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Genetic effects on the commensal microbiota in inflammatory bowel disease patients

Several bacteria in the gut microbiota have been shown to be associated with inflammatory bowel disease (IBD), and dozens of IBD genetic variants have been identified in genome-wide association studies. However, the role of the microbiota in the etiology of IBD in terms of host genetic susceptibilit...

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Autores principales: Aschard, Hugues, Laville, Vincent, Tchetgen, Eric Tchetgen, Knights, Dan, Imhann, Floris, Seksik, Philippe, Zaitlen, Noah, Silverberg, Mark S., Cosnes, Jacques, Weersma, Rinse K., Xavier, Ramnik, Beaugerie, Laurent, Skurnik, David, Sokol, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426259/
https://www.ncbi.nlm.nih.gov/pubmed/30849075
http://dx.doi.org/10.1371/journal.pgen.1008018
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author Aschard, Hugues
Laville, Vincent
Tchetgen, Eric Tchetgen
Knights, Dan
Imhann, Floris
Seksik, Philippe
Zaitlen, Noah
Silverberg, Mark S.
Cosnes, Jacques
Weersma, Rinse K.
Xavier, Ramnik
Beaugerie, Laurent
Skurnik, David
Sokol, Harry
author_facet Aschard, Hugues
Laville, Vincent
Tchetgen, Eric Tchetgen
Knights, Dan
Imhann, Floris
Seksik, Philippe
Zaitlen, Noah
Silverberg, Mark S.
Cosnes, Jacques
Weersma, Rinse K.
Xavier, Ramnik
Beaugerie, Laurent
Skurnik, David
Sokol, Harry
author_sort Aschard, Hugues
collection PubMed
description Several bacteria in the gut microbiota have been shown to be associated with inflammatory bowel disease (IBD), and dozens of IBD genetic variants have been identified in genome-wide association studies. However, the role of the microbiota in the etiology of IBD in terms of host genetic susceptibility remains unclear. Here, we studied the association between four major genetic variants associated with an increased risk of IBD and bacterial taxa in up to 633 IBD cases. We performed systematic screening for associations, identifying and replicating associations between NOD2 variants and two taxa: the Roseburia genus and the Faecalibacterium prausnitzii species. By exploring the overall association patterns between genes and bacteria, we found that IBD risk alleles were significantly enriched for associations concordant with bacteria-IBD associations. To understand the significance of this pattern in terms of the study design and known effects from the literature, we used counterfactual principles to assess the fitness of a few parsimonious gene-bacteria-IBD causal models. Our analyses showed evidence that the disease risk of these genetic variants were likely to be partially mediated by the microbiome. We confirmed these results in extensive simulation studies and sensitivity analyses using the association between NOD2 and F. prausnitzii as a case study.
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spelling pubmed-64262592019-04-01 Genetic effects on the commensal microbiota in inflammatory bowel disease patients Aschard, Hugues Laville, Vincent Tchetgen, Eric Tchetgen Knights, Dan Imhann, Floris Seksik, Philippe Zaitlen, Noah Silverberg, Mark S. Cosnes, Jacques Weersma, Rinse K. Xavier, Ramnik Beaugerie, Laurent Skurnik, David Sokol, Harry PLoS Genet Research Article Several bacteria in the gut microbiota have been shown to be associated with inflammatory bowel disease (IBD), and dozens of IBD genetic variants have been identified in genome-wide association studies. However, the role of the microbiota in the etiology of IBD in terms of host genetic susceptibility remains unclear. Here, we studied the association between four major genetic variants associated with an increased risk of IBD and bacterial taxa in up to 633 IBD cases. We performed systematic screening for associations, identifying and replicating associations between NOD2 variants and two taxa: the Roseburia genus and the Faecalibacterium prausnitzii species. By exploring the overall association patterns between genes and bacteria, we found that IBD risk alleles were significantly enriched for associations concordant with bacteria-IBD associations. To understand the significance of this pattern in terms of the study design and known effects from the literature, we used counterfactual principles to assess the fitness of a few parsimonious gene-bacteria-IBD causal models. Our analyses showed evidence that the disease risk of these genetic variants were likely to be partially mediated by the microbiome. We confirmed these results in extensive simulation studies and sensitivity analyses using the association between NOD2 and F. prausnitzii as a case study. Public Library of Science 2019-03-08 /pmc/articles/PMC6426259/ /pubmed/30849075 http://dx.doi.org/10.1371/journal.pgen.1008018 Text en © 2019 Aschard 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Aschard, Hugues
Laville, Vincent
Tchetgen, Eric Tchetgen
Knights, Dan
Imhann, Floris
Seksik, Philippe
Zaitlen, Noah
Silverberg, Mark S.
Cosnes, Jacques
Weersma, Rinse K.
Xavier, Ramnik
Beaugerie, Laurent
Skurnik, David
Sokol, Harry
Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title_full Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title_fullStr Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title_full_unstemmed Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title_short Genetic effects on the commensal microbiota in inflammatory bowel disease patients
title_sort genetic effects on the commensal microbiota in inflammatory bowel disease patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426259/
https://www.ncbi.nlm.nih.gov/pubmed/30849075
http://dx.doi.org/10.1371/journal.pgen.1008018
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