Abstract
Pyricularia oryzae (rice blast) conidial development at pre-penetration stage determines success or otherwise of infection inside the rice host plants. Studies on conidial germination and growth on the leaf surface in commercial rice (Oryza sativa) report differently, dependent upon host type and level of blast resistance. Although wild rice (O. australiensis) is known to be an alternative host of blast, the interaction between P. oryzae conidia and wild O. australiensis on its leaf surface has not been previously studied. We found significant (P < 0.001) differences in conidial development between two blast isolates with different virulence in terms of conidial germination, germ tube growth and appressoria formation on both wild and cultivated rice. Conidial germination at 6 h post-inoculation (hpi) for the virulent isolate was significantly (P < 0.001) delayed. Germ tubes of the avirulent isolate conidia grew significantly (P < 0.001) faster and with significantly (P < 0.001) longer germ tubes than from virulent conidia. Appressoria development for the virulent isolate was significantly (P < 0.001) faster at its later growth stages of 12 and 18 hpi when approximately 100% of germ tubes formed appressoria. In contrast, formation rate of appressoria for the avirulent isolate was significantly (P < 0.001) slower and only reached 76% of germ tubes forming appressoria. Appressoria formation on O. australiensis was significantly (P < 0.001) greater than the formation on O. sativa for both virulent and avirulent P. oryzae at 12 hpi, a clear indication that host type influences the extent of appressoria formation.
Similar content being viewed by others
References
Barksdale, T. H., & Jones, M. W. (1965). Minimum values of dew period and temperature required for infection by Pyricularia oryzae. Phytopathology, 55, 503.
Campbell, M., Chen, D., & Ronald, P. (2004). Development of co-dominant amplified polymorphic sequence markers in rice that flank the Magnaporthe grisea resistance gene Pi7 (t) in recombinant inbred line 29. Phytopathology, 94, 302–307.
Cockfield, G., Mushtaq, S., & White, N. (2012). Relocation of intensive agriculture to northern Australia: The case of the rice industry. Toowoomba: University of Southern Queensland.
Dean, R. A., Talbot, N. J., Ebbole, D. J., Farman, M. L., Mitchell, T. K., Orbach, M. J., Thon, M., Kulkarni, R., Xu, J.-R., & Pan, H. (2005). The genome sequence of the rice blast fungus Magnaporthe grisea. Nature, 434, 980–986.
Ebbole, D. J. (2007). Magnaporthe as a model for understanding host-pathogen interactions. Annual Review of Phytopathology, 45, 437–456.
Fang, X., Snell, P., Barbetti, M. J., & Lanoiselet, V. (2017a). Rice cultivars with resistance to multiple races of Magnaporthe oryzae offers an opportunity to manage rice blast in Australia. Annals of Applied Biology, 170, 160–1694.
Fang, X., Snell, P., Barbetti, M. J., & Lanoiselet, V. (2017b). Races of Magnaporthe oryzae in Australia and genes with resistance to these races revealed through host resistance screening inmonogenic lines of Oryza sativae. European Journal of Plant Pathology, 148, 647–556.
Garg, H., Li, H., Sivasithamparam, K., Kuo, J., & Barbetti, M. J. (2010). The infection processes of Sclerotinia sclerotiorum in cotyledon tissue of a resistant and a susceptible genotype of Brassica napus. Annals of Botany, 106, 897–908.
Gilbert, R. D., Johnson, A. M., & Dean, R. A. (1996). Chemical signals responsible for appressorium formation in the rice blast fungus Magnaporthe grisea. Physiological and Molecular Plant Pathology, 48, 335–346.
Greer, C. A., & Webster, R. K. (2001). Occurrence, distribution, epidemiology, cultivar reaction, and management of rice blast disease in California. Plant Disease, 85, 1096–1102.
Hamer, J. E., & Talbot, N. J. (1998). Infection-related development in the rice blast fungus Magnaporthe grisea. Current Opinion in Microbiology, 1, 693–697.
Hamer, J. E., Howard, R. J., Chumley, F. G., & Valent, B. (1988). A mechanism for surface attachment in spores of a plant pathogenic fungus. Science, 239, 288–290.
Heaton, J. B. (1964). Rice blast disease (Pyricularia grisea Cav) of the northern territory. The Australian Journal of Science, 27, 81.
Hegde, Y., & Kolattukudy, P. E. (1997). Cuticular waxes relieve self-inhibition of germination and appressorium formation by the conidia of Magnaporthe grisea. Physiological and Molecular Plant Pathology, 51, 75–84.
Henry, R. J., Rice, N., Waters, D. L. E., Kasem, S., Ishikawa, R., Hao, Y., Dillon, S., Crayn, D., Wing, R., & Vaughan, D. (2010). Australian Oryza: Utility and conservation. Rice, 3, 235–241.
