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人体肠微生物组药物代谢图谱问世
作者:小柯机器人 发布时间:2020/6/12 13:20:35

近日,美国普林斯顿大学Mohamed S. Donia及其课题组绘制了人体肠微生物组对药物代谢的个性化图谱。相关论文于2020年6月10日在线发表在《细胞》杂志上。

研究人员开发了一个定量实验框架,用于绘制人类肠道微生物组代谢小分子药物的能力:微生物组衍生代谢(MDM)—筛选。这些实验包括用于个体特异性肠道微生物群落持续生长的分批培养系统、离体药物代谢筛选以及靶向和非靶向功能宏基因组筛选(用于鉴定特定代谢事件的微生物编码基因)。
 
这一框架确定了个体之间不同的新型药物与微生物组相互作用,并展示了肠道微生物组能够如何被用于药物开发和个性化医疗。
 
据悉,人类肠道微生物组拥有数百种具有多种生化能力的细菌。数十种药物被发现能够由肠道微生物组的单个分离株所代谢,但是这种现象的程度在微生物群落的背景下很少被探索。
 
附:英文原文

Title: Personalized Mapping of Drug Metabolism by the Human Gut Microbiome

Author: Bahar Javdan, Jaime G. Lopez, Pranatchareeya Chankhamjon, Ying-Chiang J. Lee, Raphaella Hull, Qihao Wu, Xiaojuan Wang, Seema Chatterjee, Mohamed S. Donia

Issue&Volume: 2020-06-10

Abstract: The human gut microbiome harbors hundreds of bacterial species with diverse biochemicalcapabilities. Dozens of drugs have been shown to be metabolized by single isolatesfrom the gut microbiome, but the extent of this phenomenon is rarely explored in thecontext of microbial communities. Here, we develop a quantitative experimental frameworkfor mapping the ability of the human gut microbiome to metabolize small molecule drugs:Microbiome-Derived Metabolism (MDM)-Screen. Included are a batch culturing systemfor sustained growth of subject-specific gut microbial communities, an ex vivo drug metabolism screen, and targeted and untargeted functional metagenomic screensto identify microbiome-encoded genes responsible for specific metabolic events. Ourframework identifies novel drug-microbiome interactions that vary between individualsand demonstrates how the gut microbiome might be used in drug development and personalized medicine.

DOI: 10.1016/j.cell.2020.05.001

Source: https://www.cell.com/cell/fulltext/S0092-8674(20)30563-8

期刊信息
Cell:《细胞》,创刊于1974年。隶属于细胞出版社,最新IF:36.216
官方网址:https://www.cell.com/