北太平洋副热带环流中巨型病毒的垂直输送和时空动力学

Md Moinuddin Sheam, Elaine Luo
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引用次数: 0

摘要

核胞质大DNA病毒,或“巨型病毒”,在海洋环境中普遍存在,感染各种真核生物谱系并影响海洋碳循环。它们的基因组包含广泛的辅助代谢基因,影响生物地球化学过程。本研究结合北太平洋副热带环流浮游(5-4000 m)和颗粒相关(4000 m)宏基因组样本,以及4000 m颗粒输出通量数据,研究了巨型病毒的垂直输送及其与碳输出的时空相关性。通过对6年15个深度的宏基因组样本进行分析,我们建立了一个包含37个巨型病毒种群基因组和1496个contigs的数据库,并研究了它们在开放海洋中的时空变异性和功能容量。我们报道了多种支持病毒穿梭假说的证据,包括从上层海洋到深海深处的巨型病毒的垂直运输及其与4000 m处颗粒碳输出通量的正相关,特别是与已知感染一种形成水华的藻类的球形Phaeocystis globosavvirus密切相关的巨型物种。我们发现了编码多种amg的巨型病毒,包括与光合作用、营养转运和能量代谢相关的基因。这些辅助代谢基因显示出深度特异性分布,我们假设这反映了沿着水柱对光能和营养有限条件的深度特异性适应。总之,本研究通过确定可以影响出口过程的关键巨型病毒和影响开放海水柱生物地球化学过程的辅助代谢基因的深度特异性分布,为巨型病毒的生物地球化学影响提供了重要见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vertical transport and spatiotemporal dynamics of giant viruses in the North Pacific Subtropical Gyre
Nucleocytoplasmic large DNA viruses, or “giant viruses,” are prevalent in marine environments, infecting diverse eukaryotic lineages and influencing the marine carbon cycle. Their genomes harbor wide range of auxiliary metabolic genes that influence biogeochemical processes. This study integrates planktonic (5–4000 m) and particle-associated (4000 m) metagenomic samples in the North Pacific Subtropical Gyre, along with particulate export flux data at 4000 m, to investigate the vertical transport of giant viruses and their correlation with carbon export through space and time. By analyzing metagenomic samples over a period of 6 years across 15 depths, we curated a database of 37 giant virus population genomes and 1496 contigs and investigated their spatiotemporal variability and functional capacity in the open ocean. We reported multiple lines of evidence supporting the viral shuttle hypothesis, including the vertical transport of giant viruses from the upper ocean to abyssal depths and their positive correlation with particulate carbon export flux at 4000 m, particularly a giant species closely related to Phaeocystis globosavirus known to infect a bloom-forming alga. We identified giant viruses encoding diverse AMGs, including genes associated with photosynthesis, nutrient transport, and energy metabolism. These auxiliary metabolic genes displayed depth-specific distributions, which we postulate reflect depth-specific adaptations to light-energy and nutrient-limited conditions along the water column. Together, this study provides critical insights into the biogeochemical impacts of giant viruses by identifying key giant viruses that can impact export processes and depth-specific distributions of auxiliary metabolic genes impacting biogeochemical processes along the open ocean water column.
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