Alcaraz C, Rodriguez F, Oviedo J M, Eiras A, De Diego M, Alonso C, Escribano J M
Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain.
J Virol Methods. 1995 Mar;52(1-2):111-9. doi: 10.1016/0166-0934(94)00150-f.
A Western blot technique using a recombinant protein has been developed to confirm positive results obtained in African swine fever (ASF)-specific antibody detection by ELISA. The new confirmatory Western blot is based on the use of protein p54, one of the most antigenic ASF virus structural proteins, expressed in Escherichia coli fused to the N-terminus of MS2 polymerase. The recombinant Western blot assay was highly specific and equally sensitive for ASF virus-infected pigs detection as the conventional Western blot, which uses virus-induced proteins ranging in molecular weight between 23 and 35 kDa. The novel Western blot assay provides a simpler interpretation of the test, eliminates the possibility of false-positive reactions produced by cellular compounds that contaminate the antigen employed in the conventional technique, and avoids the use of live virus in antigen production.
已开发出一种使用重组蛋白的蛋白质印迹技术,以确认通过酶联免疫吸附测定(ELISA)进行非洲猪瘟(ASF)特异性抗体检测所获得的阳性结果。新的确认性蛋白质印迹基于使用p54蛋白,它是最具抗原性的非洲猪瘟病毒结构蛋白之一,在大肠杆菌中表达,并与MS2聚合酶的N端融合。重组蛋白质印迹分析具有高度特异性,对于检测感染非洲猪瘟病毒的猪,其灵敏度与传统蛋白质印迹相同,传统蛋白质印迹使用分子量在23至35 kDa之间的病毒诱导蛋白。这种新型蛋白质印迹分析对检测结果的解读更简单,消除了传统技术中因污染所用抗原的细胞化合物产生假阳性反应的可能性,并且避免了在抗原生产中使用活病毒。