Variable phylosymbiosis and cophylogeny patterns in wild fish gut microbiota of a large subtropical river.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-03-28 DOI:10.1128/msphere.00982-24
Yaqiu Liu, Xinhui Li, Konstantinos Ar Kormas, Yuefei Li, Huifeng Li, Jie Li
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引用次数: 0

Abstract

The persistence and specificity of fish host-microbial interaction during evolution is an important part of exploring the host-microbial symbiosis mechanism. However, it remains unclear how the environmental and host factors shape fish host-microbe symbiotic relationships in subtropical rivers with complex natural environments. Freshwater fish are important consumers in rivers and lakes and are considered keystone species in maintaining the stability of food webs there. In this study, patterns and mechanisms shaping gut microbiota community in 42 fish species from the Pearl River, in the subtropical zone of China, were investigated. The results showed that fish host specificity is a key driver of gut microbiota evolution and diversification. Different taxonomic levels of the host showed different degrees of contribution to gut microbiota variation. Geographical location and habitat type were the next most important factors in shaping gut microbiota across the 42 fishes, followed by diet and gut trait. Our results emphasized the contribution of stochastic processes (drift and homogenizing dispersal) in the gut microbial community assembly of freshwater fishes in the middle and lower reaches of the Pearl River. Phylosymbiosis is evident at both global and local levels, which are jointly shaped by complex factors including ecological or host physiological filtration and evolutionary processes. The core microbiota showed co-evolutionary relationships of varying degrees with different taxonomic groups. We speculate that host genetic isolation or habitat variation facilitates the heterogeneous selection (deterministic process), which occurs and results in different host-core bacterium specificity.

Importance: Freshwater fish are regarded as the dominant consumers in rivers and lakes. Due to their diverse feeding modes, fish significantly enhance the trophic link and nutrient recycling/retention in aquatic habitats. For this, they are often considered keystone species in maintaining the stability of food webs in rivers and lakes. A significant part of fish nutrition is essentially mediated by their gut microbiota, which can enhance fish tolerance to fluctuations in external resources and improve the efficiency of nutrients extracted from various food sources. As gut bacterial symbionts have a profound impact on the nutrition and development of their hosts, as well as their overall fitness, it is critical to answer the question of how hosts maintain these benefits by procuring or inheriting these vital symbionts, which is still largely unanswered, especially for freshwater fish. Our study provides new insights into the co-evolutionary relationship between wild fish and their symbiotic microbiome, the hidden diversity of gut microbiome, and the ecological adaptation potential of wild freshwater fish.

亚热带大河野生鱼类肠道微生物群的不同系统共生和共生体发育模式。
鱼类宿主-微生物相互作用在进化过程中的持续性和特异性是探索宿主-微生物共生机制的重要组成部分。然而,在自然环境复杂的亚热带河流中,环境和宿主因素如何影响鱼类宿主-微生物的共生关系尚不清楚。淡水鱼是河流和湖泊的重要消费者,被认为是维持食物网稳定的关键物种。本研究对中国亚热带珠江流域42种鱼类肠道微生物群落的形成模式和机制进行了研究。结果表明,鱼类宿主特异性是肠道微生物群进化和多样化的关键驱动因素。不同的寄主分类水平对肠道菌群变异的贡献程度不同。地理位置和栖息地类型是影响42种鱼类肠道微生物群的第二重要因素,其次是饮食和肠道特征。我们的研究结果强调了随机过程(漂移和均质扩散)在珠江中下游淡水鱼肠道微生物群落聚集中的作用。系统共生在全球和局部层面都很明显,这是由生态或宿主生理过滤和进化过程等复杂因素共同形成的。核心微生物群与不同分类类群表现出不同程度的共同进化关系。我们推测宿主的遗传隔离或栖息地的变化促进了异质选择(确定性过程),这种选择发生并导致不同的宿主-核心细菌特异性。重要性:淡水鱼被认为是河流和湖泊中主要的消费者。鱼类因其多样化的摄食方式,显著增强了水生生境的营养联系和养分循环/保留。因此,它们通常被认为是维持河流和湖泊食物网稳定的关键物种。鱼类营养的很大一部分本质上是由肠道菌群介导的,肠道菌群可以增强鱼类对外部资源波动的耐受性,提高从各种食物来源中提取的营养物质的效率。肠道细菌共生体对宿主的营养和发育及其整体健康有着深远的影响,因此,宿主如何通过获取或遗传这些重要的共生体来维持这些益处,这一问题的答案至关重要,尤其是对淡水鱼而言。我们的研究为野生鱼类与其共生微生物群的共同进化关系、肠道微生物群的隐藏多样性以及野生淡水鱼的生态适应潜力提供了新的见解。
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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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