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QIAGEN QIAsymphony SP 系统与 bioMérieux NucliSens easyMAG 自动化提取平台在临床病毒学实验室的比较评估。

Comparative evaluation of the QIAGEN QIAsymphony® SP system and bioMérieux NucliSens easyMAG automated extraction platforms in a clinical virology laboratory.

机构信息

Department of Infection (HPA Lead Microbiology Laboratory for London), Barts and The London NHS Trust, London, E1 2ES, UK.

出版信息

J Clin Virol. 2011 Dec;52(4):339-43. doi: 10.1016/j.jcv.2011.08.016. Epub 2011 Oct 20.

Abstract

BACKGROUND

The QIAGEN QIAsymphony(®) SP is an automated system that can process a variety of different sample types for nucleic acid extraction.

OBJECTIVES

To compare this system against the bioMérieux NucliSens easyMAG using a range of common clinical sample types.

STUDY DESIGN

Nucleic acid extracts were tested on 6 in-house real time viral PCR assays: quantitative cytomegalovirus (CMV); respiratory and enteric multiplex (10 viruses); influenza A H1N1 2009 specific H1 and N1 assays (sH1/N1); herpes simplex virus (HSV) 1, HSV 2 and varicella zoster virus (VZV) multiplex; norovirus genogroups I and II (Noro GI/II) multiplex.

RESULTS

Extraction of the clinical sample by either QIAsymphony(®) SP or NucliSens easyMAG gave similar results for each PCR; CMV viral loads, 52 plasma samples had a mean difference (easyMAG-QIAsymphony(®)) of 0.002 log(10)copies/ml (s.d. 0.536), 52 whole blood samples had a mean difference of -0.232 log(10)copies/ml (s.d. 0.490). Concordance for the qualitative assays were; 64/67 (95.5%) for the respiratory and enteric multiplex, all 28 (100%) for the sH1, sN1 and influenza A matrix multiplex, 33/34 (97%) for the HSV1/HSV2/VZV multiplex and all 15 (100%) for the Noro GI/II. Inter- and intra-run variation, determined for a 10-fold dilution series of CMV (5.20-3.20 log(10)copies/ml), was less than 0.63 log(10)copies/ml.

CONCLUSIONS

Our evaluation found the performance of the QIAsymphony(®) SP comparable to the NucliSens easyMAG for a range of sample types commonly extracted in a clinical virology laboratory. In total, 331/343 (96.5%) PCR results were concordant on samples extracted by both platforms.

摘要

背景

QIAGEN QIAsymphony(®)SP 是一种自动化系统,可用于处理各种不同类型的样本,以提取核酸。

目的

使用一系列常见的临床样本类型,比较该系统与 bioMérieux NucliSens easyMAG 的性能。

研究设计

对 6 种内部实时病毒 PCR 检测进行核酸提取测试:定量巨细胞病毒(CMV);呼吸道和肠道多重检测(10 种病毒);流感 A H1N1 2009 特异性 H1 和 N1 检测(sH1/N1);单纯疱疹病毒(HSV)1、HSV 2 和水痘带状疱疹病毒(VZV)多重检测;诺如病毒基因组 I 和 II(Noro GI/II)多重检测。

结果

通过 QIAsymphony(®)SP 或 NucliSens easyMAG 对临床样本进行提取,对于每种 PCR,结果相似;CMV 病毒载量,52 个血浆样本的平均差异(easyMAG-QIAsymphony(®))为 0.002 log(10)拷贝/ml(标准差 0.536),52 个全血样本的平均差异为-0.232 log(10)拷贝/ml(标准差 0.490)。定性检测的一致性为:呼吸道和肠道多重检测为 64/67(95.5%),sH1、sN1 和流感 A 基质多重检测为 28/28(100%),HSV1/HSV2/VZV 多重检测为 33/34(97%),Noro GI/II 为 15/15(100%)。CMV(5.20-3.20 log(10)拷贝/ml)的 10 倍稀释系列的内和日间变异小于 0.63 log(10)拷贝/ml。

结论

我们的评估发现,QIAsymphony(®)SP 的性能与临床病毒学实验室中常用的一系列样本类型的 NucliSens easyMAG 相当。在总共 343 个 PCR 样本中,有 331 个(96.5%)结果在两个平台提取的样本上是一致的。

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