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Detection of bacterial pathogens in Mongolia meningitis surveillance with a new real-time PCR assay to detect Haemophilus influenzae.应用新型实时 PCR 检测方法检测流感嗜血杆菌在蒙古脑膜炎监测中的细菌病原体检测。
Int J Med Microbiol. 2011 Apr;301(4):303-9. doi: 10.1016/j.ijmm.2010.11.004. Epub 2011 Jan 26.
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The burden of hospitalized lower respiratory tract infection due to respiratory syncytial virus in rural Thailand.泰国农村因呼吸道合胞病毒导致的住院下呼吸道感染负担。
PLoS One. 2010 Nov 30;5(11):e15098. doi: 10.1371/journal.pone.0015098.
3
Comparison of commercial systems for extraction of nucleic acids from DNA/RNA respiratory pathogens.商业系统从 DNA/RNA 呼吸道病原体中提取核酸的比较。
J Virol Methods. 2011 Jan;171(1):195-9. doi: 10.1016/j.jviromet.2010.10.024. Epub 2010 Oct 27.
4
Etiology of community-acquired pneumonia: increased microbiological yield with new diagnostic methods.社区获得性肺炎的病因:新诊断方法提高了微生物学检出率。
Clin Infect Dis. 2010 Jan 15;50(2):202-9. doi: 10.1086/648678.
5
Evaluation of tetramethylrhodamine and black hole quencher 1 labeled probes and five commercial amplification mixes in TaqMan real-time RT-PCR assays for respiratory pathogens.评价四甲基罗丹明和黑洞猝灭剂 1 标记探针以及五种商业扩增混合物在 TaqMan 实时 RT-PCR 检测呼吸道病原体中的应用。
J Virol Methods. 2009 Dec;162(1-2):288-90. doi: 10.1016/j.jviromet.2009.08.004. Epub 2009 Aug 20.
6
Evaluation of two real-time PCR chemistries for the detection of Chlamydophila pneumoniae in clinical specimens.两种实时 PCR 化学方法检测临床标本中肺炎衣原体的评价。
Mol Cell Probes. 2009 Dec;23(6):309-11. doi: 10.1016/j.mcp.2009.07.005. Epub 2009 Jul 30.
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Dual detection of Legionella pneumophila and Legionella species by real-time PCR targeting the 23S-5S rRNA gene spacer region.采用实时 PCR 靶向 23S-5S rRNA 基因间隔区检测嗜肺军团菌和军团菌属。
Clin Microbiol Infect. 2010 Mar;16(3):255-61. doi: 10.1111/j.1469-0691.2009.02766.x. Epub 2009 Apr 25.
8
Rapid group-, serotype-, and vaccine strain-specific identification of poliovirus isolates by real-time reverse transcription-PCR using degenerate primers and probes containing deoxyinosine residues.使用含有次黄嘌呤脱氧核苷残基的简并引物和探针,通过实时逆转录聚合酶链反应对脊髓灰质炎病毒分离株进行快速的群特异性、血清型特异性和疫苗株特异性鉴定。
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9
Robust global micro-RNA profiling with formalin-fixed paraffin-embedded breast cancer tissues.利用福尔马林固定石蜡包埋的乳腺癌组织进行可靠的全基因组微小RNA分析。
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10
A TaqMan low-density array to predict outcome in advanced Hodgkin's lymphoma using paraffin-embedded samples.一种用于通过石蜡包埋样本预测晚期霍奇金淋巴瘤预后的TaqMan低密度阵列。
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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.

DOI:10.1128/JCM.02270-10
PMID:21471348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3122721/
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。