Moore Carrie Julia, Bornemann Till L V, Figueroa-Gonzalez Perla Abigail, Esser Sarah P, Moraru Cristina, Soares André Rodrigues, Hinzke Tjorven, Trautwein-Schult Anke, Maaß Sandra, Becher Dörte, Starke Joern, Plewka Julia, Rothe Lousia, Probst Alexander J
Environmental Metagenomics, Research Centre One Health Ruhr of the University Alliance Ruhr, Faculty of Chemistry, University Duisburg-Essen, 45141 Essen, Germany.
Centre of Water and Environmental Research (ZWU), University of Duisburg-Essen, Universitätsstraße 5, 45141 Essen, Germany.
Microlife. 2024 May 20;5:uqae011. doi: 10.1093/femsml/uqae011. eCollection 2024.
Ecosystems subject to mantle degassing are of particular interest for understanding global biogeochemistry, as their microbiomes are shaped by prolonged exposure to high CO and have recently been suggested to be highly active. While the genetic diversity of bacteria and archaea in these deep biosphere systems have been studied extensively, little is known about how viruses impact these microbial communities. Here, we show that the viral community in a high-CO cold-water geyser (Wallender Born, Germany) undergoes substantial fluctuations over a period of 12 days, although the corresponding prokaryotic community remains stable, indicating a newly observed "infect to keep in check" strategy that maintains prokaryotic community structure. We characterized the viral community using metagenomics and metaproteomics, revealing 8 654 viral operational taxonomic units (vOTUs). CRISPR spacer-to-protospacer matching linked 278 vOTUs to 32 hosts, with many vOTUs sharing hosts from different families. High levels of viral structural proteins present in the metaproteome (several structurally annotated based on AlphaFold models) indicate active virion production at the time of sampling. Viral genomes expressed many proteins involved in DNA metabolism and manipulation, and encoded for auxiliary metabolic genes, which likely bolster phosphate and sulfur metabolism of their hosts. The active viral community encodes genes to facilitate acquisition and transformation of host nutrients, and appears to consist of many nutrient-demanding members, based on abundant virion proteins. These findings indicate viruses are inextricably linked to the biogeochemical cycling in this high-CO environment and substantially contribute to prokaryotic community stability in the deep biosphere hotspots.
受地幔脱气影响的生态系统对于理解全球生物地球化学具有特别重要的意义,因为它们的微生物群落因长期暴露于高浓度一氧化碳而形成,并且最近有研究表明其具有高度活性。虽然这些深层生物圈系统中细菌和古菌的遗传多样性已得到广泛研究,但对于病毒如何影响这些微生物群落却知之甚少。在这里,我们表明,在德国瓦伦德博恩的一个高一氧化碳冷水间歇泉中,病毒群落在12天内经历了显著波动,尽管相应的原核生物群落保持稳定,这表明一种新观察到的“感染以控制”策略维持了原核生物群落结构。我们使用宏基因组学和宏蛋白质组学对病毒群落进行了表征,揭示了8654个病毒操作分类单元(vOTU)。CRISPR间隔序列与原间隔序列的匹配将278个vOTU与32个宿主联系起来,许多vOTU共享来自不同家族的宿主。宏蛋白质组中存在高水平的病毒结构蛋白(基于AlphaFold模型进行了几种结构注释)表明在采样时病毒粒子有活跃的产生。病毒基因组表达了许多参与DNA代谢和操纵的蛋白质,并编码辅助代谢基因,这些基因可能增强其宿主的磷和硫代谢。活跃的病毒群落编码促进宿主营养获取和转化的基因,并且基于丰富的病毒粒子蛋白,似乎由许多需要营养的成员组成。这些发现表明病毒与这种高一氧化碳环境中的生物地球化学循环紧密相连,并对深层生物圈热点中原核生物群落的稳定性有重大贡献。