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Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates
Dengue is the most prevalent human arboviral disease. The morbidity related to dengue infection supports the need for an early, quick and effective diagnostic test. Brazil is a hotspot for dengue, but no serological diagnostic test has been produced using Brazilian dengue virus isolates. This study...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239016/ https://www.ncbi.nlm.nih.gov/pubmed/25412181 http://dx.doi.org/10.1371/journal.pone.0110620 |
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author | Zanluca, Camila Mazzarotto, Giovanny Augusto Camacho Antevere Bordignon, Juliano Duarte dos Santos, Claudia Nunes |
author_facet | Zanluca, Camila Mazzarotto, Giovanny Augusto Camacho Antevere Bordignon, Juliano Duarte dos Santos, Claudia Nunes |
author_sort | Zanluca, Camila |
collection | PubMed |
description | Dengue is the most prevalent human arboviral disease. The morbidity related to dengue infection supports the need for an early, quick and effective diagnostic test. Brazil is a hotspot for dengue, but no serological diagnostic test has been produced using Brazilian dengue virus isolates. This study aims to improve the development of immunodiagnostic methods for dengue virus (DENV) detection through the production and characterization of 22 monoclonal antibodies (mAbs) against Brazilian isolates of DENV-1, -2 and -3. The mAbs include IgG2bκ, IgG2aκ and IgG1κ isotypes, and most were raised against the envelope or the pre-membrane proteins of DENV. When the antibodies were tested against the four DENV serotypes, different reactivity patterns were identified: group-specific, subcomplex specific (DENV-1, -3 and -4 and DENV-2 and -3) and dengue serotype-specific (DENV-2 or -3). Additionally, some mAbs cross-reacted with yellow fever virus (YFV), West Nile virus (WNV) and Saint Louis encephalitis virus (SLEV). None of the mAbs recognized the alphavirus Venezuelan equine encephalitis virus (VEEV). Furthermore, mAbs D3 424/8G, D1 606/A12/B9 and D1 695/12C/2H were used to develop a capture enzyme-linked immunosorbent assay (ELISA) for anti-dengue IgM detection in sera from patients with acute dengue. To our knowledge, these are the first monoclonal antibodies raised against Brazilian DENV isolates, and they may be of special interest in the development of diagnostic assays, as well as for basic research. |
format | Online Article Text |
id | pubmed-4239016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42390162014-11-26 Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates Zanluca, Camila Mazzarotto, Giovanny Augusto Camacho Antevere Bordignon, Juliano Duarte dos Santos, Claudia Nunes PLoS One Research Article Dengue is the most prevalent human arboviral disease. The morbidity related to dengue infection supports the need for an early, quick and effective diagnostic test. Brazil is a hotspot for dengue, but no serological diagnostic test has been produced using Brazilian dengue virus isolates. This study aims to improve the development of immunodiagnostic methods for dengue virus (DENV) detection through the production and characterization of 22 monoclonal antibodies (mAbs) against Brazilian isolates of DENV-1, -2 and -3. The mAbs include IgG2bκ, IgG2aκ and IgG1κ isotypes, and most were raised against the envelope or the pre-membrane proteins of DENV. When the antibodies were tested against the four DENV serotypes, different reactivity patterns were identified: group-specific, subcomplex specific (DENV-1, -3 and -4 and DENV-2 and -3) and dengue serotype-specific (DENV-2 or -3). Additionally, some mAbs cross-reacted with yellow fever virus (YFV), West Nile virus (WNV) and Saint Louis encephalitis virus (SLEV). None of the mAbs recognized the alphavirus Venezuelan equine encephalitis virus (VEEV). Furthermore, mAbs D3 424/8G, D1 606/A12/B9 and D1 695/12C/2H were used to develop a capture enzyme-linked immunosorbent assay (ELISA) for anti-dengue IgM detection in sera from patients with acute dengue. To our knowledge, these are the first monoclonal antibodies raised against Brazilian DENV isolates, and they may be of special interest in the development of diagnostic assays, as well as for basic research. Public Library of Science 2014-11-20 /pmc/articles/PMC4239016/ /pubmed/25412181 http://dx.doi.org/10.1371/journal.pone.0110620 Text en © 2014 Zanluca et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zanluca, Camila Mazzarotto, Giovanny Augusto Camacho Antevere Bordignon, Juliano Duarte dos Santos, Claudia Nunes Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title | Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title_full | Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title_fullStr | Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title_full_unstemmed | Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title_short | Development, Characterization and Application of Monoclonal Antibodies against Brazilian Dengue Virus Isolates |
title_sort | development, characterization and application of monoclonal antibodies against brazilian dengue virus isolates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239016/ https://www.ncbi.nlm.nih.gov/pubmed/25412181 http://dx.doi.org/10.1371/journal.pone.0110620 |
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