Abstract
The sterol regulatory element binding proteins (SREBPs) are key regulators for sterol homeostasis in most fungi. In the citrus postharvest pathogen Penicillium digitatum, the SREBP homolog is required for fungicide resistance and regulation of CYP51 expression. In this study, we identified another SREBP transcription factor PdSreB in P. digitatum, and the biological functions of both SREBPs were characterized and compared. Inactivation of PdsreA, PdsreB or both genes in P. digitatum reduced ergosterol contents and increased sensitivities to sterol 14-α-demethylation inhibitors (DMIs) and cobalt chloride. Fungal strains impaired at PdsreA but not PdsreB increased sensitivity to tridemorph and an iron chelator 2,2’-dipyridyl. Virulence assays on citrus fruit revealed that fungal strains impaired at PdsreA, PdsreB or both induce maceration lesions similar to those induced by wild-type. However, ΔPdsreA, ΔPdsreB or the double mutant strain rarely produce aerial mycelia on infected citrus fruit peels. RNA-Seq analysis showed the broad regulatory functions of both SREBPs in biosynthesis, transmembrane transportation and stress responses. Our results provide new insights into the conserved and differentiated regulatory functions of SREBP homologs in plant pathogenic fungi.
Highlights
Green mold, caused by Penicillium digitatum (Pers.: Fr.) Sacc., is the most destructive postharvest disease of citrus fruits
A phylogenetic tree constructed using ribosomal proteins revealed a close relationship between A. fumigatus and P. digitatum (S2 Fig)
The results showed that the A. fumigatus SrbA binding sites were found in the promoter regions of the genes encoding Erg10A, Hmg2, Erg12, Idi1, Erg1, Cyp51A, Cyp51B, Erg25, Erg27, Erg3B, and Erg4B (S4 Table)
Summary
Green mold, caused by Penicillium digitatum (Pers.: Fr.) Sacc., is the most destructive postharvest disease of citrus fruits. The disease causes severe losses of citrus fruits during packaging, storage, transportation, and marketing [1,2]. Application of sterol 14-α-demethylation inhibitors (DMIs), such as imazalil and prochloraz, is the most effective and economical method for green mold control. Control efficacy of DMI fungicides is compromised as resistant strains emerged worldwide [3,4,5,6,7]. DMI fungicides inhibit the activity of the cytochrome P450-dependent sterol 14α-demethylase (Cyp51) and block C14-demethylation of lanosterol in fungal pathogens [8,9]. DMI resistance has been reported in many phytopathogenic fungi, and major mechanisms leading
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