Evidence map›Paper›PMID 39155368›Full record

ArticleBMC microbiology2024

Vaginal colonization with virulent and methicillin resistant Staphylococcus aureus among Ugandan women in Labour.

Freddie Bwanga, Claudine Mukashyaka, David Patrick Kateete, Josephine Tumuhamye, Alfred Okeng, Emmanuel Aboce, Olive Namugga, Richard Kwizera, Halvor Sommerfelt, Victoria Nankabirwa

Abstract read
In one paragraph

Article in BMC microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Antibiotics (Basel, Switzerland) · 2025
    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

10 authors.

Freddie Bwanga *Department of Immunology and Molecular Biology, School of Biomedical Sciences, Makerere University College of Health Sciences, P. O Box 7072, Kampala, Uganda.
Claudine Mukashyaka *Department of Immunology and Molecular Biology, School of Biomedical Sciences, Makerere University College of Health Sciences, P. O Box 7072, Kampala, Uganda. fabclau7@gmail.com.
David Patrick KateeteDepartment of Immunology and Molecular Biology, School of Biomedical Sciences, Makerere University College of Health Sciences, P. O Box 7072, Kampala, Uganda.
Josephine TumuhamyeCentre for Intervention Science in Maternal and Child Health, University of Bergen, Bergen, Norway.
Alfred OkengMBN Clinical Laboratories, Kampala, Uganda.
Emmanuel AboceMBN Clinical Laboratories, Kampala, Uganda.
Olive NamuggaSchool of Public Health, Makerere University College of Health Sciences, Kampala, Uganda.
Richard KwizeraInfectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.
Halvor SommerfeltCentre for Intervention Science in Maternal and Child Health, University of Bergen, Bergen, Norway.
Victoria NankabirwaCentre for Intervention Science in Maternal and Child Health, University of Bergen, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStaphylococcus aureus (S. aureus) often colonizes the human skin, upper respiratory and genital tracts. In the female genital tract, it can be passed on to the newborn during vaginal delivery leading to either ordinary colonization, or neonatal infections notably umbilical stump sepsis, scalded skin syndrome, arthritis, or bacteraemia/sepsis. These infections are mediated by staphylococcal virulence factors such as (i) Staphylococcal Enterotoxins A, B, C, D, and E encoded by the sea, seb, sec, sed, see genes, (ii) Exfoliative Toxins A and B encoded by the eta and etb genes, (iii) Toxic Shock Syndrome Toxin 1 (TSST-1) encoded by the tst gene, (iv) Panton-Valentine Leukocidin (PVL) encoded by the pvl gene, and (v) Hemolysins alpha and delta encoded by the hla and hld genes, respectively. We determined the prevalence of S. aureus possessing one or more virulence factor genes and of methicillin resistant Staphylococcus aureus (MRSA) in this population.

methodsThis was a cross-sectional study, which used 85 S. aureus isolates from the Chlorohexidine (CHX) clinical trial study in Uganda. The isolates had been obtained by culturing vaginal swabs (VS) from 1472 women in labour, frozen at minus 80

resultsOf the 85 S. aureus isolates 13 (15.3%) were positive for one or more virulence factor genes, as follows: pvl 9/85 (10.6%), hld 5/85 (5.9%), sea 1/85 (1.2%) and seb genes 1/85 (1.2%). The other virulence genes (sec, sed, see, eta, etb, hla and tst) were not detected in any of the isolates. MRSA was detected in 55.3% (47/85) of the isolates, but only two of these carried the pvl virulence gene.

conclusionThis study demonstrated that 15% of the S. aureus colonizing the female lower genital tract of mothers in labour in central Uganda carried one or more virulence genes, mostly pvl, indicating potential for newborn infection with S. aureus acquired in the maternal birth canal. More than half of the isolates were MRSA.

Indexed as

Methicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsVaginaVirulence FactorsAdultCarrier StateCross-Sectional StudiesFemaleHumansLabor, ObstetricPregnancyPrevalenceStaphylococcus aureusUgandaYoung AdultVirulence FactorsFemale genital tractMRSAStaphylococcus aureusVaginal colonizationVirulence factorsVirulence genes

Identifiers

PMID39155368
PMCPMC11331675

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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.