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建立并验证了一种新型 SYBR Green 实时 RT-PCR 检测方法,用于检测经典猪瘟病毒,该方法在不同实时 PCR 平台上进行了评估。

Development and validation of a novel SYBR Green real-time RT-PCR assay for the detection of classical swine fever virus evaluated on different real-time PCR platforms.

机构信息

Centro Nacional de Sanidad Agropecuaria (CENSA), San Jose de las Lajas, La Habana, Apdo. 10, Cuba.

出版信息

J Virol Methods. 2011 Jun;174(1-2):53-9. doi: 10.1016/j.jviromet.2011.03.022. Epub 2011 Mar 31.

Abstract

Classical swine fever is a highly contagious viral disease that causes significant economic losses in pig production on a global scale. The rapid dissemination of the virus and the variability of the clinical signs merit the development of swift and accurate classical swine fever virus (CSFV) detection methods, which can assist in disease control. The development and evaluation of a novel quantitative real-time RT-PCR assay for CSFV detection, based on SYBR Green coupled to melting curve analysis, is described. The analytical and diagnostic performances of the method using two real-time PCR instruments were compared. The assay was specific and detected the major genotypes of CSFV. The limit of detection in cell culture medium and serum was 0.1 TCID50/reaction, while in tissue homogenate for both platforms, it was 1 TCID50/reaction. The limit of detection was 1, 10 and 10² gene copies/μL when nuclease-free water, serum and tissue homogenate, respectively, were used as sample matrices for both instruments. The analysis of 108 tissue homogenate and serum samples from animals infected with CSFV naturally and experimentally and non-infected animals showed that the assay provided a highly sensitive and specific method for classical swine fever.

摘要

经典猪瘟是一种高度传染性的病毒性疾病,在全球范围内给养猪业造成了重大的经济损失。病毒的快速传播和临床表现的可变性使得快速准确的经典猪瘟病毒(CSFV)检测方法的开发变得尤为重要,这有助于疾病的控制。本研究描述了一种基于 SYBR Green 结合熔解曲线分析的新型定量实时 RT-PCR 检测方法的开发和评估。比较了两种实时 PCR 仪器对该方法的分析和诊断性能。该方法具有特异性,可检测到 CSFV 的主要基因型。在细胞培养基和血清中的检测限为 0.1 TCID50/反应,而在两种平台的组织匀浆中,检测限为 1 TCID50/反应。当使用无核酸酶水、血清和组织匀浆作为两种仪器的样品基质时,检测限分别为 1、10 和 10² 基因拷贝/μL。对 108 份来自自然和实验感染 CSFV 以及非感染动物的组织匀浆和血清样本的分析表明,该检测方法为经典猪瘟提供了一种高度敏感和特异的方法。

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