Evidence map›Paper›PMID 32070310›Full record

ArticleBMC pediatrics2020

Dynamics of toxigenic Clostridium perfringens colonisation in a cohort of prematurely born neonatal infants.

Alexander G Shaw, Emma Cornwell, Kathleen Sim, Hannah Thrower, Hannah Scott, Joseph C S Brown, Ronald A Dixon, J Simon Kroll

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01102738 (The Microbiota of the Premature Neonatal Gastrointestinal Tract), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 17% 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.

NCT01102738 completednot on this map

The Microbiota of the Premature Neonatal Gastrointestinal Tract: Its Development and Relation to Necrotizing Enterocolitis and Bloodstream Infection

TypeobservationalSponsorImperial College LondonRan2011 to 2014Enrolled369ConditionsPremature Intestinal Microbiota, Necrotizing Enterocolitis, Late Onset Bloodstream Infection
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Gut microbes · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Severe Intravascular Hemolysis fromInfection and drug resistance · 2022
    Article
  8. Prevalence and Genetic Diversity ofInfection and drug resistance · 2021
    Article
  9. Article
  10. 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

8 authors at 3 institutions in 1 country.

Alexander G ShawDepartment of Infectious Disease Epidemiology, Imperial College London, London, UK. a.shaw@imperial.ac.uk.ORCID 0000-0002-3166-872X
Emma CornwellDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
Kathleen SimDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
Hannah ThrowerDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
Hannah ScottDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
Joseph C S BrownSchool of Life Sciences, University of Lincoln, Lincoln, UK.
Ronald A DixonSchool of Life Sciences, University of Lincoln, Lincoln, UK.
J Simon KrollDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
Imperial College London · GBUniversity of Lincoln · GBNIHR Imperial Biomedical Research Centre · GB

Funding

Innovate UK KTP9440Micropathology Ltd P25076National Institute for Health Research (NIHR) Biomedical Research Centre P35969The Winnicott Foundation P26859
6 · The paper itself

Abstract

backgroundClostridium perfringens forms part of the human gut microbiota and has been associated with life-threatening necrotising enterocolitis (NEC) in premature infants. Whether specific toxigenic strains are responsible is unknown, as is the extent of diversity of strains in healthy premature babies. We investigated the C. perfringens carrier status of premature infants in the neonatal intensive care unit, factors influence this status, and the toxic potential of the strains.

methodsC. perfringens was isolated by culture from faecal samples from 333 infants and their toxin gene profiles analysed by PCR. A survival analysis was used to identify factors affecting probability of carriage. Competitive growth experiments were used to explore the results of the survival analysis.

results29.4% of infants were colonized with C. perfringens before they left hospital. Three factors were inversely associated with probability of carriage: increased duration of maternal milk feeds, CPAP oxygen treatment and antibiotic treatment. C. perfringens grew poorly in breast milk and was significantly outperformed by Bifidobacterium infantis, whether grown together or separately. Toxin gene screening revealed that infants carried isolates positive for collagenase, perfringolysin O, beta 2, beta, becA/B, netB and enterotoxin toxin genes, yet none were observed to be associated with the development of NEC.

conclusionsApproximately a third of preterm infants are colonised 3 weeks after birth with toxin gene-carrying C. perfringens. We speculate that increased maternal breast milk, oxygen and antibiotic treatment creates an environment in the gut hostile to growth of C. perfringens. Whilst potentially toxigenic C. perfringens isolates were frequent, no toxin type was associated with NEC.

trial registrationclinicaltrials.gov NCT01102738, registered 13th April 2010.

Indexed as

Clostridium InfectionsClostridium perfringensGastrointestinal MicrobiomeEnterotoxinsFecesFemaleHumansInfantInfant, NewbornInfant, PrematureMalePregnancyEnterotoxinsBreast milkClostridium perfringensNecrotising enterocolitisToxins

Identifiers

PMID32070310
PMCPMC7027286
OpenAlexW3012933586

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.