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Published on: March 24, 2023
Plasmid-mediated quinolone resistance genes transfer among enteric bacteria isolated from human and animal sources
Ehwarieme Daniel Ayobola1, Whiliki Onoriadjeren Oscar2, Ejukonemu Francis Ejovwokoghene2
1Department of Microbiology, Faculty of Science, Delta State University, Abraka, Nigeria.
Abstract:
This research investigates the transferability of plasmid-mediated quinolone resistance (PMQR) genes among enteric bacteria isolates in human and animal samples, as well as its implication on resistance of recipient cells. A total of 1,964 strains of five different enteric bacteria species (Escherichia coli, Salmonella sp., Shigella sp., Klebsiella sp. and Aeromonas sp.) were screened for plasmid-mediated quinolone resistance (PMQR) genes from a population of quinolone resistant (Q-r) isolates. Screening for PMQR isolates was achieved by plasmid curing using sub-lethal concentration of Sodium Dodecyl Sulphate and PMQR genes (qnrA, qnrB, qnrS, Aac(6')-Ib-crand Qep A) were detected by polymerase chain reaction (PCR). Conjugation and transformation experiments were attempted to ascertain transfer of genes from the Q-r isolates to a susceptible, standard recipient, E. coli J53-2. The minimum inhibitory concentration (MIC) was determined before and after gene transfer, using E-test strips. Results indicate that percentage resistance to the quinolones (Qs): Nalidixic acid, Ciprofloxacin, Pefloxacin and Ofloxacin determined by agar plate diffusion technique stood at 52.6, 47.3, 50.5, 70.6 and 46.0% for Escherichia coli, Salmonella sp., Shigellasp., Klebsiella sp. and Aeromonas sp. respectively. Analysis of variance indicated the occurrence of significant differences (F, 46.77-613.30; 0.00) in the resistance to each tested Qs. Generally, Human isolates showed greater resistance than Animal isolates (57.4 vs 47.2%). Investigation with specific primers indicated 11, 15, 7, 1 and 0 for qnrA, qnrB, qnrS, qepA and Aac(6')-Ib-cr genes respectively, out of 1018 Q-r and 29 PMQR isolates. Gene transfer experiments indicated the transfer of all genes except qepA either by conjugation or transformation. The MIC of tested Qs on recipient bacterium before gene transfer greatly increased from 0.0625 to 0.25 µg/mL, after transfer. This study demonstrates that PMQR genes amongst enteric bacteria in the Niger delta of Nigeria were transferable and transfer conferred a higher Q- resistance on recipient bacterium.
Insights
Plasmid-mediated quinolone resistance (PMQR) genes are transferable among enteric bacteria in Nigeria, increasing quinolone resistance in recipient cells. This highlights the need for monitoring and control strategies to combat antimicrobial resistance.
Area of Science:
- Microbiology
- Genetics
- Public Health
Background:
- Antimicrobial resistance is a growing global health concern.
- Plasmid-mediated quinolone resistance (PMQR) genes contribute to the spread of resistance among bacteria.
- Enteric bacteria are common causes of human and animal infections.
Purpose of the Study:
- To investigate the transferability of PMQR genes among enteric bacteria from human and animal samples.
- To determine the impact of PMQR gene transfer on quinolone resistance in recipient bacteria.
Main Methods:
- Screening of 1,964 enteric bacteria isolates for PMQR genes using plasmid curing and PCR.
- Detection of specific PMQR genes (qnrA, qnrB, qnrS, Aac(6')-Ib-cr, QepA).
- Conjugation and transformation experiments to assess gene transfer, with Minimum Inhibitory Concentration (MIC) determination before and after transfer.
Main Results:
- High prevalence of quinolone resistance (46.0–70.6%) observed in enteric bacteria.
- PMQR genes (qnrA, qnrB, qnrS) were detected in resistant isolates.
- Successful transfer of PMQR genes (except qepA) via conjugation or transformation, leading to increased quinolone MICs in recipient bacteria.
Conclusions:
- PMQR genes are transferable among enteric bacteria in the Niger Delta, Nigeria.
- Gene transfer significantly enhances quinolone resistance in recipient bacteria.
- Findings underscore the importance of surveillance and control of PMQR gene dissemination.
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