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Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi
Few studies investigate the major protein antigens targeted by the antibody diversity of infected mice with Trypanosoma cruzi. To detect global IgG antibody specificities, sera from infected mice were immunoblotted against whole T. cruzi extracts. By proteomic analysis, we were able to identify the...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909033/ https://www.ncbi.nlm.nih.gov/pubmed/29706955 http://dx.doi.org/10.3389/fimmu.2018.00671 |
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author | Montalvão, Fabricio Nascimento, Danielle Oliveira Nunes, Marise P. Koeller, Carolina M. Morrot, Alexandre Lery, Leticia Miranda S. Bisch, Paulo M. Teixeira, Santuza M. R. Vasconcellos, Rita Freire-de-Lima, Leonardo Lopes, Marcela F. Heise, Norton DosReis, George A. Freire-de-Lima, Célio Geraldo |
author_facet | Montalvão, Fabricio Nascimento, Danielle Oliveira Nunes, Marise P. Koeller, Carolina M. Morrot, Alexandre Lery, Leticia Miranda S. Bisch, Paulo M. Teixeira, Santuza M. R. Vasconcellos, Rita Freire-de-Lima, Leonardo Lopes, Marcela F. Heise, Norton DosReis, George A. Freire-de-Lima, Célio Geraldo |
author_sort | Montalvão, Fabricio |
collection | PubMed |
description | Few studies investigate the major protein antigens targeted by the antibody diversity of infected mice with Trypanosoma cruzi. To detect global IgG antibody specificities, sera from infected mice were immunoblotted against whole T. cruzi extracts. By proteomic analysis, we were able to identify the most immunogenic T. cruzi proteins. We identified three major antigens as pyruvate phosphate dikinase, Hsp-85, and β-tubulin. The major protein band recognized by host IgG was T. cruzi β-tubulin. The T. cruzi β-tubulin gene was cloned, expressed in E. coli, and recombinant T. cruzi β-tubulin was obtained. Infection increased IgG reactivity against recombinant T. cruzi β-tubulin. A single immunization of mice with recombinant T. cruzi β-tubulin increased specific IgG reactivity and induced protection against T. cruzi infection. These results indicate that repertoire analysis is a valid approach to identify antigens for vaccines against Chagas disease. |
format | Online Article Text |
id | pubmed-5909033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59090332018-04-27 Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi Montalvão, Fabricio Nascimento, Danielle Oliveira Nunes, Marise P. Koeller, Carolina M. Morrot, Alexandre Lery, Leticia Miranda S. Bisch, Paulo M. Teixeira, Santuza M. R. Vasconcellos, Rita Freire-de-Lima, Leonardo Lopes, Marcela F. Heise, Norton DosReis, George A. Freire-de-Lima, Célio Geraldo Front Immunol Immunology Few studies investigate the major protein antigens targeted by the antibody diversity of infected mice with Trypanosoma cruzi. To detect global IgG antibody specificities, sera from infected mice were immunoblotted against whole T. cruzi extracts. By proteomic analysis, we were able to identify the most immunogenic T. cruzi proteins. We identified three major antigens as pyruvate phosphate dikinase, Hsp-85, and β-tubulin. The major protein band recognized by host IgG was T. cruzi β-tubulin. The T. cruzi β-tubulin gene was cloned, expressed in E. coli, and recombinant T. cruzi β-tubulin was obtained. Infection increased IgG reactivity against recombinant T. cruzi β-tubulin. A single immunization of mice with recombinant T. cruzi β-tubulin increased specific IgG reactivity and induced protection against T. cruzi infection. These results indicate that repertoire analysis is a valid approach to identify antigens for vaccines against Chagas disease. Frontiers Media S.A. 2018-04-13 /pmc/articles/PMC5909033/ /pubmed/29706955 http://dx.doi.org/10.3389/fimmu.2018.00671 Text en Copyright © 2018 Montalvão, Nascimento, Nunes, Koeller, Morrot, Lery, Bisch, Teixeira, Vasconcellos, Freire-de-Lima, Lopes, Heise, DosReis and Freire-de-Lima. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Montalvão, Fabricio Nascimento, Danielle Oliveira Nunes, Marise P. Koeller, Carolina M. Morrot, Alexandre Lery, Leticia Miranda S. Bisch, Paulo M. Teixeira, Santuza M. R. Vasconcellos, Rita Freire-de-Lima, Leonardo Lopes, Marcela F. Heise, Norton DosReis, George A. Freire-de-Lima, Célio Geraldo Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title | Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title_full | Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title_fullStr | Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title_full_unstemmed | Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title_short | Antibody Repertoires Identify β-Tubulin as a Host Protective Parasite Antigen in Mice Infected With Trypanosoma cruzi |
title_sort | antibody repertoires identify β-tubulin as a host protective parasite antigen in mice infected with trypanosoma cruzi |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909033/ https://www.ncbi.nlm.nih.gov/pubmed/29706955 http://dx.doi.org/10.3389/fimmu.2018.00671 |
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