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Changes in the initial activity of the compounds (MIC0) after 10 subsequent passages (MIC1–10) of exposure of clinical SA isolates to the compounds (0.5 × MIC). For fusidic acid and SA 10, MIC10 (128 mg/L) is not shown. Data are not shown for erythromycin (strains SA 2, 7 and 8) and mupirocin (strains SA 4, 8, 9 and 10)—the compounds were inactive towards the isolates at the tested concentrations (512 mg/L).
