利用培养的人类粪便微生物群对秀丽隐杆线虫定殖研究宿主-微生物相互作用

Katrine V. Møller, Jonas Bruhn Wesseltoft, Richelle Malazarte, Sabrina J. Kousgaard, Hans L. Nielsen, Erika Yashiro, Anders Olsen
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引用次数: 0

摘要

微生物群在健康和疾病中的作用是学术界和工业界非常关注的一个研究领域。一个人的微生物群是指主要在肠道中发现的微生物群落。据估计,人体表面和体内大约有39万亿个细菌,越来越多的证据表明它们影响着人类健康。测序技术的进步正在彻底改变人类微生物组的特征。然而,由于人类微生物组及其与宿主的相互作用的复杂性,因果关系和潜在的分子机制在很大程度上仍然未知。转向更简单的宿主生物和使用定义明确的微生物组是加强因果关系和机制研究的两种方法。在这里,我们展示了秀丽隐杆线虫可以作为宿主来研究从人类粪便样品中提取的亚微生物群,这些样品准备用于粪便微生物群移植,遵循简单的喂养方案。在与人类粪便微生物群样本移植后,在蠕虫肠道中鉴定出大约200个扩增子序列变异。我们发现肠道微生物群并不仅仅反映最初喂给蠕虫的细菌群落。因此,我们的实验装置可用于识别和表征塑造微生物群的宿主遗传因素,并提高我们对宿主-人类微生物群相互作用的理解。
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Usage of Cultured Human Fecal Microbiota for Colonization of Caenorhabditis elegans to Study Host–Microbe Interaction
The role of the microbiota in health and disease is a research area receiving much attention in academia and industry. A person’s microbiota refers to a community of microorganisms found mainly in the gut. It is estimated that around 39 trillion bacteria can be found on and inside the human body and there is increasing evidence that they influence human health. Advances in sequencing techniques are revolutionizing characterization of the human microbiome. However, causality and underlying molecular mechanisms are still largely unknown due to the complexity of the human microbiome and its interaction with the host. Turning towards simpler host organisms and using well-defined microbiomes are two ways to strengthen studies of causality and mechanism. Here, we show that the nematode Caenorhabditis elegans can be used as host to study sub-microbiomes derived from human feces samples prepared for fecal microbiota transplantation following a simple feeding protocol. Approximately 200 amplicon sequence variants were identified in the worm gut following transplantation with human fecal microbiota samples. We find that the gut microbiome does not simply reflect the bacterial community initially fed to the worms. Hence, our experimental setup can be used to identify and characterize host genetic factors shaping the microbiota and improving our understanding of host–human microbiome interactions.
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