Yunshi Li, Na Qu, Shuang Li, Huaizhe Zhou, Ming Yue
{"title":"Ecological mechanisms of microbial assembly in clonal plant <i>Glechoma longituba</i>: from soil to endosphere.","authors":"Yunshi Li, Na Qu, Shuang Li, Huaizhe Zhou, Ming Yue","doi":"10.1128/aem.00336-25","DOIUrl":null,"url":null,"abstract":"<p><p>Climate change presents significant challenges to plant growth and reproduction. Clonal plants, with low genetic diversity, are particularly vulnerable due to their limited adaptive capacity. Plant-associated microbiomes can play a crucial role in enhancing clonal plant survival and adaptability, yet the mechanisms governing microbial community assembly along the soil-episphere-endosphere continuum remain unclear. In this study, we investigated microbial community assembly patterns in the clonal plant <i>Glechoma longituba</i>. Our findings demonstrate that the assembly of microbial communities is primarily driven by host-related factors rather than external environmental filtering. First, host selection reduced α-diversity and network complexity while increasing β-diversity and community stability. Second, the mechanisms of microbial assembly transitioned from stochastic dominance in bulk soil and epiphytic compartments to deterministic processes within endophytic niches. Third, the taxonomic structure exhibited significant turnover along the soil-episphere-endosphere continuum, accompanied by functional redundancy to maintain ecosystem functions. The results support the hypothesis that host selection optimizes the functional composition of microbial communities by reducing diversity and network complexity while ensuring the stability of key functional microorganisms. The study emphasizes the critical role of host-microbe interactions in sustaining the adaptive and functional advantages of clonal plants, offering insights into managing sustainable plant communities under climate change.IMPORTANCEThis study highlights the vital role of plant-associated microbiomes in helping clonal plants, which have low genetic diversity, adapt to climate change. By examining the clonal plant <i>Glechoma longituba</i>, the research reveals that the plant itself plays a key role in shaping its microbial communities, rather than external environmental factors. Host selection simplifies microbial diversity and network complexity but enhances community stability and functional efficiency. These findings suggest that clonal plants can optimize their microbiomes to maintain critical functions. This work provides valuable insights into how plants and microbes interact to improve resilience, offering potential strategies for managing plant communities in a changing climate. By understanding these mechanisms, we can better support sustainable ecosystems and agricultural practices in the face of global environmental challenges.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0033625"},"PeriodicalIF":3.9000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.00336-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Climate change presents significant challenges to plant growth and reproduction. Clonal plants, with low genetic diversity, are particularly vulnerable due to their limited adaptive capacity. Plant-associated microbiomes can play a crucial role in enhancing clonal plant survival and adaptability, yet the mechanisms governing microbial community assembly along the soil-episphere-endosphere continuum remain unclear. In this study, we investigated microbial community assembly patterns in the clonal plant Glechoma longituba. Our findings demonstrate that the assembly of microbial communities is primarily driven by host-related factors rather than external environmental filtering. First, host selection reduced α-diversity and network complexity while increasing β-diversity and community stability. Second, the mechanisms of microbial assembly transitioned from stochastic dominance in bulk soil and epiphytic compartments to deterministic processes within endophytic niches. Third, the taxonomic structure exhibited significant turnover along the soil-episphere-endosphere continuum, accompanied by functional redundancy to maintain ecosystem functions. The results support the hypothesis that host selection optimizes the functional composition of microbial communities by reducing diversity and network complexity while ensuring the stability of key functional microorganisms. The study emphasizes the critical role of host-microbe interactions in sustaining the adaptive and functional advantages of clonal plants, offering insights into managing sustainable plant communities under climate change.IMPORTANCEThis study highlights the vital role of plant-associated microbiomes in helping clonal plants, which have low genetic diversity, adapt to climate change. By examining the clonal plant Glechoma longituba, the research reveals that the plant itself plays a key role in shaping its microbial communities, rather than external environmental factors. Host selection simplifies microbial diversity and network complexity but enhances community stability and functional efficiency. These findings suggest that clonal plants can optimize their microbiomes to maintain critical functions. This work provides valuable insights into how plants and microbes interact to improve resilience, offering potential strategies for managing plant communities in a changing climate. By understanding these mechanisms, we can better support sustainable ecosystems and agricultural practices in the face of global environmental challenges.
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.