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红霉素耐药性、接种物生长阶段及孵育时间对RP 59500(奎奴普丁-达福普汀)针对耐万古霉素屎肠球菌杀菌活性评估的影响

Influence of erythromycin resistance, inoculum growth phase, and incubation time on assessment of the bactericidal activity of RP 59500 (quinupristin-dalfopristin) against vancomycin-resistant Enterococcus faecium.

作者信息

Caron F, Gold H S, Wennersten C B, Farris M G, Moellering R C, Eliopoulos G M

机构信息

Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215, USA.

出版信息

Antimicrob Agents Chemother. 1997 Dec;41(12):2749-53. doi: 10.1128/AAC.41.12.2749.

Abstract

RP 59500, a mixture of two semisynthetic streptogramin antibiotics (quinupristin and dalfopristin), is one of a few investigational agents currently in clinical trials with inhibitory activity against multiple-drug-resistant strains of Enterococcus faecium. We evaluated the bactericidal activity of this antimicrobial against 30 recent clinical isolates of vancomycin-resistant E. faecium, including 23 erythromycin-resistant (MIC, >256 microg/ml) and 7 erythromycin-intermediate (MIC, 2 to 4 microg/ml) strains. All isolates were inhibited by RP 59500 at 0.25 to 1.0 microg/ml. The bactericidal activity of RP 59500 was markedly influenced by the erythromycin susceptibility of the strains and by several technical factors, such as inoculum growth phase and time of incubation of counting plates. As determined by time-kill methods, RP 59500 at a concentration of 2 or 8 microg/ml failed to kill erythromycin-resistant organisms under any conditions. Bactericidal activity was observed against all seven erythromycin-intermediate isolates when log-phase inocula were used and the cells were counted after 48 h of incubation (mean reductions in viable bacteria for RP 59500 at concentrations of 2 and 8 microg/ml, 3.45 and 3.50 log10 CFU/ml, respectively), but killing was diminished when the plates were examined at 72 h (mean killing, 3.06 and 2.95 log10, CFU/ml, respectively). No bactericidal activity was observed when stationary-phase cultures were used. On the basis of these data, we expect that bactericidal activity of RP 59500 against the multiple-drug-resistant E. faecium strains currently encountered would be distinctly uncommon.

摘要

RP 59500是两种半合成链阳菌素抗生素(奎奴普丁和达福普汀)的混合物,是目前正在进行临床试验的少数几种对粪肠球菌多重耐药菌株具有抑制活性的研究药物之一。我们评估了这种抗菌药物对30株近期临床分离的耐万古霉素粪肠球菌的杀菌活性,其中包括23株耐红霉素菌株(MIC,>256μg/ml)和7株红霉素中介菌株(MIC,2至4μg/ml)。所有分离株在0.25至1.0μg/ml的RP 59500浓度下均受到抑制。RP 59500的杀菌活性受到菌株对红霉素的敏感性以及几个技术因素的显著影响,如接种物生长阶段和计数平板的孵育时间。通过时间杀菌法测定,浓度为2或8μg/ml的RP 59500在任何条件下均未能杀死耐红霉素的生物体。当使用对数期接种物并在孵育48小时后对细胞进行计数时,观察到对所有7株红霉素中介分离株均有杀菌活性(RP 59500浓度为2和8μg/ml时,活菌平均减少量分别为3.45和3.50 log10 CFU/ml),但在72小时检查平板时杀菌作用减弱(平均杀菌量分别为3.06和2.95 log10 CFU/ml)。当使用稳定期培养物时未观察到杀菌活性。基于这些数据,我们预计RP 59500对目前遇到的多重耐药粪肠球菌菌株的杀菌活性将极为罕见。

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