首页> 外文期刊>Research in Microbiology >Double triplex real-time PCR assay for simultaneous detection of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus hominis, and Staphylococcus haemolyticus and determination of their methicillin resistance directly from positive blood culture bottles
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Double triplex real-time PCR assay for simultaneous detection of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus hominis, and Staphylococcus haemolyticus and determination of their methicillin resistance directly from positive blood culture bottles

机译:双重三重实时荧光定量PCR技术可同时从阳性血培养瓶中同时检测金黄色葡萄球菌,表皮葡萄球菌,人型葡萄球菌和溶血性葡萄球菌并测定其对甲氧西林的耐药性

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We developed and validated here a double triplex real-time PCR assay to simultaneously detect and identify Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus hominis, Staphylococcus haemolyticus and their methicillin resistance in a single reaction directly from Gram-positive cocci-in-clusters (GPCs)-positive blood culture bottles. From August 15, 2009 through February 15, 2010, 238 GPC-positive samples were collected and identified by conventional methods as 11 methicillin-resistant S. aureus (MRSA), 28 methicillin-susceptible S. aureus (MSSA), 176 MR coagulase-negative staphylococci (MRCoNS), 21 MSCoNS and two Enterococcus faecalis. The double triplex real-time PCR assay was targeted and detected tuf, nuc and mecA genes in the first tube and atlE, gap and mvaA genes in the second tube which could be run simultaneously. The detection limit of the assay was found at 103 CFU/ml for the atleE gene, 104 CFU/ml for the mva gene and 105 CFU/ml for gap, nuc, mecA and tuf genes based on seeding experiments. All Staphylococcus species except two S. epidermidis were correctly identified by the assay. The double triplex real-time PCR assay quickly and accurately detects S. aureus, S. epidermidis, S. hominis and S. haemolyticus and their methicillin resistance in a single reaction directly from positive blood culture bottles within 83 min.
机译:我们在这里开发并验证了双重三重实时荧光定量PCR检测方法,可直接从革兰氏阳性球菌簇(GPC)直接反应,从而同时检测和鉴定金黄色葡萄球菌,表皮葡萄球菌,人葡萄球菌,溶血性葡萄球菌及其耐甲氧西林阳性血液培养瓶。从2009年8月15日至2010年2月15日,通过常规方法收集并鉴定了238个GPC阳性样品,分别为11株耐甲氧西林的金黄色葡萄球菌(MRSA),28株耐甲氧西林的金黄色葡萄球菌(MSSA),176 MR凝固酶-阴性葡萄球菌(MRCoNS),21个MSCoNS和两个粪肠球菌。靶向双重三重实时荧光定量PCR检测并检测了第一支试管中的tuf,nuc和mecA基因以及第二支试管中的atlE,gap和mvaA基因,这些基因可以同时运行。根据播种实验,atleE基因的检测限为103 CFU / ml,mva基因的检测限为104 CFU / ml,gap,nuc,mecA和tuf基因的检测限为105 CFU / ml。通过分析正确鉴定了除两个表皮葡萄球菌外的所有葡萄球菌种类。双重三重实时荧光定量PCR快速,准确地在83分钟内直接从阳性血培养瓶中进行单个反应,快速,准确地检测到金黄色葡萄球菌,表皮葡萄球菌,人沙门氏菌和溶血链球菌及其耐甲氧西林。

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