Evidence map›Paper›PMID 40672762›Full record

ArticleOpen forum infectious diseases2025

Decreased Antimicrobial Resistance Gene Richness Following Fecal Microbiota, Live-jslm (REBYOTA®) Administration: Post Hoc Analysis of PUNCH CD3.

Elizabeth Adamowicz, Colleen S Kraft, Tonya Ward, Nirja Mehta, William D Shannon, Rohan Mishra, Ken F Blount

Registry-linked trialAbstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03244644 (A Phase 3 Prospective, Randomized, Double-blinded, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of RBX2660), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT03244644 phase3completednot on this map

A Phase 3 Prospective, Randomized, Double-blinded, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of RBX2660 (Microbiota Suspension) for the Prevention of Clostridium Difficile Infection

TypeinterventionalSponsorRebiotix Inc.Ran2017 to 2020Enrolled320ConditionsClostridium Difficile Infection (CDI)ArmsRBX2660, Placebo, Open label RBX2660 (only for confirmed CDI recurrence)
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

7 authors.

Elizabeth AdamowiczFerring Pharmaceuticals, Roseville, Minnesota, USA.
Colleen S KraftDivision of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Atlanta, Georgia, USA.
Tonya WardFerring Pharmaceuticals, Roseville, Minnesota, USA.
Nirja MehtaDivision of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0001-6324-0077
William D ShannonBioRankings, St Louis, Missouri, USA.
Rohan MishraBioRankings, St Louis, Missouri, USA.
Ken F BlountFerring Pharmaceuticals, Roseville, Minnesota, USA.ORCID https://orcid.org/0000-0002-2062-5484

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The human gastrointestinal microbiome helps maintain vital functions related to overall health, including resistance to pathogen colonization. Disruption of the microbiome, leading to loss of colonization resistance, can be caused by multiple factors, including antimicrobial use. The loss of colonization resistance may lead to establishment or proliferation of opportunistic bacteria that carry genes associated with antimicrobial resistance, potentially increasing the risk of infection by such antimicrobial-resistant bacteria. A potential approach to mitigating this risk involves restoration of healthier microbiota and pathogen colonization resistance. Methods: A metagenomic sequencing method was used to conduct a post hoc analysis of antibiotic resistance gene richness among fecal samples from participants administered fecal microbiota, live-jslm (REBYOTA; abbreviated as RBL) or placebo in the PUNCH CD3 study (NCT03244644) for the prevention of recurrent Results: At baseline, participants had higher antibiotic resistance gene richness than a representative healthy cohort. Over time, RBL responders had lower antibiotic resistance gene richness at the class, group, and mechanism levels as compared with placebo responders. These differences were evident as early as 1 week after administration and sustained for at least 6 months. RBL responders also had decreased richness of antibiotic resistance genes deemed high risk based on designated bacterial public health threats. Conclusions: These data support a model in which microbiota-based products, including RBL, may reduce antibiotic resistance gene richness, thereby possibly reducing the risk of antimicrobial-resistant organism infection. Trial registration: NCT03244644 (https://clinicaltrials.gov/study/NCT03244644; 9 August 2017).

Indexed as

antimicrobial resistance genesantimicrobial-resistant organismsCDIClostridioides difficile infection

Identifiers

PMID40672762
PMCPMC12264430

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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 Socratic graph.