Staphylococcus aureus Mutants Selected by BMS-284756

Author:

Discotto L. F.1,Lawrence L. E.1,Denbleyker K. L.1,Barrett J. F.1

Affiliation:

1. Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, Connecticut

Abstract

ABSTRACT BMS-284756, a novel des-fluoro(6)-quinolone, was used to select for in vitro mutants of Staphylococcus aureus ISP794. Step mutants were obtained, and the quinolone resistance-determining regions of four target genes, gyrA, gyrB, grlA , and grlB , were sequenced. The data suggest that DNA gyrase is the primary target for BMS-284756 in S. aureus .

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference7 articles.

1. Antibacterial Spectrum of a Novel Des-Fluoro(6) Quinolone, BMS-284756

2. Hartman-Neumann S. K. DenBleyker L. A. Pelosi L. E. Lawrence J. F. Barrett and T. J. Dougherty. Selection and genetic characterization of Streptococcus pneumoniae mutants resistant to the des-F(6)-quinolone BMS-284756. Antimicrob. Agents Chemother in press.

3. In vitro and in vivo antibacterial activities of AM-1155, a new 6-fluoro-8-methoxy quinolone

4. Mechanisms and Frequency of Resistance to Premafloxacin in Staphylococcus aureus : Novel Mutations Suggest Novel Drug-Target Interactions

5. National Committee for Clinical Library Standards Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically 4th ed. M7–A4. National Committee for Clinical Laboratory Standards Wayne Pa. 1997

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