LaeA Controls Virulence and Secondary Metabolism in Apple Canker Pathogen
Overview
Affiliations
Apple Valsa canker is a destructive disease caused by the ascomycete and poses a serious threat to apple production. Toxins synthesized by secondary metabolite biosynthetic gene clusters (SMBGCs) have been proven to be crucial for pathogen virulence. A previous study showed that genome contains remarkably expanded SMBGCs and some of their genes were significantly upregulated during infection. In this study, we focus on LaeA, a known regulator of secondary metabolism, for its role in SMBGC regulation, toxin production, and virulence of . Deletion of led to greatly reduced virulence with lesion length reduced by 48% on apple twigs. Toxicity tests proved that toxicity of secondary metabolites (SMs) produced by deletion mutant (Δ) was markedly decreased in comparison with wild-type (WT). Transcriptomic and proteomic analyses of WT and Δ indicated that a portion of transporters and about half (31/60) SMBGCs are regulated by Function analysis of eight gene clusters including , , , , , , , and that were differentially expressed at both transcriptional and translational levels showed that four of them (i.e., , , , and ) were involved in pigment production and contributed to virulence. Our findings will provide new insights and gene resources for understanding the role of pathogenicity-related toxins in .
Calvo A, Dabholkar A, Wyman E, Lohmar J, Cary J Appl Environ Microbiol. 2024; 90(10):e0081924.
PMID: 39230285 PMC: 11497805. DOI: 10.1128/aem.00819-24.
Hou X, Liu L, Xu D, Lai D, Zhou L J Fungi (Basel). 2024; 10(8).
PMID: 39194887 PMC: 11355368. DOI: 10.3390/jof10080561.
Zhang Y, Wang X, Ran Y, Zhang K, Li G Microbiol Spectr. 2023; 11(4):e0018623.
PMID: 37358432 PMC: 10434191. DOI: 10.1128/spectrum.00186-23.
Wu Y, Wang Y, Han S, Li Q, Kong L Front Plant Sci. 2023; 14:1132507.
PMID: 36909432 PMC: 9994621. DOI: 10.3389/fpls.2023.1132507.
A putative terpene cyclase gene () is required for fungal development and virulence in .
Yang Y, Yu L, Qiu X, Xiong D, Tian C Front Microbiol. 2023; 14:1084828.
PMID: 36891381 PMC: 9986285. DOI: 10.3389/fmicb.2023.1084828.