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TaqMan 低密度基因芯片在同时检测多种呼吸道病原体中的应用。

Application of TaqMan low-density arrays for simultaneous detection of multiple respiratory pathogens.

机构信息

Division of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

J Clin Microbiol. 2011 Jun;49(6):2175-82. doi: 10.1128/JCM.02270-10. Epub 2011 Apr 6.

Abstract

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 (C(T)) cutoff of 43. The TLDA card approach offers promise for rapid and simultaneous identification of multiple respiratory pathogens for outbreak investigations and disease surveillance.

摘要

负责呼吸道感染的大量且不断增加的病毒和细菌病原体对寻求提供快速和全面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) 卡在实时 PCR 检测 21 种呼吸道病原体靶标中的新应用。使用(i)从 21 种病原体株和 66 种密切相关的病毒和细菌中提取的核酸,以及(ii)292 份临床呼吸道标本,将 TLDA 的性能与具有相同引物和探针的单个实时 PCR (IRTP) 检测进行了比较。在加标样本中,TLDA 卡比 IRTP 检测低约 10 倍。通过使用 292 份临床标本生成 2238 对单独的检测,TLDA 卡的总体灵敏度为 89%(95%置信区间 [CI],86 至 92%;每个靶标范围,47 至 100%)和 98%(95% CI,97 至 99%;每个靶标范围,85 至 100%),与 IRTP 检测相比,IRTP 检测作为金标准,阈值循环 (C(T)) 截止值为 43。TLDA 卡方法有望用于快速同时鉴定多种呼吸道病原体,用于暴发调查和疾病监测。

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