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Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes
The archaeal tailed viruses (arTV), evolutionarily related to tailed double-stranded DNA (dsDNA) bacteriophages of the class Caudoviricetes, represent the most common isolates infecting halophilic archaea. Only a handful of these viruses have been genomically characterized, limiting our appreciation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651126/ https://www.ncbi.nlm.nih.gov/pubmed/34752450 http://dx.doi.org/10.1371/journal.pbio.3001442 |
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author | Liu, Ying Demina, Tatiana A. Roux, Simon Aiewsakun, Pakorn Kazlauskas, Darius Simmonds, Peter Prangishvili, David Oksanen, Hanna M. Krupovic, Mart |
author_facet | Liu, Ying Demina, Tatiana A. Roux, Simon Aiewsakun, Pakorn Kazlauskas, Darius Simmonds, Peter Prangishvili, David Oksanen, Hanna M. Krupovic, Mart |
author_sort | Liu, Ying |
collection | PubMed |
description | The archaeal tailed viruses (arTV), evolutionarily related to tailed double-stranded DNA (dsDNA) bacteriophages of the class Caudoviricetes, represent the most common isolates infecting halophilic archaea. Only a handful of these viruses have been genomically characterized, limiting our appreciation of their ecological impacts and evolution. Here, we present 37 new genomes of haloarchaeal tailed virus isolates, more than doubling the current number of sequenced arTVs. Analysis of all 63 available complete genomes of arTVs, which we propose to classify into 14 new families and 3 orders, suggests ancient divergence of archaeal and bacterial tailed viruses and points to an extensive sharing of genes involved in DNA metabolism and counterdefense mechanisms, illuminating common strategies of virus–host interactions with tailed bacteriophages. Coupling of the comparative genomics with the host range analysis on a broad panel of haloarchaeal species uncovered 4 distinct groups of viral tail fiber adhesins controlling the host range expansion. The survey of metagenomes using viral hallmark genes suggests that the global architecture of the arTV community is shaped through recurrent transfers between different biomes, including hypersaline, marine, and anoxic environments. |
format | Online Article Text |
id | pubmed-8651126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86511262021-12-08 Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes Liu, Ying Demina, Tatiana A. Roux, Simon Aiewsakun, Pakorn Kazlauskas, Darius Simmonds, Peter Prangishvili, David Oksanen, Hanna M. Krupovic, Mart PLoS Biol Research Article The archaeal tailed viruses (arTV), evolutionarily related to tailed double-stranded DNA (dsDNA) bacteriophages of the class Caudoviricetes, represent the most common isolates infecting halophilic archaea. Only a handful of these viruses have been genomically characterized, limiting our appreciation of their ecological impacts and evolution. Here, we present 37 new genomes of haloarchaeal tailed virus isolates, more than doubling the current number of sequenced arTVs. Analysis of all 63 available complete genomes of arTVs, which we propose to classify into 14 new families and 3 orders, suggests ancient divergence of archaeal and bacterial tailed viruses and points to an extensive sharing of genes involved in DNA metabolism and counterdefense mechanisms, illuminating common strategies of virus–host interactions with tailed bacteriophages. Coupling of the comparative genomics with the host range analysis on a broad panel of haloarchaeal species uncovered 4 distinct groups of viral tail fiber adhesins controlling the host range expansion. The survey of metagenomes using viral hallmark genes suggests that the global architecture of the arTV community is shaped through recurrent transfers between different biomes, including hypersaline, marine, and anoxic environments. Public Library of Science 2021-11-09 /pmc/articles/PMC8651126/ /pubmed/34752450 http://dx.doi.org/10.1371/journal.pbio.3001442 Text en © 2021 Liu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Liu, Ying Demina, Tatiana A. Roux, Simon Aiewsakun, Pakorn Kazlauskas, Darius Simmonds, Peter Prangishvili, David Oksanen, Hanna M. Krupovic, Mart Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title | Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title_full | Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title_fullStr | Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title_full_unstemmed | Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title_short | Diversity, taxonomy, and evolution of archaeal viruses of the class Caudoviricetes |
title_sort | diversity, taxonomy, and evolution of archaeal viruses of the class caudoviricetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651126/ https://www.ncbi.nlm.nih.gov/pubmed/34752450 http://dx.doi.org/10.1371/journal.pbio.3001442 |
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