Genotyping and Antimicrobial Susceptibility of Carbapenem-resistant Acinetobacter baumannii: ISAba-1-blaOXA-23 association and plasmid analysis

Auteurs

  • Wejdene Mansour Laboratory of Biophysical Metabolic Research and Applied Pharmacology, LR12ES02, Ibn Al Jazzar Faculty of Medicine of Sousse, University of Sousse, Sousse 4002, Tunisia
  • Karama Charfi Laboratory of Biophysical Metabolic Research and Applied Pharmacology, LR12ES02, Ibn Al Jazzar Faculty of Medicine of Sousse, University of Sousse, Sousse 4002, Tunisia
  • Raoudha Grami Laboratory of Biophysical Metabolic Research and Applied Pharmacology, LR12ES02, Ibn Al Jazzar Faculty of Medicine of Sousse, University of Sousse, Sousse 4002, Tunisia
  • Aziza Massaoudi Laboratory of Biophysical Metabolic Research and Applied Pharmacology, LR12ES02, Ibn Al Jazzar Faculty of Medicine of Sousse, University of Sousse, Sousse 4002, Tunisia
  • Tounes Ben Romdhane Department of Pharmacy, Sahloul University Hospital, Sousse, Tunisia
  • Ikram El Ahmer Laboratory of Microbiology, Hopital Tahar Sfar, Mahdia, Tunisia
  • Anis Bel Haj Khlifa Faculty of Pharmacy of Monastir, University of Monastir, Tunisia
  • Mahjoub Aouni Laboratory of Transmissible Diseases and Biologically Active Substances LR99ES27, Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia

DOI :

https://doi.org/10.71599/bhr.v6i1.187

Mots-clés :

Acinetobacter baumannii, OXA-23, OXA-66, ISAba1, imipenem, Tunisia

Résumé

Objectives: To characterize the mechanisms responsible for carbapenem resistance among a collection of Acinetobacter baumannii isolates recovered at the Tahar Sfar University hospital in Tunisia.

Methods: Antimicrobial susceptibility testing were studied on Muller Hinton agar plates. Southern blot and PCR-based replicon typing (PBRT) were performed. Beta-lactamases genes were screened by PCR and sequencing. Conjugation experiments were carried out to determine whether the resistance determinants were transferable. Clonality of isolates was assessed by PFGE.

Results: Sixteen carbapenem-resistant Acientobacter baumannii strains  were collected over a 3-years period from patient hospitalized in different wards of the Tahar Sfar University hospital. Resistance to carbapenems was mostly due to the expression of the acquired blaOXA-23 and the intrinsic blaOXA-66 genes, both genes being associated with the ISAbaI insertion sequence. Mating-out assays showed that all carbapenem-resistant isolates carried the blaOXA-23 gene on plasmids that all belonged to the GR6 replicase group.

Conclusions: This study reports on the molecular characterization of carbapenem resistance determinants in A. baumannii isolates. There is an urgent need for control measures to prevent dissemination of those multi-drug resistant strains.

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Publiée

2026-01-30

Comment citer

Mansour, W., Charfi, K., Grami, R., Massaoudi, A., Ben Romdhane, T., El Ahmer, I., Bel Haj Khlifa, A., & Aouni, M. (2026). Genotyping and Antimicrobial Susceptibility of Carbapenem-resistant Acinetobacter baumannii: ISAba-1-blaOXA-23 association and plasmid analysis. Biomedicine & Healthcare Research, 6(1), 2–8. https://doi.org/10.71599/bhr.v6i1.187

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Original paper