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Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions

Many human genes have adapted to the constant threat of exposure to infectious agents; according to the “hygiene hypothesis,” lack of exposure to parasites in modern settings results in immune imbalances, augmenting susceptibility to the development of autoimmune and allergic conditions. Here, by es...

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Autores principales: Fumagalli, Matteo, Pozzoli, Uberto, Cagliani, Rachele, Comi, Giacomo P., Riva, Stefania, Clerici, Mario, Bresolin, Nereo, Sironi, Manuela
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715056/
https://www.ncbi.nlm.nih.gov/pubmed/19468064
http://dx.doi.org/10.1084/jem.20082779
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author Fumagalli, Matteo
Pozzoli, Uberto
Cagliani, Rachele
Comi, Giacomo P.
Riva, Stefania
Clerici, Mario
Bresolin, Nereo
Sironi, Manuela
author_facet Fumagalli, Matteo
Pozzoli, Uberto
Cagliani, Rachele
Comi, Giacomo P.
Riva, Stefania
Clerici, Mario
Bresolin, Nereo
Sironi, Manuela
author_sort Fumagalli, Matteo
collection PubMed
description Many human genes have adapted to the constant threat of exposure to infectious agents; according to the “hygiene hypothesis,” lack of exposure to parasites in modern settings results in immune imbalances, augmenting susceptibility to the development of autoimmune and allergic conditions. Here, by estimating the number of pathogen species/genera in a specific geographic location (pathogen richness) for 52 human populations and analyzing 91 interleukin (IL)/IL receptor genes (IL genes), we show that helminths have been a major selective force on a subset of these genes. A population genetics analysis revealed that five IL genes, including IL7R and IL18RAP, have been a target of balancing selection, a selection process that maintains genetic variability within a population. Previous identification of polymorphisms in some of these loci, and their association with autoimmune conditions, prompted us to investigate the relationship between adaptation and disease. By searching for variants in IL genes identified in genome-wide association studies, we verified that six risk alleles for inflammatory bowel (IBD) or celiac disease are significantly correlated with micropathogen richness. These data support the hygiene hypothesis for IBD and provide a large set of putative targets for susceptibility to helminth infections.
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spelling pubmed-27150562009-12-08 Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions Fumagalli, Matteo Pozzoli, Uberto Cagliani, Rachele Comi, Giacomo P. Riva, Stefania Clerici, Mario Bresolin, Nereo Sironi, Manuela J Exp Med Article Many human genes have adapted to the constant threat of exposure to infectious agents; according to the “hygiene hypothesis,” lack of exposure to parasites in modern settings results in immune imbalances, augmenting susceptibility to the development of autoimmune and allergic conditions. Here, by estimating the number of pathogen species/genera in a specific geographic location (pathogen richness) for 52 human populations and analyzing 91 interleukin (IL)/IL receptor genes (IL genes), we show that helminths have been a major selective force on a subset of these genes. A population genetics analysis revealed that five IL genes, including IL7R and IL18RAP, have been a target of balancing selection, a selection process that maintains genetic variability within a population. Previous identification of polymorphisms in some of these loci, and their association with autoimmune conditions, prompted us to investigate the relationship between adaptation and disease. By searching for variants in IL genes identified in genome-wide association studies, we verified that six risk alleles for inflammatory bowel (IBD) or celiac disease are significantly correlated with micropathogen richness. These data support the hygiene hypothesis for IBD and provide a large set of putative targets for susceptibility to helminth infections. The Rockefeller University Press 2009-06-08 /pmc/articles/PMC2715056/ /pubmed/19468064 http://dx.doi.org/10.1084/jem.20082779 Text en © 2009 Fumagalli et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Fumagalli, Matteo
Pozzoli, Uberto
Cagliani, Rachele
Comi, Giacomo P.
Riva, Stefania
Clerici, Mario
Bresolin, Nereo
Sironi, Manuela
Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title_full Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title_fullStr Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title_full_unstemmed Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title_short Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
title_sort parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715056/
https://www.ncbi.nlm.nih.gov/pubmed/19468064
http://dx.doi.org/10.1084/jem.20082779
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