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The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon
Unlike the pandemic form of HIV-1 (group M), group O viruses are endemic in west central Africa, especially in Cameroon. However, little is known about group O’s genetic evolution, and why this highly divergent lineage has not become pandemic. Using a unique and large set of group O sequences from s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524642/ https://www.ncbi.nlm.nih.gov/pubmed/26241860 http://dx.doi.org/10.1371/journal.ppat.1005029 |
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author | Leoz, Marie Feyertag, Felix Kfutwah, Anfumbom Mauclère, Philippe Lachenal, Guillaume Damond, Florence De Oliveira, Fabienne Lemée, Véronique Simon, François Robertson, David L Plantier, Jean-Christophe |
author_facet | Leoz, Marie Feyertag, Felix Kfutwah, Anfumbom Mauclère, Philippe Lachenal, Guillaume Damond, Florence De Oliveira, Fabienne Lemée, Véronique Simon, François Robertson, David L Plantier, Jean-Christophe |
author_sort | Leoz, Marie |
collection | PubMed |
description | Unlike the pandemic form of HIV-1 (group M), group O viruses are endemic in west central Africa, especially in Cameroon. However, little is known about group O’s genetic evolution, and why this highly divergent lineage has not become pandemic. Using a unique and large set of group O sequences from samples collected from 1987 to 2012, we find that this lineage has evolved in successive slow and fast phases of diversification, with a most recent common ancestor estimated to have existed around 1930 (1914–1944). The most rapid periods of diversification occurred in the 1950s and in the 1980s, and could be linked to favourable epidemiological contexts in Cameroon. Group O genetic diversity reflects this two-phase evolution, with two distinct populations potentially having different viral properties. The currently predominant viral population emerged in the 1980s, from an ancient population which had first developed in the 1950s, and is characterized by higher growth and evolutionary rates, and the natural presence of the Y181C resistance mutation, thought to confer a phenotypic advantage. Our findings show that although this evolutionary pattern is specific to HIV-1 group O, it paralleled the early spread of HIV-1 group M in the Democratic Republic of Congo. Both viral lineages are likely to have benefited from similar epidemiological contexts. The relative role of virological and social factors in the distinct epidemic histories of HIV-1 group O and M needs to be reassessed. |
format | Online Article Text |
id | pubmed-4524642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45246422015-08-06 The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon Leoz, Marie Feyertag, Felix Kfutwah, Anfumbom Mauclère, Philippe Lachenal, Guillaume Damond, Florence De Oliveira, Fabienne Lemée, Véronique Simon, François Robertson, David L Plantier, Jean-Christophe PLoS Pathog Research Article Unlike the pandemic form of HIV-1 (group M), group O viruses are endemic in west central Africa, especially in Cameroon. However, little is known about group O’s genetic evolution, and why this highly divergent lineage has not become pandemic. Using a unique and large set of group O sequences from samples collected from 1987 to 2012, we find that this lineage has evolved in successive slow and fast phases of diversification, with a most recent common ancestor estimated to have existed around 1930 (1914–1944). The most rapid periods of diversification occurred in the 1950s and in the 1980s, and could be linked to favourable epidemiological contexts in Cameroon. Group O genetic diversity reflects this two-phase evolution, with two distinct populations potentially having different viral properties. The currently predominant viral population emerged in the 1980s, from an ancient population which had first developed in the 1950s, and is characterized by higher growth and evolutionary rates, and the natural presence of the Y181C resistance mutation, thought to confer a phenotypic advantage. Our findings show that although this evolutionary pattern is specific to HIV-1 group O, it paralleled the early spread of HIV-1 group M in the Democratic Republic of Congo. Both viral lineages are likely to have benefited from similar epidemiological contexts. The relative role of virological and social factors in the distinct epidemic histories of HIV-1 group O and M needs to be reassessed. Public Library of Science 2015-08-04 /pmc/articles/PMC4524642/ /pubmed/26241860 http://dx.doi.org/10.1371/journal.ppat.1005029 Text en © 2015 Leoz et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Leoz, Marie Feyertag, Felix Kfutwah, Anfumbom Mauclère, Philippe Lachenal, Guillaume Damond, Florence De Oliveira, Fabienne Lemée, Véronique Simon, François Robertson, David L Plantier, Jean-Christophe The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title | The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title_full | The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title_fullStr | The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title_full_unstemmed | The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title_short | The Two-Phase Emergence of Non Pandemic HIV-1 Group O in Cameroon |
title_sort | two-phase emergence of non pandemic hiv-1 group o in cameroon |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524642/ https://www.ncbi.nlm.nih.gov/pubmed/26241860 http://dx.doi.org/10.1371/journal.ppat.1005029 |
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