Evidence map›Paper›PMID 32526207›Full record

ArticleCell2020

Personalized Mapping of Drug Metabolism by the Human Gut Microbiome.

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

Abstract read
In one paragraph

Article in Cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 249 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
249citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

249 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Gut microbes · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Harnessing the microbiome for cancer therapy.Nature reviews. Microbiology · 2026
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

189 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Bahar JavdanDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Jaime G LopezLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Pranatchareeya ChankhamjonDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Ying-Chiang J LeeDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Raphaella HullDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Qihao WuDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Xiaojuan WangDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Seema ChatterjeeDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Mohamed S DoniaDepartment 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.

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Uncultivated bacterial symbionts of humans: an untapped resource for drug discoveryDP2AI124441 · NIAID · PRINCETON UNIVERSITY · PI ABOU DONIA, MOHAMED · 2015 to 2015
$2.4M
NIAID NIH HHS DP2 AI124441NIGMS NIH HHS T32 GM007388
6 · The paper itself

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.

Indexed as

AdultAnimalsBacteriaBiomarkers, PharmacologicalDrug Evaluation, PreclinicalFecesFemaleGastrointestinal MicrobiomeHealthy VolunteersHumansMaleMetagenomeMetagenomicsMiceMice, Inbred C57BLMicrobiotaBiomarkers, PharmacologicalPharmaceutical PreparationsRNA, Ribosomal, 16Sdrug metabolismdrug-microbiome interactionsfunctional metagenomicsgut microbiomemicrobial communitypersonalized medicine

Identifiers

PMID32526207
PMCPMC8591631

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.