Identification of the blaOXA-23 Gene in the First Mucoid XDR Acinetobacter baumannii Isolated from a Patient with Cystic Fibrosis

Author:

Rossitto Martina12ORCID,Vrenna Gianluca34,Tuccio Guarna Assanti Vanessa3,Essa Nour3,De Santis Maria Luisa3,Granaglia Annarita3,Fini Vanessa3,Costabile Valentino3ORCID,Onori Manuela3,Cristiani Luca5,Boni Alessandra5ORCID,Cutrera Renato5ORCID,Perno Carlo Federico3,Bernaschi Paola3

Affiliation:

1. Multimodal Laboratory Medicine, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy

2. Major School in Microbiology and Virology, University Campus Bio-Medico, 00128 Rome, Italy

3. Microbiology and Diagnostic Immunology Unit, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy

4. Department of Molecular Medicine, Sapienza University of Rome, 00185 Rome, Italy

5. Pneumology and Cystic Fibrosis Unit, Bambino Gesù Children Hospital, IRCCS, 00165 Rome, Italy

Abstract

Acinetobacter baumannii is one of the pathogens most involved in health care-associated infections in recent decades. Known for its ability to accumulate several antimicrobial resistance mechanisms, it possesses the oxacillinase blaoxa-23, a carbapenemase now endemic in Italy. Acinetobacter species are not frequently observed in patients with cystic fibrosis, and multidrug-resistant A. baumannii is a rare event in these patients. Non-mucoid A. baumannii carrying the blaoxa-23 gene has been sporadically detected. Here, we describe the methods used to detect blaoxa-23 in the first established case of pulmonary infection via a mucoid strain of A. baumannii producing carbapenemase in a 24-year-old cystic fibrosis patient admitted to Bambino Gesù Children’s Hospital in Rome, Italy. This strain, which exhibited an extensively drug-resistant antibiotype, also showed a great ability to further increase its resistance in a short time.

Funder

NextGenerationEU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases

Publisher

MDPI AG

Subject

General Medicine

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