Identification and Characterization of a Novel Calcium-Activated Apyrase from Cryptosporidium Parasites and Its Potential Role in Pathogenesis

• DOI: 10.1371/journal.pone.0031030
• Publication Date: 2012-02-07T22:20:45Z
• Authors: Patricio A. Manque; Ute Woehlbier; Ana M. Lara; Fernando Tenjo; João M. Alves; Gregory A. Buck
• Keywords: Glycosylation; Science; Molecular Sequence Data; Protozoan Proteins; Antibodies, Protozoan; Cryptosporidiosis; Cryptosporidium; Guanosine Diphosphate; Protein Refolding; Mice; 03 medical and health sciences; Medicine and Health Sciences; Animals; Humans; Parasites; Amino Acid Sequence; Phylogeny; 0303 health sciences; Q; Apyrase; R; Epithelial Cells; 3. Good health; Enzyme Activation; Protein Transport; Medicine; Calcium; Research Article; Protein Binding

Herein, we report the biochemical and functional characterization of a novel Ca(2+)-activated nucleoside diphosphatase (apyrase), CApy, of the intracellular gut pathogen Cryptosporidium. The purified recombinant CApy protein displayed activity, substrate specificity and calcium dependency strikingly similar to the previously described human apyrase, SCAN-1 (soluble calcium-activated nucleotidase 1). CApy was found to be expressed in both Cryptosporidium parvum oocysts and sporozoites, and displayed a polar localization in the latter, suggesting a possible co-localization with the apical complex of the parasite. In vitro binding experiments revealed that CApy interacts with the host cell in a dose-dependent fashion, implying the presence of an interacting partner on the surface of the host cell. Antibodies directed against CApy block Cryptosporidium parvum sporozoite invasion of HCT-8 cells, suggesting that CApy may play an active role during the early stages of parasite invasion. Sequence analyses revealed that the capy gene shares a high degree of homology with apyrases identified in other organisms, including parasites, insects and humans. Phylogenetic analysis argues that the capy gene is most likely an ancestral feature that has been lost from most apicomplexan genomes except Cryptosporidium, Neospora and Toxoplasma.