The secreted lipase FGL1 is sufficient to restore the initial infection step to the apathogenic Fusarium graminearum MAP kinase disruption mutant Δgpmk1

European Journal of Plant Pathology

Volumn 134, Issue 1, 2012, Pages 23-37

  Salomon, Siegfried ^a   Gácser, Attila ^b   Frerichmann, Sebastian ^a   Kröger, Cathrin ^a   Schäfer, Wilhelm ^a   Voigt, Christian A ^a  

^a UNIVERSITY OF HAMBURG   (Germany)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

Fusarium head blight; Gibberella zeae; Type II resistance; Wheat infection

Indexed keywords

DISEASE RESISTANCE; ENZYME ACTIVITY; FUNGUS; GENE EXPRESSION; HOST-PATHOGEN INTERACTION; INFECTIVITY; INOCULATION; PATHOGEN; PATHOGENICITY; PROTEIN; SIGNALING; VIRULENCE;

COCHLIOBOLUS HETEROSTROPHUS; FUSARIUM; GIBBERELLA; GIBBERELLA ZEAE; TRITICUM AESTIVUM;

EID: 84864398575     PISSN: 09291873     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10658-012-0017-2     Document Type: Article

References (41)

1. Baidyaroy, D., Brosch, G., Ahn, J. H., Graessle, S., Wegener, S., Tonukari, N. J., et al. (2001). A gene related to yeast HOS2 histone deacetylase affects extracellular depolymerase expression and virulence in a plant pathogenic fungus. The Plant Cell, 13, 1609-1624.
2. Bluhm, B. H., Zhao, X., Flaherty, J. E., Xu, J. R., & Dunkle, L. D. (2007). RAS2 regulates growth and pathogenesis in Fusarium graminearum. Molecular Plant-Microbe Interactions, 20, 627-636.
3. Comménil, P., Belingheri, L., & Dehorter, B. (1998). Antilipase antibodies prevent infection of tomato leaves by Botrytis cinerea. Physiological and Molecular Plant Pathology, 52, 1-14.
4. Dohlman, H. G., Thorner, J., Caron, M. G., & Lefkowitz, R. J. (1991). Model systems for the study of seven-transmembrane-segment receptors. Annual Review of Biochemistry, 60, 653-688.
5. Feng, J., Liu, G., Selvaraj, G., Hughes, G. R., & Wei, Y. (2005). A secreted lipase encoded by LIP1 is necessary for efficient use of saturated triglyceride lipids in Fusarium graminearum. Microbiology, 151, 3911-3921.
6. Horwitz, B. A., Sharon, A., Lu, S. W., Ritter, V., Sandrock, T. M., Yoder, O. C., et al. (1999). A G protein alpha subunit from Cochliobolus heterostrophus involved in mating and appressorium formation. Fungal Genetics and Biology, 26, 19-32.
7. Ilgen, P., Hadeler, B., Maier, F. J., & Schäfer, W. (2009). Developing kernel and rachis node induce the trichothecene pathway of Fusarium graminearum during wheat head infection. Molecular Plant-Microbe Interactions, 22, 899-908.
8. Jansen, C., von Wettstein, D., Schäfer, W., Kogel, K. H., Felk, A., & Maier, F. J. (2005). Infection patterns in barley and wheat spikes inoculated with wild-type and trichodiene synthase gene disrupted Fusarium graminearum. Proceedings of the National Academy of Sciences of the United States of America, 102, 16892-16897.
9. Jenczmionka, N. J., & Schäfer, W. (2005). The Gpmk1 MAP kinase of Fusarium graminearum regulates the induction of specific secreted enzymes. Current Genetics, 47, 29-36.
10. Jenczmionka, N. J., Maier, F. J., Lösch, A. P., & Schäfer, W. (2003). Mating, conidiation and pathogenicity of Fusarium graminearum, the main causal agent of the head-blight disease of wheat, are regulated by the MAP kinase gpmk1. Current Genetics, 43, 87-95.
11. Klittich, C. J. R., & Leslie, J. F. (1988). Nitrate reduction mutants of Fusarium moniliforme (Giberella fujikuroi). Genetics, 118, 417-423.
12. Lengeler, K. B., Davidson, R. C., D'Souza, C., Harashima, T., Shen, W. C., Wang, P., et al. (2000). Signal transduction cascades regulating fungal development and virulence. Microbiology and Molecular Biology Reviews, 64, 746-785.
13. Lev, S., & Horwitz, B. A. (2003). A mitogen-activated protein kinase pathway modulates the expression of two cellulase genes in Cochliobolus heterostrophus during plant infection. The Plant Cell, 15, 835-844.
14. Lysøe, E., Seong, K. Y., & Kistler, H. C. (2011). The transcriptome of Fusarium graminearum during the infection of wheat. Molecular Plant-Microbe Interactions, 24, 995-1000.
15. Maier, F. J., Malz, S., Lösch, A. P., Lacour, T., & Schäfer, W. (2005). Development of a highly efficient gene targeting system for Fusarium graminearum using the disruption of a polyketide synthase gene as a visible marker. FEMS Yeast Research, 5, 653-662.
16. Miedaner, T., Reinbrecht, C., & Schilling, A. G. (2000). Association among aggressiveness, fungal colonization, and mycotoxin production of 26 isolates of Fusarium graminearum in winter rye head blight. Journal of Plant Diseases and Protection, 107, 124-134.
17. Mönke, E., & Schäfer, W. (1993). Transient and stable gene expression in the fungal maize pathogen Cochliobolus heterostrophus after transformation with the beta-glucuronidase (GUS) gene. Molecular and General Genetics, 241, 73-80.
