The activation of wheat resistance against powdery mildew by combination of biotic elicitor and NO donor
Abstract
Aim. The aim of research was to analyze the activation of Triticum aestivum L. non-specific resistance by the effect of ferulic acid and NO on H2O2 content against fungal pathogen from environment in field trials. Methods. Content of endogenous H2O2 was measured in elicitor treated and infected wheat plants (cv. Oberig myronivskij and Svitanok myronivskij) during different ontogenesis phases. The extent of disease development, morphometric parameters and yield structure were analyzed. Results. The data obtained suggest that different levels of endogenous hydrogen peroxide were induced in wheat leaves by treatment. The growth and yield were stimulated. The infection damage decreased. Conclusions. The role of endogenous hydrogen peroxide is crucial for wheat defense during all vegetation period. The elicitor and donor NO induced effective defense responses and resistance in winter wheat against Erysiphe graminis.
Keywords: Triticum aestivum L., ferulic acid, NO, induced resistance, powdery mildew.
References
Babayants O.V., Babayants L.T. Basis of selection and methodology of wheat tolerance estimation to diseases agents. Odessa, 2014. 401 p. [in Russian]
Zhuk I.V., Dmitriev A.P., Lysova G.M., Kucherova L.O. Participation of ferulic acid in elicitation of winter wheat plants resistance against Septoria tritici infection. Factors in experimental evolution of organisms. 2017. Vol. 20. P. 190–193. doi: 10.7124/FEEO.v20.761. [in Ukrainian]
Zhuk I.V, Dmitriev A.P., Lysova G.M., Kucherova L.O. The combination of NO donor and ferulic acid effect on the elicitation of Triticum aestivum tolerance against Septoria tritici. Factors in experimental evolution of organisms. 2018. Vol. 23. P. 240–245. doi: 10.7124/FEEO.v22.955. [in Ukrainian]
Zhuk I.V., Dmitriev A.P., Shylina J.V., Lysova G.M., Kucherova L.O. The estimation of organic acids effectiveness as biotic elicitors via changes of endogenous peroxide content. Factors in experimental evolution of organisms. 2020. Vol. 26. P. 202–206. doi: 10.7124/FEEO.v26.1266. [in Ukrainian]
Chen L.-M., Kao Ch.-H. Effect of excess copper on rice leaves: evidence involvement of lipid peroxidation. Bot. Bull. Acad. Sin. 1999. Vol. 40. P. 283–287.
Foyer C.H. Reactive oxygen species, oxidative signaling and the regulation of photosynthesis. Environmental and Experimental Botany. 2018. doi: 10.1016/j.envexpbot.2018.05.003.
Appiano M., Catalano D., Martínez M. S., Lotti C., Zheng Z., Visser R. G. F., Ricciardi L., Bai Y., Pavan S. Monocot and dicot MLO powdery mildew susceptibility factors are functionally conserved in spite of the evolution of class-specific molecular features. BMC Plant Biology. 2015. Vol. 15. P. 257. doi: 10.1186/s12870-015-0639-6.
Liu Z., Zhao Y; Wang X., Yang M., Guo C., Xiao K. TaNBP1, a guanine nucleotide-binding subunit gene of wheat, is essential in the regulation of N starvation adaptation via modulating N acquisition and ROS homeostasis. BMC Plant Biology. 2018. Vol. 18. P. 167. doi: 10.1186/s12870-018-1374-6.
Goto Y., Maki N., Sklenar J., Derbyshire P., Menke F.L.H., Zipfel C., Kadota Y., Shirasu K. The phagocytosis oxidase/Bem1p (PB1) domain-containing protein PB1CP negatively regulates the NADPH oxidase RBOHD in plant immunity. bioRxiv. 2020. doi: 10.1101/2020.12.28.423414.
Wu F., Chi Y., Jiang Z., Xu Y., Xie L., Huang F. et al. Hydrogen peroxide sensor HPCA1 is an LRR receptor kinase in Arabidopsis. Nature. 2020. Vol. 578. P. 577–581. doi: 10.1038/s41586-020-2032-3.
Bleau J.R., Spoel S.H. Selective redox signaling shapes plant-pathogen interactions. Plant Physiology. 2021. doi: 10.1093/plphys/kiaa088.
Gallego-Giraldo L., Posé S., Sivakumar P., Peralta A G. Hahn M. G., Ayre B.G., Sunuwar J., Hernandez J., Patel M., Shah J., Rao X., Knox J.P., Dixon R.A. Elicitors and defense gene induction in plants with altered lignin compositions. New Phytologist. 2018. Vol. 219. P. 1235–1251. doi: 10.1111/nph.15258.
Smirnoff N., Arnaud D. Hydrogen peroxide metabolism and functions in plants. New Phytologist. 2019. Vol. 221. P. 1197–1214. doi: 10.1111/nph.15488.
Kang Y. Zhou M., Merry A., Barry K. Mechanisms of powdery mildew resistance of wheat – a review of molecular breeding. Plant Pathology. 2020. Vol. 69. P. 601–617. doi: 10.1111/ppa.13166.
Sandalio L.M., Peláez-Vico M.A., Molina-Moya E., Romero-Puertas M.C. Peroxisomes as redox-signaling nodes in intracellular communication and stress responses. Plant Physiol. 2021. doi: 10.1093/plphys/kiab060.