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 , Huijiao Lin , Liguang Liu , Tiantian Lu , Yifeng Xu , Jiayi Peng , Yujie Ren , Jun Peng , Tianwei Xu , 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 , Huijiao Lin , Liguang Liu , Tiantian Lu , Yifeng Xu , Jiayi Peng , Yujie Ren , Jun Peng , Tianwei Xu , 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}
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.
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.