区室特异性微生物群落强调真菌在亚热带海草生态系统中的生态作用。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-07-23 Epub Date: 2025-07-02 DOI:10.1128/aem.00606-25
Xiao Wang, Jiawei Chen, Sangwook Lee, Zhicheng Ju, Anirban Akhand, Hongbin Liu
{"title":"区室特异性微生物群落强调真菌在亚热带海草生态系统中的生态作用。","authors":"Xiao Wang, Jiawei Chen, Sangwook Lee, Zhicheng Ju, Anirban Akhand, Hongbin Liu","doi":"10.1128/aem.00606-25","DOIUrl":null,"url":null,"abstract":"<p><p>Plant-associated compartments provide habitats for various microbes. Seagrasses are the only submerged marine angiosperms. However, the simultaneous investigation of fungi and prokaryotes inhabiting different seagrass-associated compartments is limited, and much remains to be learned about the functional roles of seagrass fungi. We examined the diversity, composition, and networks of fungal and prokaryotic communities in multiple compartments associated with the seagrass <i>Halophila ovalis</i> to shed light on the significance of fungi in the seagrass ecosystem. Seagrass compartments primarily differentiated the microbial communities. Notably, the root and rhizome tissues of visually healthy <i>H. ovalis</i> exhibited a very narrow, single-species dominated and enriched fungal spectrum, leading us to hypothesize the possible establishment of a symbiotic relationship between the Lulworthiaceae mycobiont, <i>Halophilomyces hongkongensis</i>, and the seagrass host. In addition, the Vibrionaceae family, represented by the genus <i>Vibrio</i>, emerged as the most abundant prokaryotic taxon enriched in the roots/rhizomes, showing exclusive positive correlations with <i>H. hongkongensis</i> within the tissues, implying a cross-kingdom reciprocal interaction between these taxa in the endosphere of <i>H. ovalis</i>. Fungal-prokaryotic interdomain network analysis identified <i>H. hongkongensis</i> as a keystone taxon, essential for coordinating microbial interactions in <i>H. ovalis</i>-associated compartments, while robustness analysis of interdomain networks suggested fungi plays a more crucial role in sustaining the network structures of <i>H. ovalis</i> inner tissues compared to surrounding compartments. These findings provide valuable insights into the seagrass-fungi relationship and emphasize the importance of fungi in the seagrass ecosystem.IMPORTANCEAlthough plant-associated microbes are key determinants of plant health, fitness, and stress resilience, microbial communities associated with seagrasses remain poorly understood compared to those in land plants, particularly concerning the diversity and ecological roles of their fungal associates. Our work provides a comprehensive assessment of fungal and prokaryotic communities across multiple above- and below-ground compartments associated with <i>Halophila ovalis</i>, the most widespread seagrass species in Hong Kong, through a year-round sampling. Our findings reveal compartment-specific patterns in diversity, network topology, and stability of microbial communities, highlighting the critical roles of fungi in seagrass-associated microbial networks and advancing our understanding of plant-fungal interactions in the marine environment.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0060625"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12285264/pdf/","citationCount":"0","resultStr":"{\"title\":\"Compartment-specific microbial communities highlight the ecological roles of fungi in a subtropical seagrass ecosystem.\",\"authors\":\"Xiao Wang, Jiawei Chen, Sangwook Lee, Zhicheng Ju, Anirban Akhand, Hongbin Liu\",\"doi\":\"10.1128/aem.00606-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plant-associated compartments provide habitats for various microbes. Seagrasses are the only submerged marine angiosperms. However, the simultaneous investigation of fungi and prokaryotes inhabiting different seagrass-associated compartments is limited, and much remains to be learned about the functional roles of seagrass fungi. We examined the diversity, composition, and networks of fungal and prokaryotic communities in multiple compartments associated with the seagrass <i>Halophila ovalis</i> to shed light on the significance of fungi in the seagrass ecosystem. Seagrass compartments primarily differentiated the microbial communities. Notably, the root and rhizome tissues of visually healthy <i>H. ovalis</i> exhibited a very narrow, single-species dominated and enriched fungal spectrum, leading us to hypothesize the possible establishment of a symbiotic relationship between the Lulworthiaceae mycobiont, <i>Halophilomyces hongkongensis</i>, and the seagrass host. In addition, the Vibrionaceae family, represented by the genus <i>Vibrio</i>, emerged as the most abundant prokaryotic taxon enriched in the roots/rhizomes, showing exclusive positive correlations with <i>H. hongkongensis</i> within the tissues, implying a cross-kingdom reciprocal interaction between these taxa in the endosphere of <i>H. ovalis</i>. Fungal-prokaryotic interdomain network analysis identified <i>H. hongkongensis</i> as a keystone taxon, essential for coordinating microbial interactions in <i>H. ovalis</i>-associated compartments, while robustness analysis of interdomain networks suggested fungi plays a more crucial role in