Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.

Host immune selection pressure influences the development of mutations that allow for HIV escape. Mutation patterns induced in HIV by the human leukocyte antigen (HLA) are HLA-allele specific. As ethnic groups have distinct and characteristic HLA allele frequencies, we can expect divergent viral evo...

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Main Authors: Manon Ragonnet-Cronin, Stéphane Aris-Brosou, Isabelle Joanisse, Harriet Merks, Dominic Vallee, Kyna Caminiti, Paul Sandstrom, James Brooks
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3365047?pdf=render
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spelling doaj-e9f43835e86140c0ac9ceca69b23007c2020-11-25T00:27:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0175e3693310.1371/journal.pone.0036933Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.Manon Ragonnet-CroninStéphane Aris-BrosouIsabelle JoanisseHarriet MerksDominic ValleeKyna CaminitiPaul SandstromJames BrooksHost immune selection pressure influences the development of mutations that allow for HIV escape. Mutation patterns induced in HIV by the human leukocyte antigen (HLA) are HLA-allele specific. As ethnic groups have distinct and characteristic HLA allele frequencies, we can expect divergent viral evolution within ethnicities. Here, we have sequenced and analyzed the HIV pol gene from 1248 subtype B infected, treatment-naïve individuals in Canada. Phylogenetic analysis showed no separation between pol sequences from five self-identified ethnic groups, yet fixation index (F(ST)) values showed significant divergence between ethnicities. A total of 17 amino acid sites showed an ethnic-specific fixation pattern (0.015<F(ST) <0.060, p<0.01), and 27 codons were inferred to be under positive selection (p<0.01), with each set of sites strongly associated with HLA sites (p = 1.78×10(-6) and p = 1.91×10(-7), respectively). Within the pol gene, eight sites under HLA selective pressure were correlated with ethnicity, indicating 'adaptive divergence' between the groups studied. Our findings highlight challenges in HIV vaccine design in ethnically diverse countries with subtype B epidemics.http://europepmc.org/articles/PMC3365047?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Manon Ragonnet-Cronin
Stéphane Aris-Brosou
Isabelle Joanisse
Harriet Merks
Dominic Vallee
Kyna Caminiti
Paul Sandstrom
James Brooks
spellingShingle Manon Ragonnet-Cronin
Stéphane Aris-Brosou
Isabelle Joanisse
Harriet Merks
Dominic Vallee
Kyna Caminiti
Paul Sandstrom
James Brooks
Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
PLoS ONE
author_facet Manon Ragonnet-Cronin
Stéphane Aris-Brosou
Isabelle Joanisse
Harriet Merks
Dominic Vallee
Kyna Caminiti
Paul Sandstrom
James Brooks
author_sort Manon Ragonnet-Cronin
title Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
title_short Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
title_full Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
title_fullStr Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
title_full_unstemmed Adaptive evolution of HIV at HLA epitopes is associated with ethnicity in Canada.
title_sort adaptive evolution of hiv at hla epitopes is associated with ethnicity in canada.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Host immune selection pressure influences the development of mutations that allow for HIV escape. Mutation patterns induced in HIV by the human leukocyte antigen (HLA) are HLA-allele specific. As ethnic groups have distinct and characteristic HLA allele frequencies, we can expect divergent viral evolution within ethnicities. Here, we have sequenced and analyzed the HIV pol gene from 1248 subtype B infected, treatment-naïve individuals in Canada. Phylogenetic analysis showed no separation between pol sequences from five self-identified ethnic groups, yet fixation index (F(ST)) values showed significant divergence between ethnicities. A total of 17 amino acid sites showed an ethnic-specific fixation pattern (0.015<F(ST) <0.060, p<0.01), and 27 codons were inferred to be under positive selection (p<0.01), with each set of sites strongly associated with HLA sites (p = 1.78×10(-6) and p = 1.91×10(-7), respectively). Within the pol gene, eight sites under HLA selective pressure were correlated with ethnicity, indicating 'adaptive divergence' between the groups studied. Our findings highlight challenges in HIV vaccine design in ethnically diverse countries with subtype B epidemics.
url http://europepmc.org/articles/PMC3365047?pdf=render
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