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Immune response to Neospora caninum live tachyzoites in prepubertal female calves

The aim of the present study was to characterize the specific immune response in prepubertal female calves inoculated with Neospora caninum . Forty-eight N. caninum- seronegative 6-month-old Angus female calves were randomly allocated into two groups: group A calves were inoculated subcutaneously (s...

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Published in:Parasitology research (1987) 2019-10, Vol.118 (10), p.2945-2955
Main Authors: Hecker, Yanina P., Regidor-Cerrillo, Javier, Fiorani, Franco, Horcajo, Pilar, Soria, Ivana, Gual, Ignacio, Torioni, Susana, Campero, Lucía M., Echaide, Ignacio E., Álvarez-García, Gema, Ortega-Mora, Luis M., Zamorano, Patricia I., Venturini, María C., Odeón, Anselmo C., Cantón, Germán J., Moore, Dadín P.
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Language:English
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Summary:The aim of the present study was to characterize the specific immune response in prepubertal female calves inoculated with Neospora caninum . Forty-eight N. caninum- seronegative 6-month-old Angus female calves were randomly allocated into two groups: group A calves were inoculated subcutaneously (sc) with 1 × 10 6 tachyzoites of the low virulence NC-Argentina LP1 isolate in sterile phosphate-buffered saline (PBS); group B calves were mock inoculated sc with sterile PBS. Calves from group A developed a specific immune response characterized by the production of IgG antibodies and the expression of IFN-γ and TNF-α cytokines. Animals did not present any febrile reaction or reactions at the site of inoculation. Although chronic N. caninum infection was developed in 50% of calves of group A after inoculation, according to the presence of antibodies against rNc-SAG4, antigen characteristic of bradyzoites, N. caninum antibodies dropped below the cut-off of ELISA from day 210 post-inoculation onwards. Future trials using the same group of inoculated animals will allow the characterization of the evolution of the immune response during pregnancy and to determine whether the immunization with the local isolate is able to prevent congenital transmission and to protect against heterologous challenges.
ISSN:0932-0113
1432-1955
DOI:10.1007/s00436-019-06447-y