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Clin Microbiol Newsl. 2007 Aug 1;29(15):113-119. doi: 10.1016/j.clinmicnews.2007.07.001. Epub 2007 Aug 2.
2
Comparison of the Luminex Respiratory Virus Panel fast assay with in-house real-time PCR for respiratory viral infection diagnosis.Luminex 呼吸道病毒Panel 快速检测与自建实时 PCR 检测在呼吸道病毒感染诊断中的比较。
J Clin Microbiol. 2010 Jun;48(6):2213-6. doi: 10.1128/JCM.02446-09. Epub 2010 Mar 31.
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A novel multiplex real-time RT-PCR assay with FRET hybridization probes for the detection and quantitation of 13 respiratory viruses.一种新型多重实时 RT-PCR 检测方法,采用荧光共振能量转移杂交探针,用于检测和定量 13 种呼吸道病毒。
J Virol Methods. 2010 May;165(2):254-60. doi: 10.1016/j.jviromet.2010.02.005. Epub 2010 Feb 11.
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Use of rapid influenza diagnostic tests under field conditions as a screening tool during an outbreak of the 2009 novel influenza virus: practical considerations.现场条件下使用快速流感诊断检测作为 2009 年新型流感病毒爆发期间的筛查工具:实际考虑因素。
J Clin Virol. 2010 Mar;47(3):229-33. doi: 10.1016/j.jcv.2009.12.015. Epub 2010 Jan 18.
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Emerging molecular assays for detection and characterization of respiratory viruses.用于呼吸道病毒检测和特征分析的新兴分子检测方法。
Clin Lab Med. 2009 Dec;29(4):673-93. doi: 10.1016/j.cll.2009.07.005.
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Enhanced viral etiological diagnosis of respiratory system infection outbreaks by use of a multitarget nucleic acid amplification assay.应用多靶点核酸扩增检测技术增强呼吸系统感染性疾病暴发的病毒病因学诊断。
J Clin Microbiol. 2009 Dec;47(12):3839-45. doi: 10.1128/JCM.01469-09. Epub 2009 Oct 14.
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8
Evaluation of multiple test methods for the detection of the novel 2009 influenza A (H1N1) during the New York City outbreak.纽约市疫情期间新型2009甲型流感(H1N1)检测多种测试方法的评估
J Clin Virol. 2009 Jul;45(3):191-5. doi: 10.1016/j.jcv.2009.06.005. Epub 2009 Jun 16.
9
Multiplex PCR tests sentinel the appearance of pandemic influenza viruses including H1N1 swine influenza.多重聚合酶链反应(Multiplex PCR)检测可监测包括H1N1猪流感在内的大流行性流感病毒的出现。
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10
Likelihood that an unsubtypeable influenza A virus result obtained with the Luminex xTAG respiratory virus panel is indicative of infection with novel A/H1N1 (swine-like) influenza virus.使用Luminex xTAG呼吸道病毒检测板获得的无法分型的甲型流感病毒结果表明感染新型A/H1N1(猪样)流感病毒的可能性。
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评估商业版 ResPlex II v2.0、MultiCode-PLx 和 xTAG 呼吸道病毒检测试剂盒在成人呼吸道病毒感染诊断中的应用。

Evaluation of commercial ResPlex II v2.0, MultiCode-PLx, and xTAG respiratory viral panels for the diagnosis of respiratory viral infections in adults.

机构信息

Clinical Microbiology, Department of Pathology, The Ohio State University Medical Center, 1492 E Broad Street, Columbus, OH 43205, United States.

出版信息

J Clin Virol. 2011 Jan;50(1):42-5. doi: 10.1016/j.jcv.2010.09.022. Epub 2010 Nov 2.

DOI:10.1016/j.jcv.2010.09.022
PMID:21050809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7185502/
Abstract

BACKGROUND

Commercial multiplex PCR panels for respiratory viruses (PRV) have been recently developed. ResPlex II Panel v2.0 (Qiagen), MultiCode-PLx (EraGen Biosciences), and xTAG (Luminex) PRV's were studied. All assays detect influenza A and B, adenovirus, parainfluenza 1-3, respiratory syncytial virus A and B, human metapneumovirus and human rhinovirus. The ResPlex II additionally detects coronavirus (229E, OC43, NL63, HKU1), coxsackie/echo virus, bocavirus and differentiates adenoviruses (B, E). The MultiCode-PLX assay detects 229E, OC43, and NL63, differentiates parainfluenza 4a, 4b and adenoviruses (B, C, E). The xTAG additionally subtypes influenza A as seasonal H1 and H3.

STUDY DESIGN

202 specimens collected from adult patients with signs of respiratory infection from November, 2008 to May, 2009 were used for evaluating the performance of the three commercial PRV assays. Viral culture and xTAG were used as the standards to assess sensitivity and specificity.

RESULTS

The PRV assays detected more viruses than culture. When compared to culture, the xTAG PRV showed a sensitivity and specificity of 100% and 91%, compared to MultiCode-PLx with 89% and 87%, and ResPlex II with 89% and 94%, respectively. Co-infection was detected in a small subset of patient specimens. Each panel showed differences in sensitivities for individual viruses.

CONCLUSIONS

While the ResPlex II and MultiCode-PLx offer a broader virus detection range and greater ease of use, the xTAG PRV showed increased sensitivity to common viral targets represented in the assays, and also had the ability to differentiate human from non-human influenza A H1.

摘要

背景

商业多重聚合酶链反应(PCR)检测呼吸道病毒(PRV)试剂盒已研发出来。我们对 ResPlex II 面板 v2.0(Qiagen)、MultiCode-PLx(EraGen Biosciences)和 xTAG(Luminex)PRV 试剂盒进行了研究。所有的检测都能检测到流感 A 和 B、腺病毒、副流感 1-3、呼吸道合胞病毒 A 和 B、人偏肺病毒和人鼻病毒。ResPlex II 试剂盒还可以检测冠状病毒(229E、OC43、NL63、HKU1)、柯萨奇/埃可病毒、博卡病毒,并能区分腺病毒(B、E)。MultiCode-PLX 试剂盒可以检测 229E、OC43 和 NL63,区分副流感 4a、4b 和腺病毒(B、C、E)。xTAG 试剂盒还能对季节性 H1 和 H3 流感病毒进行亚型分析。

设计

我们使用 2008 年 11 月至 2009 年 5 月期间,从出现呼吸道感染症状的成年患者中采集的 202 份标本,用于评估三种商业 PRV 试剂盒的性能。我们使用病毒培养和 xTAG 作为评估标准,来检测试剂盒的灵敏度和特异性。

结果

PRV 试剂盒比病毒培养检测到了更多的病毒。与病毒培养相比,xTAG PRV 的灵敏度和特异性分别为 100%和 91%,MultiCode-PLx 为 89%和 87%,ResPlex II 为 89%和 94%。在一小部分患者标本中检测到了混合感染。每个试剂盒对个别病毒的检测敏感性都有差异。

结论

虽然 ResPlex II 和 MultiCode-PLx 提供了更广泛的病毒检测范围,且操作更简便,但 xTAG PRV 对检测试剂盒中常见病毒靶标具有更高的灵敏度,而且还具有区分人类和非人类流感 A H1 的能力。