Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences University of Florida, Gainesville, 32611-0700, FL, USA.
Biological Sciences, Universidade Federal do Pampa, São Gabriel, 97300-000, Brazil.
Nat Commun. 2019 Aug 9;10(1):3621. doi: 10.1038/s41467-019-11460-x.
Susceptibility to many human autoimmune diseases is under strong genetic control by class II human leukocyte antigen (HLA) allele combinations. These genes remain by far the greatest risk factors in the development of type 1 diabetes and celiac disease. Despite this, little is known about HLA influences on the composition of the human gut microbiome, a potential source of environmental influence on disease. Here, using a general population cohort from the All Babies in Southeast Sweden study, we report that genetic risk for developing type 1 diabetes autoimmunity is associated with distinct changes in the gut microbiome. Both the core microbiome and beta diversity differ with HLA risk group and genotype. In addition, protective HLA haplotypes are associated with bacterial genera Intestinibacter and Romboutsia. Thus, general population cohorts are valuable in identifying potential environmental triggers or protective factors for autoimmune diseases that may otherwise be masked by strong genetic control.
许多人类自身免疫性疾病的易感性受人类白细胞抗原(HLA)II 类等位基因组合的强烈遗传控制。这些基因仍然是 1 型糖尿病和乳糜泻发展的最大风险因素。尽管如此,人们对 HLA 对人类肠道微生物组组成的影响知之甚少,而肠道微生物组是环境对疾病影响的潜在来源。在这里,我们使用来自瑞典东南部所有婴儿研究的一般人群队列,报告称,1 型糖尿病自身免疫发病的遗传风险与肠道微生物组的明显变化相关。核心微生物组和β多样性均因 HLA 风险组和基因型而异。此外,保护性 HLA 单倍型与细菌属 Intestinibacter 和 Romboutsia 相关。因此,一般人群队列在确定自身免疫性疾病的潜在环境触发因素或保护因素方面具有价值,否则这些因素可能会被强烈的遗传控制所掩盖。