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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Fine level epitope mapping and conservation analysis of two novel linear B-cell epitopes of the avian infectious bronchitis coronavirus nucleocapsid protein
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Fine level epitope mapping and conservation analysis of two novel linear B-cell epitopes of the avian infectious bronchitis coronavirus nucleocapsid protein

机译:禽传染性支气管炎冠状病毒核衣壳蛋白的两个新型线性B细胞表位的精细水平表位作图和保守性分析

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The nucleocapsid (N) protein of the infectious bronchitis virus (IBV) may play an essential role in the replication and translation of viral RNA. The N protein can also induce high titers of cross-reactive antibodies and cell-mediated immunity, which protects chickens from acute infection. In this study, we generated two monoclonal antibodies (mAbs), designated as 6D10 and 4F10, which were directed against the N protein of IBV using the whole viral particles as immunogens. Both of the mAbs do not cross react with Newcastle disease virus (NDV), infectious laryngotracheitis virus (ILTV) and subtype H9 avian influenza virus (AIV). After screening a phage display peptide library and peptide scanning, we identified two linear B-cell epitopes that were recognized by the mAbs 6D10 and 4F10, which corresponded to the amino acid sequences 242FGPRTK247 and 195DLIARAAKI203, respectively, in the IBV N protein. Alignments of amino acid sequences from a large number of IBV isolates indicated that the two epitopes, especially 242FGPRTK247, were well conserved among IBV strains. This conclusion was further confirmed by the relationships of 18 heterologous sequences to the 2 mAbs. The novel mAbs and the epitopes identified will be useful for developing diagnostic assays for IBV infections. ? 2012 Elsevier B.V.
机译:传染性支气管炎病毒(IBV)的核衣壳(N)蛋白可能在病毒RNA的复制和翻译中起重要作用。 N蛋白还可以诱导高滴度的交叉反应抗体和细胞介导的免疫,从而保护鸡免受急性感染。在这项研究中,我们生成了两个单克隆抗体(mAb),分别命名为6D10和4F10,它们使用整个病毒颗粒作为免疫原针对IBV的N蛋白。两种单克隆抗体均不会与新城疫病毒(NDV),传染性喉气管炎病毒(ILTV)和H9亚型禽流感病毒(AIV)发生交叉反应。在筛选了噬菌体展示肽库并进行了肽扫描后,我们确定了两个线性B细胞表位,它们被mAbs 6D10和4F10识别,分别对应于IBV N蛋白中的氨基酸序列242FGPRTK247和195DLIARAAKI203。来自大量IBV分离株的氨基酸序列的比对表明,两个表位,尤其是242FGPRTK247,在IBV菌株之间是非常保守的。 18个异源序列与2个mAb的关系进一步证实了这一结论。鉴定出的新颖mAb和表位将可用于开发针对IBV感染的诊断测定。 ? 2012年Elsevier B.V.

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