Design, construction, and in vivo augmentation of a complex gut microbiome

生物 微生物群 粪便 大肠杆菌 殖民地化 人体微生物群 殖民抵抗 微生物学 粪便细菌疗法 肠道菌群 限制 寄主(生物学) 表型 计算生物学 遗传学 基因 免疫学 抗生素 工程类 机械工程 艰难梭菌
作者
Alice G. Cheng,Po-Yi Ho,Andrés Aranda-Díaz,Sunit Jain,Feiqiao Brian Yu,Xiandong Meng,Min Wang,Mikhail Iakiviak,Kazuki Nagashima,Aishan Zhao,Pallavi P. Murugkar,Advait Patil,Katayoon Atabakhsh,Allison M. Weakley,Yan Jia,Ariel R. Brumbaugh,Steven K. Higginbottom,Alejandra Dimas,Anthony L. Shiver,Adam M. Deutschbauer
出处
期刊:Cell [Cell Press]
卷期号:185 (19): 3617-3636.e19 被引量:243
标识
DOI:10.1016/j.cell.2022.08.003
摘要

Efforts to model the human gut microbiome in mice have led to important insights into the mechanisms of host-microbe interactions. However, the model communities studied to date have been defined or complex, but not both, limiting their utility. Here, we construct and characterize in vitro a defined community of 104 bacterial species composed of the most common taxa from the human gut microbiota (hCom1). We then used an iterative experimental process to fill open niches: germ-free mice were colonized with hCom1 and then challenged with a human fecal sample. We identified new species that engrafted following fecal challenge and added them to hCom1, yielding hCom2. In gnotobiotic mice, hCom2 exhibited increased stability to fecal challenge and robust colonization resistance against pathogenic Escherichia coli. Mice colonized by either hCom2 or a human fecal community are phenotypically similar, suggesting that this consortium will enable a mechanistic interrogation of species and genes on microbiome-associated phenotypes.
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