Activity of moxifloxacin against intracellular community-acquired methicillin-resistant Staphylococcus aureus: comparison with clindamycin, linezolid and co-trimoxazole and attempt at defining an intracellular susceptibility breakpoint
Author(s) -
Sandrine Lemaire,
Klaudia Kosowska-Shick,
Peter C. Appelbaum,
Y. Glupczynski,
Françoise Van Bambeke,
Paul M. Tulkens
Publication year - 2010
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkq478
Subject(s) - moxifloxacin , linezolid , clindamycin , staphylococcus aureus , microbiology and biotechnology , methicillin resistant staphylococcus aureus , antibiotics , antibacterial agent , intracellular , biology , medicine , chemistry , bacteria , vancomycin , biochemistry , genetics
Co-trimoxazole, clindamycin and linezolid are used to treat community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) infections, but little is known about intracellular activity. Moxifloxacin is active against intracellular methicillin-susceptible S. aureus (MSSA), but CA-MRSA has not been studied.
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