Evidence map›Paper›PMID 41734161›Full record

ArticlePloS one2026

High burden and genetic diversity of β-lactamase-producing Escherichia coli and Klebsiella pneumoniae causing community-acquired urinary tract infections in Southeastern Gabon.

Yann Mouanga-Ndzime, Cyrille Bisseye, Annicet-Clotaire Dikoumba, Désiré Otsaghe Ekore, Michelle Bignoumba, Marie-Louise Mawili Mounguengui, Neil-Michel Longo-Pendy, Sylvain Godreuil, Barthélémy Ngoubangoye, Bolni Marius Nagalo and 1 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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
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

1 citing paper in PubMed.

  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

11 authors.

Yann Mouanga-NdzimeBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.ORCID https://orcid.org/0000-0003-1280-1211
Cyrille BisseyeResearch Unit in Biological Sciences (URSB), Laboratory of Molecular and Cellular Biology, University of Science and Technology of Masuku (USTM), Franceville, Gabon.
Annicet-Clotaire DikoumbaBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Désiré Otsaghe EkoreBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Michelle BignoumbaBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Marie-Louise Mawili MounguenguiBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Neil-Michel Longo-PendyResearch Unit for the Ecology of Health, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Sylvain GodreuilLaboratoire de Bactériologie, CHU de Montpellier, UMR MIVEGEC (IRD, CNRS, Université de Montpelier), Montpellier, France.
Barthélémy NgoubangoyeBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.
Bolni Marius NagaloDepartment of Pharmacology and Physiology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Richard OnangaBacteriology Unit and One Health Laboratory, Interdisciplinary Centre for Medical Research of Franceville, Franceville, Gabon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing prevalence of β-lactamase-producing Escherichia coli and Klebsiella pneumoniae in community-acquired urinary tract infections (CA-UTIs) represents a growing public health challenge in low-resource settings. Data from Central Africa remain limited. This study investigated antimicrobial resistance profiles and phylogenetic diversity of these pathogens in southeastern Gabon.

methodsPatients presenting with CA-UTIs were screened, and isolates of E. coli and K. pneumoniae were collected. Antimicrobial susceptibility testing was performed using the Kirby-Bauer disk diffusion method and interpreted according to EUCAST 2024 guidelines. Phenotypic screening identified extended-spectrum β-lactamase (ESBL), AmpC, and carbapenemase production. Polymerase chain reaction (PCR) was used to detect ESBL genes (bla-CTX-M-gp1, bla-CTX-M-gp2, bla-CTX-M-gp9, bla-TEM, bla-SHV), plasmid-mediated AmpC genes (bla-CMY-1, bla-CMY-2, bla-ACT-1, bla-ACC, bla-FOX, bla-DHA), and the carbapenemase gene bla-OXA-48. Phylogenetic grouping of ESBL-producing E. coli was determined using PCR targeting chuA, yjaA, TspE4.C2, and arpA.

resultsAmong 3,026 screened patients, 949 CA-UTIs were confirmed, including 589 cystitis and 360 pyelonephritis cases, yielding 200 isolates: E. coli (124) and K. pneumoniae (76). Of these, 68 (34.0%) were ESBL producers, 17 (9.0%) AmpC producers, and 2 (1.0%) carbapenemase producers. ESBL producing isolates were significantly associated with male sex (47.0%, p = 0.02) and children ≤5 years of age (48.2%, p = 0.007). ESBL- and AmpC-producing isolates exhibited high resistance rates (20-100%) to β-lactams, fluoroquinolones, and trimethoprim-sulfamethoxazole, while retaining susceptibility to carbapenems, ceftazidime-avibactam, and nitrofurantoin (up to 100%). Molecular analysis showed predominance of bla-CTX-M-gp1 in E. coli (40% alone; 31% in combination with bla-TEM). In K. pneumoniae, bla-SHV + bla-TEM (49%) and bla-SHV + bla-CTX-M-gp1 + bla-TEM (42%) were the most frequent gene combinations; one isolate carried bla-OXA-48. ESBL-producing E. coli predominantly belonged to phylogroup A (48.6%).

conclusionMultidrug-resistant ESBL-, AmpC-, and OXA-48-producing E. coli and K. pneumoniae are circulating in community settings in southeastern Gabon. These findings underscore the need for strengthened antimicrobial resistance surveillance and evidence-based community-level interventions.

Indexed as

beta-LactamasesCommunity-Acquired InfectionsEscherichia coliEscherichia coli InfectionsGenetic VariationKlebsiella InfectionsKlebsiella pneumoniaeUrinary Tract InfectionsAdolescentAgedAnti-Bacterial AgentsBacterial ProteinsChildChild, PreschoolFemaleGabonAnti-Bacterial AgentsBacterial Proteinsbeta-Lactamases

Identifiers

PMID41734161
PMCPMC12931754

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