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, Angel Sergio O, Zamorano Patricia, Odeón Anselmo C, Leunda María R, Campero Carlos M, Morein Bror, Moore Dadín P
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina; Instituto Nacional de Tecnología Agropecuaria (INTA), Balcarce, CC 276, 7620 Balcarce, Argentina.
Laboratorio de Parasitología Molecular, UB2, IIB INTECH, CONICET-UNSAM, CC 164, B7130IWA, Chascomús, Argentina.
Vet Immunol Immunopathol. 2014 Dec 15;162(3-4):142-53. doi: 10.1016/j.vetimm.2014.11.001. Epub 2014 Nov 8.
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.
本研究的目的是评估用免疫刺激复合物(ISCOMs)配制的重组蛋白rNcSAG1、rNcHSP20和rNcGRA7在怀孕小母牛中对犬新孢子虫垂直传播的免疫原性和保护效力。12头怀孕小母牛被分为3组,每组4头,在配种前接受不同的制剂。免疫原皮下注射两次:A组动物接种用ISCOMs配制的三种重组蛋白(rNcSAG1、rNcHSP20、rNcGRA7);B组动物接受ISCOM-MATRIX(无抗原),C组仅接受无菌磷酸盐缓冲盐水(PBS)。重组蛋白在大肠杆菌中表达并用镍树脂纯化。所有组在妊娠第70天静脉注射犬新孢子虫NC-1株,并在实验第17周宰杀母畜。A组小母牛在攻毒前产生了针对rNcSAG1、rNcHSP20和rNcGRA7的特异性抗体。免疫后,在第5、13和16周时,与B组和C组动物相比,A组所有动物中针对rNcSAG1和rNcHSP20的抗体有统计学意义的增加(P<0.001)。在第5周和16周时,A组动物中针对rNcGRA7的抗体水平与B组和C组相比有统计学意义的升高(P>0.001)。在任何时间点,实验组之间的IFN-γ产生均无差异(P>0.05)。通过蛋白质印迹、免疫组织化学和巢式PCR在A、B和C组的所有胎儿中测定经胎盘传播情况。这项工作表明,rNcSAG1、rNcHSP20和rNcGRA7蛋白虽然在牛中具有免疫原性,但未能预防妊娠第70天受到攻毒的怀孕母牛的胎儿感染。