深海沉积物中太古菌的生态位分配及种内变异

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2025-01-08 DOI:10.1111/1462-2920.70018
Ronghua Liu, Xinxin He, Gaoyang Ren, Da-Wei Li, Meixun Zhao, Laura Lehtovirta-Morley, Jonathan D. Todd, Xiao-Hua Zhang, Jiwen Liu
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引用次数: 0

摘要

深海沉积物中含有大量的古细菌,它们在系统发育上与远洋同类不同。然而,它们的生态学和进化适应并没有得到很好的理解。对从马里亚纳海沟挑战者深处收集的750厘米沉积物岩心的不同深度的样本进行了宏基因组分析。古细菌和古细菌amoA的丰度随着深度的增加而减少,除了在岩心中间出现一个意想不到的高峰。这些元基因组组装的Thaumarchaeota基因组被划分为不同的系统发育簇,分别与氨氧化Thaumarchaeota和非氨氧化taumarchaeota谱系的amoA-NP-γ、amoA-NP-θ和amoA-NP-δ相关。最丰富的类群是amoA-NP-γ,通常在沿海和浅海生境中发现,表明生态位可能从海洋浅海环境扩展到hadal环境。与之前发现的Hadal水组相比,该底栖生物组显示出种内基因组变异,表明Hadal Thaumarchaeota的微多样化以及底栖和远洋环境之间的生态位分离。与底栖向远洋过渡相关的进化适应包括基因组大小减少、运动/细胞粘附性丧失、能量代谢改变以及不同的底物获取和调节机制(如铵)。这些发现为hadal Thaumarchaeota的进化提供了新的见解,并首次证明了Thaumarchaeota种内水平的基因组变异与深海底栖与远洋生态位分配有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Niche Partitioning and Intraspecific Variation of Thaumarchaeota in Deep Ocean Sediments

Deep-sea sediments contain a large number of Thaumarchaeota that are phylogenetically distinct from their pelagic counterparts. However, their ecology and evolutionary adaptations are not well understood. Metagenomic analyses were conducted on samples from various depths of a 750-cm sediment core collected from the Mariana Trench Challenger Deep. The abundance of Thaumarchaeota and archaeal amoA generally decreased with depth, except for an unexpected peak midway through the core. The thaumarchaeotal metagenome-assembled genomes were classified into diverse phylogenetic clusters associated with amoA-NP-γ, amoA-NP-θ, and amoA-NP-δ of ammonia-oxidising Thaumarchaeota and non-ammonia-oxidising lineages. The most abundant group was within amoA-NP-γ, which is usually found in coastal and shallow habitats, indicating potential niche expansion from marine shallow to hadal environments. This benthic group showed within-species genomic variations compared to the previously identified Hadal water group, suggesting microdiversification of hadal Thaumarchaeota along with niche separation between benthic and pelagic environments. Evolutionary adaptations associated with the benthic-to-pelagic transition included reduced genome size, loss of motility/cell adhesion, altered energy metabolism, and different mechanisms for substrate acquisition and regulation (e.g., ammonium). These findings offer new insights into the evolution of hadal Thaumarchaeota and demonstrate, for the first time, intraspecies-level genomic variation in Thaumarchaeota related to the benthic-versus-pelagic niche partitioning in the deep ocean.

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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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