The apicomplexan parasite is the primary agent of human babesiosis, a malaria-like illness and potentially fatal tick-borne disease. Unlike its close relatives, the agents of human malaria, develops within human and mouse red blood cells in the absence of a parasitophorous vacuole, and its secreted antigens lack trafficking motifs found in malarial secreted antigens. Here, we show that after invasion of erythrocytes, undergoes a major morphogenic change during which it produces an interlacement of vesicles (IOV); the IOV system extends from the plasma membrane of the parasite into the cytoplasm of the host erythrocyte. We developed antibodies against two immunodominant antigens of the parasite and used them in cell fractionation studies and fluorescence and immunoelectron microscopy analyses to monitor the mode of secretion of antigens. These analyses demonstrate that the IOV system serves as a major export mechanism for important antigens of and represents a novel mechanism for delivery of parasite effectors into the host by this apicomplexan parasite.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572159 | PMC |
http://dx.doi.org/10.26508/lsa.201900382 | DOI Listing |
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