Unbound MEDLINE

Diminished in vitro antibacterial activity of oxacillin against clinical isolates of borderline oxacillin-resistant Staphylococcus aureus. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases [Clin Microbiol Infect] Journal article

 
TitleDiminished in vitro antibacterial activity of oxacillin against clinical isolates of borderline oxacillin-resistant Staphylococcus aureus.
Author(s)Croes S, Beisser PS, Terporten PH, Neef C, Deurenberg RH, Stobberingh EE 
InstitutionDepartment of Medical Microbiology, Maastricht University Medical Centre, Maastricht, the Netherlands.
SourceClin Microbiol Infect 2009 Oct 22.
AbstractClin Microbiol InfectAbstract Since it is unknown whether beta-lactam antimicrobial agents can be used effectively against borderline oxacillin-resistant Staphylococcus aureus (BORSA) with oxacillin MICs >/=4 mg/L, the in vitro bactericidal activity and pharmacodynamic effect of oxacillin against clinical BORSA isolates was evaluated. Time-kill experiments with oxacillin were performed and the results compared with those obtained with vancomycin, daptomycin and linezolid against BORSA with oxacillin MICs >/=4 mg/L and BORSA with oxacillin MICs </=2 mg/L. Furthermore, the effect of beta-lactamase production and plasmid profile analysis were taken into account to clarify responses to oxacillin. Oxacillin killing activity was attenuated against BORSA compared with ATCC 29213 since the pharmacodynamic parameters revealed that the potency of oxacillin was markedly reduced (c. ten-fold) against BORSA with oxacillin MICs >/=4 mg/L. pBORa53-like plasmid-containing BORSA with oxacillin MICs </=2 mg/L showed markedly more regrowth. In conclusion, oxacillin was non-effective in the eradication of either (i) BORSA with oxacillin MICs >/=4 mg/L or (ii) beta-lactamase-hyperproducing BORSA (MICs </=2 mg/L). Further investigation into beta-lactam dosing strategies against different BORSA strains is warranted in order to avoid possible therapy failure.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19849702
  
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