Clavijo Alfonso, Zhou En-Min, Hole Kate, Galic Boris, Kitching Paul
National Centre for Foreign Animal Disease, 1015 Arlington Street, Winnipeg, Man., R3E 3M4, Canada.
J Virol Methods. 2004 Sep 15;120(2):217-27. doi: 10.1016/j.jviromet.2004.05.007.
A biotinylated 3ABC recombinant protein was developed and used in a competitive ELISA (cELISA) to detect foot-and-mouth disease virus (FMDV) antibodies in cattle, sheep and pigs. In this report, we describe the cloning and expression of 3ABC protein in Escherichia coli cells as fusion protein with 6xHis and biotin. This cELISA uses streptavidin to capture bacterially expressed and in vivo biotinylated 3ABC antigen. The antigen capture strategy provides a simple and reliable method, which does not require purification of recombinant antigen before the serological assay. An hyperimmune guinea pig antiserum produced against purified 6xHis-3ABC was used as competitor in the test. The potential use of this cELISA for the identification of antibodies induced by FMD virus infection from those induced by vaccination is discussed.
开发了一种生物素化的3ABC重组蛋白,并将其用于竞争ELISA(cELISA)中,以检测牛、羊和猪中的口蹄疫病毒(FMDV)抗体。在本报告中,我们描述了3ABC蛋白在大肠杆菌细胞中作为与6xHis和生物素的融合蛋白的克隆和表达。这种cELISA使用链霉亲和素捕获细菌表达且在体内生物素化的3ABC抗原。抗原捕获策略提供了一种简单可靠的方法,在血清学检测之前无需纯化重组抗原。用针对纯化的6xHis-3ABC产生的超免疫豚鼠抗血清作为检测中的竞争剂。讨论了这种cELISA在区分口蹄疫病毒感染诱导的抗体和疫苗诱导的抗体方面的潜在用途。