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首页> 外文期刊>Journal of Clinical Microbiology >Application of TaqMan Low-Density Arrays for Simultaneous Detection of Multiple Respiratory Pathogens
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Application of TaqMan Low-Density Arrays for Simultaneous Detection of Multiple Respiratory Pathogens

机译:TaqMan低密度阵列在同时检测多种呼吸道病原体中的应用

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摘要

The large and growing number of viral and bacterial pathogens responsible for respiratory infections poses a challenge for laboratories seeking to provide rapid and comprehensive pathogen identification. We evaluated a novel application of the TaqMan low-density array (TLDA) cards for real-time PCR detection of 21 respiratory-pathogen targets. The performance of the TLDA was compared to that of individual real-time PCR (IRTP) assays with the same primers and probes using (i) nucleic acids extracted from the 21 pathogen strains and 66 closely related viruses and bacteria and (ii) 292 clinical respiratory specimens. With spiked samples, TLDA cards were about 10-fold less sensitive than IRTP assays. By using 292 clinical specimens to generate 2,238 paired individual assays, the TLDA card exhibited 89% sensitivity (95% confidence interval [CI], 86 to 92%; range per target, 47 to 100%) and 98% specificity (95% CI, 97 to 99%; range per target, 85 to 100%) overall compared to IRTP assays as the gold standard with a threshold cycle (CT) cutoff of 43. The TLDA card approach offers promise for rapid and simultaneous identification of multiple respiratory pathogens for outbreak investigations and disease surveillance.
机译:负责呼吸道感染的病毒和细菌病原体的数量不断增加,这对寻求快速,全面的病原体鉴定的实验室构成了挑战。我们评估了TaqMan低密度阵列(TLDA)卡在21种呼吸道病原体靶标的实时PCR检测中的新型应用。使用(i)从21种病原体菌株和66种密切相关的病毒和细菌中提取的核酸和(ii)292种临床方法,将TLDA的性能与使用相同引物和探针的单个实时PCR(IRTP)分析的性能进行了比较呼吸道标本。对于加标样品,TLDA卡的灵敏度比IRTP分析低约10倍。通过使用292个临床标本生成2238个配对的独立测定,TLDA卡显示出89%的敏感性(95%置信区间[CI],86至92%;每个靶标的范围为47%至100%)和98%的特异性(95%CI) (97%至99%;每个目标范围为85%至100%),而IRTP分析作为金标准,其阈值循环( C T )截止值为43。 TLDA卡方法为快速,同时识别多种呼吸道病原体以进行暴发调查和疾病监测提供了希望。

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