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应用原核表达的非结构蛋白建立鉴别感染口蹄疫病毒动物与疫苗免疫动物的 dot 免疫印迹方法。

Development of a dot immunoblot method for differentiation of animals infected with foot-and-mouth disease virus from vaccinated animals using non-structural proteins expressed prokaryotically.

机构信息

Lanzhou Veterinary Research Institute of Chinese Academy of Agriculture Science, State Key Laboratory of Veterinary Etiological Biology, Lanzhou, Gansu, China.

出版信息

J Virol Methods. 2011 Jan;171(1):234-40. doi: 10.1016/j.jviromet.2010.11.006. Epub 2010 Nov 16.

Abstract

Five non-structural proteins (NSPs) of foot-and-mouth disease virus (FMDV) were expressed in E. coli to develop a dot immunoblot (dot blot) assay for the differentiation of FMDV infected animals from vaccinated animals (DIVA). The five NSPs were 3A (24 kDa), 3B (15 kDa), major B-cell epitope regions of 2C (23 kDa), partial 3D (44 kDa) and 3ABC (59 kDa). The criteria for the dot blot were determined and are described as follows: a test sample is considered positive if four or more NSPs demonstrate staining densities equal to or higher than those of their appropriate controls; a sample is considered negative if two or more antigens demonstrate densities below their negative control. A specificity of 100% was observed based on testing of sera from clinical healthy animals with or without vaccination; the sensitivity of the dot blot was 96.1% and 65.8% for testing of samples from infected cattle and swine, respectively, at an early stage of the infection. Meanwhile, high rates of concordance were observed between the dot blot and the PrioCHECK® FMDV-NS test. The dot blot has the potential to act as a confirmatory method for DIVA by 3ABC-ELISA.

摘要

为了开发一种区分口蹄疫病毒(FMDV)感染动物和接种疫苗动物的区分免疫分析(DIVA)检测方法,本研究在大肠杆菌中表达了 FMDV 的 5 种非结构蛋白(NSPs)。这 5 种 NSPs 分别为 3A(24kDa)、3B(15kDa)、2C 的主要 B 细胞表位区域(23kDa)、部分 3D(44kDa)和 3ABC(59kDa)。本研究确定了斑点印迹的标准,并描述如下:如果四个或更多 NSP 的染色密度等于或高于其相应对照,则认为测试样品为阳性;如果两个或更多抗原的密度低于其阴性对照,则认为样品为阴性。基于对临床健康动物接种或不接种血清的检测,观察到该方法的特异性为 100%;在感染的早期阶段,对牛和猪样本的检测中,斑点印迹的敏感性分别为 96.1%和 65.8%。同时,斑点印迹与 PrioCHECK®FMDV-NS 检测之间的一致性很高。该斑点印迹法有望成为 3ABC-ELISA 方法的 DIVA 确认方法。

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