In vitro activities of six quinolones and mechanisms of resistance in Staphylococcus aureus and coagulase-negative staphylococci

Linde, Hans-Joerg and Schmidt, Mario and Fuchs, Emmi and Reischl, Udo and Niller, Hans Helmut and Lehn, Norbert (2001) In vitro activities of six quinolones and mechanisms of resistance in Staphylococcus aureus and coagulase-negative staphylococci. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 45 (5). pp. 1553-1557. ISSN 0066-4804

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Abstract

Of 94 clinical isolates of Staphylococcus aureus (n = 51) acid coagulase-negative staphylococci (CNS) (n 43), mutations in the quinolone resistance-determining region of topoisomerases Gr1A, Gr1B, GyrA, and GyrB together with MICs of six quinolones were analyzed. Amino acid substitutions at identical residues (Gr1A residues 80 and 84; GyrA residues 83 and 88) were found in S, aureus and CNS, Active efflux, as suggested by blocking by reserpine, contributed substantially to the resistance phenotype in some strains. Among ciprofloxacin, clinafloxacin, levofloxacin, nalidixic acid, trovafloxacin, and sparfloxacin, a 0.5-mug/ml concentration of sparfloxacin discriminated best between strains with two or three mutations and those with no mutations.

Item Type: Article
Uncontrolled Keywords: DNA TOPOISOMERASE-IV; CIPROFLOXACIN RESISTANCE; WILD-TYPE; GYRA; MUTATIONS; GRLA; CLINAFLOXACIN; TROVAFLOXACIN; MOXIFLOXACIN; SPARFLOXACIN;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Medizinische Mikrobiologie und Hygiene
Depositing User: Dr. Gernot Deinzer
Date Deposited: 31 Jan 2022 10:27
Last Modified: 31 Jan 2022 10:27
URI: https://pred.uni-regensburg.de/id/eprint/41444

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