Characterization of a cDNA-clone encoding Nc-p43, a major Neospora caninum tachyzoite surface protein

• Published in: Parasitology Vol. 115 ( Pt 6); p. 581
• Main Authors: Hemphill, A, Felleisen, R, Connolly, B, Gottstein, B, Hentrich, B, Müller, N
• Format: Journal Article
• Language: English
• Published: England 01-12-1997
• Subjects: Amino Acid Sequence; Animals; Antigens, Protozoan - chemistry; Antigens, Protozoan - genetics; Antigens, Surface - chemistry; Antigens, Surface - genetics; Cercopithecus aethiops; DNA Transposable Elements; DNA, Complementary; DNA, Protozoan - genetics; Fluorescent Antibody Technique; Gene Library; Host-Parasite Interactions; Immunoblotting; Immunohistochemistry; Membrane Glycoproteins - chemistry; Membrane Glycoproteins - genetics; Membrane Proteins - chemistry; Membrane Proteins - genetics; Membrane Proteins - immunology; Molecular Sequence Data; Neospora - chemistry; Neospora - genetics; Neospora - immunology; Neospora - ultrastructure; Protozoan Proteins - chemistry; Protozoan Proteins - genetics; Protozoan Proteins - immunology; Toxoplasma - chemistry; Toxoplasma - genetics; Vero Cells
• ISSN: 0031-1820
• DOI: 10.1017/S0031182097001650

Neospora caninum is an apicomplexan parasite of veterinary importance which invades many different cell types and tissues. N. caninum tachyzoites proliferate intracellularly by endodyogeny. Eventually the massive proliferation of tachyzoites leads to host cell lysis and the newly formed parasites are released and invade neighbouring cells. Tachyzoite cell surface molecules could serve as ligands, mediating host cell adhesion and invasion. Nc-p43 is a recently identified N. caninum tachyzoite surface protein which is functionally involved in the processes leading to host cell invasion in vitro. Affinity-purified antibodies directed against Nc-p43 were used to screen a lambda gt22A-cDNA expression library constructed from N. caninum tachyzoites. The cDNA insert of one immunoreactive clone was subcloned and expressed in E. coli as a poly-histidine fusion protein. The identity of the resulting recombinant antigen termed recNc-p43 was confirmed by immunoblotting, immunofluorescence and electron microscopy using affinity-purified antibodies. The sequence of the cDNA insert encoding recNc-p43 was determined. Analysis of the deduced amino acid sequence revealed that Nc-p43 exhibited similarity to SAG1 (p30) and SAG3 (p43), 2 major surface antigens of Toxoplasma gondii tachyzoites. These similarities were not reflected on the immunochemical level, since no cross-antigenicity between SAG1, SAG3 and Nc-p43 was observed.