Wichelhaus T, Schäfer V, Brade V, Böddinghaus B
Institute of Medical Microbiology, University Hospital, Paul-Ehrlich-Strasse 40, 60596 Frankfurt am Main, Germany.
J Antimicrob Chemother. 2001 Feb;47(2):153-6. doi: 10.1093/jac/47.2.153.
The in vitro antibacterial activities of the rifamycin derivatives rifampicin and KRM-1648 against 150 Staphylococcus aureus isolates were determined. The MICs of rifampicin and KRM-1648 for 90% of rifampicin-susceptible S. aureus isolates (n = 100) were 0.016 and 0.001 mg/L, respectively. In rifampicin-resistant S. aureus isolates (n = 50), different levels of resistance to rifamycins were associated with mutations at different sites in rpoB. Mutations at some sites were associated with high-level resistance to both rifamycins, while certain mutations were associated with the activity of KRM-1648 being < or = 100-fold better than that of rifampicin.
测定了利福霉素衍生物利福平与KRM-1648对150株金黄色葡萄球菌分离株的体外抗菌活性。利福平与KRM-1648对90%的利福平敏感金黄色葡萄球菌分离株(n = 100)的最低抑菌浓度(MIC)分别为0.016和0.001 mg/L。在耐利福平的金黄色葡萄球菌分离株(n = 50)中,对利福霉素的不同耐药水平与rpoB基因不同位点的突变相关。某些位点的突变与对两种利福霉素的高水平耐药相关,而某些突变则与KRM-1648的活性比利福平高100倍或更低相关。