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Personalized Mapping of Drug Metabolism by the Human Gut Microbiome.
Javdan, Bahar; Lopez, Jaime G; Chankhamjon, Pranatchareeya; Lee, Ying-Chiang J; Hull, Raphaella; Wu, Qihao; Wang, Xiaojuan; Chatterjee, Seema; Donia, Mohamed S.
Affiliation
  • Javdan B; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Lopez JG; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
  • Chankhamjon P; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Lee YJ; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Hull R; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Wu Q; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Wang X; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Chatterjee S; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Donia MS; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA. Electronic address: donia@princeton.edu.
Cell ; 181(7): 1661-1679.e22, 2020 06 25.
Article in En | MEDLINE | ID: mdl-32526207
ABSTRACT
The human gut microbiome harbors hundreds of bacterial species with diverse biochemical capabilities. Dozens of drugs have been shown to be metabolized by single isolates from the gut microbiome, but the extent of this phenomenon is rarely explored in the context of microbial communities. Here, we develop a quantitative experimental framework for mapping the ability of the human gut microbiome to metabolize small molecule drugs Microbiome-Derived Metabolism (MDM)-Screen. Included are a batch culturing system for sustained growth of subject-specific gut microbial communities, an ex vivo drug metabolism screen, and targeted and untargeted functional metagenomic screens to identify microbiome-encoded genes responsible for specific metabolic events. Our framework identifies novel drug-microbiome interactions that vary between individuals and demonstrates how the gut microbiome might be used in drug development and personalized medicine.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Evaluation, Preclinical / Microbiota / Gastrointestinal Microbiome Limits: Adult / Animals / Female / Humans / Male Language: En Journal: Cell Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Evaluation, Preclinical / Microbiota / Gastrointestinal Microbiome Limits: Adult / Animals / Female / Humans / Male Language: En Journal: Cell Year: 2020 Type: Article Affiliation country: United States