BMC Microbiology · 2019 · 29 citations · 26 references
Life SciencesMicrobiologyMolecular BiologyBacteriologyDiagnostic MicrobiologyMedical MicrobiologyAntibiotic ResistanceAntimicrobial Susceptibility TestingClinical BacteriologyDiagnostic BacteriologyPathogen DetectionResistance GenesAcinetobacter Baumannii ResistanceAntimicrobial Resistance Gene DetectionBacterial DetectionBacterial Resistance DetectionMolecular Detection AssaysMolecular Detection Of BacteriaRapid Detection AssaysResistance In Clinical Isolates
BACKGROUND: Acinetobacter baumannii is a cosmopolitan bacterium that is frequently reported from hospitalized patients, especially those patients who admitted in the intensive care unit. Recently, multiplex real-time PCR has been introduced for rapid detection of the resistance genes in clinical isolates of bacteria. The current study aimed to develop and evaluate multiplex real-time PCR to detect common resistance genes among clinical isolates of A. baumannii. RESULTS: corresponding to the amplified fragment consisted of 83.5 °C, 93.3 °C and 89.3 °C for blaIMP, blaVIM and blaNDM, respectively. Results of multiplex real-time PCR showed that the prevalence of blaIMP, blaVIM and blaNDM among the clinical isolates of A. baumannii were 5/128(3.9%), 9/128(7.03%) and 0/128(0%), respectively. Multiplex real-time PCR was able to simultaneously identify the resistance genes, while showed 100% concordance with the results of conventional PCR. CONCLUSIONS: The current study showed that blaVIM, was the most prevalent MBL gene among the clinical isolates of A. baumannii while no amplification of blaNDM was seen. Multiplex real-time PCR can be sensitive and reliable technique for rapid detection of resistance genes in clinical isolates.
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