construction and in vitro expression analyses of a dna plasmid encoding dense granule gra5 antigen of toxoplasma gondii

toxoplasmosis is an infection caused by the protozoan parasite toxoplasma gondii (t.gondii) throughout the world. although usually asymptomatic, the infection can cause serious medical problems in immunocompromised individuals and fetuses. toxoplasmosis also causes considerable economic loss because of abortion in livestock. dna vaccination is a promising approach against intracellular parasites such as t.gondii. the goal of this study was to construct and evaluate functionality of a mammalian plasmid expressing gra5 anti-gen of t.gondii as a possible dna vaccine. gra5 gene fragment, devoid of the signal sequence, was amplified from genomic dna of t.gondii rh strain, and cloned into pcdna3.1 plasmid. the pcdna3.1-gra5 (pgra5) was analyzed by restriction enzyme digestion followed by sequence determination. the pgra5 was transfected into hek 239-t human kidney cells, and expression of gra5 antigen was investigated by western blotting and immunofluorescence staining. the sequence encoding gra5 was cloned into pcdna3.1 plasmid. restriction digestion of pgra5 with pst i enzyme showed correct insertion of gra5 dna into the plasmid. sequence analysis revealed 100% homology with the published sequence of gra5. immunofluorescence and western blotting analyses of hek 293-t cells transfected with pgra5 showed specific expression of gra5. immunogenicity of pgra5 will be evaluated in mice.