Evidence map›Paper›PMID 26488281›Full record

ReviewAnnual review of microbiology2015

Interactions Between the Gastrointestinal Microbiome and Clostridium difficile.

Casey M Theriot, Vincent B Young

Abstract readReview
In one paragraph

Review in Annual review of microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed, 2 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

187 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Impact of a Purified Microbiome Therapeutic on Abundance of Antimicrobial Resistance Genes in Patients With Recurrent Clostridioides difficile Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Trial
  6. Trial
  7. Trial
  8. Trial
  9. SER-109, an Investigational Microbiome Drug to Reduce Recurrence After Clostridioides difficile Infection: Lessons Learned From a Phase 2 Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Trial
  10. Trial
  11. Review
  12. Review
  13. Pathogens (Basel, Switzerland) · 2026
    Review
  14. Biomarkers for Early Severity Prediction inMedicina (Kaunas, Lithuania) · 2026
    Review
  15. Article
  16. Article
  17. Characterization of the Gut Microbiome of Patients withPathogens (Basel, Switzerland) · 2026
    Article
  18. Article
  19. Cytoplasmic membrane vesicles fromFrontiers in microbiology · 2026
    Article
  20. Review

127 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

2 authors.

Casey M TheriotDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina 27607.
Vincent B Young

Funding

University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
The Interplay Between Host Immunity and Clostridium difficile PathogenesisU19AI090871 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YOUNG, VINCENT B · 2010 to 2014
$7.5M
Shifts in the Gastrointestinal Metabolome During Clostridium difficile InfectionK01GM109236 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THERIOT, CASEY MICHELLE · 2013 to 2015
$371k
NIAID NIH HHS U19 AI090871NIAID NIH HHS U19AI090871NIDDK NIH HHS 5P30 DK034933NIDDK NIH HHS P30 DK034933NIGMS NIH HHS K01 GM109236NIGMS NIH HHS K01GM109236
6 · The paper itself

Abstract

Antibiotics have significant and long-lasting effects on the intestinal microbiota and consequently reduce colonization resistance against pathogens, including Clostridium difficile. By altering the community structure of the gut microbiome, antibiotics alter the intestinal metabolome, which includes both host- and microbe-derived metabolites. The mechanisms by which antibiotics reduce colonization resistance against C. difficile are unknown yet important for development of preventative and therapeutic approaches against this pathogen. This review focuses on how antibiotics alter the structure of the gut microbiota and how this alters microbial metabolism in the intestine. Interactions between gut microbial products and C. difficile spore germination, growth, and toxin production are discussed. New bacterial therapies to restore changes in bacteria-driven intestinal metabolism following antibiotics will have important applications for treatment and prevention of C. difficile infection.

Indexed as

Gastrointestinal MicrobiomeAnimalsAnti-Bacterial AgentsClostridioides difficileClostridium InfectionsFermentationHumansImmune EvasionMicrobial InteractionsMicrobiotaAnti-Bacterial Agentsantibioticsbacterial metabolismbile acidsClostridium difficilecolonization resistancegut microbiota

Identifiers

PMID26488281
PMCPMC4892173

What OpenQuestion holds

Textmetadata
LicenceTDM
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.