Malate Synthase Gene Regulates Vegetative Growth, Spore Germination, Toxin Production, Pathogenicity and Sensitivity to Fungicides in Fusarium graminearum

IF 1.1 4区 农林科学 Q3 PLANT SCIENCES
Tongyu Hao, Huiming Li, Xuelian Duan, Yikai Zhang, Jia Jiang, Le Qian, Shengming Liu
{"title":"Malate Synthase Gene Regulates Vegetative Growth, Spore Germination, Toxin Production, Pathogenicity and Sensitivity to Fungicides in Fusarium graminearum","authors":"Tongyu Hao,&nbsp;Huiming Li,&nbsp;Xuelian Duan,&nbsp;Yikai Zhang,&nbsp;Jia Jiang,&nbsp;Le Qian,&nbsp;Shengming Liu","doi":"10.1111/jph.70081","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p><i>Fusarium graminearum</i> is a fungal pathogen that causes Fusarium head blight (FHB) in wheat. The glyoxylate cycle serves as an essential complement to the tricarboxylic acid (TCA) cycle, critically regulating cellular energy homeostasis and fungal virulence biosynthesis. Nevertheless, the biological functions of glyoxylate cycle-related genes and their regulatory mechanisms in <i>F. graminearum</i> pathogenesis require systematic characterisation. The <i>FgMS</i> knockout mutant <i>ΔFgMS</i> and complemented strain <i>ΔFgMS-C</i> were generated from wild-type <i>F. graminearum</i> strain AY1801 using targeted gene replacement. Compared with AY1801 and <i>ΔFgMS-C</i>, several significant defects were observed in <i>ΔFgMS</i>, which include a reduced growth rate, decreased sporulation, weakened spore germination, diminished virulence, lower toxin production, increased sensitivity to cell wall stress, and reduced sensitivity to carbendazim, pydiflumetofen, difenoconazole, tebuconazole and phenamacril. The dynamic <i>FgMS</i> expression patterns during distinct developmental stages and infection phases were determined by qRT-PCR. <i>FgMS</i> was expressed at a high level during the spore stage. In addition, its expression level increased rapidly as the infection progressed. These findings demonstrate that <i>FgMS</i> is indispensable for vegetative growth, spore formation and germination, virulence and toxin production in <i>F. graminearum</i>.</p>\n </div>","PeriodicalId":16843,"journal":{"name":"Journal of Phytopathology","volume":"173 3","pages":""},"PeriodicalIF":1.1000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jph.70081","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Fusarium graminearum is a fungal pathogen that causes Fusarium head blight (FHB) in wheat. The glyoxylate cycle serves as an essential complement to the tricarboxylic acid (TCA) cycle, critically regulating cellular energy homeostasis and fungal virulence biosynthesis. Nevertheless, the biological functions of glyoxylate cycle-related genes and their regulatory mechanisms in F. graminearum pathogenesis require systematic characterisation. The FgMS knockout mutant ΔFgMS and complemented strain ΔFgMS-C were generated from wild-type F. graminearum strain AY1801 using targeted gene replacement. Compared with AY1801 and ΔFgMS-C, several significant defects were observed in ΔFgMS, which include a reduced growth rate, decreased sporulation, weakened spore germination, diminished virulence, lower toxin production, increased sensitivity to cell wall stress, and reduced sensitivity to carbendazim, pydiflumetofen, difenoconazole, tebuconazole and phenamacril. The dynamic FgMS expression patterns during distinct developmental stages and infection phases were determined by qRT-PCR. FgMS was expressed at a high level during the spore stage. In addition, its expression level increased rapidly as the infection progressed. These findings demonstrate that FgMS is indispensable for vegetative growth, spore formation and germination, virulence and toxin production in F. graminearum.

苹果酸合成酶基因调控稻谷镰刀菌营养生长、孢子萌发、毒素产生、致病性和对杀菌剂的敏感性
小麦赤霉病(Fusarium graminearum)是一种引起小麦赤霉病的真菌病原体。乙醛酸循环作为三羧酸(TCA)循环的重要补充,关键调节细胞能量稳态和真菌毒力生物合成。然而,乙醛酸循环相关基因的生物学功能及其调控机制在禾谷镰刀菌发病机制中需要系统的表征。FgMS敲除突变体ΔFgMS和互补菌株ΔFgMS-C是利用靶向基因置换从野生型禾谷F. graminearum菌株AY1801中获得的。与AY1801和ΔFgMS-C相比,ΔFgMS的生长速度减慢,产孢量减少,孢子萌发减弱,毒力减弱,产毒量降低,对细胞壁应激敏感性增加,对多菌灵、吡氟甲醚、异丙康唑、替布康唑和非那马克利敏感性降低。采用qRT-PCR检测不同发育阶段和感染阶段FgMS的动态表达模式。FgMS在孢子期高水平表达。随着感染的进展,其表达量迅速增加。这些发现表明,FgMS对禾粒镰刀菌的营养生长、孢子形成和萌发、毒力和毒素产生都是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Phytopathology
Journal of Phytopathology 生物-植物科学
CiteScore
2.90
自引率
0.00%
发文量
88
审稿时长
4-8 weeks
期刊介绍: Journal of Phytopathology publishes original and review articles on all scientific aspects of applied phytopathology in agricultural and horticultural crops. Preference is given to contributions improving our understanding of the biotic and abiotic determinants of plant diseases, including epidemics and damage potential, as a basis for innovative disease management, modelling and forecasting. This includes practical aspects and the development of methods for disease diagnosis as well as infection bioassays. Studies at the population, organism, physiological, biochemical and molecular genetic level are welcome. The journal scope comprises the pathology and epidemiology of plant diseases caused by microbial pathogens, viruses and nematodes. Accepted papers should advance our conceptual knowledge of plant diseases, rather than presenting descriptive or screening data unrelated to phytopathological mechanisms or functions. Results from unrepeated experimental conditions or data with no or inappropriate statistical processing will not be considered. Authors are encouraged to look at past issues to ensure adherence to the standards of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信