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Plasmid-Mediated Quinolone Resistance in Pseudomonas aeruginosa Isolated from Burn Patients in Tehran, Iran
Azam Molapour1, Amir Peymani2, Parvaneh Saffarain1
1Department of Microbiology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Introduction:
Plasmid-induced quinolone resistance has raised a great concern in the treatment of serious infections worldwide. The aims of this study were to determine the antibiotic susceptibility, the frequency of qepA, aac(6')-Ib and qnr genes by PCR and sequencing, and typing of the resistant isolates using repetitive extragenic palindromic sequence-based PCR (REPPCR) in Pseudomonas aeruginosa isolated from burn wound infections.
Methods:
In the current cross-sectional study, 149 P. aeruginosa were isolated from the burn wound samples of patients admitted to Motahari hospital in Tehran, Iran, from February to December 2016. The bacterial isolates were identified using standard laboratory methods and their antibiotic susceptibility to quinolones was evaluated using the standard Kirby-Bauer method, according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. The presence of aac(6')-Ib, qepA, qnrA, qnrB4, qnrB and qnrS genes was assessed using PCR and sequencing methods and clonal relationship of the resistant isolates was evaluated using REP-PCR method.
Results:
All (100%) isolates showed complete resistance to used quinolone compounds in this study. The qnr and qepA genes were not found, but all (100%) isolates were positive for the presence of aac(6')-Ib gene and the sequencing revealed that all (100%) belong to the aac(6')-Ib-cr variant. REP-PCR showed that the studied isolates belonged to three distinct clones of A (77.9%), B (18.1%), and C (4%).
Conclusion:
The findings of the present study indicated the presence of aac(6')-Ib-cr variant and lack of the contribution of qnr and qepA in the emergence of resistance to quinolones in P. aeruginosa isolated from burn patients. Considering the importance of clonal spread of these resistant isolates and their significant role in the development of clinical infections, especially in patients with burns, more attention should be paid to the prevention of the dissemination of these resistant isolates.
Insights
Pseudomonas aeruginosa from burn infections showed complete quinolone resistance due to the aac(6')-Ib-cr gene. This highlights the need to prevent the spread of these resistant bacterial clones.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Plasmid-mediated quinolone resistance is a growing global health concern.
- Pseudomonas aeruginosa is a significant pathogen, particularly in burn wound infections.
- Understanding resistance mechanisms is crucial for effective treatment.
Purpose of the Study:
- To determine antibiotic susceptibility of P. aeruginosa from burn infections.
- To identify the frequency of specific resistance genes (qepA, aac(6 times')-Ib, qnr).
- To analyze the clonal types of resistant P. aeruginosa isolates.
Main Methods:
- Isolation and identification of P. aeruginosa from burn wound samples.
- Antibiotic susceptibility testing using Kirby-Bauer method.
- Detection of resistance genes via PCR and sequencing.
- Clonal typing using repetitive extragenic palindromic sequence-based PCR (REP-PCR).
Main Results:
- All P. aeruginosa isolates (100%) exhibited complete resistance to quinolones.
- The qnr and qepA genes were not detected.
- The aac(6 times')-Ib gene was present in all isolates, identified as the aac(6 times')-Ib-cr variant.
- REP-PCR identified three distinct clones (A, B, and C) among the resistant isolates.
Conclusions:
- The aac(6 times')-Ib-cr variant is the primary mechanism of quinolone resistance in these P. aeruginosa isolates.
- The qnr and qepA genes do not contribute to quinolone resistance in this context.
- Clonal spread of resistant P. aeruginosa is significant in burn infections, necessitating infection control measures.
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