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The molecular characterization of colistin-resistant isolates of Acinetobacter baumannii from patients at intensive care units

BACKGROUND AND OBJECTIVES: The objective of this study was to determine molecular characterization and genetic diversity of colistin-resistant A. baumannii clinical isolates in Intensive Care Unit hospitalized patients. MATERIALS AND METHODS: A total of 127 A. baumannii clinical isolates were evalua...

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Detalles Bibliográficos
Autores principales: Farajnia, Safar, Lotfi, Fariba, Dehnad, Alireza, Shojaie, Maryam, Raisi, Roya, Rahbarnia, Leila, Bazmani, Ahad, Naghili, Behrooz, Shiry, Samaneh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132339/
https://www.ncbi.nlm.nih.gov/pubmed/37124847
http://dx.doi.org/10.18502/ijm.v14i3.9768
Descripción
Sumario:BACKGROUND AND OBJECTIVES: The objective of this study was to determine molecular characterization and genetic diversity of colistin-resistant A. baumannii clinical isolates in Intensive Care Unit hospitalized patients. MATERIALS AND METHODS: A total of 127 A. baumannii clinical isolates were evaluated for antimicrobial susceptibility. PCR reaction and sequencing were performed for the detection of mutations in pmrAB and lpx ACD genes. RESULTS: Based on antimicrobial susceptibility testing, 40.94% and 33.85% of the isolates were MDR and XDR respectively whereas 3.93% of them were found to be PDR. Results of agar dilution MIC and E-test indicated that 76% of the isolates were sensitive to colistin. All of the isolates were positive for bla(OXA-51) and 50% of them were positive for both bla(OXA-23) -like and bla(OXA-143) -like genes while only 25% of the isolates were positive for bla(OXA-72) . None of them were positive for the bla(OXA-58) -like gene. There is no mutation in pmrA. The V162A substitution for pmrB gene was repeated in two isolates, and E(394)D and Y(292)H substitutions in lpxA were observed in two isolates; also, C(120)R and F(165)L substitutions in lpxC gene was repeated in two isolates. Analysis of phylogenetic tree based on alterations in lpxACD and pmrB genes indicated the appearance of new isolates compared to the reference strain ATCC17978 A. baumannii isolates. CONCLUSION: The present study indicated the prevalence of MDR and XDR A. baumannii isolates and the emergence of PDR isolates in the northwest portion of Iran. The appearance of colistin-resistant isolates with new mutations in pmrB, lpxACD genes indicates new resistance mechanisms.