Suppression of red light-induced resistance in broad beans to Botrytis cinerea by salicylic acid

We investigated the effect of salicylic acid (SA) on red light-induced resistance in broad beans to Botrytis cinerea. Both lesion formation and fungal development were suppressed on broad bean leaves kept under red light, producing anti-fungal compound(s). However, SA pre-treatment inhibited express...

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Published inPhysiological and molecular plant pathology Vol. 66; no. 1; pp. 20 - 29
Main Authors Khanam, Nurun Nahar, Ueno, Makoto, Kihara, Junichi, Honda, Yuichi, Arase, Sakae
Format Journal Article
LanguageEnglish
Published London Elsevier India Pvt Ltd 01.01.2005
Elsevier
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Summary:We investigated the effect of salicylic acid (SA) on red light-induced resistance in broad beans to Botrytis cinerea. Both lesion formation and fungal development were suppressed on broad bean leaves kept under red light, producing anti-fungal compound(s). However, SA pre-treatment inhibited expression of red light-induced resistance dose-dependently, generating hydrogen peroxide (H 2O 2). Red light-induced resistance was recovered in the presence of a H 2O 2 scavenger, ascorbic acid or a NADPH oxidase inhibitor, diphenylene iodonium even in SA-pre-treated broad bean leaves. These results suggest that breakdown of red light-induced resistance in broad beans to B. cinerea is induced by membrane-mediated H 2O 2 generation. On the other hand, catalase activity in broad bean leaves was significantly enhanced under red light, but not in those pre-treated with SA and aminotriazole. We hypothesize that enhanced antioxidant enzyme catalase activity contributes to the inhibition of cell death in broad beans scavenging endogenous H 2O 2 generated by B. cinerea infection and to elicitor-dependent production of anti-fungal component(s) by living host cells; as a consequence, red light-induced resistance may be established. It is possible that an SA-dependent signaling pathway in broad beans is playing different roles in the plant-pathogen pathosystem.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0885-5765
1096-1178
DOI:10.1016/j.pmpp.2005.03.006