sustaining the network structures of <i>H. ovalis</i> inner tissues compared to surrounding compartments. These findings provide valuable insights into the seagrass-fungi relationship and emphasize the importance of fungi in the seagrass ecosystem.IMPORTANCEAlthough plant-associated microbes are key determinants of plant health, fitness, and stress resilience, microbial communities associated with seagrasses remain poorly understood compared to those in land plants, particularly concerning the diversity and ecological roles of their fungal associates. Our work provides a comprehensive assessment of fungal and prokaryotic communities across multiple above- and below-ground compartments associated with <i>Halophila ovalis</i>, the most widespread seagrass species in Hong Kong, through a year-round sampling. Our findings reveal compartment-specific patterns in diversity, network topology, and stability of microbial communities, highlighting the critical roles of fungi in seagrass-associated microbial networks and advancing our understanding of plant-fungal interactions in the marine environment.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":\" \",\"pages\":\"e0060625\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-07-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12285264/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.00606-25\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/2 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.00606-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/2 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

植物相关的隔室为各种微生物提供栖息地。海草是唯一的水下被子植物。然而,真菌和原核生物同时居住在不同的海草相关室室的研究是有限的,关于海草真菌的功能作用还有很多需要了解。为了揭示真菌在海草生态系统中的重要意义,我们研究了与Halophila ovalis相关的多个室室真菌和原核生物群落的多样性、组成和网络。海草区室主要区分微生物群落。值得注意的是,视觉健康的卵圆螺杆菌的根和根茎组织显示出一个非常狭窄的、单种优势的和丰富的真菌谱,这使我们假设Lulworthiaceae真菌、香港嗜盐菌和海草宿主之间可能建立了共生关系。此外,以弧菌属为代表的弧菌科(Vibrionaceae)是根/根状茎中含量最多的原核生物分类群,与H. hongkongensis在组织内呈排他正相关,表明这些分类群在卵圆桃的内球层中存在着跨界的相互作用。真菌-原核生物结构域间网络分析表明,H. hongkongensis是协调卵圆虫相关区室中微生物相互作用的关键分类单元,而结构域间网络的鲁棒性分析表明,真菌在维持卵圆虫内部组织的网络结构方面起着比周围区室更重要的作用。这些发现为海草与真菌的关系提供了有价值的见解,并强调了真菌在海草生态系统中的重要性。尽管植物相关微生物是植物健康、适应性和抗逆性的关键决定因素,但与陆地植物相比,与海草相关的微生物群落仍然知之甚少,特别是关于其真菌伴生物的多样性和生态作用。我们的工作提供了一个全面的评估真菌和原核生物群落在多个地上和地下隔室与Halophila ovalis有关,Halophila ovalis是香港最广泛的海草物种,通过全年采样。我们的研究结果揭示了微生物群落多样性、网络拓扑结构和稳定性的区室特异性模式,突出了真菌在海草相关微生物网络中的关键作用,并推进了我们对海洋环境中植物-真菌相互作用的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Compartment-specific microbial communities highlight the ecological roles of fungi in a subtropical seagrass ecosystem.

Plant-associated compartments provide habitats for various microbes. Seagrasses are the only submerged marine angiosperms. However, the simultaneous investigation of fungi and prokaryotes inhabiting different seagrass-associated compartments is limited, and much remains to be learned about the functional roles of seagrass fungi. We examined the diversity, composition, and networks of fungal and prokaryotic communities in multiple compartments associated with the seagrass Halophila ovalis to shed light on the significance of fungi in the seagrass ecosystem. Seagrass compartments primarily differentiated the microbial communities. Notably, the root and rhizome tissues of visually healthy H. ovalis exhibited a very narrow, single-species dominated and enriched fungal spectrum, leading us to hypothesize the possible establishment of a symbiotic relationship between the Lulworthiaceae mycobiont, Halophilomyces hongkongensis, and the seagrass host. In addition, the Vibrionaceae family, represented by the genus Vibrio, emerged as the most abundant prokaryotic taxon enriched in the roots/rhizomes, showing exclusive positive correlations with H. hongkongensis within the tissues, implying a cross-kingdom reciprocal interaction between these taxa in the endosphere of H. ovalis. Fungal-prokaryotic interdomain network analysis identified H. hongkongensis as a keystone taxon, essential for coordinating microbial interactions in H. ovalis-associated compartments, while robustness analysis of interdomain networks suggested fungi plays a more crucial role in sustaining the network structures of H. ovalis inner tissues compared to surrounding compartments. These findings provide valuable insights into the seagrass-fungi relationship and emphasize the importance of fungi in the seagrass ecosystem.IMPORTANCEAlthough plant-associated microbes are key determinants of plant health, fitness, and stress resilience, microbial communities associated with seagrasses remain poorly understood compared to those in land plants, particularly concerning the diversity and ecological roles of their fungal associates. Our work provides a comprehensive assessment of fungal and prokaryotic communities across multiple above- and below-ground compartments associated with Halophila ovalis, the most widespread seagrass species in Hong Kong, through a year-round sampling. Our findings reveal compartment-specific patterns in diversity, network topology, and stability of microbial communities, highlighting the critical roles of fungi in seagrass-associated microbial networks and advancing our understanding of plant-fungal interactions in the marine environment.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信