National Key Laboratory for Swine Genetic Improvement and Production Technology, Ministry of Science and Technology of China, Jiangxi Agricultural University, Nanchang, PR China.
Unit of Animal Genomics, GIGA-Institute and Faculty of Veterinary Medicine, University of Liege, Liege, Belgium.
Nature. 2022 Jun;606(7913):358-367. doi: 10.1038/s41586-022-04769-z. Epub 2022 Apr 27.
The composition of the intestinal microbiome varies considerably between individuals and is correlated with health. Understanding the extent to which, and how, host genetics contributes to this variation is essential yet has proved to be difficult, as few associations have been replicated, particularly in humans. Here we study the effect of host genotype on the composition of the intestinal microbiota in a large mosaic pig population. We show that, under conditions of exacerbated genetic diversity and environmental uniformity, microbiota composition and the abundance of specific taxa are heritable. We map a quantitative trait locus affecting the abundance of Erysipelotrichaceae species and show that it is caused by a 2.3 kb deletion in the gene encoding N-acetyl-galactosaminyl-transferase that underpins the ABO blood group in humans. We show that this deletion is a ≥3.5-million-year-old trans-species polymorphism under balancing selection. We demonstrate that it decreases the concentrations of N-acetyl-galactosamine in the gut, and thereby reduces the abundance of Erysipelotrichaceae that can import and catabolize N-acetyl-galactosamine. Our results provide very strong evidence for an effect of the host genotype on the abundance of specific bacteria in the intestine combined with insights into the molecular mechanisms that underpin this association. Our data pave the way towards identifying the same effect in rural human populations.
肠道微生物组的组成在个体之间差异很大,与健康有关。了解宿主遗传因素在多大程度上以及如何导致这种变化至关重要,但事实证明这很困难,因为很少有相关性得到证实,特别是在人类中。在这里,我们研究了宿主基因型对大型马赛克猪群体肠道微生物组组成的影响。我们表明,在遗传多样性加剧和环境均匀的条件下,微生物组组成和特定分类群的丰度是可遗传的。我们绘制了一个影响肠杆菌科物种丰度的数量性状基因座,并表明它是由人类 ABO 血型基因编码 N-乙酰半乳糖胺基转移酶的 2.3kb 缺失引起的。我们表明,这种缺失是一种在平衡选择下存在了≥350 万年的跨物种多态性。我们证明它降低了肠道中 N-乙酰半乳糖胺的浓度,从而减少了可以摄取和代谢 N-乙酰半乳糖胺的肠杆菌科的丰度。我们的研究结果为宿主基因型对肠道中特定细菌丰度的影响提供了非常有力的证据,并深入了解了支持这种关联的分子机制。我们的数据为在农村人群中识别相同的影响铺平了道路。