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Detection of heterogeneous vancomycin-intermediate Staphylococcus aureus isolates using a combination of delta-hemolysis assay and Etest

机译:结合溶血分析和Etest检测万古霉素中间型金黄色葡萄球菌分离株

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This study evaluated the delta-hemolysis assay for detection of heterogeneous vancomycin-intermediate Staphylococcus aureus (hVISA) isolates. The assay was performed using Columbia or trypticase soy blood agar plates without vancomycin at 37 degrees C with 5% CO2, and the test isolate was streaked perpendicularly 1 mm away from S. aureus RN4220. One hundred thirty-eight methicillin-resistant S. aureus (MRSA) bloodstream isolates with vancomycin MICs of 0.75-2 mu g/mL were screened for hVISA by the delta-hemolysis assay and Etest glycopeptide resistance detection (GRD) method. The delta-hemolysis assay could be read at 24 h and was more sensitive and specific than the Etest GRD at 24 h and 48 h for detection of hVISA. Because most hVISA isolates have a vancomycin MIC of 2 mu g/mL, we recommend screening MRSA isolates first using Etest for those with an MIC of 2 mu g/mL and then performing the delta-hemolysis assay on these isolates for hVISA. (C) 2015 Elsevier Inc. All rights reserved.
机译:这项研究评估了三角洲溶血测定法检测异种万古霉素中间金黄色葡萄球菌(hVISA)分离株。使用不含万古霉素的Columbia或胰蛋白酶大豆血琼脂平板在37°C,5%CO2下进行测定,并将测试分离株垂直于距金黄色葡萄球菌RN4220 1毫米处划线。通过δ-溶血分析和Etest糖肽耐药性检测(GRD)方法,筛选出具有万古霉素MIC值为0.75-2μg/ mL的138个耐甲氧西林金黄色葡萄球菌(MRSA)血流分离株。 δ-溶血测定法可在24 h读取,并且比etest GRD在24 h和48 h检测hVISA更为灵敏和特异。由于大多数hVISA分离株的万古霉素MIC为2μg / mL,我们建议首先使用Etest筛选MIC为2μg / mL的MRSA分离株,然后对这些分离株进行hVISA的δ-溶血分析。 (C)2015 Elsevier Inc.保留所有权利。

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