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Single Cell Genomics Reveals Viruses Consumed by Marine Protists

The predominant model of the role of viruses in the marine trophic web is that of the “viral shunt,” where viral infection funnels a substantial fraction of the microbial primary and secondary production back to the pool of dissolved organic matter. Here, we analyzed the composition of non-eukaryoti...

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Autores principales: Brown, Julia M., Labonté, Jessica M., Brown, Joseph, Record, Nicholas R., Poulton, Nicole J., Sieracki, Michael E., Logares, Ramiro, Stepanauskas, Ramunas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541821/
https://www.ncbi.nlm.nih.gov/pubmed/33072003
http://dx.doi.org/10.3389/fmicb.2020.524828
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author Brown, Julia M.
Labonté, Jessica M.
Brown, Joseph
Record, Nicholas R.
Poulton, Nicole J.
Sieracki, Michael E.
Logares, Ramiro
Stepanauskas, Ramunas
author_facet Brown, Julia M.
Labonté, Jessica M.
Brown, Joseph
Record, Nicholas R.
Poulton, Nicole J.
Sieracki, Michael E.
Logares, Ramiro
Stepanauskas, Ramunas
author_sort Brown, Julia M.
collection PubMed
description The predominant model of the role of viruses in the marine trophic web is that of the “viral shunt,” where viral infection funnels a substantial fraction of the microbial primary and secondary production back to the pool of dissolved organic matter. Here, we analyzed the composition of non-eukaryotic DNA associated with individual cells of small, planktonic protists in the Gulf of Maine (GoM) and the Mediterranean Sea. We found viral DNA associated with a substantial fraction cells from the GoM (51%) and the Mediterranean Sea (35%). While Mediterranean SAGs contained a larger proportion of cells containing bacterial sequences (49%), a smaller fraction of cells contained bacterial sequences in the GoM (19%). In GoM cells, nearly identical bacteriophage and ssDNA virus sequences where found across diverse lineages of protists, suggesting many of these viruses are non-infective. The fraction of cells containing viral DNA varied among protistan lineages and reached 100% in Picozoa and Choanozoa. These two groups also contained significantly higher numbers of viral sequences than other identified taxa. We consider mechanisms that may explain the presence of viral DNA in protistan cells and conclude that protistan predation on free viral particles contributed to the observed patterns. These findings confirm prior experiments with protistan isolates and indicate that the viral shunt is complemented by a viral link in the marine microbial food web. This link may constitute a sink of viral particles in the ocean and has implications for the flow of carbon through the microbial food web.
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spelling pubmed-75418212020-10-17 Single Cell Genomics Reveals Viruses Consumed by Marine Protists Brown, Julia M. Labonté, Jessica M. Brown, Joseph Record, Nicholas R. Poulton, Nicole J. Sieracki, Michael E. Logares, Ramiro Stepanauskas, Ramunas Front Microbiol Microbiology The predominant model of the role of viruses in the marine trophic web is that of the “viral shunt,” where viral infection funnels a substantial fraction of the microbial primary and secondary production back to the pool of dissolved organic matter. Here, we analyzed the composition of non-eukaryotic DNA associated with individual cells of small, planktonic protists in the Gulf of Maine (GoM) and the Mediterranean Sea. We found viral DNA associated with a substantial fraction cells from the GoM (51%) and the Mediterranean Sea (35%). While Mediterranean SAGs contained a larger proportion of cells containing bacterial sequences (49%), a smaller fraction of cells contained bacterial sequences in the GoM (19%). In GoM cells, nearly identical bacteriophage and ssDNA virus sequences where found across diverse lineages of protists, suggesting many of these viruses are non-infective. The fraction of cells containing viral DNA varied among protistan lineages and reached 100% in Picozoa and Choanozoa. These two groups also contained significantly higher numbers of viral sequences than other identified taxa. We consider mechanisms that may explain the presence of viral DNA in protistan cells and conclude that protistan predation on free viral particles contributed to the observed patterns. These findings confirm prior experiments with protistan isolates and indicate that the viral shunt is complemented by a viral link in the marine microbial food web. This link may constitute a sink of viral particles in the ocean and has implications for the flow of carbon through the microbial food web. Frontiers Media S.A. 2020-09-24 /pmc/articles/PMC7541821/ /pubmed/33072003 http://dx.doi.org/10.3389/fmicb.2020.524828 Text en Copyright © 2020 Brown, Labonté, Brown, Record, Poulton, Sieracki, Logares and Stepanauskas. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Brown, Julia M.
Labonté, Jessica M.
Brown, Joseph
Record, Nicholas R.
Poulton, Nicole J.
Sieracki, Michael E.
Logares, Ramiro
Stepanauskas, Ramunas
Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title_full Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title_fullStr Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title_full_unstemmed Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title_short Single Cell Genomics Reveals Viruses Consumed by Marine Protists
title_sort single cell genomics reveals viruses consumed by marine protists
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541821/
https://www.ncbi.nlm.nih.gov/pubmed/33072003
http://dx.doi.org/10.3389/fmicb.2020.524828
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