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HIV-1 Subtype A Gag Variability and Epitope Evolution
OBJECTIVE: The aim of this study was to examine the course of time-dependent evolution of HIV-1 subtype A on a global level, especially with respect to the dynamics of immunogenic HIV gag epitopes. METHODS: We used a total of 1,893 HIV-1 subtype A gag sequences representing a timeline from 1985 thro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043486/ https://www.ncbi.nlm.nih.gov/pubmed/24892852 http://dx.doi.org/10.1371/journal.pone.0093415 |
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author | Abidi, Syed Hani Kalish, Marcia L. Abbas, Farhat Rowland-Jones, Sarah Ali, Syed |
author_facet | Abidi, Syed Hani Kalish, Marcia L. Abbas, Farhat Rowland-Jones, Sarah Ali, Syed |
author_sort | Abidi, Syed Hani |
collection | PubMed |
description | OBJECTIVE: The aim of this study was to examine the course of time-dependent evolution of HIV-1 subtype A on a global level, especially with respect to the dynamics of immunogenic HIV gag epitopes. METHODS: We used a total of 1,893 HIV-1 subtype A gag sequences representing a timeline from 1985 through 2010, and 19 different countries in Africa, Europe and Asia. The phylogenetic relationship of subtype A gag and its epidemic dynamics was analysed through a Maximum Likelihood tree and Bayesian Skyline plot, genomic variability was measured in terms of G→A substitutions and Shannon entropy, and the time-dependent evolution of HIV subtype A gag epitopes was examined. Finally, to confirm observations on globally reported HIV subtype A sequences, we analysed the gag epitope data from our Kenyan, Pakistani, and Afghan cohorts, where both cohort-specific gene epitope variability and HLA restriction profiles of gag epitopes were examined. RESULTS: The most recent common ancestor of the HIV subtype A epidemic was estimated to be 1956±1. A period of exponential growth began about 1980 and lasted for approximately 7 years, stabilized for 15 years, declined for 2–3 years, then stabilized again from about 2004. During the course of evolution, a gradual increase in genomic variability was observed that peaked in 2005–2010. We observed that the number of point mutations and novel epitopes in gag also peaked concurrently during 2005–2010. CONCLUSION: It appears that as the HIV subtype A epidemic spread globally, changing population immunogenetic pressures may have played a role in steering immune-evolution of this subtype in new directions. This trend is apparent in the genomic variability and epitope diversity of HIV-1 subtype A gag sequences. |
format | Online Article Text |
id | pubmed-4043486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40434862014-06-09 HIV-1 Subtype A Gag Variability and Epitope Evolution Abidi, Syed Hani Kalish, Marcia L. Abbas, Farhat Rowland-Jones, Sarah Ali, Syed PLoS One Research Article OBJECTIVE: The aim of this study was to examine the course of time-dependent evolution of HIV-1 subtype A on a global level, especially with respect to the dynamics of immunogenic HIV gag epitopes. METHODS: We used a total of 1,893 HIV-1 subtype A gag sequences representing a timeline from 1985 through 2010, and 19 different countries in Africa, Europe and Asia. The phylogenetic relationship of subtype A gag and its epidemic dynamics was analysed through a Maximum Likelihood tree and Bayesian Skyline plot, genomic variability was measured in terms of G→A substitutions and Shannon entropy, and the time-dependent evolution of HIV subtype A gag epitopes was examined. Finally, to confirm observations on globally reported HIV subtype A sequences, we analysed the gag epitope data from our Kenyan, Pakistani, and Afghan cohorts, where both cohort-specific gene epitope variability and HLA restriction profiles of gag epitopes were examined. RESULTS: The most recent common ancestor of the HIV subtype A epidemic was estimated to be 1956±1. A period of exponential growth began about 1980 and lasted for approximately 7 years, stabilized for 15 years, declined for 2–3 years, then stabilized again from about 2004. During the course of evolution, a gradual increase in genomic variability was observed that peaked in 2005–2010. We observed that the number of point mutations and novel epitopes in gag also peaked concurrently during 2005–2010. CONCLUSION: It appears that as the HIV subtype A epidemic spread globally, changing population immunogenetic pressures may have played a role in steering immune-evolution of this subtype in new directions. This trend is apparent in the genomic variability and epitope diversity of HIV-1 subtype A gag sequences. Public Library of Science 2014-06-03 /pmc/articles/PMC4043486/ /pubmed/24892852 http://dx.doi.org/10.1371/journal.pone.0093415 Text en © 2014 Abidi 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 Abidi, Syed Hani Kalish, Marcia L. Abbas, Farhat Rowland-Jones, Sarah Ali, Syed HIV-1 Subtype A Gag Variability and Epitope Evolution |
title | HIV-1 Subtype A Gag Variability and Epitope Evolution |
title_full | HIV-1 Subtype A Gag Variability and Epitope Evolution |
title_fullStr | HIV-1 Subtype A Gag Variability and Epitope Evolution |
title_full_unstemmed | HIV-1 Subtype A Gag Variability and Epitope Evolution |
title_short | HIV-1 Subtype A Gag Variability and Epitope Evolution |
title_sort | hiv-1 subtype a gag variability and epitope evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043486/ https://www.ncbi.nlm.nih.gov/pubmed/24892852 http://dx.doi.org/10.1371/journal.pone.0093415 |
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