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A Neospora caninum vaccine using recombinant proteins fails to prevent foetal infection in pregnant cattle after experimental intravenous challenge
- Hecker, Yanina P., Cóceres, Verónica, Wilkowsky, Silvina E., Jaramillo Ortiz, José M., Morrell, Eleonora L., Verna, Andrea E., Ganuza, Agustina, Cano, Dora B., Lischinsky, Lilian, Ángel, Sergio O., Zamorano, Patricia, Odeón, Anselmo C., Leunda, María R., Campero, Carlos M., Morein, Bror, Moore, Dadín P.
- Veterinary immunology and immunopathology 2014 v.162 no.3-4 pp. 142-153
- Escherichia coli, Neospora caninum, Western blotting, antibodies, antigens, fetus, heifers, immune response, immunization, immunohistochemistry, interferon-gamma, intravenous injection, nickel, polymerase chain reaction, pregnancy, protein synthesis, recombinant proteins, transplacental transmission, vaccines
- The aim of the present study was to evaluate the immunogenicity and protective efficacy of rNcSAG1, rNcHSP20 and rNcGRA7 recombinant proteins formulated with immune stimulating complexes (ISCOMs) in pregnant heifers against vertical transmission of Neospora caninum. Twelve pregnant heifers were divided into 3 groups of 4 heifers each, receiving different formulations before mating. Immunogens were administered twice subcutaneously: group A animals were inoculated with three recombinant proteins (rNcSAG1, rNcHSP20, rNcGRA7) formulated with ISCOMs; group B animals received ISCOM-MATRIX (without antigen) and group C received sterile phosphate-buffered saline (PBS) only. The recombinant proteins were expressed in Escherichia coli and purified nickel resin. All groups were intravenously challenged with the NC-1 strain of N. caninum at Day 70 of gestation and dams slaughtered at week 17 of the experiment. Heifers from group A developed specific antibodies against rNcSAG1, rNcHSP20 and rNcGRA7 prior to the challenge. Following immunization, an statistically significant increase of antibodies against rNcSAG1 and rNcHSP20 in all animals of group A was detected compared to animals in groups B and C at weeks 5, 13 and 16 (P<0.001). Levels of antibodies against rNcGRA7 were statistical higher in group A animals when compared with groups B and C at weeks 5 and 16 (P>0.001). There were no differences in IFN-γ production among the experimental groups at any time point (P>0.05). Transplacental transmission was determined in all foetuses of groups A, B and C by Western blot, immunohistochemistry and nested PCR. This work showed that rNcSAG1, rNcHSP20 and rNcGRA7 proteins while immunogenic in cattle failed to prevent the foetal infection in pregnant cattle challenged at Day 70 of gestation.