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    Comparative bactericidal activities of daptomycin, glycopeptides, linezolid and tigecycline against blood isolates of Gram-positive bacteria in Taiwan.

    Authors

    Huang YT, Liao CH, Teng LJ, et al. 

    Institution

    Department of Internal Medicine, Far Eastern Memorial Hospital, Taipei County, Taipei, Taiwan.

    Source

    Clin Microbiol Infect 2008 Feb; 14(2) :124-9.

    Abstract

    In-vitro MICs and minimum bactericidal concentrations (MBCs) of daptomycin, linezolid, tigecycline, vancomycin and teicoplanin against Gram-positive bacteria were determined using the broth microdilution method for ten blood isolates each of methicillin-susceptible Staphylococcus aureus (MSSA), methicillin-resistant S. aureus (MRSA), including two vancomycin-intermediate S. aureus (VISA), vancomycin-resistant Enterococcus faecium and Enterococcus faecalis. One strain of VISA was tested in a time-kill synergism assay of daptomycin combined with oxacillin, imipenem, rifampicin and isepamicin. Daptomycin showed excellent in-vitro bactericidal activity against all the isolates tested, with no tolerance or synergism effects when combined with other agents, except with rifampicin against VISA. Vancomycin had better bactericidal activity against MRSA and MSSA than did teicoplanin. Linezolid had the poorest bactericidal activity against the isolates tested, with 100% tolerance by the MSSA and VRE isolates, and 80% tolerance by the MRSA isolates. Tolerance towards tigecycline was exhibited by 40% of the MRSA isolates, 100% of the MSSA and vancomycin-resistant E. faecalis isolates, and 90% of the vancomycin-resistant E. faecium isolates.

    Mesh

    Acetamides
    Anti-Infective Agents
    Daptomycin
    Drug Resistance, Bacterial
    Drug Therapy, Combination
    Glycopeptides
    Gram-Positive Bacterial Infections
    Gram-Positive Cocci
    Humans
    Microbial Sensitivity Tests
    Minocycline
    Oxazolidinones
    Staphylococcus aureus
    Streptococcaceae
    Taiwan
    Teicoplanin
    Time Factors
    Vancomycin

    Language

    eng

    Pub Type(s)

    Journal Article

    PubMed ID

    18076671

    Content Manager
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