Journal
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2022.1010038
Keywords
Apicomplexa; Toxoplasma gondii; cytoskeleton; basal complex; myosin heavy chain (MHC); constriction; cell-cell communication; expansion microscopy
Categories
Funding
- Preciput 2019 from the department Sciences Biologiques et Medicales of theUniversity of Bordeaux
- LabEX ParaFrap [ANR-11-LABX-0024]
- Ministry of Higher Education, Research and Innovation
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This study identified new basal complex components (BCC) of Toxoplasma gondii tachyzoite and revealed their localization within different sub-compartments of the basal complex. These components play important roles in cell motility, division, and intravacuolar cell-cell communication. It was found that one BCC is critical for the constriction of the basal complex and gliding motility, while four other BCCs are involved in the formation and/or maintenance of intravacuolar parasite connection.
The Toxoplasma gondii tachyzoite is a singled-cell obligate intracellular parasite responsible for the acute phase of toxoplasmosis. This polarized cell exhibits an apical complex, a hallmark of the phylum Apicomplexa, essential for motility, invasion, and egress from the host cell. Located on the opposite end of the cell is the basal complex, an elaborated cytoskeletal structure that also plays critical roles in the lytic cycle of the parasite, being involved in motility, cell division, constriction and cytokinesis, as well as intravacuolar cell-cell communication. Nevertheless, only a few proteins of this structure have been described and functionally assessed. In this study, we used spatial proteomics to identify new basal complex components (BCC), and in situ imaging, including ultrastructure expansion microscopy, to position them. We thus confirmed the localization of nine BCCs out of the 12 selected candidates and assigned them to different sub-compartments of the basal complex, including two new domains located above the basal ring and below the posterior cup. Their functional investigation revealed that none of these BCCs are essential for parasite growth in vitro. However, one BCC is critical for constricting of the basal complex, likely through direct interaction with the class VI myosin heavy chain J (MyoJ), and for gliding motility. Four other BCCs, including a phosphatase and a guanylate-binding protein, are involved in the formation and/or maintenance of the intravacuolar parasite connection, which is required for the rosette organization and synchronicity of cell division.
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