{"title":"Decoupling Responses of Phyllosphere and Rhizosphere Bacterial Communities to Spatiotemporal Environmental Changes","authors":"Wei Chen, Biao Zhu, Caiqin Yang, Chunqiang Wei, Yifan He, Long Zheng, Xiaoyan Liu, Jingyuan Yang, Leho Tedersoo, Xinmin Lu, Rutger A. Wilschut","doi":"10.1111/gcb.70175","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Understanding and predicting how plant-associated microbes respond to environmental changes is of key importance to understanding future plant performance. Yet, how aboveground and belowground plant-associated microbial communities, which may interactively affect plant performance, simultaneously respond to environmental changes, remains unknown. To fill this gap, we monitored temporal changes of phyllosphere and rhizosphere bacterial communities of three perennial species at 18 sites spanning a 1500 m elevational gradient. We showed distinct temporal trajectories of these community types, likely reflecting their differential responses to abiotic (e.g., air moisture) and biotic (e.g., plant specific leaf area) environmental factors. Further, using a transplantation experiment with the same plant species and their rhizosphere soils, we show that a portion of bacterial taxa from transplanted communities persisted in plants' rhizosphere 2 months after being transplanted to warmer sites. In contrast, phyllosphere communities were primarily harbored by taxa colonizing from local communities. Notably, the relative growth rate of transplanted plants at new versus original sites was positively correlated with the compositional dissimilarity between their phyllosphere and rhizosphere bacterial communities. Together, our results highlight the role of compartment-by-environment interactions in shaping the plant holobiome communities and emphasize the need to understand the impacts of such interactions on plant performance under global change.</p>\n </div>","PeriodicalId":175,"journal":{"name":"Global Change Biology","volume":"31 4","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global Change Biology","FirstCategoryId":"93","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gcb.70175","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIODIVERSITY CONSERVATION","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding and predicting how plant-associated microbes respond to environmental changes is of key importance to understanding future plant performance. Yet, how aboveground and belowground plant-associated microbial communities, which may interactively affect plant performance, simultaneously respond to environmental changes, remains unknown. To fill this gap, we monitored temporal changes of phyllosphere and rhizosphere bacterial communities of three perennial species at 18 sites spanning a 1500 m elevational gradient. We showed distinct temporal trajectories of these community types, likely reflecting their differential responses to abiotic (e.g., air moisture) and biotic (e.g., plant specific leaf area) environmental factors. Further, using a transplantation experiment with the same plant species and their rhizosphere soils, we show that a portion of bacterial taxa from transplanted communities persisted in plants' rhizosphere 2 months after being transplanted to warmer sites. In contrast, phyllosphere communities were primarily harbored by taxa colonizing from local communities. Notably, the relative growth rate of transplanted plants at new versus original sites was positively correlated with the compositional dissimilarity between their phyllosphere and rhizosphere bacterial communities. Together, our results highlight the role of compartment-by-environment interactions in shaping the plant holobiome communities and emphasize the need to understand the impacts of such interactions on plant performance under global change.
期刊介绍:
Global Change Biology is an environmental change journal committed to shaping the future and addressing the world's most pressing challenges, including sustainability, climate change, environmental protection, food and water safety, and global health.
Dedicated to fostering a profound understanding of the impacts of global change on biological systems and offering innovative solutions, the journal publishes a diverse range of content, including primary research articles, technical advances, research reviews, reports, opinions, perspectives, commentaries, and letters. Starting with the 2024 volume, Global Change Biology will transition to an online-only format, enhancing accessibility and contributing to the evolution of scholarly communication.