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Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus

Dengue is one of the major public health concerns in the world. Since all the four serotypes are actively circulating in Mexico, there is a need to develop an efficient diagnosis system to improve case management of the patients. There exist few studies evaluating the use of the NS3 protein as a pro...

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Autores principales: Álvarez-Rodríguez, Laura Mónica, Ramos-Ligonio, Angel, Rosales-Encina, José Luis, Martínez-Cázares, María Teresa, Parissi-Crivelli, Aurora, López-Monteon, Aracely
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518973/
https://www.ncbi.nlm.nih.gov/pubmed/23258983
http://dx.doi.org/10.1155/2012/956875
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author Álvarez-Rodríguez, Laura Mónica
Ramos-Ligonio, Angel
Rosales-Encina, José Luis
Martínez-Cázares, María Teresa
Parissi-Crivelli, Aurora
López-Monteon, Aracely
author_facet Álvarez-Rodríguez, Laura Mónica
Ramos-Ligonio, Angel
Rosales-Encina, José Luis
Martínez-Cázares, María Teresa
Parissi-Crivelli, Aurora
López-Monteon, Aracely
author_sort Álvarez-Rodríguez, Laura Mónica
collection PubMed
description Dengue is one of the major public health concerns in the world. Since all the four serotypes are actively circulating in Mexico, there is a need to develop an efficient diagnosis system to improve case management of the patients. There exist few studies evaluating the use of the NS3 protein as a protective antigen against dengue virus (DENV). In this paper we show the expression of a recombinant NS3 protein from all serotypes of dengue virus (GST-DVNS3-1-4) and report a reliable “in-house detection system” for the diagnosis of dengue infection which was field-tested in a small village (Tezonapa) in the state of Veracruz, Mexico. The fusion proteins were immunogenic, inducing antibodies to be able to recognize to antigens up to a 1 : 3200 dilution. The purified proteins were used to develop an in-house detection system (ELISA) and were further tested with a panel of 239 serum samples. The in-house results were in excellent agreement with the commercial kits with κ = 0.934 ± 0.064 (95%  CI = 0.808–1.061), and κ = 0.872 ± 0.048 (95%  CI = 0.779–0.965) for IgM and IgG, respectively. The agreement between the NS1 antigen detection versus the rNS3 ELISA, κ = 0.837 ± 0.066 (95%  CI = 0.708–0.966), was very good. Thus, these results demonstrate that recombinant NS3 proteins have potential in early diagnosis of dengue infections.
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spelling pubmed-35189732012-12-20 Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus Álvarez-Rodríguez, Laura Mónica Ramos-Ligonio, Angel Rosales-Encina, José Luis Martínez-Cázares, María Teresa Parissi-Crivelli, Aurora López-Monteon, Aracely J Trop Med Research Article Dengue is one of the major public health concerns in the world. Since all the four serotypes are actively circulating in Mexico, there is a need to develop an efficient diagnosis system to improve case management of the patients. There exist few studies evaluating the use of the NS3 protein as a protective antigen against dengue virus (DENV). In this paper we show the expression of a recombinant NS3 protein from all serotypes of dengue virus (GST-DVNS3-1-4) and report a reliable “in-house detection system” for the diagnosis of dengue infection which was field-tested in a small village (Tezonapa) in the state of Veracruz, Mexico. The fusion proteins were immunogenic, inducing antibodies to be able to recognize to antigens up to a 1 : 3200 dilution. The purified proteins were used to develop an in-house detection system (ELISA) and were further tested with a panel of 239 serum samples. The in-house results were in excellent agreement with the commercial kits with κ = 0.934 ± 0.064 (95%  CI = 0.808–1.061), and κ = 0.872 ± 0.048 (95%  CI = 0.779–0.965) for IgM and IgG, respectively. The agreement between the NS1 antigen detection versus the rNS3 ELISA, κ = 0.837 ± 0.066 (95%  CI = 0.708–0.966), was very good. Thus, these results demonstrate that recombinant NS3 proteins have potential in early diagnosis of dengue infections. Hindawi Publishing Corporation 2012 2012-12-03 /pmc/articles/PMC3518973/ /pubmed/23258983 http://dx.doi.org/10.1155/2012/956875 Text en Copyright © 2012 Laura Mónica Álvarez-Rodríguez et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Álvarez-Rodríguez, Laura Mónica
Ramos-Ligonio, Angel
Rosales-Encina, José Luis
Martínez-Cázares, María Teresa
Parissi-Crivelli, Aurora
López-Monteon, Aracely
Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title_full Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title_fullStr Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title_full_unstemmed Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title_short Expression, Purification, and Evaluation of Diagnostic Potential and Immunogenicity of a Recombinant NS3 Protein from All Serotypes of Dengue Virus
title_sort expression, purification, and evaluation of diagnostic potential and immunogenicity of a recombinant ns3 protein from all serotypes of dengue virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518973/
https://www.ncbi.nlm.nih.gov/pubmed/23258983
http://dx.doi.org/10.1155/2012/956875
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