{"title":"在拟南芥中,宿主介导的根系内生菌-病原体竞争使真菌无症状定植成为可能。","authors":"Kei Hiruma, Kuldanai Pathompitaknukul, Hiroyuki Tanaka, Yuki Iwaguchi, Shunsuke Miyashima, Nanami Kawamura, Atsushi Toyoda, Takehiko Itoh, Yusuke Saijo","doi":"10.1093/pcp/pcaf126","DOIUrl":null,"url":null,"abstract":"<p><p>Seed plants frequently accommodate pathogenic microbes without showing disease symptoms. However, the mechanisms preventing disease progression within the host remain poorly understood. Here, we reveal a root-colonizing endophytic fungus, Colletotrichum fructicola (designated CfE), and a closely related pathogen, C. gloeosporioides (CgP), from asymptomatic field-grown Brassicaceae plants. In Arabidopsis thaliana, CgP grows hyphae into the central cylinder of the root and causes necrosis, an outcome that is effectively suppressed in the presence of CfE co-colonization. Transcriptome analyses of roots inoculated individually and simultaneously with CfE and CgP revealed over 700 CfE genes specifically induced during co-inoculation, while the extent of reprogramming in the host transcriptome was much less pronounced. These induced genes were enriched in secondary metabolism pathways, suggesting that CfE suppresses pathogenic fungal growth through the production of antifungal metabolites. Moreover, the endophytic colonization and host-protective function of CfE depend on host-derived tryptophan-based antimicrobial metabolites. Our findings highlight a critical role for fungus-fungus competition, mediated by anti-microbial metabolites and potentially orchestrated by the host, in enabling asymptomatic colonization and maintaining plant health.</p>","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Host-mediated endophyte-pathogen competition in roots enables asymptomatic fungal colonization in Arabidopsis thaliana.\",\"authors\":\"Kei Hiruma, Kuldanai Pathompitaknukul, Hiroyuki Tanaka, Yuki Iwaguchi, Shunsuke Miyashima, Nanami Kawamura, Atsushi Toyoda, Takehiko Itoh, Yusuke Saijo\",\"doi\":\"10.1093/pcp/pcaf126\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Seed plants frequently accommodate pathogenic microbes without showing disease symptoms. However, the mechanisms preventing disease progression within the host remain poorly understood. Here, we reveal a root-colonizing endophytic fungus, Colletotrichum fructicola (designated CfE), and a closely related pathogen, C. gloeosporioides (CgP), from asymptomatic field-grown Brassicaceae plants. In Arabidopsis thaliana, CgP grows hyphae into the central cylinder of the root and causes necrosis, an outcome that is effectively suppressed in the presence of CfE co-colonization. Transcriptome analyses of roots inoculated individually and simultaneously with CfE and CgP revealed over 700 CfE genes specifically induced during co-inoculation, while the extent of reprogramming in the host transcriptome was much less pronounced. These induced genes were enriched in secondary metabolism pathways, suggesting that CfE suppresses pathogenic fungal growth through the production of antifungal metabolites. Moreover, the endophytic colonization and host-protective function of CfE depend on host-derived tryptophan-based antimicrobial metabolites. Our findings highlight a critical role for fungus-fungus competition, mediated by anti-microbial metabolites and potentially orchestrated by the host, in enabling asymptomatic colonization and maintaining plant health.</p>\",\"PeriodicalId\":20575,\"journal\":{\"name\":\"Plant and Cell Physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant and Cell Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/pcp/pcaf126\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant and Cell Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/pcp/pcaf126","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Host-mediated endophyte-pathogen competition in roots enables asymptomatic fungal colonization in Arabidopsis thaliana.
Seed plants frequently accommodate pathogenic microbes without showing disease symptoms. However, the mechanisms preventing disease progression within the host remain poorly understood. Here, we reveal a root-colonizing endophytic fungus, Colletotrichum fructicola (designated CfE), and a closely related pathogen, C. gloeosporioides (CgP), from asymptomatic field-grown Brassicaceae plants. In Arabidopsis thaliana, CgP grows hyphae into the central cylinder of the root and causes necrosis, an outcome that is effectively suppressed in the presence of CfE co-colonization. Transcriptome analyses of roots inoculated individually and simultaneously with CfE and CgP revealed over 700 CfE genes specifically induced during co-inoculation, while the extent of reprogramming in the host transcriptome was much less pronounced. These induced genes were enriched in secondary metabolism pathways, suggesting that CfE suppresses pathogenic fungal growth through the production of antifungal metabolites. Moreover, the endophytic colonization and host-protective function of CfE depend on host-derived tryptophan-based antimicrobial metabolites. Our findings highlight a critical role for fungus-fungus competition, mediated by anti-microbial metabolites and potentially orchestrated by the host, in enabling asymptomatic colonization and maintaining plant health.
期刊介绍:
Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels.
Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.