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Antimicrobial Activity of Quinupristin-Dalfopristin Combined with Other Antibiotics against Vancomycin-Resistant Enterococci

机译:奎奴普林汀-达福普汀与其他抗生素联用对耐万古霉素的肠球菌的抗菌活性

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摘要

Interactions between quinupristin-dalfopristin and six other antimicrobials were examined by checkerboard arrays against 50 clinical isolates of vancomycin-resistant Enterococcus faecium selected to represent a range of susceptibilities to individual agents. Unequivocal synergistic or antagonistic interactions at clinically relevant concentrations were infrequently encountered when the streptogramin was combined with chloramphenicol, ampicillin, imipenem, vancomycin, or teicoplanin. Combinations with doxycycline resulted in synergistic inhibition in 36% of checkerboards. Against 10 strains of Enterococcus faecalis, synergistic interactions were found when quinupristin-dalfopristin was combined with doxycycline (four strains), either glycopeptide (three strains), or ampicillin (two strains). Combination with quinupristin-dalfopristin increased the ampicillin MIC from 1 to 4 μg/ml for one strain. For 10 strains of E. faecium, interactions were also assessed by time-kill methods using concentrations of the agents attainable in human serum. Most of these antimicrobials augmented killing by quinupristin-dalfopristin to a minor degree. Against 2 of the 12 strains in this collection that were not highly resistant to gentamicin, the combination of quinupristin-dalfopristin (2 μg/ml) plus gentamicin (5 μg/ml) resulted in killing approaching 3 log10 CFU/ml. With the exception of doxycycline, inhibitory interactions between quinupristin-dalfopristin and other agents tested against vancomycin-resistant strains of E. faecium were uncommon at clinically relevant concentrations.
机译:通过棋盘阵列针对50个对万古霉素耐药的粪便肠球菌临床分离株进行了检查,检查了奎奴普丁-达福普汀与其他六种抗菌剂之间的相互作用,以筛选出对个别药物敏感的范围。当链霉素与氯霉素,氨苄青霉素,亚胺培南,万古霉素或替考拉宁联用时,在临床相关浓度下很少出现明确的协同或拮抗作用。与多西环素合用可在36%的棋盘格中产生协同抑制作用。当奎奴普丁-达福普汀与强力霉素(4株),糖肽(3株)或氨苄西林(2株)联合使用时,针对10株粪肠球菌,发现了协同作用。与奎奴普丁-达福普汀合用可使一株氨苄青霉素的MIC从1μg/ ml增加到4μg/ ml。对于10株屎肠球菌,还使用人血清中可达到的药物浓度,通过时间杀灭法评估了相互作用。这些抗微生物剂中的大多数会在较小程度上增强奎奴普丁-达福普汀的杀伤力。对于该集合中对庆大霉素不是高度抗性的菌株中的2个,奎奴普丁-达福普汀(2μg/ ml)加庆大霉素(5μg/ ml)的组合导致杀死率接近3 log10 CFU / ml。除强力霉素外,奎奴普丁-达福普汀与其他针对粪便的耐万古霉素菌株测试的药物在临床相关浓度下的抑制性相互作用并不常见。

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