首页> 外文期刊>Journal of Clinical Microbiology >StaphPlex System for Rapid and Simultaneous Identification of Antibiotic Resistance Determinants and Panton-Valentine Leukocidin Detection of Staphylococci from Positive Blood Cultures
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StaphPlex System for Rapid and Simultaneous Identification of Antibiotic Resistance Determinants and Panton-Valentine Leukocidin Detection of Staphylococci from Positive Blood Cultures

机译:StaphPlex系统,用于快速同时鉴定抗生素抗性决定簇和潘通-华伦丁白细胞介素从阳性血培养物中检测葡萄球菌

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Phenotypic methods take several days for identification and antimicrobial susceptibility testing of staphylococcal isolates after gram-positive cocci in clusters (GPCC) are observed in positive blood cultures. We developed and validated a StaphPlex system that amplifies and detects 18 gene targets simultaneously in 1 reaction for species-level identification of staphylococci, detection of genes encoding Panton-Valentine leukocidin (PVL), and antimicrobial resistance determinants of staphylococci. The StaphPlex system was compared to phenotypic methods for organism identification and antimicrobial resistance detection for positive blood culture specimens in which GPCC were observed. Among a total of 360 GPCC specimens, 273 (75.8%), 37 (10.3%), 37 (10.3%), 1 (0.3%), 3 (0.8%), and 9 (2.5%) were identified by StaphPlex as coagulase-negative Staphylococcus (CoNS), methicillin-resistant Staphylococcus aureus (MRSA), methicillin-susceptible S. aureus (MSSA), or mixed infections of CoNS and MRSA, CoNS and MSSA, or nonstaphylococci, respectively, with an overall accuracy of 91.7%. The 277 CoNS-containing specimens were further identified to the species level as containing 203 (73.3%) Staphylococcus epidermidis isolates, 10 (3.6%) Staphylococcus haemolyticus isolates, 27 (9.7%) Staphylococcus hominis isolates, 1 (0.4%) Staphylococcus lugdunensis isolate, and 36 (13.0%) other CoNS isolates, with an overall accuracy of 80.1% compared to an API STAPH test and CDC reference identification. Numerous very major errors were noticed when detection of aacA, ermA, ermC, tetM, and tetK was used to predict in vitro antimicrobial resistance, but relatively few major errors were observed when the absence of these genes was used to predict susceptibility. The StaphPlex system demonstrated 100% sensitivity and specificity, ranging from 95.5% to 100.0% when used for staphylococcal cassette chromosome mec typing and PVL detection. StaphPlex provides simultaneous staphylococcal identification and detection of PVL and antimicrobial resistance determinants within 5 h, significantly shortening the time needed for phenotypic identification and antimicrobial susceptibility testing.
机译:在阳性血液培养物中观察到革兰氏阳性球菌簇(GPCC)后,表型方法需要几天的时间进行鉴定和葡萄球菌分离物的抗菌药敏测试。我们开发并验证了一个StaphPlex系统,该系统可在1个反应中同时扩增和检测18个基因靶标,用于葡萄球菌的物种级鉴定,编码潘顿-华伦特白介素(PVL)的基因以及葡萄球菌的抗药性决定因素。对于观察到GPCC的阳性血液培养标本,将StaphPlex系统与表型方法进行了有机体鉴定和抗菌素耐药性检测的比较。在总共360个GPCC标本中,通过StaphPlex将273个(75.8%),37个(10.3%),37个(10.3%),1个(0.3%),3个(0.8%)和9个(2.5%)鉴定为凝固酶。阴性葡萄球菌(CoNS),耐甲氧西林的金黄色葡萄球菌(MRSA),易受甲氧西林的 S。金黄色葡萄球菌(MSSA)或CoNS和MRSA,CoNS和MSSA的混合感染或非葡萄球菌,总准确率为91.7%。进一步确定了277个含有CoNS的标本,使其在物种水平上分别为203个(73.3%)表皮葡萄球菌分离株,10个(3.6%)溶血性葡萄球菌分离株27(9.7) %)人型葡萄球菌分离株,1(0.4%) lugdunensis 分离株和36(13.0%)其他CoNS分离株,与API相比,总准确性为80.1% STAPH测试和CDC参考标识。检测到 aacA ermA ermC tetM tetK时,发现了许多非常重要的错误。 用于预测体外抗药性,但是当不使用这些基因来预测药敏性时,观察到的主要错误相对较少。 StaphPlex系统用于葡萄球菌盒式染色体 mec 分型和PVL检测时,具有100%的敏感性和特异性,范围从95.5%到100.0%。 StaphPlex可在5小时内同时进行葡萄球菌鉴定和PVL和抗菌素耐药性决定因素的检测,从而显着缩短了进行表型鉴定和药敏试验所需的时间。

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