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单独及联合使用奎奴普丁/达福普汀对肠球菌属耐药菌株和金黄色葡萄球菌的体外杀菌活性

In-vitro bactericidal activity of quinupristin/dalfopristin alone and in combination against resistant strains of Enterococcus species and Staphylococcus aureus.

作者信息

Kang S L, Rybak M J

机构信息

School of Pharmacy, University of the Pacific, Santa Barbara, CA, USA.

出版信息

J Antimicrob Chemother. 1997 May;39 Suppl A:33-9. doi: 10.1093/jac/39.suppl_1.33.

Abstract

In-vitro activities of quinupristin/dalfopristin, a semisynthetic injectable streptogramin, and vancomycin were compared against multidrug-resistant Enterococcus faecium and Enterococcus faecalis, methicillin-susceptible Staphylococcus aureus ATCC 25923 and a methicillin-resistant S. aureus (MRSA). Combinations of quinupristin/dalfopristin and/or vancomycin with ofloxacin or gentamicin were evaluated using the chequerboard technique. The only synergy observed was that between quinupristin/dalfopristin plus vancomycin and quinupristin/dalfopristin plus gentamicin against E. faecium (FIC index < 0.5). Time-kill curves were performed over 24 h with an inoculum of 1 x 10(7) cfu/mL and clinically achievable concentrations of quinupristin/dalfopristin, vancomycin, ofloxacin and gentamicin (6, 30, 5 and 5 mg/L, respectively). In time-kill studies, combinations of quinupristin/dalfopristin plus vancomycin and quinupristin/dalfopristin plus gentamicin were additive, not synergic, against E. faecium and achieved 99.9% killing in 21.2 h and 19.6 h, respectively. None of the combination regimens suppressed the regrowth of E. faecalis. Quinupristin/dalfopristin combined with vancomycin demonstrated consistent synergy against ATCC 25923 and the MRSA, achieving 99.9% killing in 12.1 h and 11.9 h, respectively. Overall, quinupristin/dalfopristin alone demonstrated inhibitory activity against E. faecium, but not against E. faecalis, and bactericidal activity was achieved only with quinupristin/dalfopristin in combination with vancomycin or gentamicin against E. faecium. Quinupristin/dalfopristin plus vancomycin was the most potent and reliable combination against both strains of S. aureus in time-kill studies.

摘要

比较了半合成注射用链阳菌素奎奴普丁/达福普汀和万古霉素对耐多药粪肠球菌和屎肠球菌、甲氧西林敏感金黄色葡萄球菌ATCC 25923以及耐甲氧西林金黄色葡萄球菌(MRSA)的体外活性。使用棋盘法评估了奎奴普丁/达福普汀和/或万古霉素与氧氟沙星或庆大霉素的联合用药情况。观察到的唯一协同作用是奎奴普丁/达福普汀加万古霉素以及奎奴普丁/达福普汀加庆大霉素对屎肠球菌的协同作用(FIC指数<0.5)。以1×10⁷ cfu/mL的接种量以及临床可达到的奎奴普丁/达福普汀、万古霉素、氧氟沙星和庆大霉素浓度(分别为6、30、5和5 mg/L)进行了24小时的时间杀菌曲线实验。在时间杀菌研究中,奎奴普丁/达福普汀加万古霉素以及奎奴普丁/达福普汀加庆大霉素对屎肠球菌的联合用药表现为相加作用,而非协同作用,分别在21.2小时和19.6小时实现了99.9%的杀菌率。没有一种联合用药方案能抑制粪肠球菌的再生长。奎奴普丁/达福普汀与万古霉素联合对ATCC 25923和MRSA表现出持续的协同作用,分别在12.1小时和11.9小时实现了99.9%的杀菌率。总体而言,单独使用奎奴普丁/达福普汀对屎肠球菌具有抑制活性,但对粪肠球菌无抑制活性,仅在奎奴普丁/达福普汀与万古霉素或庆大霉素联合使用时对屎肠球菌具有杀菌活性。在时间杀菌研究中,奎奴普丁/达福普汀加万古霉素是针对两种金黄色葡萄球菌菌株最有效且可靠的联合用药方案。

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