Evidence map›Paper›PMID 39701818›Full record

ArticleJournal of applied microbiology2025

Perturbations in the gut microbiome of C57BL/6 mice by the sobriety aid Antabuse® (disulfiram).

Sarah E Evans, Meagan E Valentine, Fallon Gallimore, Yogesh Meka, Samuel I Koehler, Hongwei D Yu, Monica A Valentovic, Timothy E Long

Abstract read
In one paragraph

Article in Journal of applied microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Sarah E EvansDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.
Meagan E ValentineDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.
Fallon GallimoreDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.
Yogesh MekaDepartment of Pharmaceutical Sciences, School of Pharmacy, Marshall University, Huntington, WV 25755, United States.
Samuel I KoehlerBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87545, United States.
Hongwei D YuDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.
Monica A ValentovicDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.
Timothy E LongDepartment of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, United States.ORCID 0000-0003-0213-4726

Funding

WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI Travis Salisbury · 2012 to 2026
$61.1M
Discovery of Disulfiram as an Anti-MRSA Antibiotic AdjuvantR15AI151970 · NIAID · MARSHALL UNIVERSITY · PI LONG, TIMOTHY EDWARD · 2020 to 2020
$434k
National Institute of Allergy and Infectious Diseases AI151970NIAID NIH HHS R15 AI151970NIGMS NIH HHS P20 GM103434NIH HHS P20GM103434
6 · The paper itself

Abstract

aimsDisulfiram (Antabuse®) is an oral alcohol sobriety medication that exhibits antimicrobial activity against Gram-positive facultative anaerobes. The aims of this study were to measure the antimicrobial activity against anaerobic bacteria of the gut human microbiome and establish the extent that disulfiram alters the microbial composition of the ileum, cecum, and feces using C57BL/6 mice. METHODS AND

resultsAntimicrobial susceptibility testing by the microdilution method revealed that disulfiram inhibits the in vitro growth of gut anaerobic species of Bacteroides, Clostridium, Peptostreptococcus, and Porphyromonas. Differential sequencing of 16S rRNA isolated from the ileum, cecum, and feces contents of treated vs. untreated mice showed that disulfiram enriches the Gram-negative enteric population. In female mice, the enrichment was greatest in the ileum, whereas the feces composition in male mice was the most heavily altered.

conclusionsDaily administration of oral disulfiram depletes the enteric Gram-positive anaerobe population as predicted by the minimum inhibitory concentration data for isolates from the human gut microbiota.

Indexed as

DisulfiramFecesGastrointestinal MicrobiomeMice, Inbred C57BLRNA, Ribosomal, 16SAlcohol DeterrentsAnimalsAnti-Bacterial AgentsBacteria, AnaerobicBacteroidesCecumClostridiumFemaleHumansIleumMaleAlcohol DeterrentsAnti-Bacterial AgentsDisulfiramRNA, Ribosomal, 16Sanaerobesantimicrobialsintestinal microbiologymicrobiomepharmaceuticals

Identifiers

PMID39701818
PMCPMC11704607

What OpenQuestion holds

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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.