Comparative Activities of Clinafloxacin, Grepafloxacin, Levofloxacin, Moxifloxacin, Ofloxacin, Sparfloxacin, and Trovafloxacin and Nonquinolones Linozelid, Quinupristin-Dalfopristin, Gentamicin, and Vancomycin against Clinical Isolates of Ciprofloxacin-Resistant and -Susceptible Staphylococcus aureus Strains
Author(s) -
Mark E. Jones,
Maarten R. Visser,
Miriam Klootwijk,
Peter Heisig,
J. Verhoef,
FranzJosef Schmitz
Publication year - 1999
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.43.2.421
Subject(s) - trovafloxacin , sparfloxacin , moxifloxacin , levofloxacin , quinupristin , dalfopristin , ofloxacin , microbiology and biotechnology , vancomycin , ciprofloxacin , gentamicin , medicine , pefloxacin , antibacterial agent , antibiotics , staphylococcus aureus , biology , genetics , bacteria
The activities of eight fluoroquinolones and linezolid, quinupristin-dalfopristin (Synercid), gentamicin, and vancomycin were tested against 96 ciprofloxacin-susceptible and 205 ciprofloxacin-resistantStaphylococcus aureus strains. Overall, clinafloxacin, followed by moxifloxacin and trovafloxacin, was the most active quinolone tested. For all isolates, linezolid and quinupristin-dalfopristin showed activities that were at least comparable to vancomycin, with no cross-resistance to any other test compound.
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