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首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >Rapid detection of Streptococcus agalactiae from swabs by peptide nucleic acid fluorescence in situ hybridization
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Rapid detection of Streptococcus agalactiae from swabs by peptide nucleic acid fluorescence in situ hybridization

机译:肽核酸荧光原位杂交技术从拭子中快速检测无乳链球菌

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摘要

The applicability of the PNA FISH (peptide nucleic acid fluorescence in situ hybridization) method for detection of Streptococcus agalactiae [group B streptococci (GBS)] from swab samples was evaluated. Three swab-sample-processing protocols with different time-to-result (TTR) values were compared: (i) direct smearing of fresh swabs onto microscope slides (n=153, TTR 2.5 h), (ii) further extraction and concentration of cells from these same swabs (n=153, TTR 2.7 h), and (iii) short-term LIM broth enrichment culture incubation (7 h, 37 °C) of fresh swabs (n=120, TTR 9.5 h). The sensitivity, specificity, positive predictive value and negative predictive value for GBS PNA FISH for sample processing procedures, with TTR values of 2.5, 2.7 and 9.5 h, were 68, 100, 100 and 95 %; 91, 100, 100 and 98 %; and 100, 100, 100 and 100 %; respectively. Improved test results were achieved by subjecting swabs to an extraction procedure or abbreviated LIM broth enrichment culture incubation prior to performing GBS PNA FISH.
机译:评估了PNA FISH(肽核酸荧光原位杂交)方法在拭子样品中检测无乳链球菌[B组链球菌(GBS)]的适用性。比较了三种具有不同结果时间(TTR)值的拭子样品处理方案:(i)将新鲜拭子直接涂在显微镜载玻片上(n = 153,TTR 2.5 h),(ii)进一步提取和浓缩来自这些相同拭子的细胞(n = 153,TTR 2.7 h),和(iii)新鲜拭子的短期LIM肉汤富集培养孵育(7 h,37°C)(n = 120,TTR 9.5 h)。 GBS PNA FISH在样品处理过程中的TTR值为2.5、2.7和9.5 h的敏感性,特异性,阳性预测值和阴性预测值分别为68%,100%,100%和95%; 91%,100%,100%和98%;和100、100、100和100%;分别。在执行GBS PNA FISH之前,通过对拭子进行提取程序或简化的LIM肉汤富集培养孵育,可以提高测试结果。

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