Evidence map›Paper›PMID 40845059›Full record

ArticlePLoS neglected tropical diseases2025

Genomic epidemiology of enteropathogenic Escherichia coli in southwestern Nigeria.

Olabisi C Akinlabi, Rotimi A Dada, Ademola A Olayinka, Ibukunoluwa O Oginni-Falajiki, Oyeniyi S Bejide, Pelumi D Adewole, Nicholas R Thomson, Aaron O Aboderin, Iruka N Okeke

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. 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
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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.

Olabisi C AkinlabiDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.ORCID 0000-0001-8510-7189
Rotimi A DadaDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.
Ademola A OlayinkaDepartment of Medical Microbiology and Parasitology, Obafemi Awolowo University, Ile-Ife, Nigeria.ORCID 0000-0001-7684-2114
Ibukunoluwa O Oginni-FalajikiDepartment of Medical Microbiology and Parasitology, Obafemi Awolowo University, Ile-Ife, Nigeria.ORCID 0000-0003-3463-7547
Oyeniyi S BejideDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.ORCID 0000-0001-7238-3096
Pelumi D AdewoleDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.ORCID 0000-0002-0229-2540
Nicholas R ThomsonLondon School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-4432-8505
Aaron O AboderinDepartment of Medical Microbiology and Parasitology, Obafemi Awolowo University, Ile-Ife, Nigeria.ORCID 0000-0002-4280-2218
Iruka N OkekeDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.ORCID 0000-0002-1694-7587

Funding

Gates Foundation INV-036234
6 · The paper itself

Abstract

backgroundEnteropathogenic Escherichia coli (EPEC) are etiological agents of diarrhea. We studied the genetic diversity and virulence factors of EPEC in southwestern Nigeria, where this pathotype is rarely characterized. METHODOLOGY/PRINCIPAL

findingsEPEC isolates (n = 96) recovered from recent southwestern Nigeria diarrhea case-control studies were whole genome-sequenced using Illumina technology. Genomes were assembled using SPAdes and quality was evaluated using QUAST. Virulencefinder, Ectyper, and ResFinder were used to identify virulence genes, serotypes, and resistance genes. Multilocus sequence typing was done by STtyping. Single nucleotide polymorphisms (SNPs) were called out of whole genome alignment using SNP-sites and a phylogenetic tree was constructed using IQtree. Thirty-nine of the 96(40.6%) EPEC isolates were from diarrhea cases diarrhea. Nine isolates from diarrhea patients and four from healthy controls were typical EPEC, harboring bundle-forming pilus (bfp) genes whilst the rest were atypical EPEC. There were 15 EPEC-EAEC hybrids. Atypical serotypes O71:H19 (16, 16.6%), O108:H21 (6, 6.3%), O157:H39 (5, 5.2%), and O165:H9 (4, 4.2%) were the most prevalent; only 8 (8.3%) isolates belonged to classical EPEC serovars. The largest, ST517 clade harbored multiple siderophore and serine protease autotransporter genes and included an O71:H19 subclade <10 SNPs apart, representing a likely outbreak involving 15 children, four with diarrhea. Likely outbreaks, of typical O119:H6(ST28) and atypical O127:H29(ST7798) were additionally identified. CONCLUSION/SIGNIFICANCE: EPEC circulating in southwestern Nigeria are diverse and differ substantially from well-characterized lineages seen previously elsewhere. EPEC carriage and outbreaks could be commonplace but are largely undetected, hence, unreported, and require genomic surveillance for identification.

Indexed as

DiarrheaEnteropathogenic Escherichia coliEscherichia coli InfectionsAdolescentAdultCase-Control StudiesChildChild, PreschoolFemaleGenetic VariationGenome, BacterialHumansInfantMaleMolecular EpidemiologyMultilocus Sequence TypingVirulence Factors

Identifiers

PMID40845059
PMCPMC12404642

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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.