Evidence map›Paper›PMID 30307842›Full record

ArticleJournal of medical microbiology2018

Sub-lethal doses of surotomycin and vancomycin have similar effects on Clostridium difficile virulence factor production in vitro.

Michael John Aldape, Savannah Nicole Rice, Kevin Patrick Field, Amy Evelyn Bryant, Dennis Leroy Stevens

Registry-linked trialAbstract read
In one paragraph

Article in Journal of medical microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05320068 (Phase III,randomized,double-blinded Clinical Trial to Evaluate the Effectiveness and Safety of Oral Vancomycin Vs Placebo in the Prevention of Recurrence of C.difficile Infection in Patients Under Treatment with Systemic Antibiotic Therapy), 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, top 89% 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.

NCT05320068 phase3completednot on this mapstarted 2022, after this paper: background citation

Phase III,randomized,double-blinded Clinical Trial to Evaluate the Effectiveness and Safety of Oral Vancomycin Vs Placebo in the Prevention of Recurrence of C.difficile Infection in Patients Under Treatment with Systemic Antibiotic Therapy

TypeinterventionalSponsorJulia OrígüenRan2022 to 2024Enrolled24ConditionsClostridioides Difficile InfectionArmsOral Vancomycin, Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Michael John Aldape1​Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Boise, ID, USA.
Savannah Nicole Rice1​Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Boise, ID, USA.
Kevin Patrick Field1​Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Boise, ID, USA.
Amy Evelyn Bryant1​Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Boise, ID, USA.
Dennis Leroy Stevens1​Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Boise, ID, USA.
University of Washington · US

Funding

The role of the innate immune response in adenovirus Ad14p1 immunopathogenesisP20GM109007 · NIGMS · IDAHO VETERANS RESEARCH / EDUCATION FDN · PI STEVENS, DENNIS L · 2016 to 2021
$10.0M
NIGMS NIH HHS P20 GM109007
6 · The paper itself

Abstract

purposeClostridium difficile is an anaerobic spore-forming bacterial pathogen that causes a spectrum of illness severity ranging from mild diarrhoea to severe life-threatening pseudomembranous colitis. C. difficile infection (CDI) is antibiotic-associated and primarily mediated by two exotoxins, Toxins A and B. We and others have shown that some antibiotics stimulate Toxin A and B production by C. difficile in a strain-specific manner. Still, the effects of newer anti-C. difficile antibiotics on this process and spore formation remain to be investigated. METHODOLOGY: Surotomycin (formally CB-183,315) is a novel, minimally absorbed, narrow-spectrum antibiotic. We determined the effects of surotomycin on C. difficile growth, toxin production and sporulation in historical and BI/NAP1/027 epidemic strains of C. difficile.Results/Key findings. While antibiotic free controls showed toxin production during the stationary phase growth, all strains exposed to sub-inhibitory concentrations of surotomycin and vancomycin demonstrated increased TcdA and TcdB production during early (log phase) growth by all strains. However, this effect was not observed at 24 or 48 h post-treatment by any of the C. difficile strains exposed to either antibiotic. Additionally, all doses of surotomycin and vancomycin suppressed spore formation in all tested strains.

conclusionIn summary, these findings demonstrate that surotomycin and vancomycin have similar effects on exotoxin production and sporulation by C. difficile in vitro. Furthermore, since spores contribute to recurrent infection, the ability of surotomycin to suppress spore formation may explain its ability to disrupt the reinfection cycle in the clinical setting.

Indexed as

Anti-Bacterial AgentsClostridioides difficileGene Expression Regulation, BacterialLipopeptidesMicrobial Sensitivity TestsPeptides, CyclicTime FactorsVancomycinVirulence FactorsAnti-Bacterial AgentsCB-183,315LipopeptidesPeptides, CyclicVancomycinVirulence FactorsClostridium difficileexotoxinsporulationsurotomycinvancomycin

Identifiers

PMID30307842
PMCPMC6557148
OpenAlexW2897250799

What OpenQuestion holds

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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 OpenQuestion graph.