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Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution
Most theories on viral evolution are speculative and lack fossil comparison. Here, we isolated a modern Pithovirus-like virus from sewage samples. This giant virus, named Pithovirus massiliensis, was compared with its prehistoric counterpart, Pithovirus sibericum, found in Siberian permafrost. Our a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010891/ https://www.ncbi.nlm.nih.gov/pubmed/27389688 http://dx.doi.org/10.1093/gbe/evw153 |
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author | Levasseur, Anthony Andreani, Julien Delerce, Jeremy Bou Khalil, Jacques Robert, Catherine La Scola, Bernard Raoult, Didier |
author_facet | Levasseur, Anthony Andreani, Julien Delerce, Jeremy Bou Khalil, Jacques Robert, Catherine La Scola, Bernard Raoult, Didier |
author_sort | Levasseur, Anthony |
collection | PubMed |
description | Most theories on viral evolution are speculative and lack fossil comparison. Here, we isolated a modern Pithovirus-like virus from sewage samples. This giant virus, named Pithovirus massiliensis, was compared with its prehistoric counterpart, Pithovirus sibericum, found in Siberian permafrost. Our analysis revealed near-complete gene repertoire conservation, including horizontal gene transfer and ORFans. Furthermore, all orthologous genes evolved under strong purifying selection with a non-synonymous and synonymous ratio in the same range as the ratio found in the prokaryotic world. The comparison between fossil and modern Pithovirus species provided an estimation of the cadence of the molecular clock, reaching up to 3 × 10(−6) mutations/site/year. In addition, the strict conservation of HGTs and ORFans in P. massiliensis revealed the stable genetic mosaicism in giant viruses and excludes the concept of a bag of genes. The genetic stability for 30,000 years of P. massiliensis demonstrates that giant viruses evolve similarly to prokaryotes by classical mechanisms of evolution, including selection and fixation of genes, followed by selective constraints. |
format | Online Article Text |
id | pubmed-5010891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50108912016-09-06 Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution Levasseur, Anthony Andreani, Julien Delerce, Jeremy Bou Khalil, Jacques Robert, Catherine La Scola, Bernard Raoult, Didier Genome Biol Evol Research Article Most theories on viral evolution are speculative and lack fossil comparison. Here, we isolated a modern Pithovirus-like virus from sewage samples. This giant virus, named Pithovirus massiliensis, was compared with its prehistoric counterpart, Pithovirus sibericum, found in Siberian permafrost. Our analysis revealed near-complete gene repertoire conservation, including horizontal gene transfer and ORFans. Furthermore, all orthologous genes evolved under strong purifying selection with a non-synonymous and synonymous ratio in the same range as the ratio found in the prokaryotic world. The comparison between fossil and modern Pithovirus species provided an estimation of the cadence of the molecular clock, reaching up to 3 × 10(−6) mutations/site/year. In addition, the strict conservation of HGTs and ORFans in P. massiliensis revealed the stable genetic mosaicism in giant viruses and excludes the concept of a bag of genes. The genetic stability for 30,000 years of P. massiliensis demonstrates that giant viruses evolve similarly to prokaryotes by classical mechanisms of evolution, including selection and fixation of genes, followed by selective constraints. Oxford University Press 2016-07-07 /pmc/articles/PMC5010891/ /pubmed/27389688 http://dx.doi.org/10.1093/gbe/evw153 Text en © The Author 2016. 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 Levasseur, Anthony Andreani, Julien Delerce, Jeremy Bou Khalil, Jacques Robert, Catherine La Scola, Bernard Raoult, Didier Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title | Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title_full | Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title_fullStr | Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title_full_unstemmed | Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title_short | Comparison of a Modern and Fossil Pithovirus Reveals Its Genetic Conservation and Evolution |
title_sort | comparison of a modern and fossil pithovirus reveals its genetic conservation and evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010891/ https://www.ncbi.nlm.nih.gov/pubmed/27389688 http://dx.doi.org/10.1093/gbe/evw153 |
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