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Production of a Recombinant Dengue Virus 2 NS5 Protein and Potential Use as a Vaccine Antigen.

Authors :
Alves RPDS
Pereira LR
Fabris DLN
Salvador FS
Santos RA
Zanotto PMA
Romano CM
Amorim JH
Ferreira LCS
Source :
Clinical and vaccine immunology : CVI [Clin Vaccine Immunol] 2016 Jun 06; Vol. 23 (6), pp. 460-469. Date of Electronic Publication: 2016 Jun 06 (Print Publication: 2016).
Publication Year :
2016

Abstract

Dengue fever is caused by any of the four known dengue virus serotypes (DENV1 to DENV4) that affect millions of people worldwide, causing a significant number of deaths. There are vaccines based on chimeric viruses, but they still are not in clinical use. Anti-DENV vaccine strategies based on nonstructural proteins are promising alternatives to those based on whole virus or structural proteins. The DENV nonstructural protein 5 (NS5) is the main target of anti-DENV T cell-based immune responses in humans. In this study, we purified a soluble recombinant form of DENV2 NS5 expressed in Escherichia coli at large amounts and high purity after optimization of expression conditions and purification steps. The purified DENV2 NS5 was recognized by serum from DENV1-, DENV2-, DENV3-, or DENV4-infected patients in an epitope-conformation-dependent manner. In addition, immunization of BALB/c mice with NS5 induced high levels of NS5-specific antibodies and expansion of gamma interferon- and tumor necrosis factor alpha-producing T cells. Moreover, mice immunized with purified NS5 were partially protected from lethal challenges with the DENV2 NGC strain and with a clinical isolate (JHA1). These results indicate that the recombinant NS5 protein preserves immunological determinants of the native protein and is a promising vaccine antigen capable of inducing protective immune responses.<br /> (Copyright © 2016, American Society for Microbiology. All Rights Reserved.)

Details

Language :
English
ISSN :
1556-679X
Volume :
23
Issue :
6
Database :
MEDLINE
Journal :
Clinical and vaccine immunology : CVI
Publication Type :
Academic Journal
Accession number :
27030586
Full Text :
https://doi.org/10.1128/CVI.00081-16