A Conserved Apicomplexan Microneme Protein Contributes to Toxoplasma gondii Invasion and Virulence

作者：Huynh My Hang; Boulanger Martin J; Carruthers Vern B^*

来源：Infection and Immunity, 2014, 82(10): 4358-4368.

DOI：10.1128/IAI.01877-14

The obligate intracellular parasite Toxoplasma gondii critically relies on host cell invasion during infection. Proteins secreted from the apical micronemes are central components for host cell recognition, invasion, egress, and virulence. Although previous work established that the sporozoite protein with an altered thrombospondin repeat (SPATR) is a micronemal protein conserved in other apicomplexan parasites, including Plasmodium, Neospora, and Eimeria, no genetic evidence of its contribution to invasion has been reported. SPATR contains a predicted epidermal growth factor domain and two thrombospondin type 1 repeats, implying a role in host cell recognition. In this study, we assess the contribution of T. gondii SPATR (TgSPATR) to T. gondii invasion by genetically ablating it and restoring its expression by genetic complementation. Delta spatr parasites were similar to 50% reduced in invasion compared to parental strains, a defect that was reversed in the complemented strain. In mouse virulence assays, Delta spatr parasites were significantly attenuated, with similar to 20% of mice surviving infection. Given the conservation of this protein among the Apicomplexa, we assessed whether the Plasmodium falciparum SPATR ortholog (PfSPATR) could complement the absence of the TgSPATR. Although PfSPATR showed correct micronemal localization, it did not reverse the invasion deficiency of Delta spatr parasites, because of an apparent failure in secretion. Overall, the results suggest that TgSPATR contributes to invasion and virulence, findings that have implications for the many genera and life stages of apicomplexans that express SPATR.

• 出版日期2014-10