DOI: 10.4103/mjbl.mjbl_326_24 ISSN: 1812-156X

Molecular Characterization of Metallo-β-Lactamase Resistance Genes (bla VIM and bla KPC ) in Pseudomonas aeruginosa Isolated from Different Clinical Specimens

Inas Ahmed Saeed, Samara Abdulhameed Alsalihi, Alaa H. Al-Charrakh

Abstract

Background:

Pseudomonas aeruginosa poses a significant challenge in modern medicine due to its inclination to infect individuals with weakened immune systems, remarkable adaptability, resistance to antibiotics, and an extensive array of dynamic defense mechanisms.

Objectives:

Detection of genetic resistance mechanisms of metallo-beta-lactamases (MBLs) in P. aeruginosa isolates.

Materials and Methods:

The present study involving 400 bacterial isolates obtained from diverse clinical sources (blood, urine, wound, and burn swabs) were collected from Hilla Teaching Hospital between February 2023 and September 2023. Antimicrobial susceptibility testing was conducted using the disk diffusion test, and molecular detection of enzymatic genes was performed through polymerase chain reaction (PCR).

Results:

In the present study, 28 P. aeruginosa isolates demonstrate pronounced resistance. The antibiotic resistance rates were notably high for piperacillin (80%) and carbenicillin (81.2%). Resistance to imipenem and meropenem was 8.4% and 19.8%, respectively, while the highest resistance was recorded against gentamicin (82%), amikacin (72.6%), cefepime (60.8%), cefotaxime (70.2%), ceftazidime (70.2%), and ceftriaxone (71.6%). Molecular detection of enzymatic genes was performed through PCR testing, revealing that all 28 isolates (100%) exhibited the presence of the 16SrRNA gene, a considered indicator for detecting bacteria by PCR. The prevailing MBL gene was the bla VIM -type gene, identified in 12 (42.8)% of the isolates. Furthermore, 10 (35.7%) of isolates carried the bla KPC -type gene.

Conclusion:

The identification of bla VIM- and bla KPC -type genes in P. aeruginosa suggests a high degree of resistance to antibiotics, especially those that target carbapenems. This restricts the options for treating infections caused by these bacteria, which is a serious concern in healthcare settings.

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