转录因子 FoAce2 调节立方镰刀菌的毒力、无性繁殖、分生孢子和细胞壁平衡

IF 3 3区 生物学 Q2 MYCOLOGY Fungal biology Pub Date : 2024-08-01 Epub Date: 2024-06-18 DOI:10.1016/j.funbio.2024.06.002
Zhaojian Ding , Huijiao Lin , Liguang Liu , Tiantian Lu , Yifeng Xu , Jiayi Peng , Yujie Ren , Jun Peng , Tianwei Xu , Xin Zhang
{"title":"转录因子 FoAce2 调节立方镰刀菌的毒力、无性繁殖、分生孢子和细胞壁平衡","authors":"Zhaojian Ding ,&nbsp;Huijiao Lin ,&nbsp;Liguang Liu ,&nbsp;Tiantian Lu ,&nbsp;Yifeng Xu ,&nbsp;Jiayi Peng ,&nbsp;Yujie Ren ,&nbsp;Jun Peng ,&nbsp;Tianwei Xu ,&nbsp;Xin Zhang","doi":"10.1016/j.funbio.2024.06.002","DOIUrl":null,"url":null,"abstract":"<div><p>Fusarium wilt of banana, caused by the fungus <em>Fusarium oxysporum</em> f. sp. <em>cubense</em> (Foc), is a serious fungal disease that affects banana plants globally. To explore the virulence mechanisms of this pathogen, we created a null mutation of the transcription factor gene <em>FoAce2</em> (encoding <em>F. oxysporum</em> angiotensin converting enzyme 2). Deletion of <em>FoAce2</em> resulted in slower growth, decreased aerial mycelia and conidiation, and a significant decrease in fungal virulence against banana hosts relative to those of the wild-type (WT) fungus. Additionally, transmission electron microscopy showed that the cell wall was thicker in the <em>FoAce2</em> deletion mutants. Consistent with this finding, the cell wall glucose level was decreased in the Δ<em>FoAce2</em> mutants compared with that in the WT and complemented strain, Δ<em>FoAce2-</em>C1. Complementation with the WT <em>FoAce2</em> gene fully reversed the mutant phenotypes. Analysis of the transcriptome of Δ<em>FoAce2</em> and the WT strain showed alterations in the expression levels of many genes associated with virulence and growth. Thus, FoAce2 appears to be essential for Foc virulence, cell wall homeostasis, conidiation, and vegetative growth.</p></div>","PeriodicalId":12683,"journal":{"name":"Fungal biology","volume":"128 5","pages":"Pages 1960-1967"},"PeriodicalIF":3.0000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcription factor FoAce2 regulates virulence, vegetative growth, conidiation, and cell wall homeostasis in Fusarium oxysporum f. sp. cubense\",\"authors\":\"Zhaojian Ding ,&nbsp;Huijiao Lin ,&nbsp;Liguang Liu ,&nbsp;Tiantian Lu ,&nbsp;Yifeng Xu ,&nbsp;Jiayi Peng ,&nbsp;Yujie Ren ,&nbsp;Jun Peng ,&nbsp;Tianwei Xu ,&nbsp;Xin Zhang\",\"doi\":\"10.1016/j.funbio.2024.06.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Fusarium wilt of banana, caused by the fungus <em>Fusarium oxysporum</em> f. sp. <em>cubense</em> (Foc), is a serious fungal disease that affects banana plants globally. To explore the virulence mechanisms of this pathogen, we created a null mutation of the transcription factor gene <em>FoAce2</em> (encoding <em>F. oxysporum</em> angiotensin converting enzyme 2). Deletion of <em>FoAce2</em> resulted in slower growth, decreased aerial mycelia and conidiation, and a significant decrease in fungal virulence against banana hosts relative to those of the wild-type (WT) fungus. Additionally, transmission electron microscopy showed that the cell wall was thicker in the <em>FoAce2</em> deletion mutants. Consistent with this finding, the cell wall glucose level was decreased in the Δ<em>FoAce2</em> mutants compared with that in the WT and complemented strain, Δ<em>FoAce2-</em>C1. Complementation with the WT <em>FoAce2</em> gene fully reversed the mutant phenotypes. Analysis of the transcriptome of Δ<em>FoAce2</em> and the WT strain showed alterations in the expression levels of many genes associated with virulence and growth. Thus, FoAce2 appears to be essential for Foc virulence, cell wall homeostasis, conidiation, and vegetative growth.</p></div>\",\"PeriodicalId\":12683,\"journal\":{\"name\":\"Fungal biology\",\"volume\":\"128 5\",\"pages\":\"Pages 1960-1967\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fungal biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1878614624000837\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/6/18 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878614624000837","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

