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Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations

BACKGROUND: Non-celiac wheat sensitivity is an emerging wheat-related syndrome showing peak prevalence in Western populations. Recent studies hypothesize that new gliadin alleles introduced in the human diet by replacement of ancient wheat with modern varieties can prompt immune responses mediated b...

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Autores principales: Sazzini, Marco, De Fanti, Sara, Cherubini, Anna, Quagliariello, Andrea, Profiti, Giuseppe, Martelli, Pier Luigi, Casadio, Rita, Ricci, Chiara, Campieri, Massimo, Lanzini, Alberto, Volta, Umberto, Caio, Giacomo, Franceschi, Claudio, Spisni, Enzo, Luiselli, Donata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968434/
https://www.ncbi.nlm.nih.gov/pubmed/27551316
http://dx.doi.org/10.1186/s12263-016-0532-4
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author Sazzini, Marco
De Fanti, Sara
Cherubini, Anna
Quagliariello, Andrea
Profiti, Giuseppe
Martelli, Pier Luigi
Casadio, Rita
Ricci, Chiara
Campieri, Massimo
Lanzini, Alberto
Volta, Umberto
Caio, Giacomo
Franceschi, Claudio
Spisni, Enzo
Luiselli, Donata
author_facet Sazzini, Marco
De Fanti, Sara
Cherubini, Anna
Quagliariello, Andrea
Profiti, Giuseppe
Martelli, Pier Luigi
Casadio, Rita
Ricci, Chiara
Campieri, Massimo
Lanzini, Alberto
Volta, Umberto
Caio, Giacomo
Franceschi, Claudio
Spisni, Enzo
Luiselli, Donata
author_sort Sazzini, Marco
collection PubMed
description BACKGROUND: Non-celiac wheat sensitivity is an emerging wheat-related syndrome showing peak prevalence in Western populations. Recent studies hypothesize that new gliadin alleles introduced in the human diet by replacement of ancient wheat with modern varieties can prompt immune responses mediated by the CXCR3-chemokine axis potentially underlying such pathogenic inflammation. This cultural shift may also explain disease epidemiology, having turned European-specific adaptive alleles previously targeted by natural selection into disadvantageous ones. METHODS: To explore this evolutionary scenario, we performed ultra-deep sequencing of genes pivotal in the CXCR3-inflammatory pathway on individuals diagnosed for non-celiac wheat sensitivity and we applied anthropological evolutionary genetics methods to sequence data from worldwide populations to investigate the genetic legacy of natural selection on these loci. RESULTS: Our results indicate that balancing selection has maintained two divergent CXCL10/CXCL11 haplotypes in Europeans, one responsible for boosting inflammatory reactions and another for encoding moderate chemokine expression. CONCLUSIONS: This led to considerably higher occurrence of the former haplotype in Western people than in Africans and East Asians, suggesting that they might be more prone to side effects related to the consumption of modern wheat varieties. Accordingly, this study contributed to shed new light on some of the mechanisms potentially involved in the disease etiology and on the evolutionary bases of its present-day epidemiological patterns. Moreover, overrepresentation of disease homozygotes for the dis-adaptive haplotype plausibly accounts for their even more enhanced CXCR3-axis expression and for their further increase in disease risk, representing a promising finding to be validated by larger follow-up studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12263-016-0532-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-49684342016-08-22 Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations Sazzini, Marco De Fanti, Sara Cherubini, Anna Quagliariello, Andrea Profiti, Giuseppe Martelli, Pier Luigi Casadio, Rita Ricci, Chiara Campieri, Massimo Lanzini, Alberto Volta, Umberto Caio, Giacomo Franceschi, Claudio Spisni, Enzo Luiselli, Donata Genes Nutr Research BACKGROUND: Non-celiac wheat sensitivity is an emerging wheat-related syndrome showing peak prevalence in Western populations. Recent studies hypothesize that new gliadin alleles introduced in the human diet by replacement of ancient wheat with modern varieties can prompt immune responses mediated by the CXCR3-chemokine axis potentially underlying such pathogenic inflammation. This cultural shift may also explain disease epidemiology, having turned European-specific adaptive alleles previously targeted by natural selection into disadvantageous ones. METHODS: To explore this evolutionary scenario, we performed ultra-deep sequencing of genes pivotal in the CXCR3-inflammatory pathway on individuals diagnosed for non-celiac wheat sensitivity and we applied anthropological evolutionary genetics methods to sequence data from worldwide populations to investigate the genetic legacy of natural selection on these loci. RESULTS: Our results indicate that balancing selection has maintained two divergent CXCL10/CXCL11 haplotypes in Europeans, one responsible for boosting inflammatory reactions and another for encoding moderate chemokine expression. CONCLUSIONS: This led to considerably higher occurrence of the former haplotype in Western people than in Africans and East Asians, suggesting that they might be more prone to side effects related to the consumption of modern wheat varieties. Accordingly, this study contributed to shed new light on some of the mechanisms potentially involved in the disease etiology and on the evolutionary bases of its present-day epidemiological patterns. Moreover, overrepresentation of disease homozygotes for the dis-adaptive haplotype plausibly accounts for their even more enhanced CXCR3-axis expression and for their further increase in disease risk, representing a promising finding to be validated by larger follow-up studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12263-016-0532-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-23 /pmc/articles/PMC4968434/ /pubmed/27551316 http://dx.doi.org/10.1186/s12263-016-0532-4 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sazzini, Marco
De Fanti, Sara
Cherubini, Anna
Quagliariello, Andrea
Profiti, Giuseppe
Martelli, Pier Luigi
Casadio, Rita
Ricci, Chiara
Campieri, Massimo
Lanzini, Alberto
Volta, Umberto
Caio, Giacomo
Franceschi, Claudio
Spisni, Enzo
Luiselli, Donata
Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title_full Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title_fullStr Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title_full_unstemmed Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title_short Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations
title_sort ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day european populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968434/
https://www.ncbi.nlm.nih.gov/pubmed/27551316
http://dx.doi.org/10.1186/s12263-016-0532-4
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