Jevitt Laura A, Thorne Grace M, Traczewski Maria M, Jones Ronald N, McGowan John E, Tenover Fred C, Brown Steven D
Division of Healthcare Quality Promotion, G-08, Centers for Disease Control and Prevention, 1600 Clifton Rd., NE, Atlanta, GA 30333, USA.
J Clin Microbiol. 2006 Sep;44(9):3098-104. doi: 10.1128/JCM.00665-06.
Daptomycin is a novel cyclic lipopeptide that is approved by the U.S. Food and Drug Administration for the treatment of complicated skin and skin structure infections associated with Staphylococcus aureus and other gram-positive pathogens and also staphylococcal bacteremia, including right-sided endocarditis. The Clinical and Laboratory Standards Institute (CLSI) established "susceptible-only" interpretive criteria for broth microdilution (BMD) and disk diffusion (DD) testing of daptomycin in 2005. However, a series of S. aureus isolates have been recovered with daptomycin MICs in the nonsusceptible range (i.e., MICs of >1 microg/ml). The objective of this study was to determine the ability of the Etest and DD methods to differentiate daptomycin-susceptible from nonsusceptible isolates of S. aureus compared to the results of the CLSI BMD reference method. There was a good correlation between Etest MIC results and the results of BMD among laboratories (r = 0.86 to 0.88), with 95.3% of the Etest MICs within a +/-1 log(2) dilution of the BMD MIC result. A total of 92 of 102 (90.2%) non-daptomycin-susceptible isolates of S. aureus identified by BMD in two participating laboratories were also classified as nonsusceptible by Etest. However, the very major and major error rates reported by one of the participating laboratories were 13.5 and 4.0%, respectively, primarily due to the absence of an intermediate category. The DD method, however, did not reliably differentiate daptomycin-susceptible from non-daptomycin-susceptible isolates. In 2005, daptomycin disks were voluntarily removed from the market by Cubist Pharmaceuticals. The disk diffusion breakpoints were subsequently removed from the CLSI M100 standard in 2006.
达托霉素是一种新型环脂肽,已获美国食品药品监督管理局批准,用于治疗由金黄色葡萄球菌和其他革兰氏阳性病原体引起的复杂性皮肤及皮肤结构感染,以及包括右侧心内膜炎在内的金黄色葡萄球菌菌血症。2005年,临床和实验室标准协会(CLSI)制定了达托霉素肉汤微量稀释(BMD)和纸片扩散法(DD)检测的“仅敏感”解释标准。然而,已分离出一系列达托霉素最低抑菌浓度(MIC)处于非敏感范围(即MIC>1μg/ml)的金黄色葡萄球菌菌株。本研究的目的是将Etest法和DD法区分达托霉素敏感与非敏感金黄色葡萄球菌菌株的能力与CLSI BMD参考方法的结果进行比较。实验室间Etest MIC结果与BMD结果具有良好的相关性(r = 0.86至0.88),95.3%的Etest MIC值在BMD MIC结果的±1 log(2)稀释范围内。在两个参与实验室中,通过BMD鉴定的102株(90.2%)非达托霉素敏感金黄色葡萄球菌菌株中,共有92株也被Etest法判定为非敏感。然而,其中一个参与实验室报告的极重大误差率和重大误差率分别为13.5%和4.0%,主要原因是没有中间类别。然而,DD法不能可靠地区分达托霉素敏感与非敏感菌株。2005年,Cubist制药公司主动将达托霉素纸片撤出市场。纸片扩散法的断点随后在2006年从CLSI M100标准中删除。