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Virus diversity and interactions with hosts in deep-sea hydrothermal vents

BACKGROUND: The deep sea harbors many viruses, yet their diversity and interactions with hosts in hydrothermal ecosystems are largely unknown. Here, we analyzed the viral composition, distribution, host preference, and metabolic potential in different habitats of global hydrothermal vents, including...

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Autores principales: Cheng, Ruolin, Li, Xiaofeng, Jiang, Lijing, Gong, Linfeng, Geslin, Claire, Shao, Zongze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789665/
https://www.ncbi.nlm.nih.gov/pubmed/36566239
http://dx.doi.org/10.1186/s40168-022-01441-6
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author Cheng, Ruolin
Li, Xiaofeng
Jiang, Lijing
Gong, Linfeng
Geslin, Claire
Shao, Zongze
author_facet Cheng, Ruolin
Li, Xiaofeng
Jiang, Lijing
Gong, Linfeng
Geslin, Claire
Shao, Zongze
author_sort Cheng, Ruolin
collection PubMed
description BACKGROUND: The deep sea harbors many viruses, yet their diversity and interactions with hosts in hydrothermal ecosystems are largely unknown. Here, we analyzed the viral composition, distribution, host preference, and metabolic potential in different habitats of global hydrothermal vents, including vent plumes, background seawater, diffuse fluids, and sediments. RESULTS: From 34 samples collected at eight vent sites, a total of 4662 viral populations (vOTUs) were recovered from the metagenome assemblies, encompassing diverse phylogenetic groups and defining many novel lineages. Apart from the abundant unclassified viruses, tailed phages are most predominant across the global hydrothermal vents, while single-stranded DNA viruses, including Microviridae and small eukaryotic viruses, also constitute a significant part of the viromes. As revealed by protein-sharing network analysis, hydrothermal vent viruses formed many novel genus-level viral clusters and are highly endemic to specific vent sites and habitat types. Only 11% of the vOTUs can be linked to hosts, which are the key microbial taxa of hydrothermal habitats, such as Gammaproteobacteria and Campylobacterota. Intriguingly, vent viromes share some common metabolic features in that they encode auxiliary genes that are extensively involved in the metabolism of carbohydrates, amino acids, cofactors, and vitamins. Specifically, in plume viruses, various auxiliary genes related to methane, nitrogen, and sulfur metabolism were observed, indicating their contribution to host energy conservation. Moreover, the prevalence of sulfur-relay pathway genes indicated the significant role of vent viruses in stabilizing the tRNA structure, which promotes host adaptation to steep environmental gradients. CONCLUSIONS: The deep-sea hydrothermal systems hold untapped viral diversity with novelty. They may affect both vent prokaryotic and eukaryotic communities and modulate host metabolism related to vent adaptability. More explorations are needed to depict global vent virus diversity and its roles in this unique ecosystem. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01441-6.
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spelling pubmed-97896652022-12-25 Virus diversity and interactions with hosts in deep-sea hydrothermal vents Cheng, Ruolin Li, Xiaofeng Jiang, Lijing Gong, Linfeng Geslin, Claire Shao, Zongze Microbiome Research BACKGROUND: The deep sea harbors many viruses, yet their diversity and interactions with hosts in hydrothermal ecosystems are largely unknown. Here, we analyzed the viral composition, distribution, host preference, and metabolic potential in different habitats of global hydrothermal vents, including vent plumes, background seawater, diffuse fluids, and sediments. RESULTS: From 34 samples collected at eight vent sites, a total of 4662 viral populations (vOTUs) were recovered from the metagenome assemblies, encompassing diverse phylogenetic groups and defining many novel lineages. Apart from the abundant unclassified viruses, tailed phages are most predominant across the global hydrothermal vents, while single-stranded DNA viruses, including Microviridae and small eukaryotic viruses, also constitute a significant part of the viromes. As revealed by protein-sharing network analysis, hydrothermal vent viruses formed many novel genus-level viral clusters and are highly endemic to specific vent sites and habitat types. Only 11% of the vOTUs can be linked to hosts, which are the key microbial taxa of hydrothermal habitats, such as Gammaproteobacteria and Campylobacterota. Intriguingly, vent viromes share some common metabolic features in that they encode auxiliary genes that are extensively involved in the metabolism of carbohydrates, amino acids, cofactors, and vitamins. Specifically, in plume viruses, various auxiliary genes related to methane, nitrogen, and sulfur metabolism were observed, indicating their contribution to host energy conservation. Moreover, the prevalence of sulfur-relay pathway genes indicated the significant role of vent viruses in stabilizing the tRNA structure, which promotes host adaptation to steep environmental gradients. CONCLUSIONS: The deep-sea hydrothermal systems hold untapped viral diversity with novelty. They may affect both vent prokaryotic and eukaryotic communities and modulate host metabolism related to vent adaptability. More explorations are needed to depict global vent virus diversity and its roles in this unique ecosystem. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01441-6. BioMed Central 2022-12-24 /pmc/articles/PMC9789665/ /pubmed/36566239 http://dx.doi.org/10.1186/s40168-022-01441-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cheng, Ruolin
Li, Xiaofeng
Jiang, Lijing
Gong, Linfeng
Geslin, Claire
Shao, Zongze
Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title_full Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title_fullStr Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title_full_unstemmed Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title_short Virus diversity and interactions with hosts in deep-sea hydrothermal vents
title_sort virus diversity and interactions with hosts in deep-sea hydrothermal vents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789665/
https://www.ncbi.nlm.nih.gov/pubmed/36566239
http://dx.doi.org/10.1186/s40168-022-01441-6
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