Cambridge University Press, Cambridge, pp 405Google Scholar
  3. 3.
    Bimpong CE, Hickman CJ (1975) Ultrastructural and cytochemical studies of zoospores, cysts, and germinating cysts of Phytophthora palmivora. Can J Bot 53: 1310–1327CrossRefGoogle Scholar
  4. 4.
    Grove SN, Bracker CE (1978) Protoplasmic changes during zoospore encystment and cyst germination in Pythium aphanidermatum. Exp Mycol 2: 51–98CrossRefGoogle Scholar
  5. 5.
    Gubler F, Hardham AR (1988) Secretion of adhesive material during encystment of Phytophthora cinnamomi zoospores, characterized by immunogold labeling with monoclonal antibodies to components of peripheral vesicles. J Cell Sci 90: 225–235Google Scholar
  6. 6.
    Gubler F, Hardham AR, Duniec J (1989) Characterising adhesiveness of Phytophthora cinnamomi zoospores during encystfnent. Protoplasma 149: 24–30CrossRefGoogle Scholar
  7. 7.
    Hardham AR (1987) Ultrastructure and serial section reconstruction of zoospores of the fungus Phytophthora cinnamomi. Exp Mycol 11: 297–306CrossRefGoogle Scholar
  8. 8.
    Hardham AR, Suzaki E, Perikin JL (1986) Monoclonal antibodies to isolate-, species-and genus-specific components on the surface of zoospores and cysts of the fungus Phytophthora cinnamomi. Can J Bot 64: 311–321CrossRefGoogle Scholar
  9. 9.
    Hemmes DE, Hohl HR (1971) Ultrastructural aspects of encystation and cyst-germin-ation in Phytophthora parasitica. J Cell Sci 9: 175–191PubMedGoogle Scholar
  10. 10.
    Hinch JM, Clarke AE (1980) Adhesion of fungal zoospores to root surfaces is mediated by carbohydrate determinants of the root slime. Physiol Plant Pathol 16: 303–307Google Scholar
  11. 11.
    Ho HH, Zachariah K, Hickman CJ (1968) The ultrastructure of zoospores of Phytophthora megasperma var. sojae. Can J Bot 46: 37–41CrossRefGoogle Scholar
  12. 12.
    Irving HR, Griffith JM, Grant BR (1984) Calcium efflux associated with encystment of Phytophthora palmivora zoospores. Cell Calcium 5: 487–500PubMedCrossRefGoogle Scholar
  13. 13.
    Jaffe LF (1983) Sources of calcium in egg activation: A review and hypothesis. Dev Biol 99:265–276PubMedCrossRefGoogle Scholar
  14. 14.
    Kubota HY, Yoshimoto Y, Yoneda M, Hiramoto Y (1987) Free calcium wave upon activation in Xenopus eggs. Dev Biol 119: 129–136PubMedCrossRefGoogle Scholar
  15. 15.
    Lehnen LP, Powell MJ (1989) The role of kinetosome-associated organelles in the attachment of encysting secondary zoospores of Saprolegnia ferax to substrates. Protoplasma 149: 163–174CrossRefGoogle Scholar
  16. 16.
    Lunney CZ, Bland CE (1976) Ultrastructural observations of mature and encysting zoospores of Pythium proliferum de Bary. Protoplasma 90: 119–137CrossRefGoogle Scholar
  17. 17.
    Pinto Da Silva P, Nogueira ML (1977) Membrane fusion during secretion. A hypothesis based on electron microscope observations of Phytophthora palmivora zoospores during encystment. J Cell Biol 73: 161–181CrossRefGoogle Scholar
  18. 18.
    Powell MJ, Bracker CE (1986) Distribution of diaminobenzidine reaction products in zoospores of Phytophthor-a palmivora. Mycologia 78: 892–900CrossRefGoogle Scholar
  19. 19.
    Sing VO, Bartnicki-Garcia S (1975a) Adhesion of Phytophthor a palmivora zoospores: electron microscopy of cell attachment and cyst wall fibril formation. J Cell Sci 18: 123–132PubMedGoogle Scholar
  20. 20.
    Sing VO, Bartnicki-Garcia S (1975b) Adhesion of Phytophthor a palmivora zoospores: detection and ultrastructural visualization of concanavalin A receptor sites appearing during encystment. J Cell Sci 19: 11–20PubMedGoogle Scholar
  21. 21.
    Swann K, Whitaker M (1986) The part played by inositol triphosphate and calcium in the propagation of the fertilization wave in sea urchin eggs. J Cell Biol 103: 2333–2342PubMedCrossRefGoogle Scholar
  22. 22.
    Zentmyer G A (1980) Phytophthor a cinnamomi and the diseases it causes. The American Phytopathological Society, St Paul, MinnesotaGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1991

Authors and Affiliations

  • Frank Gubler
    • 1
  • Adrienne R. Hardham
    • 1
  1. 1.Plant Cell Biology Group, Research School of Biological SciencesThe Australian National UniversityCanberraAustralia

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