Evidence map›Paper›PMID 37823484›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2024

Impact of a Purified Microbiome Therapeutic on Abundance of Antimicrobial Resistance Genes in Patients With Recurrent Clostridioides difficile Infection.

Timothy J Straub, Mary-Jane Lombardo, Jessica A Bryant, Liyang Diao, Thomas P Lodise, Daniel E Freedberg, Jennifer R Wortman, Kevin D Litcofsky, Brooke R Hasson, Barbara H McGovern and 2 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Microbes as medicine.Annals of the New York Academy of Sciences · 2024
    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

12 authors at 3 institutions in 1 country.

Timothy J StraubSeres Therapeutics, Cambridge, Massachusetts, USA.
Mary-Jane LombardoSeres Therapeutics, Cambridge, Massachusetts, USA.
Jessica A BryantSeres Therapeutics, Cambridge, Massachusetts, USA.
Liyang DiaoSeres Therapeutics, Cambridge, Massachusetts, USA.
Thomas P LodiseAlbany College of Pharmacy and Health Sciences, Albany, New York, USA.ORCID 0000-0002-4730-0655
Daniel E FreedbergDivision of Digestive and Liver Diseases, Columbia University Irving Medical Center-New York Presbyterian Hospital, New York, New York, USA.
Jennifer R WortmanSeres Therapeutics, Cambridge, Massachusetts, USA.
Kevin D LitcofskySeres Therapeutics, Cambridge, Massachusetts, USA.
Brooke R HassonSeres Therapeutics, Cambridge, Massachusetts, USA.
Barbara H McGovernSeres Therapeutics, Cambridge, Massachusetts, USA.ORCID 0000-0003-4451-2393
Christopher B FordSeres Therapeutics, Cambridge, Massachusetts, USA.
Matthew R HennSeres Therapeutics, Cambridge, Massachusetts, USA.
Seres Therapeutics (United States) · USAlbany College of Pharmacy and Health Sciences · USNewYork–Presbyterian Hospital · US

Funding

Seres Therapeutics
6 · The paper itself

Abstract

backgroundThe gastrointestinal microbiota is an important line of defense against colonization with antimicrobial resistant (AR) bacteria. In this post hoc analysis of the phase 3 ECOSPOR III trial, we assessed impact of a microbiota-based oral therapeutic (fecal microbiota spores, live; VOWST Oral Spores [VOS], formerly SER-109]; Seres Therapeutics) compared with placebo, on AR gene (ARG) abundance in patients with recurrent Clostridioides difficile infection (rCDI).

methodsAdults with rCDI were randomized to receive VOS or placebo orally for 3 days following standard-of-care antibiotics. ARG and taxonomic profiles were generated using whole metagenomic sequencing of stool at baseline and weeks 1, 2, 8, and 24 posttreatment.

resultsBaseline (n = 151) and serial posttreatment stool samples collected through 24 weeks (total N = 472) from 182 patients (59.9% female; mean age: 65.5 years) in ECOSPOR III as well as 68 stool samples obtained at a single time point from a healthy cohort were analyzed. Baseline ARG abundance was similar between arms and significantly elevated versus the healthy cohort. By week 1, there was a greater decline in ARG abundance in VOS versus placebo (P = .003) in association with marked decline of Proteobacteria and repletion of spore-forming Firmicutes, as compared with baseline. We observed abundance of Proteobacteria and non-spore-forming Firmicutes were associated with ARG abundance, while spore-forming Firmicutes abundance was negatively associated.

conclusionsThis proof-of-concept analysis suggests that microbiome remodeling with Firmicutes spores may be a potential novel approach to reduce ARG colonization in the gastrointestinal tract.

Indexed as

Clostridioides difficileClostridium InfectionsMicrobiotaAdultAgedAnti-Bacterial AgentsBacillotaBacteriaDrug Resistance, BacterialFecal Microbiota TransplantationFemaleHumansMaleAnti-Bacterial Agentsantimicrobial resistanceClostridioides difficile infectionmicrobiome therapeuticsSER-109VOWST

Identifiers

PMID37823484
PMCPMC11006105
OpenAlexW4387564179

What OpenQuestion holds

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LicenceCC BY
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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.