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首页> 外文期刊>Journal of Clinical Microbiology >Antigenic Characterization of Hantaan and Seoul Virus Nucleocapsid Proteins Expressed by Recombinant Baculovirus: Application of a Truncated Protein, Lacking an Antigenic Region Common to the Two Viruses, as a Serotyping Antigen
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Antigenic Characterization of Hantaan and Seoul Virus Nucleocapsid Proteins Expressed by Recombinant Baculovirus: Application of a Truncated Protein, Lacking an Antigenic Region Common to the Two Viruses, as a Serotyping Antigen

机译:重组杆状病毒表达的汉坦和汉城病毒核蛋白的抗原表征:一种截短蛋白的应用,缺乏两种病毒的共同抗原区域,作为血清分型抗原。

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摘要

Hantaan virus (HTN) and Seoul virus (SEO) are members of the genusHantavirus in the family Bunyaviridae and are causative agents of hemorrhagic fever with renal syndrome. The complete and truncated nucleocapsid proteins (NP) of HTN and SEO were expressed by a recombinant baculovirus system. Antigenic characterization of the NP using monoclonal antibodies (MAbs) indicated that the binding sites for the serotype-specific MAbs were located between amino acids (aa) 155 and 429. A Western blot assay indicated that the serotype-specific epitopes were conformation dependent. An indirect immunofluorescence antibody (IFA) assay with the truncated NP (aa 155 to 429) was able to distinguish convalescent-phase sera from HTN and SEO patients. However, the antibody titers with the truncated NP were lower than those with the whole NP. The truncated NP of SEO (aa 155 to 429) could be used as an enzyme-linked immunosorbent assay (ELISA) antigen, but the truncated NP from HTN lost its reactivity when used for ELISA. The IFA assay using baculovirus-expressed truncated NP as an antigen is a rapid, simple, and safe test for distinguishing between HTN and SEO infections by serotype.
机译:汉坦病毒(HTN)和汉城病毒(SEO)是 Bunyaviridae 家族的 Hantavirus 属,并且是肾综合征出血热的病原体。通过重组杆状病毒系统表达完整和截短的HTN和SEO核衣壳蛋白(NP)。使用单克隆抗体(MAb)对NP进行抗原学表征表明,血清型特异性MAb的结合位点位于氨基酸(aa)155和429之间。蛋白质印迹分析表明,血清型特异性表位是构象依赖性的。用截短的NP(aa 155至429)进行的间接免疫荧光抗体(IFA)测定能够区分HTN和SEO患者的恢复期血清。但是,截短的NP的抗体滴度低于整个NP的抗体滴度。 SEO的截短的NP(氨基酸155至429)可用作酶联免疫吸附测定(ELISA)抗原,但是来自HTN的截短的NP在用于ELISA时会失去反应性。使用杆状病毒表达的截短的NP作为抗原的IFA分析是一种快速,简单且安全的测试,可通过血清型区分HTN和SEO感染。

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