Fluoroquinolone resistance conferred by gyrA, parC mutations, and AbaQ efflux pump among Acinetobacter baumannii clinical isolates causing ventilator-associated pneumonia
Nancy M Attia1, Amira Elbaradei2,3
11Microbiology Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Abstract:
Acinetobacter baumannii has emerged as an important nosocomial pathogen due to its ability to survive in hospital settings and its antimicrobial resistance. It is one of the key pathogens in ventilator-associated pneumonia (VAP). The aim of this study was to characterize the mechanisms of quinolone resistance among A. baumannii isolates causing VAP and to investigate the presence of the novel abaQ gene among them. Quinolone-resistant A. baumannii isolates causing VAP were collected over a period of 4 months. Mutations within gyrA and parC were analyzed and the presence of qnrA, qnrB, qnrS, and abaQ was investigated genotypically. Twenty-one A. baumannii isolates were collected, most of them (76.2%) were extensively drug-resistant (XDR) and only one isolate (4.8%) was pandrug-resistant (PDR). All isolates showed high level of resistance to ciprofloxacin, while qnrA, qnrB and qnrS were absent among our isolates. This is the first report of A. baumannii isolates co-harboring Ser81Leu in gyrA and Ser84Leu in parC together with the novel abaQ gene. Interestingly, a new mutation in gyrA quinolone resistance-determining region Arg89Cys was detected among two of our isolates. The emergence of XDR and PDR isolates among A. baumannii causing VAP is an alarming threat.
Insights
This study investigated quinolone resistance in Acinetobacter baumannii causing ventilator-associated pneumonia (VAP). Novel mutations and the abaQ gene were identified in extensively drug-resistant strains, highlighting a significant threat.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Acinetobacter baumannii is a critical nosocomial pathogen, frequently implicated in ventilator-associated pneumonia (VAP).
- High rates of antimicrobial resistance in A. baumannii complicate treatment and infection control.
- Understanding resistance mechanisms is crucial for managing VAP caused by this pathogen.
Purpose of the Study:
- To characterize quinolone resistance mechanisms in A. baumannii isolates from VAP patients.
- To investigate the prevalence of the novel abaQ gene in these isolates.
- To identify new mutations conferring quinolone resistance.
Main Methods:
- Genotypic analysis of mutations in gyrA and parC genes.
- Investigation of qnrA, qnrB, qnrS, and abaQ gene presence.
- Phenotypic characterization of drug resistance patterns.
Main Results:
- Twenty-one A. baumannii isolates were analyzed, with 76.2% exhibiting extensively drug-resistance (XDR) and 4.8% pandrug-resistance (PDR).
- All isolates demonstrated high-level ciprofloxacin resistance; qnrA, qnrB, and qnrS genes were absent.
- Co-occurrence of gyrA (Ser81Leu) and parC (Ser84Leu) mutations with the abaQ gene was observed for the first time.
- A novel gyrA mutation (Arg89Cys) was detected in two isolates.
Conclusions:
- The study identified novel quinolone resistance mechanisms in A. baumannii associated with VAP.
- The emergence of XDR and PDR A. baumannii strains poses a significant clinical threat.
- The findings underscore the need for enhanced surveillance and novel therapeutic strategies against resistant A. baumannii.
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