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Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics
Rapid warming in the highly productive western Antarctic Peninsula (WAP) region of the Southern Ocean has affected multiple trophic levels, yet viral influences on microbial processes and ecosystem function remain understudied in the Southern Ocean. Here we use cultivation-independent quantitative e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737935/ https://www.ncbi.nlm.nih.gov/pubmed/26296067 http://dx.doi.org/10.1038/ismej.2015.125 |
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author | Brum, Jennifer R Hurwitz, Bonnie L Schofield, Oscar Ducklow, Hugh W Sullivan, Matthew B |
author_facet | Brum, Jennifer R Hurwitz, Bonnie L Schofield, Oscar Ducklow, Hugh W Sullivan, Matthew B |
author_sort | Brum, Jennifer R |
collection | PubMed |
description | Rapid warming in the highly productive western Antarctic Peninsula (WAP) region of the Southern Ocean has affected multiple trophic levels, yet viral influences on microbial processes and ecosystem function remain understudied in the Southern Ocean. Here we use cultivation-independent quantitative ecological and metagenomic assays, combined with new comparative bioinformatic techniques, to investigate double-stranded DNA viruses during the WAP spring–summer transition. This study demonstrates that (i) temperate viruses dominate this region, switching from lysogeny to lytic replication as bacterial production increases, and (ii) Southern Ocean viral assemblages are genetically distinct from lower-latitude assemblages, primarily driven by this temperate viral dominance. This new information suggests fundamentally different virus–host interactions in polar environments, where intense seasonal changes in bacterial production select for temperate viruses because of increased fitness imparted by the ability to switch replication strategies in response to resource availability. Further, temperate viral dominance may provide mechanisms (for example, bacterial mortality resulting from prophage induction) that help explain observed temporal delays between, and lower ratios of, bacterial and primary production in polar versus lower-latitude marine ecosystems. Together these results suggest that temperate virus–host interactions are critical to predicting changes in microbial dynamics brought on by warming in polar marine systems. |
format | Online Article Text |
id | pubmed-4737935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47379352016-02-19 Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics Brum, Jennifer R Hurwitz, Bonnie L Schofield, Oscar Ducklow, Hugh W Sullivan, Matthew B ISME J Original Article Rapid warming in the highly productive western Antarctic Peninsula (WAP) region of the Southern Ocean has affected multiple trophic levels, yet viral influences on microbial processes and ecosystem function remain understudied in the Southern Ocean. Here we use cultivation-independent quantitative ecological and metagenomic assays, combined with new comparative bioinformatic techniques, to investigate double-stranded DNA viruses during the WAP spring–summer transition. This study demonstrates that (i) temperate viruses dominate this region, switching from lysogeny to lytic replication as bacterial production increases, and (ii) Southern Ocean viral assemblages are genetically distinct from lower-latitude assemblages, primarily driven by this temperate viral dominance. This new information suggests fundamentally different virus–host interactions in polar environments, where intense seasonal changes in bacterial production select for temperate viruses because of increased fitness imparted by the ability to switch replication strategies in response to resource availability. Further, temperate viral dominance may provide mechanisms (for example, bacterial mortality resulting from prophage induction) that help explain observed temporal delays between, and lower ratios of, bacterial and primary production in polar versus lower-latitude marine ecosystems. Together these results suggest that temperate virus–host interactions are critical to predicting changes in microbial dynamics brought on by warming in polar marine systems. Nature Publishing Group 2016-02 2015-08-21 /pmc/articles/PMC4737935/ /pubmed/26296067 http://dx.doi.org/10.1038/ismej.2015.125 Text en Copyright © 2016 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Brum, Jennifer R Hurwitz, Bonnie L Schofield, Oscar Ducklow, Hugh W Sullivan, Matthew B Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title | Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title_full | Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title_fullStr | Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title_full_unstemmed | Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title_short | Seasonal time bombs: dominant temperate viruses affect Southern Ocean microbial dynamics |
title_sort | seasonal time bombs: dominant temperate viruses affect southern ocean microbial dynamics |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737935/ https://www.ncbi.nlm.nih.gov/pubmed/26296067 http://dx.doi.org/10.1038/ismej.2015.125 |
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