Decoding the resistome, virulome and mobilome of clinical versus aquatic Acinetobacter baumannii in southern Romania

Acinetobacter baumannii, a notorious opportunistic pathogen, presents a formidable challenge in both clinical and environmental fields due to its resilience and ability to acquire resistance. This study undertook a comprehensive analysis of 183 A. baumannii isolates collected between 2019 and 2022 f...

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Published inHeliyon Vol. 10; no. 13; p. e33372
Main Authors Gheorghe-Barbu, Irina, Surleac, Marius, Barbu, Ilda Czobor, Paraschiv, Simona, Bănică, Leontina Mirela, Rotaru, Liviu-Iulian, Vrâncianu, Corneliu Ovidiu, Niță Lazăr, Mihai, Oțelea, Dan, Chifiriuc, Mariana Carmen
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 15.07.2024
Elsevier
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Summary:Acinetobacter baumannii, a notorious opportunistic pathogen, presents a formidable challenge in both clinical and environmental fields due to its resilience and ability to acquire resistance. This study undertook a comprehensive analysis of 183 A. baumannii isolates collected between 2019 and 2022 from intra-hospital infections (IHI), hospital sewages (Hs), wastewater treatment plants (WWTP), and adjacent river waters from two Southern cities, focusing on their resistome, virulome, and mobilome through isolation on chromogenic media, identification by MALDI-TOF-MS and antibiotic susceptibility testing by disk diffusion) followed by genotypic characterization [Whole Genome Sequencing (WGS), 3rd generation sequencing through the MinION (ONT) platform, pangenome description, and respectively horizontal gene transfer through conjugation assays]. Our findings reveal significant genomic plasticity and the prevalence of high-risk international clones, underlining the potential of these isolates to act as reservoirs for antibiotic resistance genes (ARGs) that could be dynamically exchanged between clinical and environmental settings through mobile genetic elements (MGEs) such as the pMAL1 plasmids and the critical role of WWTPs in the persistence and spread of A. baumannii. Moreover, our study presents the first report of the co-occurrence of blaOXA-23 and blaOXA-72 in A. baumannii ST2 clone. Thus, our research underscores the necessity for integrated surveillance and targeted interventions across healthcare and environmental sectors to mitigate the risk posed by this adaptable pathogen. •A. baumannii persists through wastewater treatment.•Variable ARG profiles in A. baumannii by region and site.•First finding of blaOXA-23 and blaOXA-72 co-occurrence.•Clinical genes in environmental strains show gene exchange risk.•Study shows A. baumannii as ARG reservoirs linking environments.
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ISSN:2405-8440
2405-8440
DOI:10.1016/j.heliyon.2024.e33372