ClearColi BL21(DE3)-based expression of Zika virus antigens illustrates a rapid method of antibody production against emerging pathogens

被引:19
作者
Viranaicken, Wildriss [1 ]
Nativel, Brice [2 ]
Krejbich-Trotot, Pascale [1 ]
Harrabi, Wissal [1 ]
Bos, Sandra [1 ]
El Kalamouni, Chaker [1 ]
Roche, Marjolaine [1 ]
Gadea, Gilles [1 ]
Despres, Philippe [1 ]
机构
[1] Univ La Reunion, CNRS 9192, INSERM, UMR 1187,PIMIT,IRD 249,Plateforme CYROI, 2 Rue Maxime Riviere, F-97490 St Clotilde, Reunion, France
[2] Univ La Reunion, INSERM, UMR 1188,Plateform CYROL, DeTROI Diabete Atherothrombose Therap Reunion, 2 Rue Maxime Riviere, F-97490 St Clotilde, Reunion, France
基金
欧盟地平线“2020”;
关键词
Polyclonal antibody; Recombinant protein; Zika antigens; inclusion bodies; Wistar rat; CROSS-REACTIVITY; DOMAIN-III; ENVELOPE; INFECTION; CELLS;
D O I
10.1016/j.biochi.2017.09.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Available rapid, simple and accurate methods for detection and diagnosis of emerging viral diseases are required. Recently, there was an urgent need for specific antibodies against mosquito-borne Zika virus (ZIKV), which is an emerging zoonotic disease of medical concern in different regions of the world. Here, we showed that overexpression of ZIKV antigens in ClearColi BL21(DE3), a bacteria strain expressing a non-endotoxic form of LPS, is suitable for the production of specific ZIKV antisera. Two major ZIKV antigenic domains, the domain III from envelope E glycoprotein, which brings the virus-specific epitopes, and the N-terminal region of nonstructural NS1 glycoprotein, which is responsible for pathophysiological conditions, were overexpressed in ClearColi BL21(DE3). Immunization of adult rat with insoluble recombinant ZIKV antigens in inclusion bodies resulted in the production of specific antibodies in a few weeks. Anti-E and anti-NS1 antibodies are efficient as biological tools for ZIKV detection by indirect ELISA and immunoblot assay. This method could successfully be applied to any emerging viruses. (C) 2017 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
引用
收藏
页码:179 / 182
页数:4
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