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Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise

Marine viruses are the most abundant biological entity in the ocean and are considered as major evolutionary drivers of microbial life [C. A. Suttle, Nat. Rev. Microbiol. 5, 801–812 (2007)]. Yet, we lack quantitative approaches to assess their impact on the marine ecosystem. Here, we provide quantif...

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Detalles Bibliográficos
Autores principales: Vincent, Flora, Sheyn, Uri, Porat, Ziv, Schatz, Daniella, Vardi, Assaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980383/
https://www.ncbi.nlm.nih.gov/pubmed/33707211
http://dx.doi.org/10.1073/pnas.2021586118
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author Vincent, Flora
Sheyn, Uri
Porat, Ziv
Schatz, Daniella
Vardi, Assaf
author_facet Vincent, Flora
Sheyn, Uri
Porat, Ziv
Schatz, Daniella
Vardi, Assaf
author_sort Vincent, Flora
collection PubMed
description Marine viruses are the most abundant biological entity in the ocean and are considered as major evolutionary drivers of microbial life [C. A. Suttle, Nat. Rev. Microbiol. 5, 801–812 (2007)]. Yet, we lack quantitative approaches to assess their impact on the marine ecosystem. Here, we provide quantification of active viral infection in the bloom forming single-celled phytoplankton Emiliania huxleyi infected by the large virus EhV, using high-throughput single-molecule messenger RNA in situ hybridization (smFISH) of both virus and host transcripts. In natural samples, viral infection reached only 25% of the population despite synchronized bloom demise exposing the coexistence of infected and noninfected subpopulations. We prove that photosynthetically active cells chronically release viral particles through nonlytic infection and that viral-induced cell lysis can occur without viral release, thus challenging major assumptions regarding the life cycle of giant viruses. We could also assess active infection in cell aggregates linking viral infection and carbon export to the deep ocean [C. P. Laber et al., Nat. Microbiol. 3, 537–547 (2018)] and suggest a potential host defense strategy by enrichment of infected cells in sinking aggregates. Our approach can be applied to diverse marine microbial systems, opening a mechanistic dimension to the study of biotic interactions in the ocean.
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spelling pubmed-79803832021-03-26 Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise Vincent, Flora Sheyn, Uri Porat, Ziv Schatz, Daniella Vardi, Assaf Proc Natl Acad Sci U S A Biological Sciences Marine viruses are the most abundant biological entity in the ocean and are considered as major evolutionary drivers of microbial life [C. A. Suttle, Nat. Rev. Microbiol. 5, 801–812 (2007)]. Yet, we lack quantitative approaches to assess their impact on the marine ecosystem. Here, we provide quantification of active viral infection in the bloom forming single-celled phytoplankton Emiliania huxleyi infected by the large virus EhV, using high-throughput single-molecule messenger RNA in situ hybridization (smFISH) of both virus and host transcripts. In natural samples, viral infection reached only 25% of the population despite synchronized bloom demise exposing the coexistence of infected and noninfected subpopulations. We prove that photosynthetically active cells chronically release viral particles through nonlytic infection and that viral-induced cell lysis can occur without viral release, thus challenging major assumptions regarding the life cycle of giant viruses. We could also assess active infection in cell aggregates linking viral infection and carbon export to the deep ocean [C. P. Laber et al., Nat. Microbiol. 3, 537–547 (2018)] and suggest a potential host defense strategy by enrichment of infected cells in sinking aggregates. Our approach can be applied to diverse marine microbial systems, opening a mechanistic dimension to the study of biotic interactions in the ocean. National Academy of Sciences 2021-03-16 2021-03-11 /pmc/articles/PMC7980383/ /pubmed/33707211 http://dx.doi.org/10.1073/pnas.2021586118 Text en Copyright © 2021 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Vincent, Flora
Sheyn, Uri
Porat, Ziv
Schatz, Daniella
Vardi, Assaf
Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title_full Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title_fullStr Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title_full_unstemmed Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title_short Visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
title_sort visualizing active viral infection reveals diverse cell fates in synchronized algal bloom demise
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980383/
https://www.ncbi.nlm.nih.gov/pubmed/33707211
http://dx.doi.org/10.1073/pnas.2021586118
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