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Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics
Giant viruses infect many unicellular eukaryotes, including algae that form massive oceanic blooms. Despite the major impact of viruses on the marine ecosystem, the ability to quantify and assess active viral infection in nature remains a major challenge. We applied single-cell RNA sequencing, to pr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569711/ https://www.ncbi.nlm.nih.gov/pubmed/37824628 http://dx.doi.org/10.1126/sciadv.adf7971 |
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author | Hevroni, Gur Vincent, Flora Ku, Chuan Sheyn, Uri Vardi, Assaf |
author_facet | Hevroni, Gur Vincent, Flora Ku, Chuan Sheyn, Uri Vardi, Assaf |
author_sort | Hevroni, Gur |
collection | PubMed |
description | Giant viruses infect many unicellular eukaryotes, including algae that form massive oceanic blooms. Despite the major impact of viruses on the marine ecosystem, the ability to quantify and assess active viral infection in nature remains a major challenge. We applied single-cell RNA sequencing, to profile virus and host transcriptomes of 12,000 single algal cells from a coccolithophore bloom. Viral infection was detected already at early exponential bloom phase, negatively correlating with the bloom intensity. A consistent percent of infected coccolithophores displayed the early phase of viral replication for several consecutive days, indicating a daily turnover and continuous virocell-associated metabolite production, potentially affecting the surrounding microbiome. Linking single-cell infection state to host physiology revealed that infected cells remained calcified even in the late infection stage. These findings stress the importance of studying host-virus dynamics in natural populations, at single-cell resolution, to better understand virus life cycle and its impact on microbial food webs. |
format | Online Article Text |
id | pubmed-10569711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105697112023-10-13 Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics Hevroni, Gur Vincent, Flora Ku, Chuan Sheyn, Uri Vardi, Assaf Sci Adv Earth, Environmental, Ecological, and Space Sciences Giant viruses infect many unicellular eukaryotes, including algae that form massive oceanic blooms. Despite the major impact of viruses on the marine ecosystem, the ability to quantify and assess active viral infection in nature remains a major challenge. We applied single-cell RNA sequencing, to profile virus and host transcriptomes of 12,000 single algal cells from a coccolithophore bloom. Viral infection was detected already at early exponential bloom phase, negatively correlating with the bloom intensity. A consistent percent of infected coccolithophores displayed the early phase of viral replication for several consecutive days, indicating a daily turnover and continuous virocell-associated metabolite production, potentially affecting the surrounding microbiome. Linking single-cell infection state to host physiology revealed that infected cells remained calcified even in the late infection stage. These findings stress the importance of studying host-virus dynamics in natural populations, at single-cell resolution, to better understand virus life cycle and its impact on microbial food webs. American Association for the Advancement of Science 2023-10-12 /pmc/articles/PMC10569711/ /pubmed/37824628 http://dx.doi.org/10.1126/sciadv.adf7971 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Earth, Environmental, Ecological, and Space Sciences Hevroni, Gur Vincent, Flora Ku, Chuan Sheyn, Uri Vardi, Assaf Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title | Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title_full | Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title_fullStr | Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title_full_unstemmed | Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title_short | Daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
title_sort | daily turnover of active giant virus infection during algal blooms revealed by single-cell transcriptomics |
topic | Earth, Environmental, Ecological, and Space Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569711/ https://www.ncbi.nlm.nih.gov/pubmed/37824628 http://dx.doi.org/10.1126/sciadv.adf7971 |
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