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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...

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Autores principales: Liu, Ying, Demina, Tatiana A., Roux, Simon, Aiewsakun, Pakorn, Kazlauskas, Darius, Simmonds, Peter, Prangishvili, David, Oksanen, Hanna M., Krupovic, Mart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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.
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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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