Publication | Open Access
In Vitro Activities of Daptomycin, Vancomycin, Linezolid, and Quinupristin-Dalfopristin against Staphylococci and Enterococci, Including Vancomycin- Intermediate and -Resistant Strains
360
Citations
11
References
2000
Year
-Resistant StrainsVancomycin- IntermediateAntimicrobial ChemotherapyAntibiotic ResistanceVitro ActivitiesDrug ResistanceGram-positive BacteriaInfection ControlAntimicrobial ResistanceHealth SciencesH. DaptomycinAntimicrobial CompoundPharmacologyClinical MicrobiologyVancomycin-intermediate S. AureusAntimicrobial SusceptibilityAntibioticsMicrobiologyMedicineDrug Discovery
The in vitro activity of daptomycin was compared with those of vancomycin, linezolid, and quinupristin-dalfopristin against a variety (n = 203) of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus and S. epidermidis (MRSA and MRSE, respectively), vancomycin-resistant enterococci (VRE), and vancomycin-intermediate S. aureus (VISA). Overall, daptomycin was more active against all organisms tested, except Enterococcus faecium and VISA, against which its activity was similar to that of quinupristin-dalfopristin. In time-kill studies with MRSA, MRSE, VRE, and VISA, daptomycin demonstrated greater bactericidal activity than all other drugs tested, killing > or =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.
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