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Protist impacts on marine cyanovirocell metabolism

The fate of oceanic carbon and nutrients depends on interactions between viruses, prokaryotes, and unicellular eukaryotes (protists) in a highly interconnected planktonic food web. To date, few controlled mechanistic studies of these interactions exist, and where they do, they are largely pairwise,...

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Autores principales: Howard-Varona, Cristina, Roux, Simon, Bowen, Benjamin P., Silva, Leslie P., Lau, Rebecca, Schwenck, Sarah M., Schwartz, Samuel, Woyke, Tanja, Northen, Trent, Sullivan, Matthew B., Floge, Sheri A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723779/
https://www.ncbi.nlm.nih.gov/pubmed/37938263
http://dx.doi.org/10.1038/s43705-022-00169-6
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author Howard-Varona, Cristina
Roux, Simon
Bowen, Benjamin P.
Silva, Leslie P.
Lau, Rebecca
Schwenck, Sarah M.
Schwartz, Samuel
Woyke, Tanja
Northen, Trent
Sullivan, Matthew B.
Floge, Sheri A.
author_facet Howard-Varona, Cristina
Roux, Simon
Bowen, Benjamin P.
Silva, Leslie P.
Lau, Rebecca
Schwenck, Sarah M.
Schwartz, Samuel
Woyke, Tanja
Northen, Trent
Sullivan, Matthew B.
Floge, Sheri A.
author_sort Howard-Varona, Cristina
collection PubMed
description The fate of oceanic carbon and nutrients depends on interactions between viruses, prokaryotes, and unicellular eukaryotes (protists) in a highly interconnected planktonic food web. To date, few controlled mechanistic studies of these interactions exist, and where they do, they are largely pairwise, focusing either on viral infection (i.e., virocells) or protist predation. Here we studied population-level responses of Synechococcus cyanobacterial virocells (i.e., cyanovirocells) to the protist Oxyrrhis marina using transcriptomics, endo- and exo-metabolomics, photosynthetic efficiency measurements, and microscopy. Protist presence had no measurable impact on Synechococcus transcripts or endometabolites. The cyanovirocells alone had a smaller intracellular transcriptional and metabolic response than cyanovirocells co-cultured with protists, displaying known patterns of virus-mediated metabolic reprogramming while releasing diverse exometabolites during infection. When protists were added, several exometabolites disappeared, suggesting microbial consumption. In addition, the intracellular cyanovirocell impact was largest, with 4.5- and 10-fold more host transcripts and endometabolites, respectively, responding to protists, especially those involved in resource and energy production. Physiologically, photosynthetic efficiency also increased, and together with the transcriptomics and metabolomics findings suggest that cyanovirocell metabolic demand is highest when protists are present. These data illustrate cyanovirocell responses to protist presence that are not yet considered when linking microbial physiology to global-scale biogeochemical processes.
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spelling pubmed-97237792023-01-04 Protist impacts on marine cyanovirocell metabolism Howard-Varona, Cristina Roux, Simon Bowen, Benjamin P. Silva, Leslie P. Lau, Rebecca Schwenck, Sarah M. Schwartz, Samuel Woyke, Tanja Northen, Trent Sullivan, Matthew B. Floge, Sheri A. ISME Commun Article The fate of oceanic carbon and nutrients depends on interactions between viruses, prokaryotes, and unicellular eukaryotes (protists) in a highly interconnected planktonic food web. To date, few controlled mechanistic studies of these interactions exist, and where they do, they are largely pairwise, focusing either on viral infection (i.e., virocells) or protist predation. Here we studied population-level responses of Synechococcus cyanobacterial virocells (i.e., cyanovirocells) to the protist Oxyrrhis marina using transcriptomics, endo- and exo-metabolomics, photosynthetic efficiency measurements, and microscopy. Protist presence had no measurable impact on Synechococcus transcripts or endometabolites. The cyanovirocells alone had a smaller intracellular transcriptional and metabolic response than cyanovirocells co-cultured with protists, displaying known patterns of virus-mediated metabolic reprogramming while releasing diverse exometabolites during infection. When protists were added, several exometabolites disappeared, suggesting microbial consumption. In addition, the intracellular cyanovirocell impact was largest, with 4.5- and 10-fold more host transcripts and endometabolites, respectively, responding to protists, especially those involved in resource and energy production. Physiologically, photosynthetic efficiency also increased, and together with the transcriptomics and metabolomics findings suggest that cyanovirocell metabolic demand is highest when protists are present. These data illustrate cyanovirocell responses to protist presence that are not yet considered when linking microbial physiology to global-scale biogeochemical processes. Nature Publishing Group UK 2022-10-01 /pmc/articles/PMC9723779/ /pubmed/37938263 http://dx.doi.org/10.1038/s43705-022-00169-6 Text en © The Author(s) 2022 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
Howard-Varona, Cristina
Roux, Simon
Bowen, Benjamin P.
Silva, Leslie P.
Lau, Rebecca
Schwenck, Sarah M.
Schwartz, Samuel
Woyke, Tanja
Northen, Trent
Sullivan, Matthew B.
Floge, Sheri A.
Protist impacts on marine cyanovirocell metabolism
title Protist impacts on marine cyanovirocell metabolism
title_full Protist impacts on marine cyanovirocell metabolism
title_fullStr Protist impacts on marine cyanovirocell metabolism
title_full_unstemmed Protist impacts on marine cyanovirocell metabolism
title_short Protist impacts on marine cyanovirocell metabolism
title_sort protist impacts on marine cyanovirocell metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723779/
https://www.ncbi.nlm.nih.gov/pubmed/37938263
http://dx.doi.org/10.1038/s43705-022-00169-6
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