18. Namiki, F., Matsunaga, M., Okuda, M., Inoue, I., Nishi, K., Fujita, Y., et al. (2001). Mutation of an arginine biosynthesis gene causes reduced pathogenicity in Fusarium oxysporum f. sp. melonis. Molecular Plant-Microbe Interactions, 14, 580-584.
19. Nguyen, L. N., Bormann, J., Le, G. T., Starkel, C., Olsson, S., Nosanchuk, J. D., et al. (2011). Autophagy-related lipase FgATG15 of Fusarium graminearum is important for lipid turnover and plant infection. Fungal Genetics and Biology, 48, 217-224.
20. Nirenberg, H. (1981). A simplified method for identifying Fusarium spp occurring on wheat. Canadian Journal of Botany, 59, 1599-1609.
21. Phalip, V., Delalande, F., Carapito, C., Goubet, F., Hatsch, D., Leize-Wagner, E., et al. (2005). Diversity of the exoproteome of Fusarium graminearum grown on plant cell wall. Current Genetics, 48, 366-379.
22. Pritsch, C., Muehlbauer, G. J., Bushnell, W. R., Somers, D. A., & Vance, C. P. (2000). Fungal development and induction of defense response genes during early infection of wheat spikes by Fusarium graminearum. Molecular Plant-Microbe Interactions, 13, 159-169.
23. Proctor, R. H., Hohn, T. M., & McCormick, S. P. (1995). Reduced virulence of Gibberella zeae caused by disruption of a trichothecene toxin biosynthetic gene. Molecular Plant-Microbe Interactions, 8, 593-601.
24. Punt, P. J., Mattern, I. E., & van den Hondel, C. A. M. J. J. (1988). A vector for Aspergillus transformation conferring phleomycin resistance. Fungal Genetics Newsletter, 35, 25-30.
25. Ramamoorthy, V., Zhao, X., Snyder, A. K., Xu, J. R., & Shah, D. M. (2007). Two mitogen-activated protein kinase signalling cascades mediate basal resistance to antifungal plant defensins in Fusarium graminearum. Cellular Microbiology, 9, 1491-1506.
26. Raper, K. B., & Thorn, C. (1949). A manual of the Penicillia. Baltimore: Waverly Press.
27. Royer, J. C., Moyer, D. L., Reiwitch, S. G., Madden, M. S., Jensen, E. B., Brown, S. H., et al. (1995). Fusarium graminearum A 3/5 as a novel host for heterologous protein production. Biotechnology (N. Y), 13, 1479-1483.
28. Schroeder, H. W., & Christensen, J. J. (1963). Factors affecting the resistance of wheat to scab caused by Gibberella zeae. Phytopathology, 53, 831-838.
29. Singh, A., & Del Poeta, M. (2011). Lipid signalling in pathogenic fungi. Cellular Microbiology, 13, 177-185.
30. Starkey, D. E., Ward, T. J., Aoki, T., Gale, L. R., Kistler, H. C., Geiser, D. M., et al. (2007). Global molecular surveillance reveals novel Fusarium head blight species and trichothecene toxin diversity. Fungal Genetics and Biology, 44, 1191-1204.
31. Urban, M., Mott, E., Farley, T., & Hammond-Kosack, K. (2003). The Fusarium graminearum MAP1 gene is essential for pathogenicity and development of perithecia. Molecular Plant Pathology, 4, 347-359.
32. Voigt, C. A., Schäfer, W., & Salomon, S. (2005). A secreted lipase of Fusarium graminearum is a virulence factor required for infection of cereals. The Plant Journal, 42, 364-375.
33. Voigt, C. A., von Scheidt, B., Gácser, A., Kassner, H., Lieberei, R., Schäfer, W., et al. (2007). Enhanced mycotoxin production of a virulence-reduced Fusarium graminearum mutant correlates to toxin-related gene expression. European Journal of Plant Pathology, 117, 1-12.
34. Wanjiru, W. M., Zhensheng, K., & Buchenauer, H. (2002). Importance of cell wall degrading enzymes produced by Fusarium graminearum during infection of wheat heads. European Journal of Plant Pathology, 108, 803-810.
35. Wu, S.-C., Ham, K.-S., Darvill, A. G., & Albersheim, P. (1997). Deletion of the two endo-β-1, 4-xylanase genes reveals additional isozymes secreted by the rice blast fungus. Molecular Plant-Microbe Interactions, 10, 700-708.
36. Xu, J. R. (2000). Map kinases in fungal pathogens. Fungal Genetics and Biology, 31, 137-152.
37. Xu, J. R., Staiger, C. J., & Hamer, J. E. (1998). Inactivation of the mitogen-activated protein kinase Mps1 from the rice blast fungus prevents penetration of host cells but allows activation of plant defense responses. Proceedings of the National Academy of Sciences of the United States of America, 95, 12713-12718.
38. Yli-Mattila, T., Gagkaeva, T., Ward, T. J., Aoki, T., Kistler, H. C., & O'Donnell, K. (2009). A novel Asian clade within the Fusarium graminearum species complex includes a newly discovered cereal head blight pathogen from the Russian Far East. Mycologia, 101, 841-852.
39. Zhang, Y., Choi, Y. E., Zou, X., & Xu, J. R. (2011). The FvMK1 mitogen-activated protein kinase gene regulates conidiation, pathogenesis, and fumonisin production in Fusarium verticillioides. Fungal Genetics and Biology, 48, 71-79.
40. Zhao, X., Mehrabi, R., & Xu, J. R. (2007). Mitogen-activated protein kinase pathways and fungal pathogenesis. Eukaryotic Cell, 6, 1701-1714.
41. Zwerger, K., & Hirt, H. (2001). Recent advances in plant MAP kinase signalling. Biological Chemistry, 382, 1123-1131.