BMC Genomics (Dec 2024)

Linking the gut microbiome to host DNA methylation by a discovery and replication epigenome-wide association study

  • Ayşe Demirkan,
  • Jenny van Dongen,
  • Casey T. Finnicum,
  • Harm-Jan Westra,
  • Soesma Jankipersadsing,
  • Gonneke Willemsen,
  • Richard G. Ijzerman,
  • Dorret I. Boomsma,
  • Erik A. Ehli,
  • Marc Jan Bonder,
  • Jingyuan Fu,
  • Lude Franke,
  • Cisca Wijmenga,
  • Eco J. C. de Geus,
  • Alexander Kurilshikov,
  • Alexandra Zhernakova

DOI
https://doi.org/10.1186/s12864-024-11136-x
Journal volume & issue
Vol. 25, no. 1
pp. 1 – 11

Abstract

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Summary Microbiome influences multiple human systems, but its effects on gene methylation is unknown. We investigated the relations between gene methylation in blood and the abundance of common gut bacteria profiled by 16s rRNA gene sequencing in two population-based Dutch cohorts: LifeLines-Deep (LLD, n = 616, discovery) and the Netherlands Twin Register (NTR, n = 296, replication). In LLD, we also explored microbial pathways using data generated by shotgun metagenomic sequencing (n = 683). Methylation in both cohorts was profiled in blood samples using the Illumina 450K array. Discovery and replication analysis identified two independent CpGs associated with the genus Eggerthella: cg16586104 (Pmeta−analysis = 3.21 × 10−11) and cg12234533 (Pmeta−analysis = 4.29 × 10−10). We also show that microbiome can mediate the effect of environmental factors on host gene methylation. In this first association study linking epigenome to microbiome, we found and replicated the associations of two CpGs to the abundance of genus Eggerthella and identified microbiome as a mediator of the exposome. These associations are observational and suggest further investigation in larger and longitudinal set-ups.

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