Article ID Journal Published Year Pages File Type
5741136 Experimental Parasitology 2017 7 Pages PDF
Abstract

•NcMIC8 is exists in the form of precursor and mature body, with the former only detected in extracellular tachyzoites.•NcMIC8 forms a complex with NcMIC3 probably during transportation, and is secreted to host cell surface.•NcMIC8 is critical in host cell invasion.

Microneme proteins play an important role in the invasion process of Apicomplexan parasites through adhesion to host cells. We discovered a new N. caninum protein, NcMIC8, which is highly identical to TgMIC8. The NcMIC8 sequence has 2049 bp and no intron in the open reading fragment. It has a molecular weight of 73.8 kDa and contains a signal peptide, a transmembrane region, a low complexity region and 10 epidermal growth factor (EGF) domains. Immuno-fluorescence assay showed that NcMIC8 is located in the microneme. NcMIC8 was secreted to culture medium under stimulation of 1% ethanol, and cleaved to form the mature body of 40 kDa before transporting to microneme or during secretion. Blocking NcMIC8 using anti-NcMIC8 serum effectively inhibited host cell invasion by tachyzoites in vitro. NcMIC8 in the form of mature body interacts with NcMIC3, and the two microneme proteins form a complex probably during transportation. NcMIC8 is a new microneme protein of N. caninum and could be an attractive target for the control of neosporosis.

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Related Topics
Life Sciences Immunology and Microbiology Parasitology
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