Lotufo Cecilia M, Bergmann Ingrid E, Mattion Nora M, Wilda Maximiliano, Grigera Pablo R
Instituto de Ciencia y Tecnología Dr. César Milstein-CONICET, Saladillo 2468 (C1440FFX), Buenos Aires, Argentina.
Arch Virol. 2017 Aug;162(8):2279-2286. doi: 10.1007/s00705-017-3359-4. Epub 2017 Apr 18.
Recombinant protein 3A-EGFP, a fusion construct between foot-and-mouth disease virus (FMDV) non-structural protein 3A and the enhanced green fluorescent protein (EGFP) was expressed in BL21-DE3 cells. The identity of the partially purified protein 3A-EGFP was confirmed by its reactivity with sera from cattle infected with FMDV and with a monoclonal antibody specific for FMDV-3ABC (MAb3H7) in Western blot assays. No reactivity was observed with sera from uninfected vaccinated animals. The performance of 3A-EGFP as an antigen in an indirect enzyme-linked immunosorbent assay (ELISA) was assessed and compared with that of a previously developed and validated capture ELISA that uses a 3ABC recombinant antigen (3ABC ELISA) and has been widely applied for serological surveys in Argentina. Parallel analysis of strongly and weakly positive reference sera from infected animals and 329 serum samples from uninfected vaccinated cattle showed that the 3A-EGFP antigen unequivocally identifies sera from FMDV-infected cattle with similar performance to its 3ABC counterpart. The 3A-EGFP ELISA is simpler and faster to perform than the 3ABC ELISA, since it does not require a capture step with a specific antibody. Moreover, the expression and storage of the recombinant 3A-EGFP is simplified by the absence of residual autoproteolytic activity associated to the 3C sequence. We conclude that the 3A-EGFP ELISA constitutes a promising screening method in serosurveys to determine whether or not animals are infected with FMDV.
重组蛋白3A-EGFP是口蹄疫病毒(FMDV)非结构蛋白3A与增强型绿色荧光蛋白(EGFP)的融合构建体,在BL21-DE3细胞中表达。在蛋白质印迹分析中,部分纯化的蛋白3A-EGFP与感染FMDV的牛血清以及针对FMDV-3ABC的单克隆抗体(MAb3H7)发生反应,从而证实了其身份。未感染疫苗接种动物的血清未观察到反应性。评估了3A-EGFP作为间接酶联免疫吸附测定(ELISA)中抗原的性能,并与先前开发并验证的使用3ABC重组抗原的捕获ELISA(3ABC ELISA)进行了比较,该捕获ELISA已在阿根廷广泛应用于血清学调查。对感染动物的强阳性和弱阳性参考血清以及329份未感染疫苗接种牛的血清样本进行平行分析表明,3A-EGFP抗原能够明确识别FMDV感染牛的血清,其性能与3ABC对应物相似。3A-EGFP ELISA比3ABC ELISA操作更简单、更快,因为它不需要用特异性抗体进行捕获步骤。此外,重组3A-EGFP的表达和储存因不存在与3C序列相关的残留自蛋白水解活性而得到简化。我们得出结论,3A-EGFP ELISA是血清学调查中一种有前景的筛查方法,可用于确定动物是否感染FMDV。