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Updated: Aug 18, 2026

Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach
Published on: December 14, 2019
Quinolone resistance in bacteria: emphasis on plasmid-mediated mechanisms
1Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3202, USA. xianzhi_li@hc-sc.gc.ca
Abstract:
Bacterial resistance to quinolones/fluoroquinolones has emerged rapidly and such resistance has traditionally been attributed to the chromosomally mediated mechanisms that alter the quinolone targets (i.e. DNA gyrase and topoisomerase IV) and/or overproduce multidrug resistance efflux pumps. However, the discovery of the plasmid-borne quinolone resistance determinant, named qnr, has substantially broadened our horizon on the molecular mechanisms of quinolone resistance. Several recent reports of Qnr or its homologues encoded by transferable plasmids in Gram-negative bacteria isolated worldwide highlight the significance of the emerging plasmid-mediated mechanism(s). This also alerts us to the potential rapid dissemination of quinolone resistance determinants. Qnr belongs to the pentapeptide repeat family and protects DNA gyrase from the action of quinolone agents including the newer fluoroquinolones. This protection interplays with chromosomal mechanisms to raise significantly the resistance levels. The qnr-bearing strains generate quinolone-resistant mutants at a much higher frequency than those qnr-free strains. Furthermore, the qnr-plasmids are integron-associated and carry multiple resistance determinants providing resistance to several classes of antimicrobials including beta-lactams and aminoglycosides. The high quinolone resistance rates in Escherichia coli are used to address issues of quinolone resistance, and possible strategies for minimising quinolone resistance are discussed.
Insights
The discovery of plasmid-borne qnr genes significantly expands understanding of bacterial quinolone resistance. These genes protect DNA gyrase, increasing resistance and facilitating rapid spread of antimicrobial resistance.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Bacterial resistance to quinolones/fluoroquinolones is a growing concern.
- Traditionally, resistance was linked to chromosomal alterations in DNA gyrase/topoisomerase IV or efflux pumps.
- The emergence of plasmid-mediated resistance mechanisms was previously underestimated.
Purpose of the Study:
- To investigate the role of plasmid-borne quinolone resistance determinants (qnr).
- To understand the molecular mechanisms and dissemination of qnr-mediated resistance.
- To explore the implications of qnr in the context of overall antimicrobial resistance.
Main Methods:
- Review of recent reports on Qnr and its homologues in Gram-negative bacteria.
- Analysis of the molecular function of Qnr in protecting DNA gyrase.
- Examination of the association of qnr-plasmids with integrons and other resistance genes.
Main Results:
- The qnr gene, encoding a pentapeptide repeat protein, protects DNA gyrase from quinolones.
- Qnr enhances resistance levels by interacting with chromosomal mechanisms.
- Qnr-bearing strains exhibit higher mutation frequencies for quinolone resistance.
- Qnr-plasmids are often integron-associated, carrying multiple antimicrobial resistance genes (e.g., beta-lactams, aminoglycosides).
Conclusions:
- Plasmid-mediated qnr genes represent a significant and emerging mechanism of bacterial quinolone resistance.
- Qnr facilitates the rapid dissemination of quinolone resistance determinants globally.
- The presence of qnr, especially on mobile genetic elements, poses a substantial threat to quinolone efficacy and necessitates strategies to minimize resistance development.
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