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Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model
The only existing preventive measure against American trypanosomosis, or Chagas disease, is the control of the transmitting insect, which has only been effective in a few South American regions. Currently, there is no vaccine available to prevent this disease. Here, we present the clinical and cardi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505182/ https://www.ncbi.nlm.nih.gov/pubmed/23148870 http://dx.doi.org/10.1186/1297-9716-43-79 |
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author | Rodríguez-Morales, Olivia Pérez-Leyva, M Magdalena Ballinas-Verdugo, Martha A Carrillo-Sánchez, Silvia C Rosales-Encina, J Luis Alejandre-Aguilar, Ricardo Reyes, Pedro A Arce-Fonseca, Minerva |
author_facet | Rodríguez-Morales, Olivia Pérez-Leyva, M Magdalena Ballinas-Verdugo, Martha A Carrillo-Sánchez, Silvia C Rosales-Encina, J Luis Alejandre-Aguilar, Ricardo Reyes, Pedro A Arce-Fonseca, Minerva |
author_sort | Rodríguez-Morales, Olivia |
collection | PubMed |
description | The only existing preventive measure against American trypanosomosis, or Chagas disease, is the control of the transmitting insect, which has only been effective in a few South American regions. Currently, there is no vaccine available to prevent this disease. Here, we present the clinical and cardiac levels of protection induced by expression to Trypanosoma cruzi genes encoding the TcSP and TcSSP4 proteins in the canine model. Physical examination, diagnostic chagasic serology, and serial electrocardiograms were performed before and after immunization, as well as after experimental infection. We found that immunization with recombinant plasmids prevented hyperthermia in the acute phase of experimental infection and produced lymphadenomegaly as an immunological response against the parasite and additionally prevented heart rate elevation (tachycardia) in the acute and/or chronic stages of infection. Immunization with T. cruzi genes encoding the TcSP and TcSSP4 antigens diminished the quality and quantity of the electrocardiographic abnormalities, thereby avoiding progression to more severe developments such as right bundle branch block or ventricular premature complexes in a greater number of dogs. |
format | Online Article Text |
id | pubmed-3505182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35051822012-11-24 Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model Rodríguez-Morales, Olivia Pérez-Leyva, M Magdalena Ballinas-Verdugo, Martha A Carrillo-Sánchez, Silvia C Rosales-Encina, J Luis Alejandre-Aguilar, Ricardo Reyes, Pedro A Arce-Fonseca, Minerva Vet Res Research The only existing preventive measure against American trypanosomosis, or Chagas disease, is the control of the transmitting insect, which has only been effective in a few South American regions. Currently, there is no vaccine available to prevent this disease. Here, we present the clinical and cardiac levels of protection induced by expression to Trypanosoma cruzi genes encoding the TcSP and TcSSP4 proteins in the canine model. Physical examination, diagnostic chagasic serology, and serial electrocardiograms were performed before and after immunization, as well as after experimental infection. We found that immunization with recombinant plasmids prevented hyperthermia in the acute phase of experimental infection and produced lymphadenomegaly as an immunological response against the parasite and additionally prevented heart rate elevation (tachycardia) in the acute and/or chronic stages of infection. Immunization with T. cruzi genes encoding the TcSP and TcSSP4 antigens diminished the quality and quantity of the electrocardiographic abnormalities, thereby avoiding progression to more severe developments such as right bundle branch block or ventricular premature complexes in a greater number of dogs. BioMed Central 2012 2012-11-13 /pmc/articles/PMC3505182/ /pubmed/23148870 http://dx.doi.org/10.1186/1297-9716-43-79 Text en Copyright ©2012 Rodríguez-Morales et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Rodríguez-Morales, Olivia Pérez-Leyva, M Magdalena Ballinas-Verdugo, Martha A Carrillo-Sánchez, Silvia C Rosales-Encina, J Luis Alejandre-Aguilar, Ricardo Reyes, Pedro A Arce-Fonseca, Minerva Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title | Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title_full | Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title_fullStr | Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title_full_unstemmed | Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title_short | Plasmid DNA immunization with Trypanosoma cruzi genes induces cardiac and clinical protection against Chagas disease in the canine model |
title_sort | plasmid dna immunization with trypanosoma cruzi genes induces cardiac and clinical protection against chagas disease in the canine model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505182/ https://www.ncbi.nlm.nih.gov/pubmed/23148870 http://dx.doi.org/10.1186/1297-9716-43-79 |
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