深海冷渗漏和热液喷口 Heimdallarchaeia 支系的元基因组研究。

IF 6.2 2区 环境科学与生态学 Q1 GENETICS & HEREDITY Environmental Microbiome Pub Date : 2024-06-22 DOI:10.1186/s40793-024-00585-2
Rui Liu, Ruining Cai, Minxiao Wang, Jing Zhang, Huan Zhang, Chaolun Li, Chaomin Sun
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引用次数: 0

摘要

海姆达尔古菌(Heimdallarchaeia)是阿斯加德古菌群(Asgardarchaeota)中的一类,是迄今为止已确定的古原核生物祖先的最可能候选者。然而,人们对它们的生活习性知之甚少,尽管它们无处不在地分布于不同的栖息地,尤其是深海环境中的海姆达尔古菌(Heimdallarchaeia)。在这项研究中,我们从深海冷渗漏和热液喷口获得了 13 个 Heimdallarchaeia 的元基因组组装基因组(MAGs)。根据基因组分类数据库(GTDB),这些MAGs属于o_Heimdallarchaeales和o_JABLTI01目,其中大部分(9个MAGs)来自f_Heimdallarchaeaceae科。这些MAG富含常见的真核生物特异性特征。我们的研究结果表明,这些 Heimdallarchaeia 具有将硫酸盐(同化作用)和硝酸盐(异化作用)分别还原成硫化物和氨的代谢潜能,这表明它们在生物地球化学循环中发挥着以前未被重视的作用。此外,我们还发现它们可以同时进行 TCA 和 rTCA 途径以及丙酮酸代谢以保存能量,并通过非典型伍德-荣格达尔途径固定二氧化碳和生成有机化合物。此外,在这些海姆达尔弓形虫 MAGs 中还发现了许多与细菌叶绿素和类胡萝卜素生物合成密切相关的基因,以及依赖氧的代谢途径,这表明色素和微氧生活方式可能利用光。总之,我们的研究结果表明,海姆达尔弓形虫具有混养的生活方式,这可能使它们更灵活地适应恶劣的深海条件。
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Metagenomic insights into Heimdallarchaeia clades from the deep-sea cold seep and hydrothermal vent.

Heimdallarchaeia is a class of the Asgardarchaeota, are the most probable candidates for the archaeal protoeukaryote ancestor that have been identified to date. However, little is known about their life habits regardless of their ubiquitous distribution in diverse habitats, which is especially true for Heimdallarchaeia from deep-sea environments. In this study, we obtained 13 metagenome-assembled genomes (MAGs) of Heimdallarchaeia from the deep-sea cold seep and hydrothermal vent. These MAGs belonged to orders o_Heimdallarchaeales and o_JABLTI01, and most of them (9 MAGs) come from the family f_Heimdallarchaeaceae according to genome taxonomy database (GTDB). These are enriched for common eukaryote-specific signatures. Our results show that these Heimdallarchaeia have the metabolic potential to reduce sulfate (assimilatory) and nitrate (dissimilatory) to sulfide and ammonia, respectively, suggesting a previously unappreciated role in biogeochemical cycling. Furthermore, we find that they could perform both TCA and rTCA pathways coupled with pyruvate metabolism for energy conservation, fix CO2 and generate organic compounds through an atypical Wood-Ljungdahl pathway. In addition, many genes closely associated with bacteriochlorophyll and carotenoid biosynthesis, and oxygen-dependent metabolic pathways are identified in these Heimdallarchaeia MAGs, suggesting a potential light-utilization by pigments and microoxic lifestyle. Taken together, our results indicate that Heimdallarchaeia possess a mixotrophic lifestyle, which may give them more flexibility to adapt to the harsh deep-sea conditions.

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来源期刊
Environmental Microbiome
Environmental Microbiome Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
2.50%
发文量
55
审稿时长
13 weeks
期刊介绍: Microorganisms, omnipresent across Earth's diverse environments, play a crucial role in adapting to external changes, influencing Earth's systems and cycles, and contributing significantly to agricultural practices. Through applied microbiology, they offer solutions to various everyday needs. Environmental Microbiome recognizes the universal presence and significance of microorganisms, inviting submissions that explore the diverse facets of environmental and applied microbiological research.
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