Ergosterol, a principal compound of the fungal plasma membrane, is regarded as a pathogen-associated molecular pattern. In the present study, the role of salicylic acid (SA), jasmonic acid (JA) and spermine signaling pathways after ergosterol elicitation were evaluated. SA, JA and spermine production, as well as accumulation of transcripts for a lipoxygenase (NaLOX3) gene, the phenylalanine-ammonia lyase gene, selected pathogenesis-related genes (PR1, PR5), and peroxidase tPOXC1 were determined in tobacco (Nicotiana tabacum L. cv. Xanthi) in response to ergosterol elicitation. To understand the sequence of the signaling cascade, several representative steps involved in the synthesis of crucial signaling molecules were targeted using specific inhibitors. SA signaling pathway, together with calmodulin-dependent protein kinases and nitric oxide, was demonstrated to play an important role in the induction of defense-related genes following ergosterol treatment. The results suggested that nitric oxide participates in defense-related gene activation following ergosterol treatment but does not directly participate in activation of reactive oxygen species production. The induction of PR5 and tPOXC1 transcripts was found to be not fully dependent on calmodulin/Ca2+ and SA signaling, contrary to the PR1a transcript. A possible candidate for this SA-independent pathway is the spermine pathway, as elevated spermine levels were detected following ergosterol treatment.
Keywords: 2-(4-carboxyphenyl-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide; 4-amino-5-methylamino-2′,7′-difluorofluorescein diacetate; Chole; DAF-FM DA; Defense; Ergo; Ergosterol; JA; Jasmonic acid; N-(6-aminohexyl)-5-chloro-1-naphthalenesulphonamide; N-methyl-l-arginine acetate salt; NO; NOS; PAL; PLA2; PR; ROS; RR; RT-qPCR; SA; Salicylic acid; Signaling; Spermine; Tobacco; W7; cPTIO; cholesterol; ergosterol; jasmonic acid; l-NMMA; nitric oxide; nitric oxide synthase; pathogenesis-related; phenylalanine-ammonia lyase; phospholipase A(2); reactive oxygen species; real-time quantitative polymerase chain reaction; ruthenium red; salicylic acid; tPOXC1; tobacco peroxidase C1.
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