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BMS284756(T-3811;一种去氟喹诺酮)对国际葡萄球菌和肠球菌菌株集合的抗菌谱及活性比较,包括体外试验开发和方法间比较。

Comparative antimicrobial spectrum and activity of BMS284756 (T-3811; a desfluoroquinolone) tested against an international collection of staphylococci and enterococci, including in vitro test development and intermethod comparisons.

作者信息

Pfaller M A, Beach M L, Gordon K A, Jones R N

机构信息

University of Iowa College of Medicine, Iowa City, USA.

出版信息

J Chemother. 2002 Feb;14(1):13-8.

PMID:11892893
Abstract

The study was initiated to determine the in vitro activity and MIC/disk test comparisons of BMS284756, a new des-fluoro(6)-quinolone, against isolates of staphylococci and enterococci from the SENTRY Antimicrobial Surveillance Program, 2000. Isolates were tested by reference broth microdilution and standardized disk diffusion methods. Against 3,789 strains of gram-positive cocci from the SENTRY Program (2000), the BMS284756 MIC90 and percentage susceptible at < or = 2 and < or = 4 microg/ml were: Staphylococcus aureus (4 microg/ml; 89.3 and 97.1%), coagulase-negative staphylococci (CoNS; 4 microg/ml; 86.1 and 96.0%) and enterococci (> 4 microg/ml; 62.0 and 76.2%). Also tested were selected staphylococci (300 strains) and enterococci (102 strains) by two standardized methods. The activity of BMS284756 was highly correlated with oxacillin resistance among staphylococci. Oxacillin-susceptible staphylococci were all inhibited by BMS284756 at < or = 0.5 microg/ml, whereas oxacillin-resistant strains required inhibitory concentrations of > or = 1 microg/ml. Excellent correlation was observed between the MIC and 5-microg disk zone diameter for staphylococci and enterococci (r=0.91 to 0.93). Among vancomycin-susceptible enterococci, 67% of Enterococcus faecalis, 25% of E. faecium, and 76% of other Enterococcus spp. isolates were inhibited by BMS284756 at < or = 2 microg/ml. All vancomycin-resistant enterococci (VRE; 11 E. faecalis and 15 E. faecium) were inhibited by > or = 2 microg/ml of BMS284756. Among the non-VRE, non-faecium enterococcal isolates (n=64), 62% were inhibited by < or = 0.5 microg/ml. BMS284756 showed excellent activity against oxacillin-susceptible staphylococci and moderate activity against enterococci other than VRE and E. faecium. Acceptable correlations were observed between MIC and disk test results for both tested genus groups.

摘要

开展该研究是为了确定新型去氟(6)-喹诺酮类药物BMS284756对2000年哨兵抗菌监测计划中葡萄球菌和肠球菌分离株的体外活性以及MIC/纸片试验比较。采用参考肉汤微量稀释法和标准化纸片扩散法对分离株进行检测。针对哨兵计划(2000年)中的3789株革兰氏阳性球菌,BMS284756的MIC90以及在≤2μg/ml和≤4μg/ml时的敏感百分比分别为:金黄色葡萄球菌(4μg/ml;89.3%和97.1%)、凝固酶阴性葡萄球菌(CoNS;4μg/ml;86.1%和96.0%)和肠球菌(>4μg/ml;62.0%和76.2%)。还通过两种标准化方法对选定的葡萄球菌(300株)和肠球菌(102株)进行了检测。BMS284756的活性与葡萄球菌中的苯唑西林耐药性高度相关。苯唑西林敏感的葡萄球菌在≤0.5μg/ml时均被BMS284756抑制,而苯唑西林耐药菌株则需要≥1μg/ml的抑菌浓度。观察到葡萄球菌和肠球菌的MIC与5μg纸片抑菌圈直径之间具有良好的相关性(r=0.91至0.93)。在对万古霉素敏感的肠球菌中,67%的粪肠球菌、25%的屎肠球菌以及76%的其他肠球菌属分离株在≤2μg/ml时被BMS284756抑制。所有万古霉素耐药肠球菌(VRE;11株粪肠球菌和15株屎肠球菌)在≥2μg/ml的BMS284756作用下被抑制。在非VRE、非屎肠球菌的肠球菌分离株(n=64)中,62%在≤0.

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