Community organization and network complexity and stability: contrasting strategies of prokaryotic versus eukaryotic microbiomes in the Bohai Sea and Yellow Sea.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2024-09-25 Epub Date: 2024-08-13 DOI:10.1128/msphere.00395-24
Xiaoxiao Wang, Hualong Wang, Yantao Liang, Andrew McMinn, Min Wang
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引用次数: 0

Abstract

Unraveling the effects of spatial gradients on microbiome assembly and association is a challenging topic that remains understudied in the coastal ecosystem. Here, we aimed to investigate the effects of spatial variation on the network complexity and stability of plankton microbiomes in the Bohai Sea and Yellow Sea. These seas serve as spawning and nursery grounds for economically important fisheries valued at billions of dollars annually. Environmental heterogeneity structures microbial communities into distinct spatial patterns, leading to complex direct/indirect relationships and broader ecological niches of bacterioplankton compared to microeukaryotic communities. Interestingly, salinity gradients positively influenced the richness of rare subgroups of bacterioplankton, while the rare microeukaryotic subgroups showed an opposite trend. Abundant subgroups of prokaryotic/eukaryotic microbiomes exhibited greater environmental niche breadth and lower phylogenetic distance compared to the rare subgroups. Stochastic processes contributed greatly to microbiome dynamics, and deterministic processes governed the bacterioplankton organization with a lower phylogenetic turnover rate. Compared to microeukaryotes, bacterioplankton exhibit higher network modularity, complexity, and robustness and lower fragmentation, and vulnerability. These observations offer vital insights into the anti-interference ability and resistance of plankton microbiomes in response to environmental gradients in terms of organization and survival strategy as well as their adaptability to environmental disturbances.IMPORTANCEAn in-depth understanding of community organization and stability of coastal microbiomes is crucial to determining the sustainability of marine ecosystems, such as the Bohai Sea and Yellow Sea. Distinct responses between prokaryotic and eukaryotic microbiomes to spatial heterogeneity were observed in terms of geographical distribution, phylogenetic distance, niche breadth, and community assembly process. Environmental variations are significantly correlated with the dynamics of rare eukaryotic plankton subcommunities compared to prokaryotic plankton subcommunities. Deterministic processes shaped prokaryotic plankton community organization with a lower phylogenic turnover rate. Rare subgroups had noticeably higher phylogenetic distance and lower niche breadth than the corresponding abundant subgroups. Prokaryotic microbiomes had higher molecular network complexity and stability compared to microeukaryotes. Results presented here show how environmental gradients alter both the geographical characteristics of the microbial organization in coastal seas and also their co-occurrence network complexity and stability and thus have critical implications for nutrient and energy cycling.

群落组织与网络的复杂性和稳定性:渤海和黄海中原核与真核微生物群落的对比策略。
揭示空间梯度对微生物组组装和关联的影响是一个具有挑战性的课题,在沿岸生态系统中的研究仍然不足。在此,我们旨在研究空间变化对渤海和黄海浮游生物微生物组网络复杂性和稳定性的影响。这些海域是每年价值数十亿美元的重要渔业产卵和育苗场。环境异质性将微生物群落构造成不同的空间模式,导致复杂的直接/间接关系,与微真核细胞群落相比,浮游细菌的生态位更为宽泛。有趣的是,盐度梯度对稀有浮游细菌亚群的丰富程度产生了积极影响,而稀有微真核细胞亚群则呈现出相反的趋势。与稀有亚群相比,原核/真核微生物群的丰富亚群表现出更大的环境生态位广度和更低的系统发育距离。随机过程对微生物群的动态变化贡献很大,而确定性过程则以较低的系统发育更替率控制着浮游细菌的组织。与微真核细胞相比,浮游细菌表现出更高的网络模块性、复杂性和稳健性,以及更低的破碎性和脆弱性。这些观察结果为了解浮游生物微生物组在组织和生存策略方面的抗干扰能力和对环境梯度的抵抗力,以及对环境干扰的适应性提供了重要启示。 重要意义 深入了解沿海微生物组的群落组织和稳定性,对于确定渤海和黄海等海洋生态系统的可持续性至关重要。在地理分布、系统发育距离、生态位广度和群落组装过程等方面,观察到原核微生物群落和真核微生物群落对空间异质性的不同反应。与原核生物浮游生物亚群落相比,环境变化与稀有真核生物浮游生物亚群落的动态密切相关。决定性过程塑造了原核浮游生物群落组织,其系统更替率较低。与相应的丰富亚群相比,稀有亚群的系统发育距离明显较高,生态位广度较低。与微真核细胞相比,原核微生物群具有更高的分子网络复杂性和稳定性。本文的研究结果表明,环境梯度既改变了近岸海域微生物组织的地理特征,也改变了它们共生网络的复杂性和稳定性,从而对营养和能量循环产生了重要影响。
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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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