Application of the distance-based F test in an mGWAS investigating β diversity of intestinal microbiota identifies variants in SLC9A8 (NHE8) and 3 other loci

Gut Microbes. 2018 Jan 2;9(1):68-75. doi: 10.1080/19490976.2017.1356979. Epub 2017 Aug 28.

Abstract

Factors shaping the human intestinal microbiota range from environmental influences, like smoking and exercise, over dietary patterns and disease to the host's genetic variation. Recently, we could show in a microbiome genome-wide association study (mGWAS) targeting genetic variation influencing the β diversity of gut microbial communities, that approximately 10% of the overall gut microbiome variation can be explained by host genetics. Here, we report on the application of a new method for genotype-β-diversity association testing, the distance-based F (DBF) test. With this we identified 4 loci with genome-wide significant associations, harboring the genes CBEP4, SLC9A8, TNFSF4, and SP140, respectively. Our findings highlight the utility of the high-performance DBF test in β diversity GWAS and emphasize the important role of host genetics and immunity in shaping the human intestinal microbiota.

Keywords: GWAS; IBD; human gut microbiota; immunity; β diversity.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Nuclear / genetics
  • Bacteria / classification
  • Bacteria / genetics*
  • Biodiversity*
  • Gastrointestinal Microbiome*
  • Genetic Loci / genetics*
  • Genetic Variation
  • Genome-Wide Association Study*
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunity / genetics
  • Models, Statistical*
  • OX40 Ligand / genetics
  • RNA-Binding Proteins / genetics
  • Reproducibility of Results
  • Sodium-Hydrogen Exchangers / genetics
  • Transcription Factors / genetics

Substances

  • Antigens, Nuclear
  • CPEB4 protein, human
  • OX40 Ligand
  • RNA-Binding Proteins
  • SLC9A8 protein, human
  • SP140 protein, human
  • Sodium-Hydrogen Exchangers
  • TNFSF4 protein, human
  • Transcription Factors