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首页> 外文期刊>Journal of Clinical Microbiology >Antigenic variability among North American and European strains of porcine reproductive and respiratory syndrome virus as defined by monoclonal antibodies to the matrix protein.
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Antigenic variability among North American and European strains of porcine reproductive and respiratory syndrome virus as defined by monoclonal antibodies to the matrix protein.

机译:北美和欧洲猪繁殖与呼吸综合征病毒株的抗原变异性,由针对基质蛋白的单克隆抗体定义。

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Two hybridoma cell lines producing monoclonal antibodies (Mabs) to the 19-kDa matrix (M) protein of porcine reproductive and respiratory syndrome virus (PRRSV) were obtained from BALB/c mice that were immunized with a reference Quebec tissue culture-adapted strain (strain IAF-Klop). The polypeptide specificities of the MAbs were determined by immunoblotting and immunoprecipitation tests with concentrated and purified preparations of the virus and by determining their reactivities with the Escherichia coli-expressed gene products of open reading frames 5 to 7. The two anti-M protein MAbs (MAbs IAFK3 and IAFK6) and another MAb (MAb IAFK8) directed to the 15-kDa nucleocapsid (N) protein were devoid of virus-neutralizing activity. A library of four anti-N protein MAbs (MAbs IAFK8, SDOW17, VO17, and EP147) and two anti-M protein MAbs (MAbs IAFK6 and IAFK3) was used to investigate, by an indirect fluorescent-antibody assay, the antigenic diversity of 15 Canadian PRRSV isolates, in comparison with those of the U.S. ATCC VR2332 attenuated vaccine strain and two reference European (Lelystad and Weybridge) PRRSV strains. The North American and European PRRSV isolates tested shared the epitopes recognized by anti-N protein MAbs IAFK8 and SDOW17, but three distinct patterns could be identified on the basis of their reactivities with the other anti-PRRSV MAbs. No reactivity to the anti-M protein MAbs was observed by either European PRRSV isolate or the attenuated U.S. vaccine strain.
机译:从BALB / c小鼠中获得了两种针对猪繁殖与呼吸综合征病毒(PRRSV)的19-kDa基质(M)蛋白产生单克隆抗体(Mabs)的杂交瘤细胞系,这些小鼠用参考魁北克组织培养适应株进行了免疫( IAF-Klop株)。通过用浓缩和纯化的病毒制剂进行免疫印迹和免疫沉淀测试,以及通过确定其与大肠杆菌表达的开放阅读框5至7的基因产物的反应性,来确定MAb的多肽特异性。两种抗M蛋白的MAb(直接针对15 kDa核衣壳(N)蛋白的单克隆抗体IAFK3和IAFK6)和另一种单克隆抗体(MAb IAFK8)没有病毒中和活​​性。使用四个抗N蛋白MAb(MAb IAFK8,SDOW17,VO17和EP147)和两个抗M蛋白MAb(MAb IAFK6和IAFK3)的文库,通过间接荧光抗体测定法来研究与美国ATCC VR2332减毒疫苗株和两种参考欧洲(Lelystad和Weybridge)PRRSV株相比,加拿大的15种PRRSV株。测试的北美和欧洲PRRSV分离株具有被抗N蛋白单抗IAFK8和SDOW17识别的表位,但根据它们与其他抗PRRSV MAb的反应性可以鉴定出三种不同的模式。欧洲PRRSV分离株或减毒的美国疫苗株均未观察到与抗M蛋白MAb的反应性。

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