calcimycin and Toxoplasmosis

calcimycin has been researched along with Toxoplasmosis* in 2 studies

Other Studies

2 other study(ies) available for calcimycin and Toxoplasmosis

ArticleYear
A novel dense granule protein, GRA41, regulates timing of egress and calcium sensitivity in Toxoplasma gondii.
    Cellular microbiology, 2017, Volume: 19, Issue:9

    Toxoplasma gondii is an obligate intracellular apicomplexan parasite with high seroprevalence in humans. Repeated lytic cycles of invasion, replication, and egress drive both the propagation and the virulence of this parasite. Key steps in this cycle, including invasion and egress, depend on tightly regulated calcium fluxes and, although many of the calcium-dependent effectors have been identified, the factors that detect and regulate the calcium fluxes are mostly unknown. To address this knowledge gap, we used a forward genetic approach to isolate mutants resistant to extracellular exposure to the calcium ionophore A23187. Through whole genome sequencing and complementation, we have determined that a nonsense mutation in a previously uncharacterised protein is responsible for the ionophore resistance of one of the mutants. The complete loss of this protein recapitulates the resistance phenotype and importantly shows defects in calcium regulation and in the timing of egress. The affected protein, GRA41, localises to the dense granules and is secreted into the parasitophorous vacuole where it associates with the tubulovesicular network. Our findings support a connection between the tubulovesicular network and ion homeostasis within the parasite, and thus a novel role for the vacuole of this important pathogen.

    Topics: Calcimycin; Calcium; Calcium Ionophores; Calcium Signaling; Cytoplasmic Vesicles; Gene Knockdown Techniques; Humans; Membrane Proteins; Protozoan Proteins; Toxoplasma; Toxoplasmosis; Vacuoles

2017
Microscopic analysis of calcium ionophore activated egress of Toxoplasma gondii from the host cell.
    Veterinary parasitology, 2010, Jan-20, Volume: 167, Issue:1

    Toxoplasma gondii invades and destroys nucleated cells of warm blooded hosts in a process which involves several steps: recognition, adhesion, penetration, multiplication inside a parasitophorous vacuole (PV) and egress. The last one is the least understood. Parasite egress from LLC-MK2 cells infected with the RH strain of T. gondii was artificially triggered with 4BrA23187 calcium ionophore. The combination of videomicroscopy, field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) showed that egress does not result from host cell rupture due to overloading with tachyzoites. Videomicroscopy showed that upon calcium ionophore administration parasite rosettes disassemble, the contour of the parasitophorous vacuole disappears and each tachyzoite takes a separate route to the extracellular medium. FESEM and TEM showed the fragmentation of the intravacuolar network, the fragmentation of parasitophorous vacuole membrane and individual tachyzoites with extruded conoids migrating through the cytosol, tightly surrounded by remnants of parasitophorous vacuole membrane or free in the cytosol. Both videomicroscopy and FESEM showed that a single parasite can cross the host cell membrane without disrupting it, while a large number of parasites, egressing simultaneously, rupture the membrane and the cell as a whole. These data suggest that invasion and egress share less similarities than previously believed.

    Topics: Animals; Calcimycin; Calcium; Cell Line; Cell Membrane; Ionophores; Macaca mulatta; Microscopy, Electron, Scanning; Microscopy, Electron, Transmission; Microscopy, Video; Toxoplasma; Toxoplasmosis; Vacuoles

2010