Department of Internal Medicine, Ghent University, Ghent, Belgium; VIB-UGent Center for Inflammation Research, VIB, Ghent, Belgium.
Maurice Müller Laboratories (DKF), Universitätsklinik für Viszerale Chirurgie und Medizin Inselspital, University of Bern, Bern, Switzerland.
Immunity. 2017 Aug 15;47(2):339-348.e4. doi: 10.1016/j.immuni.2017.07.011. Epub 2017 Aug 8.
The gut microbiota regulate susceptibility to multiple human diseases. The Nlrp6-ASC inflammasome is widely regarded as a hallmark host innate immune axis that shapes the gut microbiota composition. This notion stems from studies reporting dysbiosis in mice lacking these inflammasome components when compared with non-littermate wild-type animals. Here, we describe microbial analyses in inflammasome-deficient mice while minimizing non-genetic confounders using littermate-controlled Nlrp6-deficient mice and ex-germ-free littermate-controlled ASC-deficient mice that were all allowed to shape their gut microbiota naturally after birth. Careful microbial phylogenetic analyses of these cohorts failed to reveal regulation of the gut microbiota composition by the Nlrp6- and ASC-dependent inflammasomes. Our results obtained in two geographically separated animal facilities dismiss a generalizable impact of Nlrp6- and ASC-dependent inflammasomes on the composition of the commensal gut microbiota and highlight the necessity for littermate-controlled experimental design in assessing the influence of host immunity on gut microbial ecology.
肠道微生物群调节多种人类疾病的易感性。Nlrp6-ASC 炎性小体被广泛认为是一种标志性的宿主先天免疫轴,它塑造了肠道微生物群的组成。这一观点源于研究报告,与非同窝野生型动物相比,缺乏这些炎性小体成分的小鼠存在菌群失调。在这里,我们描述了在炎性小体缺陷小鼠中进行的微生物分析,同时使用同窝对照 Nlrp6 缺陷小鼠和体外定植的同窝对照 ASC 缺陷小鼠最小化非遗传混杂因素,这些小鼠在出生后都允许其自然形成肠道微生物群。对这些队列进行仔细的微生物系统发育分析未能揭示 Nlrp6 和 ASC 依赖性炎性小体对肠道微生物群组成的调节作用。我们在两个地理位置分离的动物设施中获得的结果否定了 Nlrp6 和 ASC 依赖性炎性小体对共生肠道微生物群组成的普遍影响,并强调了在评估宿主免疫对肠道微生物生态的影响时,同窝对照实验设计的必要性。