FgVAC1 is an Essential Gene Required for Golgi-to-Vacuole Transport and Fungal Development in Fusarium graminearum.

IF 3.3 4区 生物学 Q2 MICROBIOLOGY Journal of Microbiology Pub Date : 2024-08-01 Epub Date: 2024-07-30 DOI:10.1007/s12275-024-00160-x
Sieun Kim, Jiyeun Park, You-Kyoung Han, Hokyoung Son
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Abstract

Fusarium graminearum is an important plant pathogen that causes head blight in cereal crops such as wheat, barley, and rice worldwide. In this study, we identified and functionally characterized FgVAC1, an essential gene in F. graminearum that encodes a Rab5 effector involved in membrane tethering functions. The essentiality of FgVAC1 was confirmed through a conditional promoter replacement strategy using the zearalenone-inducible promoter (PZEAR). Cytological analyses revealed that FgVac1 colocalizes with FgRab51 on early endosomes and regulates the proper transport of the vacuolar hydrolase FgCpy1 to the vacuole. Suppression of FgVAC1 led to inhibited vegetative growth, reduced asexual and sexual reproduction, decreased deoxynivalenol (DON) biosynthesis, and diminished pathogenicity. Our findings highlight the significant role of FgVac1 in vacuolar protein sorting, fungal development, and plant infection in F. graminearum.

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FgVAC1 是禾谷镰刀菌高尔基体到液泡转运和真菌发育所需的重要基因
禾本科镰刀菌是一种重要的植物病原菌,会引起全球小麦、大麦和水稻等谷类作物的头枯病。在这项研究中,我们发现并从功能上鉴定了禾谷镰刀菌中的一个重要基因 FgVAC1,该基因编码一种参与膜拴系功能的 Rab5 效应子。通过使用玉米赤霉烯酮诱导型启动子(PZEAR)的条件启动子替换策略,证实了 FgVAC1 的必需性。细胞学分析表明,FgVac1与FgRab51共定位在早期内体上,并调节液泡水解酶FgCpy1向液泡的正常运输。抑制 FgVAC1 可抑制无性生殖,减少无性和有性生殖,降低脱氧雪腐镰刀菌烯醇(DON)的生物合成,并降低致病性。我们的研究结果突显了 FgVac1 在禾谷镰孢的液泡蛋白分选、真菌发育和植物感染中的重要作用。
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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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