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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
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.
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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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