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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.

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。

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