Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-19T22:41:11.566Z Has data issue: false hasContentIssue false

Pathogenic fungal protein-induced resistance and its effects on vegetable diseases

Published online by Cambridge University Press:  31 March 2017

T.-C. LIN
Affiliation:
Department of Plant Pathology, College of Agriculture and Natural Resources, National Chung-Hsing University (NCHU), Taichung 40227, Taiwan Plant Pathology Division, Taiwan Agricultural Research Institute, Wufeng, Taichung 41362, Taiwan
C.-L. LIN
Affiliation:
Department of Plant Pathology, College of Agriculture and Natural Resources, National Chung-Hsing University (NCHU), Taichung 40227, Taiwan
W.-C. CHUNG
Affiliation:
Section of Biotechnology, Seed Improvement and Propagation Station, Hsinshe, Taichung 42642, Taiwan
K.-R. CHUNG
Affiliation:
Department of Plant Pathology, College of Agriculture and Natural Resources, National Chung-Hsing University (NCHU), Taichung 40227, Taiwan Biotechnology Center, NCHU, Taichung 40227, Taiwan NCHU-UCD Plant and Food Biotechnology Center, NCHU, Taichung 40227, Taiwan
J.-W. HUANG*
Affiliation:
Department of Plant Pathology, College of Agriculture and Natural Resources, National Chung-Hsing University (NCHU), Taichung 40227, Taiwan NCHU-UCD Plant and Food Biotechnology Center, NCHU, Taichung 40227, Taiwan
*
*To whom all correspondence should be addressed. Email: [email protected]

Summary

Plant defence systems can be induced by biotic and abiotic stress. Experiments were undertaken to explore the feasibility of different fungal proteins for the reduction of vegetable diseases. Total proteins purified from three soil-borne and five foliar fungal pathogens had no fungistatic effects nor did they trigger hypersensitive reactions on test plants. The abilities to promote plant growth and to reduce disease severity varied among test proteins and plants. Depending on test proteins, experiments have demonstrated that exogenous application of fungal proteins could reduce Alternaria brassicicola-induced black spot severity on cabbage, Colletotrichum spp.-induced anthracnose on Chinese cabbage and cucumber, Rhizoctonia solani-induced damping-off on sweet pepper and Chinese cabbage, and powdery mildew on cucumber seedlings. An Alternariaprotein effector 1 (Ape1)-coding gene was cloned from two Alternaria spp. and expressed in Escherichia coli. The expressed Ape1 reduced anthracnose incidence on cucumber leaves, indicating that Ape1 was the primary activator in the crude protein extracts responsible for disease reduction. Application of Alternaria proteins onto Chinese cabbage seedlings caused an increase of phenylalanine ammonia lyase and peroxidase activities in treated seedlings, which may have played a role in host defence.

