Mechanism and Spread of Qnr-Mediated Resistance. Quinolones are widely used antimicrobial agents because of their broad antibacterial spectrum, low toxicity, and reliable action against otherwise resistant pathogens. Bacterial resistance to quinolones, however, is increasing and has reached alarming levels in some parts of Europe and the Far East. Various chromosomal mutations contribute to this resistance. Plasmid-mediated resistance was long thought not to exist. We discovered a plasmid-encoded protein termed Qnr that protects DNA gyrase from quinolone inhibition. Qnr acts additively with chromosomal mechanisms for quinolone resistance, belongs to the pentapeptide repeat family of proteins and, by a gel displacement assay, binds to the gyrase tetramer as well as to the GyrA and GyrB subunits with differing affinities. Although initially found at a single hospital in the United States, the qnr gene has recently been discovered in clinical Escherichia coli isolates from the Far East and in about 10% of quinolone resistant Klebsiella pneumoniae strains from the US.
The aims of this proposal are to explore the hypothesis that Qnr blocks quinolone binding to gyrase, to study Qnr binding kinetics by surface plasmon resonance, to investigate whether Qnr can also protect gyrase from such protein inhibitors as MccB17, CcdB, and Gyrl, to study further the prevalence of qnr and the genetic basis of its acquisition by plasmids, and to explore whether Qnr and an active gyrase fragment can co-crystallize for structural analysis by x-ray diffraction. These studies are important not only for understanding an emerging resistance mechanism but should also reveal details of how DNA gyrase and related topoisomerases function and how proteins in the pentapeptide family interact with and regulate the activity of other proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI057576-01
Application #
6705185
Study Section
Special Emphasis Panel (ZRG1-BM-1 (01))
Program Officer
Peters, Kent
Project Start
2004-01-01
Project End
2008-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
1
Fiscal Year
2004
Total Cost
$216,876
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Monárrez, Rubén; Wang, Yin; Fu, Yingmei et al. (2018) Genes and Proteins Involved in qnrS1 Induction. Antimicrob Agents Chemother 62:
Vinué, Laura; Hooper, David C; Jacoby, George A (2018) Chromosomal mutations that accompany qnr in clinical isolates of Escherichia coli. Int J Antimicrob Agents 51:479-483
Hooper, David C; Jacoby, George A (2016) Topoisomerase Inhibitors: Fluoroquinolone Mechanisms of Action and Resistance. Cold Spring Harb Perspect Med 6:
Vinué, Laura; Hooper, David C (2016) A simple technique for suppressor detection in Escherichia coli. FEMS Microbiol Lett :
Vinué, Laura; Corcoran, Marian A; Hooper, David C et al. (2015) Mutations That Enhance the Ciprofloxacin Resistance of Escherichia coli with qnrA1. Antimicrob Agents Chemother 60:1537-45
Hooper, David C; Jacoby, George A (2015) Mechanisms of drug resistance: quinolone resistance. Ann N Y Acad Sci 1354:12-31
Jacoby, George A; Corcoran, Marian A; Hooper, David C (2015) Protective effect of Qnr on agents other than quinolones that target DNA gyrase. Antimicrob Agents Chemother 59:6689-95
Chen, Chunhui; Villet, Regis; Jacoby, George A et al. (2015) Functions of a GyrBA fusion protein and its interaction with QnrB and quinolones. Antimicrob Agents Chemother 59:7124-7
Kwak, Yee Gyung; Jacoby, George A; Hooper, David C (2015) Effect of Qnr on Plasmid Gyrase Toxins CcdB and ParE. Antimicrob Agents Chemother 59:5078-9
Kim, Eu Suk; Chen, Chunhui; Braun, Molly et al. (2015) Interactions between QnrB, QnrB mutants, and DNA gyrase. Antimicrob Agents Chemother 59:5413-9

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