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首页> 外文期刊>Journal of Clinical Microbiology >Synergy of β-Lactams with Vancomycin against Methicillin-Resistant Staphylococcus aureus: Correlation of Disk Diffusion and Checkerboard Methods
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Synergy of β-Lactams with Vancomycin against Methicillin-Resistant Staphylococcus aureus: Correlation of Disk Diffusion and Checkerboard Methods

机译:β-内酰胺与万古霉素对耐甲氧西林金黄色葡萄球菌的协同作用:磁盘扩散和棋盘方法的相关性

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摘要

Modified disk diffusion (MDD) and checkerboard tests were employed to assess the synergy of combinations of vancomycin and β-lactam antibiotics for 59 clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) and Mu50 (ATCC 700699). Bacterial inocula equivalent to 0.5 and 2.0 McFarland standard were inoculated on agar plates containing 0, 0.5, 1, and 2 μg/ml of vancomycin. Oxacillin-, cefazolin-, and cefoxitin-impregnated disks were applied to the surface, and the zones of inhibition were measured at 24 h. The CLSI-recommended checkerboard method was used as a reference to detect synergy. The MICs for vancomycin were determined using the Etest method, broth microdilution, and the Vitek 2 automated system. Synergy was observed with the checkerboard method in 51% to 60% of the isolates when vancomycin was combined with any β-lactam. The fractional inhibitory concentration indices were significantly lower in MRSA isolates with higher vancomycin MIC combinations (P < 0.05). The overall agreement between the MDD and checkerboard methods to detect synergy in MRSA isolates with bacterial inocula equivalent to McFarland standard 0.5 were 33.0% and 62.5% for oxacillin, 45.1% and 52.4% for cefazolin, and 43.1% and 52.4% for cefoxitin when combined with 0.5 and 2 μg/ml of vancomycin, respectively. Based on our study, the simple MDD method is not recommended as a replacement for the checkerboard method to detect synergy. However, it may serve as an initial screening method for the detection of potential synergy when it is not feasible to perform other labor-intensive synergy tests.
机译:改良的磁盘扩散(MDD)和棋盘格测试用于评估万古霉素和β-内酰胺抗生素组合对59株耐甲氧西林金黄色葡萄球菌(MRSA)和Mu50(ATCC 700699)临床分离株的协同作用。在含有0、0.5、1和2μg/ ml万古霉素的琼脂平板上接种相当于0.5和2.0 McFarland标准的细菌接种物。将奥沙西林,头孢唑啉和头孢西丁浸渍的片涂在表面上,并在24小时内测量抑制区域。 CLSI推荐的棋盘格方法被用作检测协同作用的参考。使用Etest方法,肉汤微量稀释和Vitek 2自动化系统确定万古霉素的MIC。万古霉素与任何β-内酰胺合用时,用棋盘法在51%至60%的分离物中观察到协同作用。万古霉素MIC组合较高的MRSA分离物的抑制分数浓度指数显着降低( P <0.05)。用MDD和棋盘法检测具有McFarland标准0.5的细菌接种量的MRSA分离株中的协同作用的总体一致性为:奥沙西林为33.0%和62.5%,头孢唑林为45.1%和52.4%,头孢西丁为43.1%和52.4%分别加入0.5和2μg/ ml的万古霉素。根据我们的研究,不建议使用简单的MDD方法代替棋盘格方法来检测协同作用。但是,当无法执行其他劳动密集型协同测试时,它可以用作检测潜在协同作用的初始筛选方法。

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