{"title":"TOX2基因与伪谷物镰刀菌的条件作用和全毒力有关。","authors":"Sen Han, Shaobo Zhao, Yajiao Wang, Qiusheng Li, Mengwei Sun, Lingxiao Kong, Xianghong Chen, Jianhai Gao, Yuxing Wu","doi":"10.3390/cimb47090714","DOIUrl":null,"url":null,"abstract":"<p><p>Fusarium crown rot, a widespread and destructive disease affecting cereal crops (particularly wheat and barley), is primarily caused by the soil-borne fungal pathogen <i>Fusarium pseudograminearum</i>. Secondary metabolites (SMs) play a crucial role in colonization and host tissue invasion by pathogenic fungi. In this study, we investigated the functional role of <i>FpTox2</i>, a secondary metabolite-related gene in <i>F. pseudograminearum</i>. An <i>FpTox2</i> deletion mutant exhibited significantly reduced radial growth compared to wild-type <i>F. pseudograminearum</i>. Notably, the mutant strain completely lost conidiation capacity under induced conditions. Furthermore, although it showed decreased sensitivity to the cell membrane inhibitor sodium dodecyl sulfate (SDS), the mutant demonstrated enhanced susceptibility to NaCl, a metal ion stressor. Most importantly, the pathogen's virulence was markedly attenuated in wheat stem base infections following <i>FpTox2</i> deletion, and we demonstrated that <i>FpTox2</i> regulates pathogen virulence by influencing deoxynivalenol production. In conclusion, <i>FpTox2</i> is crucial for vegetative growth, asexual development, abiotic stress responses, and full virulence in <i>F. pseudograminearum</i>.</p>","PeriodicalId":10839,"journal":{"name":"Current Issues in Molecular Biology","volume":"47 9","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12468165/pdf/","citationCount":"0","resultStr":"{\"title\":\"The TOX2 Gene Is Responsible for Conidiation and Full Virulence in <i>Fusarium pseudograminearum</i>.\",\"authors\":\"Sen Han, Shaobo Zhao, Yajiao Wang, Qiusheng Li, Mengwei Sun, Lingxiao Kong, Xianghong Chen, Jianhai Gao, Yuxing Wu\",\"doi\":\"10.3390/cimb47090714\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fusarium crown rot, a widespread and destructive disease affecting cereal crops (particularly wheat and barley), is primarily caused by the soil-borne fungal pathogen <i>Fusarium pseudograminearum</i>. Secondary metabolites (SMs) play a crucial role in colonization and host tissue invasion by pathogenic fungi. In this study, we investigated the functional role of <i>FpTox2</i>, a secondary metabolite-related gene in <i>F. pseudograminearum</i>. An <i>FpTox2</i> deletion mutant exhibited significantly reduced radial growth compared to wild-type <i>F. pseudograminearum</i>. Notably, the mutant strain completely lost conidiation capacity under induced conditions. Furthermore, although it showed decreased sensitivity to the cell membrane inhibitor sodium dodecyl sulfate (SDS), the mutant demonstrated enhanced susceptibility to NaCl, a metal ion stressor. Most importantly, the pathogen's virulence was markedly attenuated in wheat stem base infections following <i>FpTox2</i> deletion, and we demonstrated that <i>FpTox2</i> regulates pathogen virulence by influencing deoxynivalenol production. In conclusion, <i>FpTox2</i> is crucial for vegetative growth, asexual development, abiotic stress responses, and full virulence in <i>F. pseudograminearum</i>.</p>\",\"PeriodicalId\":10839,\"journal\":{\"name\":\"Current Issues in Molecular Biology\",\"volume\":\"47 9\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12468165/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Issues in Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/cimb47090714\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Issues in Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/cimb47090714","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
The TOX2 Gene Is Responsible for Conidiation and Full Virulence in Fusarium pseudograminearum.
Fusarium crown rot, a widespread and destructive disease affecting cereal crops (particularly wheat and barley), is primarily caused by the soil-borne fungal pathogen Fusarium pseudograminearum. Secondary metabolites (SMs) play a crucial role in colonization and host tissue invasion by pathogenic fungi. In this study, we investigated the functional role of FpTox2, a secondary metabolite-related gene in F. pseudograminearum. An FpTox2 deletion mutant exhibited significantly reduced radial growth compared to wild-type F. pseudograminearum. Notably, the mutant strain completely lost conidiation capacity under induced conditions. Furthermore, although it showed decreased sensitivity to the cell membrane inhibitor sodium dodecyl sulfate (SDS), the mutant demonstrated enhanced susceptibility to NaCl, a metal ion stressor. Most importantly, the pathogen's virulence was markedly attenuated in wheat stem base infections following FpTox2 deletion, and we demonstrated that FpTox2 regulates pathogen virulence by influencing deoxynivalenol production. In conclusion, FpTox2 is crucial for vegetative growth, asexual development, abiotic stress responses, and full virulence in F. pseudograminearum.
期刊介绍:
Current Issues in Molecular Biology (CIMB) is a peer-reviewed journal publishing review articles and minireviews in all areas of molecular biology and microbiology. Submitted articles are subject to an Article Processing Charge (APC) and are open access immediately upon publication. All manuscripts undergo a peer-review process.