Evidence map›Paper›PMID 42842059›Full record

ArticleWorld journal of microbiology & biotechnology2026

Emergence of multidrug resistant Enterobacter spp. in Nigeria: a genomic study.

Ayodele Timilehin Adesoji, Vittoria Mattioni Marchetti, Claudia Cortimiglia, Francesca Piscopiello, Ilaria Petrizzi, Aurora Piazza, Emmanuel Dayo Alabi, Pier Sandro Cocconcelli, Roberta Migliavacca

Abstract read
In one paragraph

Article in World journal of microbiology & biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Ayodele Timilehin AdesojiDepartment of Microbiology, Federal University Dutsin-Ma, Dutsin-Ma, Katsina State, Nigeria.
Vittoria Mattioni Marchetti *S.C.C.D.P. Department, Microbiology and Clinical Microbiology Unit, University of Pavia, Pavia, Italy. vittoria.mattionimarchetti@unipv.it.
Claudia Cortimiglia *Dipartimento di Scienze e Tecnologie Alimentari per la Sostenibilità della Filiera Agro-Alimentare, Facoltà di Scienze Agrarie Alimentari ed Ambientali, Università Cattolica del Sacro Cuore, Via Emilia Parmense 84, Piacenza-Cremona, 29122, Italy.
Francesca PiscopielloS.C.C.D.P. Department, Microbiology and Clinical Microbiology Unit, University of Pavia, Pavia, Italy.
Ilaria PetrizziS.C.C.D.P. Department, Microbiology and Clinical Microbiology Unit, University of Pavia, Pavia, Italy.
Aurora PiazzaS.C.C.D.P. Department, Microbiology and Clinical Microbiology Unit, University of Pavia, Pavia, Italy.
Emmanuel Dayo AlabiDepartment of Microbiology, Federal University Dutsin-Ma, Dutsin-Ma, Katsina State, Nigeria.
Pier Sandro CocconcelliDipartimento di Scienze e Tecnologie Alimentari per la Sostenibilità della Filiera Agro-Alimentare, Facoltà di Scienze Agrarie Alimentari ed Ambientali, Università Cattolica del Sacro Cuore, Via Emilia Parmense 84, Piacenza-Cremona, 29122, Italy.
Roberta MigliavaccaS.C.C.D.P. Department, Microbiology and Clinical Microbiology Unit, University of Pavia, Pavia, Italy.

Funding

NextGenerationEU-MUR PNRR P E00000007, INF-ACT
6 · The paper itself

Abstract

backgroundExtended-spectrum β-lactamases (ESBL) and AmpC β-lactamase-producing Enterobacter species are pathogens of public health concern. In this study, we investigated the resistome, virulome, and plasmidome of circulating Enterobacter hormaechei isolated from humans, animals, and ready-to-eat (RTE) food in Dutsin-Ma, northwest Nigeria. MATERIALS AND

methodsEnterobacter species were isolated from human, and RTE food samples using MacConkey and CHROM agar. Species identification and antibiotics susceptibility testing (AST) were performed using Microscan autoSCAN-4 and MALDI-TOF MS, respectively. Whole-genome sequencing (WGS) and bioinformatics analysis were performed to validate the species identities. WGS also determined sequence types (STs), resistome, plasmidome, and virulome using PubMLST, ResFinder, PlasmidFinder, and Virulence Factors Database (VFDB) via ABRicate, respectively.

resultsE. hormaechei subs. xiangfangensis was the dominant species isolated from humans (6/8, 75%) and animals (1/8, 12.5%), while E. hormaechei subs. oharae was exclusively found in RTE food (1/8, 12.5%). The most frequent sequence type (ST) was ST813, found solely in humans, along with ST511, ST454, and the emerging high-risk ST171. ST68 was identified in food, and novel ST (ST3186) were identified in animal and human samples, respectively. All isolates exhibited 100% resistance to ampicillin and amoxicillin-clavulanic acid, with 62.5% resistant to each of aztreonam, ceftazidime, ciprofloxacin, gentamicin, tobramycin and cefotaxime, and 25% to colistin. E. hormaechei (62.5%) isolates carried the blaCTX-M-15 gene, encoding ESBL-production, along with AmpC genes such as blaCMH-3, and also harbored resistance genes for aminoglycosides, fluoroquinolones, sulfonamides, tetracyclines, and trimethoprim. The IncHI2 (50%) was identified as the dominant plasmid type followed by Col (pHAD28) (25%), IncFIB (25%), and IncFII (11.1%). The most (62.5%) prevalence virulence gene among the isolates is ompA encoding adhesion while each of entA, entB and fepD encoding iron acquisition were least (12.5%) occurred.

conclusionThis study provides the first genomic insight into Enterobacter species in northwest Nigeria, highlighting their role in the spread of antimicrobial resistance. E. hormaechei subsp. xiangfangensis was identified as the main reservoir of ESBL and AmpC β-lactamases in this study. The discovery of novel STs with diverse virulence factors and plasmid replicon indicates potential horizontal gene transfer across different ecological niches. Our findings underscore the need for robust surveillance and control measures to combat the spread of MDR Enterobacter species across human, animal, and food niches.

Indexed as

Drug Resistance, Multiple, BacterialEnterobacterEnterobacteriaceae InfectionsAnimalsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesFood MicrobiologyGenome, BacterialGenomicsHumansMicrobial Sensitivity TestsNigeriaPlasmidsThird Generation CephalosporinsVirulence FactorsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesThird Generation CephalosporinsVirulence FactorsDrug resistanceE. cloacaeEnterobacter hormaecheiEnterobacter spp.NigeriaSequence typesWhole-genome sequencing

Identifiers

PMID42842059
PMCPMC13645906

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