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用于在阳性血培养物中直接检测金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌的分子BD GeneOhm StaphSR检测法的临床验证

Clinical validation of the molecular BD GeneOhm StaphSR assay for direct detection of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus in positive blood cultures.

作者信息

Stamper Paul D, Cai Mian, Howard Tracy, Speser Sharon, Carroll Karen C

机构信息

Division of Medical Microbiology, Department of Pathology, Johns Hopkins University School of Medicine, Johns Hopkins Hospital, Baltimore, Maryland 21287, USA.

出版信息

J Clin Microbiol. 2007 Jul;45(7):2191-6. doi: 10.1128/JCM.00552-07. Epub 2007 May 23.

Abstract

The rapid detection of Staphylococcus aureus bacteremia and a swift determination of methicillin susceptibility has serious clinical implications affecting patient mortality. This study evaluated the StaphSR assay (BD GeneOhm, San Diego, CA), a real-time PCR assay, for the identification and differentiation of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) from 300 positive blood cultures. The BD GeneOhm StaphSR assay was performed and interpreted according to the manufacturer's recommendations. Positive blood cultures (containing predominantly gram-positive cocci in clusters) were subcultured on 5% sheep blood agar plates. After 18 to 24 h of incubation, isolates morphologically consistent with S. aureus were presumptively identified by latex agglutination (Staphaurex Plus; Remel, Lenexa, KS). Susceptibility testing was initially performed with the Phoenix automated microbiology system (BD Diagnostics, Sparks, MD). Additional susceptibility testing of samples with discrepant results was done using BBL oxacillin screen agar (BD Diagnostics, Sparks, MD), oxacillin and cefoxitin Etests (AB Biodisk, Solna, Sweden) on Mueller-Hinton agar, an immunoassay for penicillin binding protein 2' (Denka Seiken Co., Tokyo, Japan), and mecA PCR. The sensitivity, specificity, and positive and negative predictive values of the BD GeneOhm StaphSR assay for MSSA detection were 98.9, 96.7, 93.6, and 99.5%, respectively. For the detection of MRSA, the BD GeneOhm StaphSR assay was 100% sensitive and 98.4% specific; positive and negative predictive values for MRSA detection were 92.6 and 100%, respectively. Inhibition was seen with only one sample, and the issue was resolved upon retesting. The BD GeneOhm StaphSR assay appears to be a valuable diagnostic tool for quickly differentiating bacteremia caused by MSSA and MRSA from that caused by other gram-positive cocci.

摘要

金黄色葡萄球菌菌血症的快速检测以及甲氧西林敏感性的迅速判定具有严重的临床意义,会影响患者死亡率。本研究评估了StaphSR检测法(BD GeneOhm,加利福尼亚州圣地亚哥),这是一种实时PCR检测法,用于从300份阳性血培养物中鉴定和区分甲氧西林敏感金黄色葡萄球菌(MSSA)和甲氧西林耐药金黄色葡萄球菌(MRSA)。BD GeneOhm StaphSR检测法按照制造商的建议进行操作和解读。将阳性血培养物(主要含有呈葡萄串状的革兰氏阳性球菌)接种于5%绵羊血琼脂平板进行传代培养。孵育18至24小时后,通过乳胶凝集试验(Staphaurex Plus;Remel,堪萨斯州莱尼克斯)初步鉴定形态学上与金黄色葡萄球菌一致的分离株。敏感性检测最初使用Phoenix自动化微生物系统(BD诊断公司,马里兰州斯帕克斯)进行。对结果不一致的样本,使用BBL苯唑西林筛选琼脂(BD诊断公司,马里兰州斯帕克斯)、苯唑西林和头孢西丁E试验(AB Biodisk,瑞典索尔纳)在Mueller-Hinton琼脂上进行额外的敏感性检测,采用青霉素结合蛋白2'免疫测定法(Denka Seiken公司,日本东京)以及mecA PCR。BD GeneOhm StaphSR检测法检测MSSA的敏感性、特异性、阳性预测值和阴性预测值分别为98.9%、96.7%、93.6%和99.5%。对于MRSA的检测,BD GeneOhm StaphSR检测法的敏感性为100%,特异性为98.4%;检测MRSA的阳性预测值和阴性预测值分别为92.6%和100%。仅一个样本出现抑制现象,重新检测后问题得到解决。BD GeneOhm StaphSR检测法似乎是一种有价值的诊断工具,可快速区分由MSSA和MRSA引起的菌血症与由其他革兰氏阳性球菌引起的菌血症。

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