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Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites

C57BL/6, BALB/c, and CBA/Ca mouse strains with different MHC-I haplotypes were compared with respect to susceptibility to Neospora caninum infection. Groups of 5 mice received 1 × 10(6), 5 × 10(6), or 25 × 10(6) tachyzoites of the NC-Liverpool isolate by intraperitoneal injection and were observed f...

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Autores principales: Mols-Vorstermans, Tanja, Hemphill, Andrew, Monney, Thierry, Schaap, Dick, Boerhout, Eveline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890932/
https://www.ncbi.nlm.nih.gov/pubmed/27335863
http://dx.doi.org/10.5402/2013/830980
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author Mols-Vorstermans, Tanja
Hemphill, Andrew
Monney, Thierry
Schaap, Dick
Boerhout, Eveline
author_facet Mols-Vorstermans, Tanja
Hemphill, Andrew
Monney, Thierry
Schaap, Dick
Boerhout, Eveline
author_sort Mols-Vorstermans, Tanja
collection PubMed
description C57BL/6, BALB/c, and CBA/Ca mouse strains with different MHC-I haplotypes were compared with respect to susceptibility to Neospora caninum infection. Groups of 5 mice received 1 × 10(6), 5 × 10(6), or 25 × 10(6) tachyzoites of the NC-Liverpool isolate by intraperitoneal injection and were observed for disease symptoms. Humoral responses, splenocyte interferon-γ (IFN-γ) production, cerebral parasite loads, and histopathology were evaluated at human end points or the latest at 34 days postinfection (PI). The mortality rates in C57BL/6 mice were the highest, and relatively high levels of IgG1 antibodies were detected in those mice surviving till 34 days PI. In lymphocyte proliferation assays, spleen cells from C57BL6 mice stimulated with N. caninum antigen extract exhibited large variations in IFN-γ production. In BALB/c mice mortality was 0% at the lowest and 100% at the highest infection dose. Serologically they responded with high levels of both IgG2a and IgG1 subclasses, and lymphocyte proliferation assays of surviving mice yielded lower IFN-γ levels. CBA/Ca mice were the most resistant, with no animal succumbing to infection at a dose of 1 × 10(6) and 5 × 10(6) tachyzoites, but 100% mortality at 25 × 10(6) tachyzoites. High IgG2a levels as well as increased IFN-γ in lymphocyte proliferation assays were measured in CBA/Ca mice infected with 1 × 10(6) tachyzoites.
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spelling pubmed-48909322016-06-22 Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites Mols-Vorstermans, Tanja Hemphill, Andrew Monney, Thierry Schaap, Dick Boerhout, Eveline ISRN Parasitol Research Article C57BL/6, BALB/c, and CBA/Ca mouse strains with different MHC-I haplotypes were compared with respect to susceptibility to Neospora caninum infection. Groups of 5 mice received 1 × 10(6), 5 × 10(6), or 25 × 10(6) tachyzoites of the NC-Liverpool isolate by intraperitoneal injection and were observed for disease symptoms. Humoral responses, splenocyte interferon-γ (IFN-γ) production, cerebral parasite loads, and histopathology were evaluated at human end points or the latest at 34 days postinfection (PI). The mortality rates in C57BL/6 mice were the highest, and relatively high levels of IgG1 antibodies were detected in those mice surviving till 34 days PI. In lymphocyte proliferation assays, spleen cells from C57BL6 mice stimulated with N. caninum antigen extract exhibited large variations in IFN-γ production. In BALB/c mice mortality was 0% at the lowest and 100% at the highest infection dose. Serologically they responded with high levels of both IgG2a and IgG1 subclasses, and lymphocyte proliferation assays of surviving mice yielded lower IFN-γ levels. CBA/Ca mice were the most resistant, with no animal succumbing to infection at a dose of 1 × 10(6) and 5 × 10(6) tachyzoites, but 100% mortality at 25 × 10(6) tachyzoites. High IgG2a levels as well as increased IFN-γ in lymphocyte proliferation assays were measured in CBA/Ca mice infected with 1 × 10(6) tachyzoites. Hindawi Publishing Corporation 2013-03-24 /pmc/articles/PMC4890932/ /pubmed/27335863 http://dx.doi.org/10.5402/2013/830980 Text en Copyright © 2013 Tanja Mols-Vorstermans et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mols-Vorstermans, Tanja
Hemphill, Andrew
Monney, Thierry
Schaap, Dick
Boerhout, Eveline
Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title_full Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title_fullStr Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title_full_unstemmed Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title_short Differential Effects on Survival, Humoral Immune Responses and Brain Lesions in Inbred BALB/C, CBA/CA, and C57BL/6 Mice Experimentally Infected with Neospora caninum Tachyzoites
title_sort differential effects on survival, humoral immune responses and brain lesions in inbred balb/c, cba/ca, and c57bl/6 mice experimentally infected with neospora caninum tachyzoites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890932/
https://www.ncbi.nlm.nih.gov/pubmed/27335863
http://dx.doi.org/10.5402/2013/830980
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