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一种结合生物标志物提取和恒温PCR的生物标志物探测器原型

A Prototype Biomarker Detector Combining Biomarker Extraction and Fixed Temperature PCR.

作者信息

Russ Patricia K, Karhade Aditya V, Bitting Anna L, Doyle Andrew, Solinas Francesca, Wright David W, Haselton Frederick R

机构信息

Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.

Department of Chemistry, Vanderbilt University, Nashville, TN, USA.

出版信息

J Lab Autom. 2016 Aug;21(4):590-8. doi: 10.1177/2211068216634072. Epub 2016 Feb 26.

Abstract

PCR is the most sensitive molecular diagnostic available for infectious diseases. The goal for low-resource settings is a simple, inexpensive instrument. Toward this goal, we previously published a self-contained sample preparation instrument that uses magnetics and prearrayed reagents in thin tubing to extract nucleic acids and perform isothermal amplification and detection of extracted biomarkers. To incorporate PCR thermal cycling, after biomarker is magnetically extracted from a patient sample, the section of tubing containing the extracted biomarker and PCR reagents is alternately positioned within two constant temperature blocks. This instrument was evaluated initially by extracting and amplifying a 140 bp fragment of the IS6110 sequence of tuberculosis from TE buffer. The mean cycle threshold for 5 × 10(6) copies of IS6110 was 25.5 ± 1.5 cycles (n = 4), which was significantly different from negative control samples (34.0 ± 2.6 cycles; n = 3). Using a more clinically relevant sample, we extracted and amplified Plasmodium falciparum DNA from malaria-infected human blood cultures. The average cycle threshold for 1% parasitemia samples was 24.7 ± 1.5 cycles (n = 3) and significantly different from negatives (31.5 ± 2.1 cycles; n = 3). This approach integrates biomarker extraction, PCR amplification, and detection in a simple, linear tubing design with potential for use as a low-resource instrument.

摘要

聚合酶链反应(PCR)是用于传染病诊断的最灵敏的分子诊断方法。对于资源匮乏地区而言,目标是拥有一种简单且价格低廉的仪器。为实现这一目标,我们此前发表了一种独立的样品制备仪器,该仪器利用磁性和细管中预排列的试剂来提取核酸,并对提取的生物标志物进行等温扩增和检测。为纳入PCR热循环,在从患者样本中磁性提取生物标志物后,将含有提取的生物标志物和PCR试剂的细管段交替放置在两个恒温块内。最初通过从TE缓冲液中提取并扩增结核分枝杆菌IS6110序列的140bp片段对该仪器进行评估。对于5×10⁶份IS6110拷贝,平均循环阈值为25.5±1.5个循环(n = 4),这与阴性对照样本(34.0±2.6个循环;n = 3)有显著差异。使用更具临床相关性的样本,我们从疟疾感染的人类血液培养物中提取并扩增了恶性疟原虫DNA。对于1%疟原虫血症样本,平均循环阈值为24.7±1.5个循环(n = 3),与阴性样本(31.5±2.1个循环;n = 3)有显著差异。这种方法在简单的线性细管设计中整合了生物标志物提取、PCR扩增和检测,有潜力用作资源匮乏地区的仪器。

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