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一种基于多重连接酶检测-PCR 和微阵列的新型诊断平台,用于同时检测猪病毒。

A novel diagnostic platform based on multiplex ligase detection-PCR and microarray for simultaneous detection of swine viruses.

机构信息

College of Life Sciences, Zhejiang Sci-Tech University, 2nd Street, Hangzhou 310018, China.

出版信息

J Virol Methods. 2011 Dec;178(1-2):171-8. doi: 10.1016/j.jviromet.2011.09.008. Epub 2011 Sep 19.

Abstract

Simultaneous detection and identification of multiple pathogens is required in many diagnostic fields. In this study a novel method based on a multiplex ligase detection (LD)-polymerase chain reaction (PCR) and microarray (MLPM) is described to detect simultaneously several swine viruses involved in reproductive and/or respiratory problems. The multiplex diagnostic system was validated using standard plasmids, and clinical samples. Using this strategy as few as 10 copies of target plasmids were detected successfully. Each probe pair yielded specific positive signal only in its target site. In addition, when six target plasmids were present simultaneously sufficient robust signals were generated in their corresponding sites of six plasmid templates and no obvious signals were detected in non-target sites. Compared to real-time PCR, the MLPM showed specificities and sensitivities of 95.7-100% and 100% for 47 clinical samples tested, respectively. The results demonstrate that this novel assay is a specific, sensitive, and multiplex diagnostic method for detection of multiple pathogens and can also be adapted easily for diagnostic purposes.

摘要

在许多诊断领域都需要同时检测和鉴定多种病原体。在这项研究中,描述了一种基于多重连接酶检测(LD)-聚合酶链反应(PCR)和微阵列(MLPM)的新型方法,用于同时检测几种与生殖和/或呼吸问题有关的猪病毒。使用标准质粒和临床样本对多重诊断系统进行了验证。使用这种策略,可以成功检测到低至 10 个拷贝的靶质粒。每个探针对仅在其靶位点产生特异性阳性信号。此外,当同时存在 6 个靶质粒时,在它们相应的质粒模板的 6 个位点产生足够强的信号,而在非靶位点未检测到明显的信号。与实时 PCR 相比,MLPM 对 47 个测试的临床样本的特异性和敏感性分别为 95.7-100%和 100%。结果表明,该新型检测方法是一种用于检测多种病原体的特异性、敏感性和多重诊断方法,也可以很容易地适应诊断目的。

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