Differential effects of intranasal vaccination with recombinant Nc PDI in different mouse models of Neospora caninum infection

In this study, mice were vaccinated intranasally with recombinant N. caninum protein disulphide isomerase (NcPDI) emulsified in cholera toxin (CT) or cholera toxin subunit B (CTB) from Vibrio cholerae . The effects of vaccination were assessed in the murine nonpregnant model and the foetal infection model, respectively. In the nonpregnant mice, previous results were confirmed, in that intranasal vaccination with recNcPDI in CT was highly protective, and low cerebral parasite loads were noted upon real‐time PCR analysis. Protection was accompanied by an IgG1‐biased anti‐NcPDI response upon infection and significantly increased expression of Th2 (IL‐4/IL‐10) and IL‐17 transcripts in spleen compared with corresponding values in mice treated with CT only. However, vaccination with recNcPDI in CT did not induce significant protection in dams and their offspring. In the dams, increased splenic Th1 (IFN‐γ/IL‐12) and Th17 mRNA expressions was detected. No protection was noted in the groups vaccinated with recNcPDI emulsified in CTB. Thus, vaccination with recNcPDI in CT in nonpregnant mice followed by challenge infection induced a protective Th2‐biased immune response, while in the pregnant mouse model, the same vaccine formulation resulted in a Th1‐biased inflammatory response and failed to protect dams and their progeny.