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基于重组血凝素蛋白片段-1 的间接 ELISA 区分针对欧洲猪流感病毒的亚型特异性抗体。

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

机构信息

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, Greifswald 17493, Germany.

出版信息

Virol J. 2013 Jul 30;10:246. doi: 10.1186/1743-422X-10-246.

DOI:10.1186/1743-422X-10-246
PMID:23898799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3733666/
Abstract

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.

摘要

背景

由于流行的病毒亚型和谱系复杂且具有地域差异,以及不断变化的疫苗接种方案,对猪流感病毒感染进行血清学调查和得出流行病学结论具有挑战性。目前,针对亚型特异性抗体的检测依赖于血凝抑制(HI)检测,这种方法难以标准化,不适合大规模调查。

方法

猪流感病毒的 5 种不同谱系(H1N1av、H1N1pdm、H1pdmN2、H1N2、H3N2)的血凝素蛋白(HA)的核衣壳蛋白(NP)和 HA1 片段在细菌中表达,并用作间接 ELISA 中的诊断抗原。

结果

蛋白质在共翻译时被单生物素化,并在体外重新折叠成具有抗原性的构象。尽管存在一些交叉反应性,尤其是在 H1 亚型的抗原之间,但 Western blot 和间接 ELISA 揭示了重组 HA1 蛋白高度的亚型特异性抗原特征。使用间接 ELISA 格式,可以区分针对德国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,提供了一种替代商业阻断 NP ELISA 和 HI 检测的方法,分别用于针对 NP 特异性和 HA 亚型特异性血清学诊断,适用于畜群基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/fa3b6b8fb022/1743-422X-10-246-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/11657e2bf860/1743-422X-10-246-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/2ee0afadfd60/1743-422X-10-246-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/503434845e76/1743-422X-10-246-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/5fa2fbbf6e4f/1743-422X-10-246-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/fa3b6b8fb022/1743-422X-10-246-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/11657e2bf860/1743-422X-10-246-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/2ee0afadfd60/1743-422X-10-246-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/503434845e76/1743-422X-10-246-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/5fa2fbbf6e4f/1743-422X-10-246-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/3733666/fa3b6b8fb022/1743-422X-10-246-5.jpg

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