Prokaryotic-virus-encoded auxiliary metabolic genes throughout the global oceans.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-08-29 DOI:10.1186/s40168-024-01876-z
Funing Tian, James M Wainaina, Cristina Howard-Varona, Guillermo Domínguez-Huerta, Benjamin Bolduc, Maria Consuelo Gazitúa, Garrett Smith, Marissa R Gittrich, Olivier Zablocki, Dylan R Cronin, Damien Eveillard, Steven J Hallam, Matthew B Sullivan
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Abstract

Background: Prokaryotic microbes have impacted marine biogeochemical cycles for billions of years. Viruses also impact these cycles, through lysis, horizontal gene transfer, and encoding and expressing genes that contribute to metabolic reprogramming of prokaryotic cells. While this impact is difficult to quantify in nature, we hypothesized that it can be examined by surveying virus-encoded auxiliary metabolic genes (AMGs) and assessing their ecological context.

Results: We systematically developed a global ocean AMG catalog by integrating previously described and newly identified AMGs and then placed this catalog into ecological and metabolic contexts relevant to ocean biogeochemistry. From 7.6 terabases of Tara Oceans paired prokaryote- and virus-enriched metagenomic sequence data, we increased known ocean virus populations to 579,904 (up 16%). From these virus populations, we then conservatively identified 86,913 AMGs that grouped into 22,779 sequence-based gene clusters, 7248 (~ 32%) of which were not previously reported. Using our catalog and modeled data from mock communities, we estimate that ~ 19% of ocean virus populations carry at least one AMG. To understand AMGs in their metabolic context, we identified 340 metabolic pathways encoded by ocean microbes and showed that AMGs map to 128 of them. Furthermore, we identified metabolic "hot spots" targeted by virus AMGs, including nine pathways where most steps (≥ 0.75) were AMG-targeted (involved in carbohydrate, amino acid, fatty acid, and nucleotide metabolism), as well as other pathways where virus-encoded AMGs outnumbered cellular homologs (involved in lipid A phosphates, phosphatidylethanolamine, creatine biosynthesis, phosphoribosylamine-glycine ligase, and carbamoyl-phosphate synthase pathways).

Conclusions: Together, this systematically curated, global ocean AMG catalog and analyses provide a valuable resource and foundational observations to understand the role of viruses in modulating global ocean metabolisms and their biogeochemical implications. Video Abstract.

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全球海洋中原核生物-病毒编码的辅助代谢基因。
背景:数十亿年来,原核微生物一直影响着海洋生物地球化学循环。病毒通过裂解、水平基因转移以及编码和表达有助于原核细胞代谢重编程的基因,也对这些循环产生了影响。虽然这种影响很难在自然界中量化,但我们假设可以通过调查病毒编码的辅助代谢基因(AMGs)并评估其生态环境来研究这种影响:结果:我们通过整合之前描述的和新发现的 AMG,系统地编制了全球海洋 AMG 目录,然后将该目录置于与海洋生物地球化学相关的生态和代谢环境中。从 7.6 terabases 的塔拉海洋配对原核生物和富含病毒的元基因组序列数据中,我们将已知的海洋病毒种群增加到了 579,904 个(增加了 16%)。然后,我们从这些病毒种群中保守地鉴定出 86913 个 AMGs,它们被归入 22779 个基于序列的基因簇,其中 7248 个(约 32%)是以前未曾报道过的。利用我们的目录和模拟群落的模型数据,我们估计约有 19% 的海洋病毒种群携带至少一种 AMG。为了从新陈代谢的角度了解 AMG,我们确定了海洋微生物编码的 340 条新陈代谢途径,并发现 AMG 与其中的 128 条途径有关联。此外,我们还确定了病毒 AMG 所针对的代谢 "热点",其中包括九条途径,在这些途径中,大多数步骤(≥ 0.75)的途径(涉及碳水化合物、氨基酸、脂肪酸和核苷酸代谢),以及病毒编码的AMG多于细胞同源物的其他途径(涉及脂质A磷酸盐、磷脂酰乙醇胺、肌酸生物合成、磷酸核糖胺-甘氨酸连接酶和氨基甲酰基磷酸合成酶途径):总之,这一系统整理的全球海洋 AMG 目录和分析为了解病毒在调节全球海洋新陈代谢中的作用及其生物地球化学影响提供了宝贵的资源和基础观测数据。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
期刊最新文献
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