Yew W W, Piddock L J, Li M S, Lyon D, Chan C Y, Cheng A F
Tuberculosis and Chest Unit, Grantham Hospital, Aberdeen, Hong Kong.
J Antimicrob Chemother. 1994 Sep;34(3):343-51. doi: 10.1093/jac/34.3.343.
The activities of eight quinolones (ciprofloxacin, clinafloxacin, levofloxacin, ofloxacin, A-80556, sparfloxacin, temafloxacin and tosufloxacin) and three macrolides (azithromycin, clarithromycin and erythromycin) against 98 clinical isolates of Mycobacterium tuberculosis and 120 isolates of five different atypical mycobacterial species including 20 Mycobacterium kansasii, 25 Mycobacterium scrofulaceum, 25 Mycobacterium avium/intracellulare, 25 Mycobacterium chelonae and 25 Mycobacterium fortuitum were determined with the Middlebrook 7H9 broth macrodilution method. Sparfloxacin, clinafloxacin, levofloxacin, ciprofloxacin and ofloxacin were active against M. tuberculosis (MIC90 0.06-0.5 mg/L; MBC90 0.125-2.0 mg/L). However, higher MIC90S and MBC90S of these quinolones were obtained for strains of multi-drug resistant M. tuberculosis. The macrolides tested had poor activity against M. tuberculosis isolates (MIC90 > 8.0 mg/L). Furthermore, high MIC90S of the quinolones and macrolides (2.0 to 8.0 mg/L) were obtained for clinical isolates of atypical mycobacteria, with the exception of clarithromycin against M. kansasii (MIC90 = 1.0 mg/L) and sparfloxacin against M. scrofulaceum (MIC90 = 1.0 mg/L).
采用Middlebrook 7H9肉汤微量稀释法测定了8种喹诺酮类药物(环丙沙星、克林沙星、左氧氟沙星、氧氟沙星、A - 80556、司帕沙星、替马沙星和妥舒沙星)以及3种大环内酯类药物(阿奇霉素、克拉霉素和红霉素)对98株结核分枝杆菌临床分离株和120株5种不同非结核分枝杆菌的抗菌活性,这5种非结核分枝杆菌包括20株堪萨斯分枝杆菌、25株瘰疬分枝杆菌、25株鸟分枝杆菌/胞内分枝杆菌、25株龟分枝杆菌和25株偶然分枝杆菌。司帕沙星、克林沙星、左氧氟沙星、环丙沙星和氧氟沙星对结核分枝杆菌有活性(MIC₉₀为0.06 - 0.5mg/L;MBC₉₀为0.125 - 2.0mg/L)。然而,对于耐多药结核分枝杆菌菌株,这些喹诺酮类药物的MIC₉₀和MBC₉₀更高。所测试的大环内酯类药物对结核分枝杆菌分离株活性较差(MIC₉₀>8.0mg/L)。此外,对于非结核分枝杆菌临床分离株,喹诺酮类药物和大环内酯类药物的MIC₉₀较高(2.0至8.0mg/L),但克拉霉素对堪萨斯分枝杆菌(MIC₉₀ = 1.0mg/L)和司帕沙星对瘰疬分枝杆菌(MIC₉₀ = 1.0mg/L)除外。