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Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae

Host-pathogen interactions can be powerful drivers of adaptive evolution, shaping the patterns of molecular variation at the genes involved. In this study, we sequenced alleles from 28 immune-related loci in wild samples of multiple genetic subpopulations of the African malaria mosquito Anopheles ga...

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Autores principales: Crawford, Jacob E., Bischoff, Emmanuel, Garnier, Thierry, Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Riehle, Michelle M., Guelbeogo, Wamdaogo M., Sagnon, N’Fale, Lazzaro, Brian P., Vernick, Kenneth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516473/
https://www.ncbi.nlm.nih.gov/pubmed/23275874
http://dx.doi.org/10.1534/g3.112.004473
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author Crawford, Jacob E.
Bischoff, Emmanuel
Garnier, Thierry
Gneme, Awa
Eiglmeier, Karin
Holm, Inge
Riehle, Michelle M.
Guelbeogo, Wamdaogo M.
Sagnon, N’Fale
Lazzaro, Brian P.
Vernick, Kenneth D.
author_facet Crawford, Jacob E.
Bischoff, Emmanuel
Garnier, Thierry
Gneme, Awa
Eiglmeier, Karin
Holm, Inge
Riehle, Michelle M.
Guelbeogo, Wamdaogo M.
Sagnon, N’Fale
Lazzaro, Brian P.
Vernick, Kenneth D.
author_sort Crawford, Jacob E.
collection PubMed
description Host-pathogen interactions can be powerful drivers of adaptive evolution, shaping the patterns of molecular variation at the genes involved. In this study, we sequenced alleles from 28 immune-related loci in wild samples of multiple genetic subpopulations of the African malaria mosquito Anopheles gambiae, obtaining unprecedented sample sizes and providing the first opportunity to contrast patterns of molecular evolution at immune-related loci in the recently discovered GOUNDRY population to those of the indoor-resting M and S molecular forms. In contrast to previous studies that focused on immune genes identified in laboratory studies, we centered our analysis on genes that fall within a quantitative trait locus associated with resistance to Plasmodium falciparum in natural populations of A. gambiae. Analyses of haplotypic and genetic diversity at these 28 loci revealed striking differences among populations in levels of genetic diversity and allele frequencies in coding sequence. Putative signals of positive selection were identified at 11 loci, but only one was shared by two subgroups of A. gambiae. Striking patterns of linkage disequilibrium were observed at several loci. We discuss these results with respect to ecological differences among these strata as well as potential implications for disease transmission.
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spelling pubmed-35164732012-12-28 Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae Crawford, Jacob E. Bischoff, Emmanuel Garnier, Thierry Gneme, Awa Eiglmeier, Karin Holm, Inge Riehle, Michelle M. Guelbeogo, Wamdaogo M. Sagnon, N’Fale Lazzaro, Brian P. Vernick, Kenneth D. G3 (Bethesda) Investigations Host-pathogen interactions can be powerful drivers of adaptive evolution, shaping the patterns of molecular variation at the genes involved. In this study, we sequenced alleles from 28 immune-related loci in wild samples of multiple genetic subpopulations of the African malaria mosquito Anopheles gambiae, obtaining unprecedented sample sizes and providing the first opportunity to contrast patterns of molecular evolution at immune-related loci in the recently discovered GOUNDRY population to those of the indoor-resting M and S molecular forms. In contrast to previous studies that focused on immune genes identified in laboratory studies, we centered our analysis on genes that fall within a quantitative trait locus associated with resistance to Plasmodium falciparum in natural populations of A. gambiae. Analyses of haplotypic and genetic diversity at these 28 loci revealed striking differences among populations in levels of genetic diversity and allele frequencies in coding sequence. Putative signals of positive selection were identified at 11 loci, but only one was shared by two subgroups of A. gambiae. Striking patterns of linkage disequilibrium were observed at several loci. We discuss these results with respect to ecological differences among these strata as well as potential implications for disease transmission. Genetics Society of America 2012-12-01 /pmc/articles/PMC3516473/ /pubmed/23275874 http://dx.doi.org/10.1534/g3.112.004473 Text en Copyright © 2012 Crawford et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Crawford, Jacob E.
Bischoff, Emmanuel
Garnier, Thierry
Gneme, Awa
Eiglmeier, Karin
Holm, Inge
Riehle, Michelle M.
Guelbeogo, Wamdaogo M.
Sagnon, N’Fale
Lazzaro, Brian P.
Vernick, Kenneth D.
Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title_full Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title_fullStr Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title_full_unstemmed Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title_short Evidence for Population-Specific Positive Selection on Immune Genes of Anopheles gambiae
title_sort evidence for population-specific positive selection on immune genes of anopheles gambiae
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516473/
https://www.ncbi.nlm.nih.gov/pubmed/23275874
http://dx.doi.org/10.1534/g3.112.004473
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