In vitro activities of daptomycin, vancomycin, linezolid, and quinupristin-dalfopristin against staphylococci and enterococci, including vancomycin-intermediate and -resistant strains

Citation
Mj. Rybak et al., In vitro activities of daptomycin, vancomycin, linezolid, and quinupristin-dalfopristin against staphylococci and enterococci, including vancomycin-intermediate and -resistant strains, ANTIM AG CH, 44(4), 2000, pp. 1062-1066
Citations number
11
Categorie Soggetti
Microbiology
Journal title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
ISSN journal
00664804 → ACNP
Volume
44
Issue
4
Year of publication
2000
Pages
1062 - 1066
Database
ISI
SICI code
0066-4804(200004)44:4<1062:IVAODV>2.0.ZU;2-9
Abstract
The in vitro activity of daptomycin was compared with those of vancomycin, linezolid, and quinupristin-dalfopristin against a variety (n = 203) of gra m-positive bacteria, including methicillin resistant Staphylococcus aureus and S. epidermidis (MRSA and MRSE, respectively), vancomycin resistant ente rococci (VRE), and vancomycin-intermediate S. aureus (VISA). Overall, dapto mycin was more active against all organisms tested, except Enterococcus fae cium and VISA, against which its activity was similar to that of quinuprist in-dalfopristin. In time-kill studies with MRSA, MRSE, VRE, and VISA, dapto mycin demonstrated greater bactericidal activity than all other drugs teste d, killing greater than or equal to 3 log CFU/ml by 8 h. Daptomycin may be a potential alternative drug therapy for multidrug-resistant gram-positive organisms and warrants further investigation.