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Remarkable Diversity of Endogenous Viruses in a Crustacean Genome
Recent studies in paleovirology have uncovered myriads of endogenous viral elements (EVEs) integrated in the genome of their eukaryotic hosts. These fragments result from endogenization, that is, integration of the viral genome into the host germline genome followed by vertical inheritance. So far,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231630/ https://www.ncbi.nlm.nih.gov/pubmed/25084787 http://dx.doi.org/10.1093/gbe/evu163 |
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author | Thézé, Julien Leclercq, Sébastien Moumen, Bouziane Cordaux, Richard Gilbert, Clément |
author_facet | Thézé, Julien Leclercq, Sébastien Moumen, Bouziane Cordaux, Richard Gilbert, Clément |
author_sort | Thézé, Julien |
collection | PubMed |
description | Recent studies in paleovirology have uncovered myriads of endogenous viral elements (EVEs) integrated in the genome of their eukaryotic hosts. These fragments result from endogenization, that is, integration of the viral genome into the host germline genome followed by vertical inheritance. So far, most studies have used a virus-centered approach, whereby endogenous copies of a particular group of viruses were searched in all available sequenced genomes. Here, we follow a host-centered approach whereby the genome of a given species is comprehensively screened for the presence of EVEs using all available complete viral genomes as queries. Our analyses revealed that 54 EVEs corresponding to 10 different viral lineages belonging to 5 viral families (Bunyaviridae, Circoviridae, Parvoviridae, and Totiviridae) and one viral order (Mononegavirales) became endogenized in the genome of the isopod crustacean Armadillidium vulgare. We show that viral endogenization occurred recurrently during the evolution of isopods and that A. vulgare viral lineages were involved in multiple host switches that took place between widely divergent taxa. Furthermore, 30 A. vulgare EVEs have uninterrupted open reading frames, suggesting they result from recent endogenization of viruses likely to be currently infecting isopod populations. Overall, our work shows that isopods have been and are still infected by a large variety of viruses. It also extends the host range of several families of viruses and brings new insights into their evolution. More generally, our results underline the power of paleovirology in characterizing the viral diversity currently infecting eukaryotic taxa. |
format | Online Article Text |
id | pubmed-4231630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42316302014-11-14 Remarkable Diversity of Endogenous Viruses in a Crustacean Genome Thézé, Julien Leclercq, Sébastien Moumen, Bouziane Cordaux, Richard Gilbert, Clément Genome Biol Evol Research Article Recent studies in paleovirology have uncovered myriads of endogenous viral elements (EVEs) integrated in the genome of their eukaryotic hosts. These fragments result from endogenization, that is, integration of the viral genome into the host germline genome followed by vertical inheritance. So far, most studies have used a virus-centered approach, whereby endogenous copies of a particular group of viruses were searched in all available sequenced genomes. Here, we follow a host-centered approach whereby the genome of a given species is comprehensively screened for the presence of EVEs using all available complete viral genomes as queries. Our analyses revealed that 54 EVEs corresponding to 10 different viral lineages belonging to 5 viral families (Bunyaviridae, Circoviridae, Parvoviridae, and Totiviridae) and one viral order (Mononegavirales) became endogenized in the genome of the isopod crustacean Armadillidium vulgare. We show that viral endogenization occurred recurrently during the evolution of isopods and that A. vulgare viral lineages were involved in multiple host switches that took place between widely divergent taxa. Furthermore, 30 A. vulgare EVEs have uninterrupted open reading frames, suggesting they result from recent endogenization of viruses likely to be currently infecting isopod populations. Overall, our work shows that isopods have been and are still infected by a large variety of viruses. It also extends the host range of several families of viruses and brings new insights into their evolution. More generally, our results underline the power of paleovirology in characterizing the viral diversity currently infecting eukaryotic taxa. Oxford University Press 2014-08-01 /pmc/articles/PMC4231630/ /pubmed/25084787 http://dx.doi.org/10.1093/gbe/evu163 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Thézé, Julien Leclercq, Sébastien Moumen, Bouziane Cordaux, Richard Gilbert, Clément Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title | Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title_full | Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title_fullStr | Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title_full_unstemmed | Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title_short | Remarkable Diversity of Endogenous Viruses in a Crustacean Genome |
title_sort | remarkable diversity of endogenous viruses in a crustacean genome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231630/ https://www.ncbi.nlm.nih.gov/pubmed/25084787 http://dx.doi.org/10.1093/gbe/evu163 |
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