Systematic assessment of the antifungal mechanism of soil fumigant methyl isothiocyanate against Fusarium oxysporum

文献类型： 外文期刊

第一作者： Zhang, Daqi

作者： Zhang, Daqi;Ren, Lirui;Wang, Qing;Li, Wenjing;Song, Zhaoxin;Fang, Wensheng;Yan, Dongdong;Li, Yuan;Wang, Qiuxia;Cao, Aocheng;He, Lin;Jin, Xi;Cao, Aocheng;Fang, Wensheng;Yan, Dongdong;Li, Yuan;Wang, Qiuxia;Cao, Aocheng;Cao, Aocheng

作者机构： Chinese Acad Agr Sci, Inst Plant Protect, Beijing 100193, Peoples R China;Southwest Univ, Coll Plant Protect, Innovat Res Team Vegetable Pests Biol, Chongqing 400716, Peoples R China;Beijing Innovat Consortium Agr Res Syst, Beijing 100193, Peoples R China;Baoding Univ, Hebei Technol Innovat Ctr Green Management Soil Bo, Baoding 071000, Hebei, Peoples R China;Chinese Acad Agr Sci, Inst Plant Protect, 2 West Yuanmingyuan Rd, Beijing 100193, Peoples R China

关键词： Methyl isothiocyanate; Antimicrobial mechanism; Transcriptome sequencing; Soil-borne fungi; Oxidative stress

期刊名称：ENVIRONMENTAL POLLUTION （ 2022影响因子：8.9； 五年影响因子：9.5 ）

ISSN： 0269-7491

年卷期： 2024 年 341 卷

页码：

收录情况： SCI

摘要： Fusarium oxysporum is an important phytopathogenic fungus, it can be controlled by the soil fumigant methyl isothiocyanate (MITC). However, the antimicrobial mechanism of MITC against F. oxysporum, especially at the transcriptional level, is still unclear. In this experiment, the antimicrobial mechanism of MITC against F. oxysporum was investigated. Our results indicated that when F. oxysporum was exposed to 6 mg/L MITC for 12 h, the inhibitory rate of MITC on F. oxysporum was 80%. Transmission electron microscopes showed that the cell wall and membrane of F. oxysporum had shrunk and folded, vacuoles increased, and mitochondria swelled and deformed. In addition, the enzyme activity of F. oxysporum treated with MITC showed a decrease of 32.50%, 8.28% and 74.04% in catalase, peroxidase and superoxide dismutase, respectively. Transcriptome sequencing of F. oxysporum was performed and the results showed that 1478 differentially expressed genes (DEGs) were produced in response to MITC exposure. GO and KEGG analysis showed that the DEGs identified were involved in substance and energy metabolism, signal transduction, transport and catalysis. MITC disrupted cell homeostasis by influencing the expression of some key genes involved in chitin synthase and detoxification enzymes production, but F. oxysporum also protected itself by up-regulating genes involved in energy synthesis (such as upregulating acnA, CS and LSC2 in TCA). qRT-PCR data validated the reliability of transcriptome data. Our research used biochemical and genetic techniques to identify molecular lesions in the mycelia of F. oxysporum exposed to MITC, and provide valuable insights into the toxic mechanism of pathogenic fungi mediated by MITC. These techniques are also likely to be useful for rapidly screening and identifying new, environmentally-friendly soil fumigants that are efficacious against fungal pathogens.

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