Comparative transcriptome analysis provides insights into the resistance regulation mechanism and inhibitory effect of fungicide phenamacril in Fusarium asiaticum

文献类型： 外文期刊

第一作者： Zheng, Zhitian

作者： Zheng, Zhitian;Liu, Huaqi;Luo, Xiao;Liu, Runze;Joe, Alexander Dumbi;Li, Haolin;Wang, Yunpeng;Liu, Huaqi;Li, Yanzhong;Sun, Haiyan;Lin, Yanling

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关键词： Comparative transcriptome; Phenamacril; Resistance regulation; Inhibitory effect; Fusarium asiaticum

期刊名称：PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY （ 影响因子：4.7； 五年影响因子：4.7 ）

ISSN： 0048-3575

年卷期： 2024 年 201 卷

页码：

收录情况： SCI

摘要： Fusarium asiaticum is a destructive phytopathogenic fungus that causes Fusarium head blight of wheat (FHB), leading to serious yield and economic losses to cereal crops worldwide. Our previous studies indicated that target -site mutations (K216R/E, S217P/L, or E420K/G/D) of Type I myosin FaMyo5 conferred high resistance to phenamacril. Here, we first constructed one sensitive strain H1S and three point mutation resistant strains HA, HC and H1R. Then we conducted comparative transcriptome analysis of these F. asiaticum strains after 1 and 10 mu g center dot mL-1 phenamacril treatment. Results indicated that 2135 genes were differentially expressed (DEGs) among the sensitive and resistant strains. The DEGs encoding ammonium transporter MEP1/MEP2, nitrate reductase, copper amine oxidase 1, 4-aminobutyrate aminotransferase, amino -acid permease inda1, succinatesemialdehyde dehydrogenase, 2, 3-dihydroxybenzoic acid decarboxylase, etc., were significantly up -regulated in all the phenamacril-resistant strains. Compared to the control group, a total of 1778 and 2097 DEGs were identified in these strains after 1 and 10 mu g center dot mL-1 phenamacril treatment, respectively. These DEGs involved in 4aminobutyrate aminotransferase, chitin synthase 1, multiprotein-bridging factor 1, transcriptional regulatory protein pro -1, amino -acid permease inda1, ATP -dependent RNA helicase DED1, acetyl -coenzyme A synthetase, sarcoplasmic/endoplasmic reticulum calcium ATPase 2, etc., showed significantly down -regulated expression in phenamacril-sensitive strain but not in resistant strains after phenamacril treatment. In addition, cyanide hydratase, mating -type protein MAT -1, putative purine nucleoside permease, plasma membrane protein yro2, etc., showed significantly co -down -regulated expression in all the strains after phenamacril treatment. Taken together, This study provides deep insights into the resistance regulation mechanism and the inhibitory effect of fungicide phenamacril and these new annotated proteins or enzymes are worth for the discovery of new fungicide targets.

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