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Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages
Subtype A is one of the rare HIV-1 group M (HIV-1M) lineages that is both widely distributed throughout the world and persists at high frequencies in the Congo Basin (CB), the site where HIV-1M likely originated. This, together with its high degree of diversity suggests that subtype A is amongst the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819727/ https://www.ncbi.nlm.nih.gov/pubmed/29484203 http://dx.doi.org/10.1093/ve/vey003 |
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author | Tongo, Marcel Harkins, Gordon W Dorfman, Jeffrey R Billings, Erik Tovanabutra, Sodsai de Oliveira, Tulio Martin, Darren P |
author_facet | Tongo, Marcel Harkins, Gordon W Dorfman, Jeffrey R Billings, Erik Tovanabutra, Sodsai de Oliveira, Tulio Martin, Darren P |
author_sort | Tongo, Marcel |
collection | PubMed |
description | Subtype A is one of the rare HIV-1 group M (HIV-1M) lineages that is both widely distributed throughout the world and persists at high frequencies in the Congo Basin (CB), the site where HIV-1M likely originated. This, together with its high degree of diversity suggests that subtype A is amongst the fittest HIV-1M lineages. Here we use a comprehensive set of published near full-length subtype A sequences and A-derived genome fragments from both circulating and unique recombinant forms (CRFs/URFs) to obtain some insights into how frequently these lineages have independently seeded HIV-1M sub-epidemics in different parts of the world. We do this by inferring when and where the major subtype A lineages and subtype A-derived CRFs originated. Following its origin in the CB during the 1940s, we track the diversification and recombination history of subtype A sequences before and during its dissemination throughout much of the world between the 1950s and 1970s. Collectively, the timings and numbers of detectable subtype A recombination and dissemination events, the present broad global distribution of the sub-epidemics that were seeded by these events, and the high prevalence of subtype A sequences within the regions where these sub-epidemics occurred, suggest that ancestral subtype A viruses (and particularly sub-subtype A1 ancestral viruses) may have been genetically predisposed to become major components of the present epidemic. |
format | Online Article Text |
id | pubmed-5819727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58197272018-02-26 Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages Tongo, Marcel Harkins, Gordon W Dorfman, Jeffrey R Billings, Erik Tovanabutra, Sodsai de Oliveira, Tulio Martin, Darren P Virus Evol Research Article Subtype A is one of the rare HIV-1 group M (HIV-1M) lineages that is both widely distributed throughout the world and persists at high frequencies in the Congo Basin (CB), the site where HIV-1M likely originated. This, together with its high degree of diversity suggests that subtype A is amongst the fittest HIV-1M lineages. Here we use a comprehensive set of published near full-length subtype A sequences and A-derived genome fragments from both circulating and unique recombinant forms (CRFs/URFs) to obtain some insights into how frequently these lineages have independently seeded HIV-1M sub-epidemics in different parts of the world. We do this by inferring when and where the major subtype A lineages and subtype A-derived CRFs originated. Following its origin in the CB during the 1940s, we track the diversification and recombination history of subtype A sequences before and during its dissemination throughout much of the world between the 1950s and 1970s. Collectively, the timings and numbers of detectable subtype A recombination and dissemination events, the present broad global distribution of the sub-epidemics that were seeded by these events, and the high prevalence of subtype A sequences within the regions where these sub-epidemics occurred, suggest that ancestral subtype A viruses (and particularly sub-subtype A1 ancestral viruses) may have been genetically predisposed to become major components of the present epidemic. Oxford University Press 2018-02-19 /pmc/articles/PMC5819727/ /pubmed/29484203 http://dx.doi.org/10.1093/ve/vey003 Text en © The Author(s) 2018. Published by Oxford University Press. 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 Tongo, Marcel Harkins, Gordon W Dorfman, Jeffrey R Billings, Erik Tovanabutra, Sodsai de Oliveira, Tulio Martin, Darren P Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title | Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title_full | Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title_fullStr | Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title_full_unstemmed | Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title_short | Unravelling the complicated evolutionary and dissemination history of HIV-1M subtype A lineages |
title_sort | unravelling the complicated evolutionary and dissemination history of hiv-1m subtype a lineages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819727/ https://www.ncbi.nlm.nih.gov/pubmed/29484203 http://dx.doi.org/10.1093/ve/vey003 |
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