由 Fusarium oxysporum f. sp. cubense(Foc)真菌引起的香蕉镰刀菌枯萎病是一种严重的真菌病害,影响着全球的香蕉植株。为了探索这种病原菌的致病机制,我们对转录因子基因 FoAce2(编码 F. oxysporum 血管紧张素转换酶 2)进行了缺失突变。与野生型(WT)真菌相比,缺失 FoAce2 会导致生长缓慢、气生菌丝和分生孢子减少,以及对香蕉寄主的毒力显著降低。此外,透射电子显微镜显示,FoAce2缺失突变体的细胞壁更厚。与这一发现一致的是,与 WT 菌株和互补菌株 ΔFoAce2-C1 相比,ΔFoAce2 突变体的细胞壁葡萄糖含量降低。与 WT FoAce2 基因的互补完全逆转了突变体的表型。对 ΔFoAce2 和 WT 菌株转录组的分析表明,许多与毒力和生长相关的基因的表达水平发生了变化。因此,FoAce2 似乎对 Foc 的毒力、细胞壁平衡、分生孢子和无性生殖至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Transcription factor FoAce2 regulates virulence, vegetative growth, conidiation, and cell wall homeostasis in Fusarium oxysporum f. sp. cubense

Fusarium wilt of banana, caused by the fungus Fusarium oxysporum f. sp. cubense (Foc), is a serious fungal disease that affects banana plants globally. To explore the virulence mechanisms of this pathogen, we created a null mutation of the transcription factor gene FoAce2 (encoding F. oxysporum angiotensin converting enzyme 2). Deletion of FoAce2 resulted in slower growth, decreased aerial mycelia and conidiation, and a significant decrease in fungal virulence against banana hosts relative to those of the wild-type (WT) fungus. Additionally, transmission electron microscopy showed that the cell wall was thicker in the FoAce2 deletion mutants. Consistent with this finding, the cell wall glucose level was decreased in the ΔFoAce2 mutants compared with that in the WT and complemented strain, ΔFoAce2-C1. Complementation with the WT FoAce2 gene fully reversed the mutant phenotypes. Analysis of the transcriptome of ΔFoAce2 and the WT strain showed alterations in the expression levels of many genes associated with virulence and growth. Thus, FoAce2 appears to be essential for Foc virulence, cell wall homeostasis, conidiation, and vegetative growth.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Fungal biology
Fungal biology MYCOLOGY-
CiteScore
5.80
自引率
4.00%
发文量
80
审稿时长
49 days
期刊介绍: Fungal Biology publishes original contributions in all fields of basic and applied research involving fungi and fungus-like organisms (including oomycetes and slime moulds). Areas of investigation include biodeterioration, biotechnology, cell and developmental biology, ecology, evolution, genetics, geomycology, medical mycology, mutualistic interactions (including lichens and mycorrhizas), physiology, plant pathology, secondary metabolites, and taxonomy and systematics. Submissions on experimental methods are also welcomed. Priority is given to contributions likely to be of interest to a wide international audience.
期刊最新文献
Fungal and algal community structures and their relationships with soluble salts at the Dazu Rock Carvings, China Cosmopolites sordidus G. as a dispersal agent of Fusarium oxysporum f. sp. cubense Tropical Race 4 (Foc TR4) in Cavendish banana crops (Musa AAA) The peroxisome RING-type E3 ubiquitin ligase-mediated peroxisome function is essential for Alternaria alternata pathogenicity: coordinated regulation of lipid metabolism homeostasis and redox balance Native fungal endophytes provide effective biocontrol against Phytophthora plurivora associated with alder decline in northern Spain Temperature and growth media affect conidia production, germination and virulence of Metarhizium spp. during simulated solid substrate fermentation conditions
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1