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首页> 外文期刊>Gut microbes. >Inflammasomes make the case for litter mate-control led experimental design in studying host-microbiota interactions
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Inflammasomes make the case for litter mate-control led experimental design in studying host-microbiota interactions

机译:炎症作用于研究宿主微生物A相互作用的垃圾伴侣控制LED实验设计

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摘要

Several human diseases are thought to evolve due to a combination of host genetic mutations and environmental factors that include alterations in intestinal microbiota composition termed dysbiosis. Although in some cases, host genetics may shape the gut microbiota and enable it to provoke disease, experimentally disentangling cause and consequence in such host-microbe interactions requires strict control over non-genetic confounding factors. Mouse genetic studies previously proposed Nlrp6/ASC inflammasomes as innate immunity regulators of the intestinal ecosystem. In contrast, using littermate-controlled experimental setups, we recently showed that Nlrp6/ASC inflammasomes do not alter the gut microbiota composition. Our analyses indicated that maternal inheritance and long-term separate housing are non-genetic confounders that preclude the use of non-littermate mice when analyzing host genetic effects on intestinal ecology. Here, we summarize and discuss our gut microbiota analyses in inflammasome-deficient mice for illustrating the importance of littermate experimental design in studying host-microbiota interactions.
机译:由于宿主遗传突变和环境因素的组合包括包括肠道微生物组成的改变而导致的肠微生物组成分所谓的亡血症,几种人类疾病被认为演变。虽然在某些情况下,宿主遗传学可能塑造肠道微生物,但使其能够引发疾病,实验性解开原因和在这种宿主微生物相互作用中的结果需要严格控制非遗传混杂因素。鼠标遗传学研究以前提出了NLRP6 / ASC炎症,是肠道生态系统的先天免疫调节剂。相比之下,使用枯结窝控制的实验设置,我们最近显示NLRP6 / ASC炎性炎症不会改变肠道微生物酵母组合物。我们的分析表明,在分析对肠生态学的宿主遗传效应时,母体遗传和长期单独的住房是非遗传混淆,这妨碍了非凋落物小鼠的使用。在这里,我们总结并讨论了炎症组缺陷小鼠中的肠道微生物群分析,用于说明凋落物实验设计在研究宿主微生物群相互作用中的重要性。

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