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Plasmid-Mediated Fluoroquinolone Resistance in Pseudomonas aeruginosa and Acinetobacter baumannii
Geetha P Venkataramana1, Aishwarya K V Lalitha1, Shanthi Mariappan1
1Department of Microbiology, Sri Ramachandra Institute of Higher Education and Research, Porur, Chennai, Tamil Nadu, India.
Abstract:
Introduction Pseudomonas aeruginosa and Acinetobacter baumannii are important pathogens in health care-associated infections. Fluoroquinolone resistance has emerged in these pathogens. In this study, we aimed to determine the occurrence of plasmid-mediated quinolone resistance (PMQR) determinants ( qnrA , qnrB , qnrS , aac(6')-Ib-cr , oqxAB , and qepA ) by polymerase chain reaction (PCR) and the transmissibility of plasmid-borne resistance determinants in clinical isolates of P. aeruginosa and A. baumannii . Materials and Methods The study included P. aeruginosa (85) and A. baumannii (45) which were nonduplicate, clinically significant, and ciprofloxacin resistant. Antibiotic susceptibility testing was done by disk diffusion method for other antimicrobial agents, namely amikacin, ceftazidime, piperacillin/tazobactam, ofloxacin, levofloxacin, and imipenem. Minimum inhibitory concentration of ciprofloxacin was determined. Efflux pump activity was evaluated using carbonyl-cyanide m-chlorophenylhydrazone (CCCP). The presence of PMQR genes was screened by PCR amplification. Transferability of PMQR genes was determined by conjugation experiment, and plasmid-based replicon typing was performed. Results Resistance to other classes of antimicrobial agents was as follows: ceftazidime (86.9%), piperacillin/tazobactam (73.8%), imipenem (69.2%), and amikacin (63.8%). The minimal inhibitory concentration (MIC)50 and MIC90 for ciprofloxacin were 64 and greater than or equal to 256 µg/mL, respectively. There was a reduction in MIC for 37 (28.4%) isolates with CCCP. In P. aeruginosa , 12 (14.1%) isolates harbored qnrB , 12 (14.1%) qnrS , 9 (10.5%) both qnrB and qnrS , 66 (77.6%) aac(6')-Ib-cr , and 3 (3.5%) oqxAB gene. In A. baumannii , qnrB was detected in 2 (4.4%), 1 (2.2%) harbored both the qnrA and qnrS , 1 isolate harbored qnrB and qnrS , 21 (46.6%) aac(6')-Ib-cr , and 1 (2.2%) isolate harbored oqxAB gene. Notably, qepA gene was not detected in any of the study isolates. Conjugation experiments revealed that 12 (9.2%) were transferable. Of the transconjugants, seven (58.3%) belonged to IncFII type plasmid replicon, followed by four (33.3%) IncA/C and one (8.3%) IncFIC type. Conclusion The plasmid-mediated resistance aac(6')-Ib-cr gene is primarily responsible for mediating fluoroquinolone resistance in clinical isolates of P . aeruginosa and A. baumannii . The predominant plasmid type is IncFII.
Insights
The plasmid-mediated aac(6')-Ib-cr gene is the main cause of fluoroquinolone resistance in Pseudomonas aeruginosa and Acinetobacter baumannii. This resistance is transferable via IncFII plasmids, highlighting a significant challenge in healthcare-associated infections.
Area of Science:
- Clinical Microbiology
- Molecular Biology
- Infectious Diseases
Background:
- Pseudomonas aeruginosa and Acinetobacter baumannii are critical pathogens in healthcare-associated infections.
- Emergence of fluoroquinolone resistance in these bacteria poses a significant treatment challenge.
- Plasmid-mediated quinolone resistance (PMQR) determinants contribute to antimicrobial resistance spread.
Purpose of the Study:
- To determine the prevalence of specific PMQR determinants (qnrA, qnrB, qnrS, aac(6">-Ib-cr, oqxAB, qepA) in clinical isolates.
- To investigate the transmissibility of plasmid-borne resistance genes.
- To identify the types of plasmids carrying these resistance determinants.
Main Methods:
- Analysis of 85 Pseudomonas aeruginosa and 45 Acinetobacter baumannii isolates resistant to ciprofloxacin.
- Polymerase chain reaction (PCR) to screen for PMQR genes.
- Conjugation experiments to assess gene transferability and plasmid replicon typing.
Main Results:
- The aac(6">-Ib-cr gene was highly prevalent (77.6% in P. aeruginosa, 46.6% in A. baumannii).
- qnrB and qnrS genes were also detected in both species.
- 12 (9.2%) of the PMQR determinants were transferable, predominantly on IncFII plasmids.
Conclusions:
- The aac(6">-Ib-cr gene is a primary mediator of fluoroquinolone resistance in these clinical isolates.
- The IncFII plasmid type is the predominant vehicle for the spread of PMQR genes.
- Findings underscore the importance of monitoring plasmid-mediated resistance in combating bacterial infections.
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