首页> 外文期刊>Journal of Virological Methods >A differential ELISA based on recombinant immunodominant epitopes of the gE gene of SHV-1 in a baculovirus-insect cell system to discriminate between pigs infected naturally with pseudorabies and vaccinated pigs
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A differential ELISA based on recombinant immunodominant epitopes of the gE gene of SHV-1 in a baculovirus-insect cell system to discriminate between pigs infected naturally with pseudorabies and vaccinated pigs

机译:基于杆状病毒-昆虫细胞系统中SHV-1 gE基因重组免疫优势表位的差异ELISA区分自然感染伪狂犬病的猪和接种的猪

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In the present study, the fragment corresponding to the immunodominant epitopes of the gE gene (gEpi) from the CL15 Argentinean strain of pseudorabies virus was expressed successfully in a baculovirus-insect cell system that contained the M6 gene of Bluetongue virus, which encodes the NS1 nonstructural protein. This protein has the ability to polymerize into highly immunogenic tubules inside infected cells that can be purified at large quantities by ultracentrifugation. Previously, the NS1 protein has been expressed by fusing it to sequences derived from viruses, such as human immunodeficiency virus type 1, hepatitis B virus, bovine leukemia virus, foot-and-mouth disease virus and influenza A virus. In the present study, a recombinant protein was obtained containing the gEpi fused to NS1 (NS1-gEpi) and used it as ELISA antigen for detection of anti-gE antibodies in order to discriminate between infected and vaccinated animals. This is the first report where gEpi was expressed in this particular baculovirus-insect cell system
机译:在本研究中,来自CL15阿根廷伪狂犬病病毒株gE基因(gEpi)免疫显性表位的片段在杆状病毒-昆虫细胞系统中成功表达,该系统包含蓝舌病毒的M6基因,该基因编码NS1非结构蛋白。该蛋白具有聚合成感染细胞内部高度免疫原性的小管的能力,可以通过超速离心大量纯化。以前,NS1蛋白是通过将其融合到病毒衍生的序列中而表达的,这些病毒例如1型人类免疫缺陷病毒,乙型肝炎病毒,牛白血病病毒,口蹄疫病毒和A型流感病毒。在本研究中,获得了含有与NS1融合的gEpi的重组蛋白(NS1-gEpi),并将其用作ELISA抗原来检测抗gE抗体,以便区分感染动物和接种疫苗的动物。这是gEpi在这种特殊的杆状病毒-昆虫细胞系统中表达的第一份报告

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