Type
Crops and Soils Research Papers
Copyright
Copyright © Cambridge University Press 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Albert, M. (2013). Peptides as triggers of plant defence. Journal of Experimental Botany 64, 52695279.CrossRefGoogle ScholarPubMed
Bradford, M. M. (1976). A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248254.CrossRefGoogle Scholar
Bridge, P. (1996). Protein extraction from fungi. Methods in Molecular Biology 59, 3948.Google ScholarPubMed
Bridge, P. D., Kokubun, T. & Simmonds, M. S. J. (2004). Protein extraction from fungi. In Protein Purification Protocols (Ed. Cutler, P.), pp. 3746. Methods in Molecular Biology 244. Totowa, NJ, USA: Humana Press Inc.Google Scholar
Burketova, L., Trda, L., Ott, P. G. & Valentova, O. (2015). Bio-based resistance inducers for sustainable plant protection against pathogens. Biotechnology Advances 33, 9941004.CrossRefGoogle ScholarPubMed
Conrath, U., Beckers, G. J. M., Langenbach, C. J. G. & Jaskiewicz, M. R. (2015). Priming for enhanced defense. Annual Review of Phytopathology 53, 97119.CrossRefGoogle ScholarPubMed
Cui, H., Tsuda, K. & Parker, J. E. (2015). Effector-triggered immunity: from pathogen perception to robust defense. Annual Review of Plant Biology 66, 487511.CrossRefGoogle ScholarPubMed
Fu, Z. Q. & Dong, X. (2013). Systemic acquired resistance: turning local infection into global defense. Annual Review of Plant Biology 64, 839863.CrossRefGoogle ScholarPubMed
Gaspar, T., Penel, C., Thorpe, T.& Greppin, H. (1982). Peroxidases 1970–1980. A Survey of their Biochemical and Physiological Roles in Higher Plants. Geneva, Switzerland: University of Geneva Press.Google Scholar
Greenberg, J. T. (1997). Programmed cell death in plant-pathogen interactions. Annual Review of Plant Physiology and Plant Molecular Biology 48, 525545.Google Scholar
Herrera-Vásquez, A., Salinas, P. & Holuigue, L. (2015). Salicylic acid and reactive oxygen species interplay in the transcriptional control of defence genes expression. Frontiers in Plant Science 6, 171.CrossRefGoogle ScholarPubMed
Hofmann, K. & Bucher, P. (1996). The UBA domain: a sequence motif present in multiple enzyme classes of the ubiquitination pathway. Trends in Biochemical Sciences 21, 172173.CrossRefGoogle ScholarPubMed
Hsieh, T. Y., Lin, T. C., Lin, C. L., Chung, K. R. & Huang, J. W. (2016). Reduction of Rhizoctonia damping-off in Chinese cabbage seedlings by fungal protein activators. Journal of Plant Medicine 58, 18.Google Scholar
Hückelhoven, R. (2007). Cell wall-associated mechanisms of disease resistance and susceptibility. Annual Review of Phytopathology 45, 101127.Google Scholar
Huystee, R. B. V. (1987). Some molecular aspects of plant peroxidase biosynthetic studies. Annual Review of Plant Physiology 38, 205219.Google Scholar
Lamb, C. & Dixon, R. A. (1997). The oxidative burst in plant disease resistance. Annual Review of Plant Physiology and Plant Molecular Biology 48, 251275.CrossRefGoogle ScholarPubMed
Lamb, C. J. & Rubery, P. H. (1976). Phenylalanine ammonia-lyase and cinnamic acid 4-hydroxylase: product repression of the level of enzyme activity in potato tuber discs. Planta 130, 283290.Google Scholar
Li, J., Qiu, D. W., Yang, X. F., Zeng, H. M., Yuan, J. J. & Zhu, J. I. (2008). Purification of an activator protein (66 kDa) from Alternaria tenuissima and its biological activity of inducing tobacco resistance to TMV disease. Journal of Agricultural University of Hebei 6, 5154.Google Scholar
Li, X., Guo, M., Xu, D., Chen, F., Zhang, H., Pan, Y., Li, M. & Gao, Z. (2015). The nascent-polypeptide-associated complex alpha subunit regulates the polygalacturonases expression negatively and influences the pathogenicity of Sclerotinia sclerotiorum . Mycologia 107, 11301137.Google Scholar
Lin, T. C., Lin, C. L. & Huang, J. W. (2014). Nonidet p-40, a novel inducer, activates cucumber disease resistance against cucumber anthracnose disease. Journal of Agricultural Science (Cambridge) 152, 932940.Google Scholar
Lithgow, T. (2000). Targeting of proteins to mitochondria. FEBS Letters 476, 2226.CrossRefGoogle ScholarPubMed
Liu, W. P., Zeng, H. M., Liu, Y. F., Yuan, J. J. & Qiu, D. W. (2007). Expression of Alternaria tenuissima peaT2 gene in Pichia pastoris and its function. Acta Microbiologica Sinica 47, 593597.Google Scholar
Mao, J., Liu, Q., Yang, X., Long, C., Zhao, M., Zeng, H., Liu, H., Yuan, J. & Qiu, D. (2010). Purification and expression of a protein elicitor from Alternaria tenuissima and elicitor-mediated defence responses in tobacco. Annals of Applied Biology 156, 411420.Google Scholar
