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Emergence of New-Delhi Metallo-Betalactamase-1 and Oxacillinase-48 Positive <i>Escherichia coli</i> in South-Eastern Nigeria


Ijeoma Maryrose Ajuba
Comfort Nne Akujobi
Iloduba Nnaemeka Aghanya
Simon Nkpeh Ushie
Akachukwu Egwu Okoro
Robinson Ogochukwu Ofiaeli
Chibuike Jesse Ezeama
Michel Chiedu Egbuniwe
Mabel Ogochukwu Okeke

Abstract

Objective: The spread of carbapenemase‑producing Enterobacteriaceae is a global challenge that leads to an increase in health-care
cost, treatment failures, high morbidity, and mortality. This study was aimed at determining the prevalence of New‑Delhi Metallo Beta‑Lactamase (NDM), and oxacillinase‑48 (OXA‑48) genes in clinical isolates of Escherichia coli obtained from a tertiary hospital in Nnewi,
South‑eastern, Nigeria. Materials and


Methods: E. coli isolated from several clinical specimens including blood, urine, and wound swabs from patients receiving care at the hospital, were screened for resistance to meropenem and ertapenem antibiotics (Oxoid, UK) by the Kirby–Bauer disk‑diffusion method. All isolates, which showed reduced sensitivity to the tested antibiotics, were then subjected to phenotypic confirmation of carbapenemase production using the Modified Hodge test. The NDM and OXA‑48 genes were then detected using the polymerase chain reaction techniques.


Results: Of the 187 E. coli isolates, 41 (21.9%) screened positive as suspected carbapenemase producers, while the prevalence of carbapenemase‑producing E. coli in this study was 21/187 (11.23%). The prevalence of NDM and OXA‑48 genes in the entire sample population was 3/187 (1.6%) and 12/187 (6.4%), respectively.


Conclusion: The results obtained showed that NDM and OXA‑48 carbapenemase‑mediated resistance occurred in the study location. Hence, a reinforcement of infection prevention and control practices in the hospital will be required to curb the propagation of these resistant organisms.


Keywords: Beta‑lactamase, carbapenemase, New‑Delhi, Nigeria, oxacillinase 


Journal Identifiers


eISSN: 2667-0526
print ISSN: 1115-2613