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The effect of host genetics on the gut microbiome

Authors :
Daisy Jonkers
Soesma A Jankipersadsing
Ad A.M. Masclee
Jingyuan Fu
Lude Franke
Marc Jan Bonder
Ramnik J. Xavier
Daria V. Zhernakova
Cisca Wijmenga
Marten H. Hofker
Floris Imhann
Tommi Vatanen
Leo A. B. Joosten
Yang Li
Alexander Kurilshikov
María Carmen Cenit
Arnau Vich Vila
Melanie Schirmer
Zlatan Mujagic
Morris A. Swertz
Rinse K. Weersma
Hermie J. M. Harmsen
Martin Jaeger
Vinod Kumar
Sanne P. Smeekens
Patrick Deelen
Ettje F. Tigchelaar
Marije Oosting
Mihai G. Netea
Alexandra Zhernakova
Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)
Microbes in Health and Disease (MHD)
Center for Liver, Digestive and Metabolic Diseases (CLDM)
Vascular Ageing Programme (VAP)
Translational Immunology Groningen (TRIGR)
Stem Cell Aging Leukemia and Lymphoma (SALL)
MUMC+: MA Med Staf Artsass Interne Geneeskunde (9)
Promovendi NTM
Interne Geneeskunde
MUMC+: MA Maag Darm Lever (9)
RS: NUTRIM - R2 - Gut-liver homeostasis
Source :
Nature Genetics, 48(11), 1407-1412. Nature Publishing Group, Nature Genetics, 48, 1407-1412, Nature Genetics, 48, 11, pp. 1407-1412
Publication Year :
2016

Abstract

Contains fulltext : 171719.pdf (Publisher’s version ) (Closed access) The gut microbiome is affected by multiple factors, including genetics. In this study, we assessed the influence of host genetics on microbial species, pathways and gene ontology categories, on the basis of metagenomic sequencing in 1,514 subjects. In a genome-wide analysis, we identified associations of 9 loci with microbial taxonomies and 33 loci with microbial pathways and gene ontology terms at P < 5 x 10-8. Additionally, in a targeted analysis of regions involved in complex diseases, innate and adaptive immunity, or food preferences, 32 loci were identified at the suggestive level of P < 5 x 10-6. Most of our reported associations are new, including genome-wide significance for the C-type lectin molecules CLEC4F-CD207 at 2p13.3 and CLEC4A-FAM90A1 at 12p13. We also identified association of a functional LCT SNP with the Bifidobacterium genus (P = 3.45 x 10-8) and provide evidence of a gene-diet interaction in the regulation of Bifidobacterium abundance. Our results demonstrate the importance of understanding host-microbe interactions to gain better insight into human health.

Details

Language :
English
ISSN :
10614036
Database :
OpenAIRE
Journal :
Nature Genetics, 48(11), 1407-1412. Nature Publishing Group, Nature Genetics, 48, 1407-1412, Nature Genetics, 48, 11, pp. 1407-1412
Accession number :
edsair.doi.dedup.....e9a35c7a8c83a2871022078cc548121d