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Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state
Microbial communities in oxygen minimum zones (OMZs) are known to have significant impacts on global biogeochemical cycles, but viral influence on microbial processes in these regions are much less studied. Here we provide baseline ecological patterns using microscopy and viral metagenomics from the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940887/ https://www.ncbi.nlm.nih.gov/pubmed/34743175 http://dx.doi.org/10.1038/s41396-021-01143-1 |
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author | Jurgensen, Sophie K. Roux, Simon Schwenck, Sarah M. Stewart, Frank J. Sullivan, Matthew B. Brum, Jennifer R. |
author_facet | Jurgensen, Sophie K. Roux, Simon Schwenck, Sarah M. Stewart, Frank J. Sullivan, Matthew B. Brum, Jennifer R. |
author_sort | Jurgensen, Sophie K. |
collection | PubMed |
description | Microbial communities in oxygen minimum zones (OMZs) are known to have significant impacts on global biogeochemical cycles, but viral influence on microbial processes in these regions are much less studied. Here we provide baseline ecological patterns using microscopy and viral metagenomics from the Eastern Tropical North Pacific (ETNP) OMZ region that enhance our understanding of viruses in these climate-critical systems. While extracellular viral abundance decreased below the oxycline, viral diversity and lytic infection frequency remained high within the OMZ, demonstrating that viral influences on microbial communities were still substantial without the detectable presence of oxygen. Viral community composition was strongly related to oxygen concentration, with viral populations in low-oxygen portions of the water column being distinct from their surface layer counterparts. However, this divergence was not accompanied by the expected differences in viral-encoded auxiliary metabolic genes (AMGs) relating to nitrogen and sulfur metabolisms that are known to be performed by microbial communities in these low-oxygen and anoxic regions. Instead, several abundant AMGs were identified in the oxycline and OMZ that may modulate host responses to low-oxygen stress. We hypothesize that this is due to selection for viral-encoded genes that influence host survivability rather than modulating host metabolic reactions within the ETNP OMZ. Together, this study shows that viruses are not only diverse throughout the water column in the ETNP, including the OMZ, but their infection of microorganisms has the potential to alter host physiological state within these biogeochemically important regions of the ocean. |
format | Online Article Text |
id | pubmed-8940887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89408872022-04-08 Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state Jurgensen, Sophie K. Roux, Simon Schwenck, Sarah M. Stewart, Frank J. Sullivan, Matthew B. Brum, Jennifer R. ISME J Article Microbial communities in oxygen minimum zones (OMZs) are known to have significant impacts on global biogeochemical cycles, but viral influence on microbial processes in these regions are much less studied. Here we provide baseline ecological patterns using microscopy and viral metagenomics from the Eastern Tropical North Pacific (ETNP) OMZ region that enhance our understanding of viruses in these climate-critical systems. While extracellular viral abundance decreased below the oxycline, viral diversity and lytic infection frequency remained high within the OMZ, demonstrating that viral influences on microbial communities were still substantial without the detectable presence of oxygen. Viral community composition was strongly related to oxygen concentration, with viral populations in low-oxygen portions of the water column being distinct from their surface layer counterparts. However, this divergence was not accompanied by the expected differences in viral-encoded auxiliary metabolic genes (AMGs) relating to nitrogen and sulfur metabolisms that are known to be performed by microbial communities in these low-oxygen and anoxic regions. Instead, several abundant AMGs were identified in the oxycline and OMZ that may modulate host responses to low-oxygen stress. We hypothesize that this is due to selection for viral-encoded genes that influence host survivability rather than modulating host metabolic reactions within the ETNP OMZ. Together, this study shows that viruses are not only diverse throughout the water column in the ETNP, including the OMZ, but their infection of microorganisms has the potential to alter host physiological state within these biogeochemically important regions of the ocean. Nature Publishing Group UK 2021-11-06 2022-04 /pmc/articles/PMC8940887/ /pubmed/34743175 http://dx.doi.org/10.1038/s41396-021-01143-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jurgensen, Sophie K. Roux, Simon Schwenck, Sarah M. Stewart, Frank J. Sullivan, Matthew B. Brum, Jennifer R. Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title | Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title_full | Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title_fullStr | Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title_full_unstemmed | Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title_short | Viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
title_sort | viral community analysis in a marine oxygen minimum zone indicates increased potential for viral manipulation of microbial physiological state |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940887/ https://www.ncbi.nlm.nih.gov/pubmed/34743175 http://dx.doi.org/10.1038/s41396-021-01143-1 |
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