Mur, L. A. J., Prats, E., Pierre, S., Hall, M. A. & Hebelstrup, K. H. (2013). Integrating nitric oxide into salicylic acid and jasmonic acid/ethylene plant defense pathways. Frontiers in Plant Science 4, Article 215 doi: 10.3389/fpls.2013.00215 CrossRefGoogle ScholarPubMed
Oliveira, M. D. M., Varanda, C. M. R. & Félix, M. R. F. (2016). Induced resistance during the interaction pathogen x plant and the use of resistance inducers. Phytochemistry Letters 15, 152158.CrossRefGoogle Scholar
Rao, G. S., Reddy, N. N. R. & Surekha, Ch. (2015). Induction of plant systemic resistance in legumes Cajanus cajan, Vigna radiata, Vigna mungo against plant pathogens Fusarium oxysporum and Alternaria alternata – a Trichoderma viride mediated reprogramming of plant defense mechanism. International Journal of Recent Scientific Research 6, 42704280.Google Scholar
Sarma, B. K., Yadav, S. K., Singh, S. & Singh, H. B. (2015). Microbial consortium-mediated plant defense against phyopathogens: readressing for enhancing efficacy. Soil Biology and Biochemistry 87, 2533.CrossRefGoogle Scholar
Scheler, C., Durner, J. & Astier, J. (2013). Nitric oxide and reactive oxygen species in plant biotic interactions. Current Opinion in Plant Biology 16, 534539.Google Scholar
Sels, J., Mathys, J., De Coninck, B. M. A., Cammue, B. P. A. & De Bolle, M. F. C. (2008). Plant pathogenesis-related (PR) proteins: a focus on PR peptides. Plant Physiology and Biochemistry 46, 941950.Google Scholar
Shoresh, M., Harman, G. E. & Mastouri, F. (2010). Induced systemic resistance and plant responses to fungal biocontrol agents. Annual Review of Phytopathology 48, 2143.CrossRefGoogle ScholarPubMed
Spoel, S. H. & Dong, X. (2012). Pathogenesis-related proteins are the executioners of plant immunity. Nature Reviews Immunology 12, 89100.Google Scholar
Su, V. & Lau, A. F. (2009). Ubiquitin-like and ubiquitin-associated domain proteins: significance in proteasomal degradation. Cellular and Molecular Life Science 66, 28192833.Google Scholar
Thakur, M. & Sohal, B. S. (2013). Role of elicitors in inducing resistance in plants against pathogen infection: a review. ISRN Biochemistry Article ID 762412. http://dx.doi.org/10.1155/2013/762412 Google Scholar
Vallad, G. E. & Goodman, R. M. (2004). Systemic acquired resistance and induced systemic resistance in conventional agriculture. Crop Science 44, 19201934.CrossRefGoogle Scholar
Van Den Bosch, F., Oliver, R., Van Den Berg, F. & Paveley, N. (2014). Governing principles can guide fungicide-resistance management tactics. Annual Review of Phytopathology 52, 175195.Google Scholar
Van Loon, L. C. & Van Strien, E. A. (1999). The families of pathogenesis-related proteins, their activities, and comparative analysis of PR-1 type proteins. Physiological and Molecular Plant Pathology 55, 8597.CrossRefGoogle Scholar
Wu, G. Y., Qiu, D. W., Yang, X. F., Wu, G. F. & Zhao, S. Y. (2007). Effects of new fungal activator protein on physiological characters of soybean. Soybean Science 26, 691694.Google Scholar
Yogev, O., Karniely, S. & Pines, O. (2007). Translation-coupled translocation of yeast fumarase into mitochondria in vivo . Journal of Biological Chemistry 282, 2922229229.CrossRefGoogle ScholarPubMed
Zhang, J. & Kirkham, M. B. (1994). Drought-stress-induced changes in activities of superoxide dismutase, catalase, and peroxidase in wheat species. Plant & Cell Physiology 35, 785791.CrossRefGoogle Scholar
Zhang, Y., Yang, X., Liu, Q., Qiu, D., Zhang, Y., Zeng, H., Yuan, J. & Mao, J. (2010). Purification of novel protein elicitor from Botrytis cinerea that induces disease resistance and drought tolerance in plants. Microbiological Research 165, 142151.Google Scholar
Zhang, W., Yang, X., Qiu, D., Guo, L., Zeng, H., Mao, J. & Gao, Q. (2011). PeaT1-induced systemic acquired resistance in tobacco follows salicylic acid-dependent pathway. Molecular Biology Reports 38, 25492556.Google Scholar
Zhao, L. H., Qiu, D. W., Liu, Z. & Yang, X. F. (2005). Effect of plant activator protein on the transcription of defense-related genes in rice seedlings. Scientia Agricultura Sinica 38, 13581363.Google Scholar
Zhao, M. Z., Yang, X. F., Zhang, M., Yuan, J. J. & Qiu, D. W. (2007). Purification and bioactivities of a protein growth-activator from Alternaria tenuissima . Chinese Journal of Biological Control 23, 170173.Google Scholar
Zucker, M. (1965). Induction of phenylalanine deaminase by light and its relation to chlorogenic acid synthesis in potato tuber tissue. Plant Physiology 40, 779784.CrossRefGoogle ScholarPubMed