Resistance Mechanisms Of Acinetobacter Baumannii In North Indian Clinical Isolates: A Molecular Study Of Β-Lactam, Carbapenem, Cephalosporin, Fluoroquinolone, And Aminoglycoside Genes

Background- The WHO recently added to priority list Carbapenem-resistant Acinetobacter baumannii (CRAB) major infection cause death throughout the developing world. With time the bacteria have become smarter so antimicrobial resistance is major problem so treatment of infection. Aim- This study explored the relationship between antimicrobial resistance patterns and identified the resistance genes responsible for β-lactam, fluoroquinolone, and aminoglycosides. A. baumannii isolates susceptibility patterns of antimicrobial agent and conventional PCR was used to detection of β-lactamase leading gene to carbapenem- resistant class ( blaSHV, blaTEM, blaVEB, blaPER, blaGES, blaKPC, blaCTX-M-1), (MBL) genes (blaIMP, blaVIM, blaNDM-1), Oxacillinase genes (blaOXA-48, blaOXA-23, blaOXA-24/40, blaOXA-58), Aminoglycoside-modifying enzyme (AME) genes (aac(3)-Ia, aac(3)-IIa, aph(3)-Ia, ant(2)-Ia), Plasmid-mediated quinolone resistance genes (qnrA, qnrB, qnrS), and DNA gyrase genes (parC, gyrA). Results- Resistance genes were detected in 62.09% of blaOXA-23, 15.3% of blaPER, 24.18% of blaNDM, 15.6% of blaSHV-1, 36.6% of parC, 20.26% of aph (3')-VIa, 23.5% of ant(1a), and 9.1% of aac(1a), predominantly in extensively drug-resistant (XDR-AB) isolates. Additionally, 2.6% of blaOXA-58-like genes were found in multidrug-resistant (MDR-AB) isolates. A high prevalence of blaOXA-23-like and specific ESBL genes in extensively drug-resistant (XDR) strains suggests the co-evolution of resistance mechanisms, contributing to enhanced resistance profiles. The co-occurrence of carbapenem resistance genes with aminoglycoside-modifying enzymes or ESBL genes shows A. baumannii versatility and flexibility to acquire several resistance mechanisms; co-resistance is more common in XDR isolates. The high prevalence of blaOXA-23, blaNDM, and parC among resistant isolates means that carbapenem and fluoroquinolone resistance has a major part in the continuing existence of A. baumannii outbreaks.

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Publication Details

Journal
International Journal of Environmental Sciences
Published
2025-08-04
DOI
https://doi.org/10.64252/pvy9b790
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.00

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article

Resistance Mechanisms Of Acinetobacter Baumannii In North Indian Clinical Isolates: A Molecular Study Of Β-Lactam, Carbapenem, Cephalosporin, Fluoroquinolone, And Aminoglycoside Genes

Vimala Venkatesh, Satya Narayan Varma, Rashmi Singh, Raj Kumar Kalyan et al.
International Journal of Environmental Sciences
Antibiotic Resistance in Bacteria
article

Resistance Mechanisms Of Acinetobacter Baumannii In North Indian Clinical Isolates: A Molecular Study Of Β-Lactam, Carbapenem, Cephalosporin, Fluoroquinolone, And Aminoglycoside Genes

Vimala Venkatesh, Satya Narayan Varma, Rashmi Singh, Raj Kumar Kalyan, Atin Singhai, Upma Singh, Parul Jain
article en

Abstract

Background- The WHO recently added to priority list Carbapenem-resistant Acinetobacter baumannii (CRAB) major infection cause death throughout the developing world. With time the bacteria have become smarter so antimicrobial resistance is major problem so treatment of infection. Aim- This study explored the relationship between antimicrobial resistance patterns and identified the resistance genes responsible for β-lactam, fluoroquinolone, and aminoglycosides. A. baumannii isolates susceptibility patterns of antimicrobial agent and conventional PCR was used to detection of β-lactamase leading gene to carbapenem- resistant class ( blaSHV, blaTEM, blaVEB, blaPER, blaGES, blaKPC, blaCTX-M-1), (MBL) genes (blaIMP, blaVIM, blaNDM-1), Oxacillinase genes (blaOXA-48, blaOXA-23, blaOXA-24/40, blaOXA-58), Aminoglycoside-modifying enzyme (AME) genes (aac(3)-Ia, aac(3)-IIa, aph(3)-Ia, ant(2)-Ia), Plasmid-mediated quinolone resistance genes (qnrA, qnrB, qnrS), and DNA gyrase genes (parC, gyrA). Results- Resistance genes were detected in 62.09% of blaOXA-23, 15.3% of blaPER, 24.18% of blaNDM, 15.6% of blaSHV-1, 36.6% of parC, 20.26% of aph (3')-VIa, 23.5% of ant(1a), and 9.1% of aac(1a), predominantly in extensively drug-resistant (XDR-AB) isolates. Additionally, 2.6% of blaOXA-58-like genes were found in multidrug-resistant (MDR-AB) isolates. A high prevalence of blaOXA-23-like and specific ESBL genes in extensively drug-resistant (XDR) strains suggests the co-evolution of resistance mechanisms, contributing to enhanced resistance profiles. The co-occurrence of carbapenem resistance genes with aminoglycoside-modifying enzymes or ESBL genes shows A. baumannii versatility and flexibility to acquire several resistance mechanisms; co-resistance is more common in XDR isolates. The high prevalence of blaOXA-23, blaNDM, and parC among resistant isolates means that carbapenem and fluoroquinolone resistance has a major part in the continuing existence of A. baumannii outbreaks.

International Journal of Environmental Sciences
Council of Scientific and Industrial Research, India, University Grants Commission
Openalex Percentile: Top 82%
Antibiotic Resistance in Bacteria
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