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Distinction of subtype-specific antibodies against European porcine influenza viruses by indirect ELISA based on recombinant hemagglutinin protein fragment-1

机译:基于重组血凝素蛋白片段1的间接ELISA区分欧洲猪流感病毒亚型特异性抗体

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Background Serological investigations of swine influenza virus infections and epidemiological conclusions thereof are challenging due to the complex and regionally variable pattern of co-circulating viral subtypes and lineages and varying vaccination regimes. Detection of subtype-specific antibodies currently depends on hemagglutination inhibition (HI) assays which are difficult to standardize and unsuitable for large scale investigations. Methods The nucleocapsid protein (NP) and HA1 fragments of the hemagglutinin protein (HA) of five different lineages (H1N1av, H1N1pdm, H1pdmN2, H1N2, H3N2) of swine influenza viruses were bacterially expressed and used as diagnostic antigens in indirect ELISA. Results Proteins were co-translationally mono-biotinylated and refolded in vitro into an antigenically authentic conformation. Western blotting and indirect ELISA revealed highly subtype-specific antigenic characteristics of the recombinant HA1 proteins although some cross reactivity especially among antigens of the H1 subtype were evident. Discrimination of antibodies directed against four swine influenza virus subtypes co-circulating in Germany was feasible using the indirect ELISA format. Conclusions Bacterially expressed recombinant NP and HA1 swine influenza virus proteins served as antigens in indirect ELISAs and provided an alternative to commercial blocking NP ELISA and HI assays concerning generic (NP-specific) and HA subtype-specific sero-diagnostics, respectively, on a herd basis.
机译:背景技术由于共同传播的病毒亚型和谱系以及变化的疫苗接种方案,猪流感病毒感染的血清学研究及其流行病学结论具有挑战性。目前,亚型特异性抗体的检测取决于血凝抑制(HI)测定法,该测定法难以标准化且不适合大规模研究。方法通过细菌表达猪流感病毒的五个不同谱系(H1N1av,H1N1pdm,H1pdmN2,H1N2,H3N2)的血凝素蛋白(HA)的核衣壳蛋白(NP)和HA1片段,并在间接ELISA中用作诊断抗原。结果蛋白质被共翻译单生物素化,并在体外重折叠成抗原真实构象。蛋白质印迹和间接ELISA显示重组HA1蛋白具有高度亚型特异性的抗原特性,尽管有明显的交叉反应性,尤其是在H1亚型抗原之间。使用间接ELISA格式可以区分针对在德国共同流行的四种猪流感病毒亚型的抗体。结论细菌表达的重组NP和HA1猪流感病毒蛋白可作为间接ELISA中的抗原,并提供了分别针对一般(NP特异性)和HA亚型特异性血清学诊断的商业封闭NP ELISA和HI测定的替代方法基础。

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