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首页> 外文期刊>Journal of Clinical Microbiology >Clinical comparison of the AutoMicrobic system gram-positive identification card, API Staph-Ident, and conventional methods in the identification of coagulase-negative Staphylococcus spp.
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Clinical comparison of the AutoMicrobic system gram-positive identification card, API Staph-Ident, and conventional methods in the identification of coagulase-negative Staphylococcus spp.

机译:AutoMicrobic系统革兰氏阳性识别卡,API Staph-Ident和常规方法在鉴定凝固酶阴性葡萄球菌中的临床比较。

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In an effort to rapidly identify coagulase-negative staphylococci (CNS), a clinical comparison was conducted with the AutoMicrobic system Gram-Positive Identification Card (GPI) (Vitek Systems, Inc.), the API Staph-Ident (Analytab Products), and the conventional methods of W. E. Kloos and K. H. Schleifer (W. E. Kloos and K. H. Schleifer, J. Clin. Microbiol. 1:82-88, 1975). CNS isolates tested included 157 from blood and 33 from urine in pure culture at greater than 10(5) CFU/ml. S. epidermidis accounted for 79.6 and 60.6% of the isolates from blood and urine, respectively. S. saprophyticus was the next most frequent urine isolate (27.4%). Other CNS species were isolated from blood and urine specimens with frequencies of less than 5%. Overall, the GPI correctly identified 158 (83.2%) of the 190 CNS, whereas the Staph-Ident identified 124 (65.3%) without further testing. This resulted in the GPI and Staph-Ident correctly identifying 95.9 and 74.5% of the S. epidermidis and 100 and 33% of the S. saprophyticus, respectively. The GPI misidentified 8 (47%) of the S. hominis and S. warneri isolates as S. saprophyticus, indicating the need for novobiocin testing. These data suggest that the GPI is a more definitive method for the rapid identification of S. epidermidis than the Staph-Ident and that both systems require additional testing to identify S. saprophyticus.
机译:为了快速识别凝固酶阴性葡萄球菌(CNS),使用AutoMicrobic系统革兰氏阳性识别卡(GPI)(Vitek Systems,Inc。),API Staph-Ident(Analytab产品)和WE Kloos和KH Schleifer的常规方法(WE Kloos和KH Schleifer,J.Clin.Microbiol.1:82-88,1975)。在纯培养物中,以大于10(5)CFU / ml的浓度测试的CNS分离物包括157血和33尿。表皮葡萄球菌分别占血液和尿液分离株的79.6和60.6%。腐生链球菌是第二常见的尿液分离株(27.4%)。从血液和尿液样本中分离出其他CNS物种的频率低于5%。总体而言,GPI正确地识别了190个CNS中的158个(占83.2%),而Staph-Ident识别了124个(65.3%),而无需进一步测试。这导致GPI和葡萄球菌身份分别正确鉴定出表皮葡萄球菌的95.9%和表皮葡萄球菌的74.5%以及腐生链球菌的100%和33%。 GPI将8株(47%)人肉链球菌和Warneri分离株误认为是腐生链球菌,表明需要进行新霉素检测。这些数据表明,与葡萄球菌身份相比,GPI是一种更快速确定表皮葡萄球菌的确定方法,并且这两个系统都需要进行额外的测试才能鉴定腐生葡萄球菌。

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