Cargando…

Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance

Toxoplasmosis is a worldwide disease with most of the infections originating through the oral route and generates various pathological manifestations, ranging from meningoencephalitis to retinochoroiditis and inflammatory bowel disease. Animal models for these pathologies are scarce and have limitat...

Descripción completa

Detalles Bibliográficos
Autores principales: Dias, Raul Ramos Furtado, de Carvalho, Eulógio Carlos Queiroz, Leite, Carla Cristina da Silva, Tedesco, Roberto Carlos, Calabrese, Katia da Silva, Silva, Antonio Carlos, DaMatta, Renato Augusto, de Fatima Sarro-Silva, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4249919/
https://www.ncbi.nlm.nih.gov/pubmed/25437299
http://dx.doi.org/10.1371/journal.pone.0113374
_version_ 1782346917595840512
author Dias, Raul Ramos Furtado
de Carvalho, Eulógio Carlos Queiroz
Leite, Carla Cristina da Silva
Tedesco, Roberto Carlos
Calabrese, Katia da Silva
Silva, Antonio Carlos
DaMatta, Renato Augusto
de Fatima Sarro-Silva, Maria
author_facet Dias, Raul Ramos Furtado
de Carvalho, Eulógio Carlos Queiroz
Leite, Carla Cristina da Silva
Tedesco, Roberto Carlos
Calabrese, Katia da Silva
Silva, Antonio Carlos
DaMatta, Renato Augusto
de Fatima Sarro-Silva, Maria
author_sort Dias, Raul Ramos Furtado
collection PubMed
description Toxoplasmosis is a worldwide disease with most of the infections originating through the oral route and generates various pathological manifestations, ranging from meningoencephalitis to retinochoroiditis and inflammatory bowel disease. Animal models for these pathologies are scarce and have limitations. We evaluated the outcome of Toxoplasma gondii oral infection with 50 or 100 cysts of the ME-49 strain in two lines of mice with extreme phenotypes of susceptibility (TS) or resistance (TR) to immune oral tolerance. Therefore, the aim of this study was to evaluate the behaviour of TS and TR mice, orally infected by T. gondii, and determine its value as a model for inflammatory diseases study. Mortality during the acute stage of the infection for TR was 50% for both dosages, while 10 and 40% of the TS died after infection with these respective dosages. In the chronic stage, the remaining TS succumbed while TR survived for 90 days. The TS displayed higher parasite load with lower intestinal inflammation and cellular proliferation, notwithstanding myocarditis, pneumonitis and meningoencephalitis. TR presented massive necrosis of villi and crypt, comparable to inflammatory bowel disease, with infiltration of lymphoid cells in the lamina propria of the intestines. Also, TR mice infected with 100 cysts presented intense cellular infiltrate within the photoreceptor layer of the eyes, changes in disposition and morphology of the retina cell layers and retinochoroiditis. During the infection, high levels of IL-6 were detected in the serum of TS mice and TR mice presented high amounts of IFN-γ and TNF-α. Both mice lineages developed different disease outcomes, but it is emphasized that TR and TS mice presented acute and chronic stages of the infection, demonstrating that the two lineages offer an attractive model for studying toxoplasmosis.
format Online
Article
Text
id pubmed-4249919
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-42499192014-12-05 Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance Dias, Raul Ramos Furtado de Carvalho, Eulógio Carlos Queiroz Leite, Carla Cristina da Silva Tedesco, Roberto Carlos Calabrese, Katia da Silva Silva, Antonio Carlos DaMatta, Renato Augusto de Fatima Sarro-Silva, Maria PLoS One Research Article Toxoplasmosis is a worldwide disease with most of the infections originating through the oral route and generates various pathological manifestations, ranging from meningoencephalitis to retinochoroiditis and inflammatory bowel disease. Animal models for these pathologies are scarce and have limitations. We evaluated the outcome of Toxoplasma gondii oral infection with 50 or 100 cysts of the ME-49 strain in two lines of mice with extreme phenotypes of susceptibility (TS) or resistance (TR) to immune oral tolerance. Therefore, the aim of this study was to evaluate the behaviour of TS and TR mice, orally infected by T. gondii, and determine its value as a model for inflammatory diseases study. Mortality during the acute stage of the infection for TR was 50% for both dosages, while 10 and 40% of the TS died after infection with these respective dosages. In the chronic stage, the remaining TS succumbed while TR survived for 90 days. The TS displayed higher parasite load with lower intestinal inflammation and cellular proliferation, notwithstanding myocarditis, pneumonitis and meningoencephalitis. TR presented massive necrosis of villi and crypt, comparable to inflammatory bowel disease, with infiltration of lymphoid cells in the lamina propria of the intestines. Also, TR mice infected with 100 cysts presented intense cellular infiltrate within the photoreceptor layer of the eyes, changes in disposition and morphology of the retina cell layers and retinochoroiditis. During the infection, high levels of IL-6 were detected in the serum of TS mice and TR mice presented high amounts of IFN-γ and TNF-α. Both mice lineages developed different disease outcomes, but it is emphasized that TR and TS mice presented acute and chronic stages of the infection, demonstrating that the two lineages offer an attractive model for studying toxoplasmosis. Public Library of Science 2014-12-01 /pmc/articles/PMC4249919/ /pubmed/25437299 http://dx.doi.org/10.1371/journal.pone.0113374 Text en © 2014 Dias 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
Dias, Raul Ramos Furtado
de Carvalho, Eulógio Carlos Queiroz
Leite, Carla Cristina da Silva
Tedesco, Roberto Carlos
Calabrese, Katia da Silva
Silva, Antonio Carlos
DaMatta, Renato Augusto
de Fatima Sarro-Silva, Maria
Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title_full Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title_fullStr Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title_full_unstemmed Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title_short Toxoplasma gondii Oral Infection Induces Intestinal Inflammation and Retinochoroiditis in Mice Genetically Selected for Immune Oral Tolerance Resistance
title_sort toxoplasma gondii oral infection induces intestinal inflammation and retinochoroiditis in mice genetically selected for immune oral tolerance resistance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4249919/
https://www.ncbi.nlm.nih.gov/pubmed/25437299
http://dx.doi.org/10.1371/journal.pone.0113374
work_keys_str_mv AT diasraulramosfurtado toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT decarvalhoeulogiocarlosqueiroz toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT leitecarlacristinadasilva toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT tedescorobertocarlos toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT calabresekatiadasilva toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT silvaantoniocarlos toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT damattarenatoaugusto toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance
AT defatimasarrosilvamaria toxoplasmagondiioralinfectioninducesintestinalinflammationandretinochoroiditisinmicegeneticallyselectedforimmuneoraltoleranceresistance