Kahn, R. P., & Libby, J. L. (1958). The effect of environmental factors and plant age on the infection of rice by the blast fungus, Pyricularia oryzae. Phytopathology, 48, 25–30.
Khemmuk, W., Shivas, R. G., Henry, R. J., et al. (2016). Fungi associated with foliar diseases of wild and cultivated rice (Oryza spp.) in northern Queensland. Australasian Plant Pathology, 45, 297–308.
Koga, H. (1989). Histopathology of resistant and susceptible rice plants inoculated with Pyricularia oryzae Cavara. Japan Agricultural. Research Quarterly, 23, 8–15.
Kolattukudy, P.E. (1980). Cutin, suberin, and waxes. The Biochemistry of Plants (eds. Stumpf, PK & Conn. EE) Academic Press: New York, 4, 571-645.
Kumar, S., & Sridhar, R. (1987). Significance of epicuticular wax in the specificity of blast fungus to rice varieties. International Journal of Tropical Plant Diseases, 5, 131–140.
Lanoiselet, V., Cother, E. J., Ash, G. J., Hind-Lanoiselef, T. L., Murray, G. M., & Harper, J. D. I. (2005). Prevalence and survival, with emphasis on stubble burning, of Rhizoctonia spp., causal agents of sheath diseases of rice in Australia. Australasian Plant Pathology, 34, 135–142.
Lee, Y.-H., & Dean, R. A. (1994). Hydrophobicity of contact surface induces appressorium formation in Magnaporthe grisea. FEMS Microbiology Letters, 115, 71–75.
Liu, Z.-M., & Kolattukudy, P. E. (1999). Early expression of the calmodulin gene, which precedes appressorium formation in Magnaporthe grisea, is inhibited by self-inhibitors and requires surface attachment. Journal of Bacteriology, 181, 3571–3577.
Pak, D., You, M. P., Lanoiselet, V., & Barbetti, M. J. (2017a). Reservoir of cultivated rice pathogens in wild rice in Australia. European Journal of Plant Pathology, 47, 295–311.
Pak, D., You, M. P., Lanoiselet, V., & Barbetti, M. J. (2017b). Azoxystrobin and propiconazole offer significant potential for rice blast (Pyricularia oryzae) management in Australia. European Journal of Plant Pathology, 48, 247–259.
Pasechnik, T. D., Lapikova, V. P., & Aver'yanov, A. A. (1997). Inhibition of pre-penetration development of blast fungus during the infection of resistant rice cultivars. European Journal of Plant Pathology, 103, 747–750.
Talbot, N. J. (2003). On the trail of a cereal killer: Exploring the biology of Magnaporthe grisea. Annual Reviews in Microbiology, 57, 177–202.
Uchiyama, T., & Okuyama, K. (1990). Participation of Oryza sativa leaf wax in appressorium formation by Pyricularia oryzae. Phytochemistry, 29, 91–92.
Uchiyama, T., Ogasawara, N., Nanba, Y., & Itô, H. (1979). Conidial germination and appressorial formation of the plant pathogenic fungi on the coverglass or cellophane coated with various lipid components of plant leaf waxes. Agricultural and Biological Chemistry, 43, 383–384.
Veneault-Fourrey, C., Barooah, M., Egan, M., Wakley, G., & Talbot, N. J. (2006). Autophagic fungal cell death is necessary for infection by the rice blast fungus. Science, 312, 580–583.
Wurm, S. A. P., Campbel, C. L., Batten, D. G., & Bellairs, M. S. (2012). Australian native rice: A new sustainable wild food enterprise. Rural Industries Research and Development Corporation.
You, M. P., Lanoiselet, V., Wang, C. P., Shivas, R. G., Li, Y., & Barbetti, M. J. (2012). First report of rice blast (Magnaporthe oryzae) on rice (Oryza sativa) in Western Australia. Plant Disease, 96, 1228–1228.
Zeigler, R. S., Leong, S. A., & Teng, P. S. (1994). Rice blast disease. (640 pp). Wallingford, Oxod, United Kingdom: CAB International.
Acknowledgements
The first author gratefully acknowledges an Australian Government Endeavour Postgraduate Scholarship funding his PhD studies. We are very grateful to the University of Western Australia and the Rural Industries Research and Development Corporation (RIRDC project PRJ-008565 ‘Characterisation of rice blast races present in Australia’) for supporting this research and to Dr. Peta Clode and Ms. Lyn Kirilak, in the Centre for Microscopic, Characterization, and Analysis at the University of Western Australia for help with microscopy studies.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Ethical statement
This research did not involve any animal and/or human participants. The authors declare that they have no conflict of interests.
Rights and permissions
About this article
Cite this article
Pak, D., You, M.P., Lanoiselet, V. et al. Comparative colonisation by virulent versus avirulent Pyricularia oryzae on wild Oryza australiensis. Eur J Plant Pathol 151, 927–936 (2018). https://doi.org/10.1007/s10658-018-1428-5
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10658-018-1428-5