Evidence map›Paper›PMID 39252007›Full record

ArticleBMC infectious diseases2024

Genomic approach to determine sources of neonatal Staphylococcus aureus infection from carriage in the Gambia.

Abdoulie Bojang, Matthew Chung, Bully Camara, Isatou Jagne, Romain Guérillot, Ebrahim Ndure, Benjamin P Howden, Anna Roca, Elodie Ghedin

Registry-linked trialAbstract read
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03199547 (Pre-delivery Administration of Azithromycin to Prevent Neonatal Sepsis and Death), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT03199547 phase3completednot on this map

Pre-delivery Administration of Azithromycin to Prevent Neonatal Sepsis and Death: a Phase III Double-blind Randomized Clinical Trial

TypeinterventionalSponsorLondon School of Hygiene and Tropical MedicineRan2017 to 2021Enrolled11,985ConditionsNeonatal SEPSISArmsAzithromycin, Placebo Oral Tablet
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Nasal microbiome inhabitants with anti-Microbiology spectrum · 2025
    Article
  6. 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

9 authors.

Abdoulie BojangSystems Genomics Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Matthew ChungSystems Genomics Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Bully CamaraMRC Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Isatou JagneMRC Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Romain GuérillotDepartment of Microbiology and Immunology, Doherty Institute, University of Melbourne, Melbourne, Australia.
Ebrahim NdureMRC Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Benjamin P HowdenDepartment of Microbiology and Immunology, Doherty Institute, University of Melbourne, Melbourne, Australia.
Anna RocaMRC Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Elodie GhedinSystems Genomics Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA. elodie.ghedin@nih.gov.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is a major cause of neonatal infections in various anatomical sites, resulting in high morbidity and mortality in The Gambia. These clinical infections are often preceded by nasal carriage of S. aureus, a known risk factor. To determine whether potential sources of newborn S. aureus infections were from carriage, and to characterize S. aureus present in different anatomical sites (blood, ear, eye, umbilical cord, skin, pus, oropharynx, breast milk and vagina), we performed whole-genome sequencing of 172 isolates from clinical sites as well as from healthy and unhealthy carriage. A random selection of mothers (n = 90) and newborns (n = 42) participating in a clinical trial and testing positive for S. aureus were considered for this study. Sequence data were analyzed to determine S. aureus multilocus sequence types and selected antimicrobial and virulence gene profiles. Our findings revealed that in The Gambia, ST15 is the dominant sequence type associated with both carriage and clinical infection. In addition, S. aureus isolates causing clinical infection among neonates were genetically similar to those colonizing their oropharynx, and the different anatomical sites were not found to be uniquely colonized by S. aureus of a single genomic profile. Furthermore, while S. aureus associated with clinical infection had similar antimicrobial resistance gene profiles to carriage isolates, only hemolysin and adhesive factor virulence genes were significantly higher among clinical isolates. In conclusion, this study confirmed S. aureus oropharyngeal colonization among neonates as a potential source of clinical infection in The Gambia. Hence, interventions aiming to reduce neonatal clinical infections in The Gambia should consider decreasing oropharyngeal S. aureus carriage.Trial registration The trial was registered at ClinicalTrials.gov NCT03199547.

Indexed as

Carrier StateStaphylococcal InfectionsStaphylococcus aureusAdultAnti-Bacterial AgentsFemaleGambiaGenome, BacterialGenomicsHumansInfant, NewbornMaleMultilocus Sequence TypingVirulence FactorsWhole Genome SequencingAnti-Bacterial AgentsVirulence FactorsAntimicrobial resistanceSequence typesStaphylococcusThe GambiaVirulence

Identifiers

PMID39252007
PMCPMC11384681

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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.