Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Nat Genet. 2022 Feb;54(2):143-151. doi: 10.1038/s41588-021-00992-y. Epub 2022 Feb 3.
Host genetics are known to influence the gut microbiome, yet their role remains poorly understood. To robustly characterize these effects, we performed a genome-wide association study of 207 taxa and 205 pathways representing microbial composition and function in 7,738 participants of the Dutch Microbiome Project. Two robust, study-wide significant (P < 1.89 × 10) signals near the LCT and ABO genes were found to be associated with multiple microbial taxa and pathways and were replicated in two independent cohorts. The LCT locus associations seemed modulated by lactose intake, whereas those at ABO could be explained by participant secretor status determined by their FUT2 genotype. Twenty-two other loci showed suggestive evidence (P < 5 × 10) of association with microbial taxa and pathways. At a more lenient threshold, the number of loci we identified strongly correlated with trait heritability, suggesting that much larger sample sizes are needed to elucidate the remaining effects of host genetics on the gut microbiome.
宿主遗传学已知会影响肠道微生物组,但它们的作用仍知之甚少。为了准确描述这些影响,我们对荷兰微生物组计划中的 7738 名参与者的 207 个分类群和代表微生物组成和功能的 205 个途径进行了全基因组关联研究。在 LCT 和 ABO 基因附近发现了两个稳健的、具有全研究意义的(P<1.89×10)信号,与多个微生物分类群和途径相关,并在两个独立的队列中得到了复制。LCT 基因座的关联似乎受到乳糖摄入的调节,而 ABO 基因座的关联可以通过参与者的 FUT2 基因型决定的分泌状态来解释。其他 22 个基因座与微生物分类群和途径存在暗示性关联(P<5×10)。在一个更宽松的阈值下,我们确定的与微生物分类群和途径相关的基因座数量与性状遗传力强烈相关,这表明需要更大的样本量来阐明宿主遗传学对肠道微生物组的剩余影响。