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Hilla University College Journal For Medical Science

Document Type

Original Study

Keywords

A.baumannii, blaOXA-51, VITEK 2 system, CHROMID

Abstract

Background: Acinetobacter baumannii, identified as an ESKAPE pathogen, is part of a group of bacteria known for their high antibiotic resistance and significant role in nosocomial infections. Objectives: The objective of the current study is to investigate the genetic sequences of the blaOXA-51 gene in A. baumannii isolates. Materials and Methods: 600 specimens were collected during the period from September 2022 to December 2022 from three hospitals in Babylon Province/ Iraq. Results: In the present study, 20 (3.33%) out of 600 isolates from (urine, Burn, blood and wound)in percentage 6(30%), 5(25%), 5(25%), and 4(20%) respectively. The identification of bacteria by VITEK 2 system and PCR techniques for the detection of blaoxa-51gene and nucleotide sequence of nucleotide to blaoxa-51gene. The specimens were immediately inoculated on MacConkey agar and then on CHROM agar incubated overnight at 37°C under aerobic conditions, and the isolated bacteria were identified by VITEK 2 system. The detection of antimicrobial activity using the Vitek 2 system. The susceptibility of A.baumannii isolates to antibiotics, including highly resistant for Amikacin, Cefepime, Ceftazidime, and Ciprofloxacin, Piperacillin, Ticarcillin, and Ticarcillin/Clavulanic Acid. Colistin 33.33%, Imipenem 93.3%, Meropenem 86.67%, and Tobramycin 80%. Genetically, PCR for the detection of bla OXA-51 genes among A.baumannii isolates revealed that 5 isolates were registered in GenBank. Conclusion: PCR of A. baumannii performed by blaOXA-51 Gene, Housekeeping genes blaOXA-51 are considered unique gene to A.baumannii and blaOXA-51 is considered a better molecular marker for the study of phylogenetic and taxonomic relationships at the species level, precisely for this bacterium. The detection of blaOXA-51 gene provides a correct and convenient method of identifying A. baumannii.

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