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使用COBAS AmpliPrep自动样本制备和LightCycler实时PCR对细小病毒B19 DNA进行定量分析。

Quantification of parvovirus B19 DNA using COBAS AmpliPrep automated sample preparation and LightCycler real-time PCR.

作者信息

Schorling Stefan, Schalasta Gunnar, Enders Gisela, Zauke Michael

机构信息

Roche Diagnostics GmbH, Penzberg, Germany.

出版信息

J Mol Diagn. 2004 Feb;6(1):37-41. doi: 10.1016/S1525-1578(10)60489-8.

Abstract

The COBAS AmpliPrep instrument (Roche Diagnostics GmbH, D-68305 Mannheim, Germany) automates the entire sample preparation process of nucleic acid isolation from serum or plasma for polymerase chain reaction analysis. We report the analytical performance of the LightCycler Parvovirus B19 Quantification Kit (Roche Diagnostics) using nucleic acids isolated with the COBAS AmpliPrep instrument. Nucleic acids were extracted using the Total Nucleic Acid Isolation Kit (Roche Diagnostics) and amplified with the LightCycler Parvovirus B19 Quantification Kit. The kit combination processes 72 samples per 8-hour shift. The lower detection limit is 234 IU/ml at a 95% hit-rate, linear range approximately 10(4)-10(10) IU/ml, and overall precision 16 to 40%. Relative sensitivity and specificity in routine samples from pregnant women are 100% and 93%, respectively. Identification of a persistent parvovirus B19-infected individual by the polymerase chain reaction among 51 anti-parvovirus B19 IgM-negative samples underlines the importance of additional nucleic acid testing in pregnancy and its superiority to serology in identifying the risk of parvovirus B19 transmission via blood or blood products. Combination of the Total Nucleic Acid Isolation Kit on the COBAS AmpliPrep instrument with the LightCycler Parvovirus B19 Quantification Kit provides a reliable and time-saving tool for sensitive and accurate detection of parvovirus B19 DNA.

摘要

COBAS AmpliPrep仪器(德国罗氏诊断有限公司,德国曼海姆68305)可自动完成从血清或血浆中分离核酸用于聚合酶链反应分析的整个样本制备过程。我们报告了使用通过COBAS AmpliPrep仪器分离的核酸的LightCycler细小病毒B19定量试剂盒(罗氏诊断)的分析性能。使用总核酸分离试剂盒(罗氏诊断)提取核酸,并使用LightCycler细小病毒B19定量试剂盒进行扩增。该试剂盒组合每8小时轮班可处理72个样本。在95%的命中率下,检测下限为234 IU/ml,线性范围约为10(4)-10(10) IU/ml,总体精密度为16%至40%。孕妇常规样本中的相对敏感性和特异性分别为100%和93%。在51份抗细小病毒B19 IgM阴性样本中通过聚合酶链反应鉴定出一名持续感染细小病毒B19的个体,这突出了孕期额外核酸检测的重要性及其在识别细小病毒B19通过血液或血液制品传播风险方面相对于血清学的优越性。COBAS AmpliPrep仪器上的总核酸分离试剂盒与LightCycler细小病毒B19定量试剂盒相结合,为灵敏准确地检测细小病毒B19 DNA提供了一种可靠且省时的工具。

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