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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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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. |
format | Online Article Text |
id | pubmed-7980383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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