Centre for Ecology and Evolution in Microbial Model Systems (EEMiS), Department of Biology and Environmental Science, Linnaeus University, Kalmar, Sweden.
Aero-Aquatic Virus Research Group, Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena, Jena, Germany.
Microbiome. 2024 Oct 24;12(1):218. doi: 10.1186/s40168-024-01902-0.
Aquatic viruses act as key players in shaping microbial communities. In polar environments, they face significant challenges such as limited host availability and harsh conditions. However, due to the restricted accessibility of these ecosystems, our understanding of viral diversity, abundance, adaptations, and host interactions remains limited.
To fill this knowledge gap, we studied viruses from atmosphere-close aquatic ecosystems in the Central Arctic and Northern Greenland. Aquatic samples for virus-host analysis were collected from ~60 cm depth and the submillimeter surface microlayer (SML) during the Synoptic Arctic Survey 2021 on icebreaker Oden in the Arctic summer. Water was sampled from a melt pond and open water before undergoing size-fractioned filtration, followed by genome-resolved metagenomic and cultivation investigations. The prokaryotic diversity in the melt pond was considerably lower compared to that of open water. The melt pond was dominated by a Flavobacterium sp. and Aquiluna sp., the latter having a relatively small genome size of 1.2 Mb and the metabolic potential to generate ATP using the phosphate acetyltransferase-acetate kinase pathway. Viral diversity on the host fraction (0.2-5 µm) of the melt pond was strikingly limited compared to that of open water. From the 1154 viral operational taxonomic units (vOTUs), of which two-thirds were predicted bacteriophages, 17.2% encoded for auxiliary metabolic genes (AMGs) with metabolic functions. Some AMGs like glycerol-3-phosphate cytidylyltransferase and ice-binding like proteins might serve to provide cryoprotection for the host. Prophages were often associated with SML genomes, and two active prophages of new viral genera from the Arctic SML strain Leeuwenhoekiella aequorea Arc30 were induced. We found evidence that vOTU abundance in the SML compared to that of ~60 cm depth was more positively correlated with the distribution of a vOTU across five different Arctic stations.
The results indicate that viruses employ elaborate strategies to endure in extreme, host-limited environments. Moreover, our observations suggest that the immediate air-sea interface serves as a platform for viral distribution in the Central Arctic. Video Abstract.
水生病毒是塑造微生物群落的关键因素。在极地环境中,它们面临着宿主可用性有限和恶劣条件等重大挑战。然而,由于这些生态系统的访问受限,我们对病毒多样性、丰度、适应性以及宿主相互作用的了解仍然有限。
为了填补这一知识空白,我们研究了来自北极中部和格陵兰北部大气接近的水生生态系统中的病毒。在北极夏季奥登号破冰船上进行的综合北极调查 2021 期间,从60 厘米深度和亚毫米表面微层(SML)采集了用于病毒-宿主分析的水样。水取自融池和开阔水域,然后进行大小分级过滤,随后进行基因组解析宏基因组和培养研究。与开阔水域相比,融池中的原核生物多样性要低得多。融池由黄杆菌属和 Aquiluna 属主导,后者基因组相对较小,为 1.2 Mb,具有利用磷酸乙酰转移酶-乙酸激酶途径生成 ATP 的代谢潜力。与开阔水域相比,融池宿主部分(0.2-5 µm)的病毒多样性明显有限。在 1154 个病毒操作分类单元(vOTU)中,其中三分之二被预测为噬菌体,有 17.2%编码具有代谢功能的辅助代谢基因(AMGs)。一些 AMGs,如甘油-3-磷酸胞苷酰转移酶和冰结合蛋白,可能为宿主提供抗冻保护。噬菌体通常与 SML 基因组相关联,并且从北极 SML 菌株 Leeuwenhoekiella aequorea Arc30 中诱导出两个新的噬菌体属的活性噬菌体。我们发现,与60 厘米深度相比,SML 中的 vOTU 丰度与 vOTU 在五个不同北极站的分布更呈正相关。
研究结果表明,病毒采用了精心设计的策略来在极端、宿主有限的环境中生存。此外,我们的观察结果表明,立即的气-海界面是病毒在北极中部分布的平台。视频摘要。