游离氨梯度分布下微生物群落的集结过程和共生网络

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-07-26 DOI:10.1128/spectrum.01051-24
Shengjie Sun, Zhiyi Qiao, Kexin Sun, Da Huo
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引用次数: 0

摘要

微生物种类繁多,数量巨大,是水生生态系统的重要组成部分。它们对维持生态服务,尤其是维持基本的生物地球化学循环至关重要。近年来,由于人类活动的增加,水生生态系统中过剩的含氮污染物大幅增加。过量的氮污染物排放导致游离氨(FA,NH3)水平升高,引起了水生生态系统的显著波动,导致水体富营养化和各种生态挑战。这些波动对水生生态系统中微生物群落的影响尚未得到广泛研究。本研究采用 16S rRNA 基因扩增子测序技术,系统研究了中国滦河引水工程中微生物群落及其亚群落(丰富、中等和稀少)的动态、共现网络和组装过程。我们的研究结果表明,NH3 浓度对微生物群落的动态变化有显著影响,在 NH3 浓度较高的条件下,群落丰富度和系统发育距离明显下降,同时群落差异性增加。分析表明,某些微生物群落,尤其是放线菌群,在 NH3 水平升高的环境中明显更为普遍,这表明它们对 NH3 压力具有潜在的恢复力或适应性反应。此外,通过共现网络分析,我们观察到了网络拓扑结构的动态变化以及在 NH3 压力下连接性的增加。被确定为连接者和模块枢纽的关键节点在维持网络结构方面发挥了至关重要的作用,尤其是蓝藻和放线菌群。此外,随机过程,尤其是漂移和扩散限制,也是形成微生物群落的主要因素。在三个亚群落中,漂移的影响越来越明显,而扩散限制的影响则越来越小。总之,阐明暴露于 NH3 的水生生态系统中微生物群落的动态变化,可以加深我们对微生物群落生态机制的理解,并为保护微生物群落多样性和生态功能提供新的见解:本文介绍的研究探讨了不同浓度的游离氨如何影响水生生态系统中的微生物群落。通过采用先进的基因测序技术,该研究揭示了微生物多样性和网络结构随着氨含量的增加而发生的显著变化。主要发现表明,高浓度氨氮会导致微生物丰富度和多样性下降,同时增加群落的差异性。值得注意的是,某些微生物群落,如放线菌,对氨压力表现出了恢复能力。这项研究加深了我们对污染如何影响微生物生态系统的理解,并强调了维持氨水平平衡对保护微生物多样性和生态系统健康的重要性。
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Assembly process and co-occurrence network of microbial community in response to free ammonia gradient distribution.

Microorganisms are crucial components of the aquatic ecosystem due to their immense diversity and abundance. They are vital in sustaining ecological services, especially in maintaining essential biogeochemical cycles. Recent years have seen a substantial increase in surplus nitrogenous pollutants in aquatic ecosystems due to the heightened occurrence of anthropogenic activities. Elevated levels of free ammonia (FA, NH3), stemming from the discharge of excess nitrogenous pollutants, have caused notable fluctuations in aquatic ecosystems, leading to water eutrophication and various ecological challenges. The impact of these oscillations on microbial communities in aquatic ecosystems has not been extensively studied. This study employed 16S rRNA gene amplicon sequencing to systematically investigate the dynamics, co-occurrence networks, and assembly processes of microbial communities and their subcommunities (abundant, moderate, and rare) in the Luanhe River Diversion Project in China. Our findings indicate that NH3 concentration significantly influences the dynamics of microbial communities, with a notable decrease in community Richness and Phylogenetic Distance alongside increased community dissimilarity under higher NH3 conditions. The analysis revealed that certain microbial groups, particularly Actinobacteriaota, were notably more prevalent in environments with elevated NH3 levels, suggesting their potential resilience or adaptive responses to NH3 stress. Additionally, through co-occurrence network analysis, we observed dynamic changes in network topology and increased connectedness under NH3 stress. Key nodes, identified as connectors and module hubs, played crucial roles in maintaining network structure, particularly Cyanobacteria and Actinobacteriaota. Furthermore, stochastic processes, particularly drift and dispersal limitation, predominantly shaped the microbial communities. Within the three subcommunities, the impact of drift became more pronounced as the effect of dispersal limitation diminished. Overall, elucidating the dynamics of microbial communities in aquatic ecosystems exposed to NH3 can enhance our comprehension of the ecological mechanisms of microbial communities and provide new insights into the conservation of microbial community diversity and ecological functions.

Importance: The research presented in this paper explores how varying concentrations of free ammonia impact microbial communities in aquatic ecosystems. By employing advanced gene sequencing techniques, the study reveals significant changes in microbial diversity and network structures in response to increased ammonia levels. Key findings indicate that high ammonia concentrations lead to a decrease in microbial richness and diversity while increasing community dissimilarity. Notably, certain microbial groups, like Actinobacteria, show resilience to ammonia stress. This research enhances our understanding of how pollution affects microbial ecosystems and underscores the importance of maintaining balanced ammonia levels to preserve microbial diversity and ecosystem health.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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