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Distinct signalling pathways control Toxoplasma egress and host-cell invasion
Distinct signalling pathways control Toxoplasma egress and host-cell invasion
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Distinct signalling pathways control Toxoplasma egress and host-cell invasion
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Distinct signalling pathways control Toxoplasma egress and host-cell invasion
Distinct signalling pathways control Toxoplasma egress and host-cell invasion
Journal Article

Distinct signalling pathways control Toxoplasma egress and host-cell invasion

2012
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Overview
Calcium signalling coordinates motility, cell invasion, and egress by apicomplexan parasites, yet the key mediators that transduce these signals remain largely unknown. One underlying assumption is that invasion into and egress from the host cell depend on highly similar systems to initiate motility. Using a chemical‐genetic approach to specifically inhibit select calcium‐dependent kinases (CDPKs), we instead demonstrate that these pathways are controlled by different kinases: both TgCDPK1 and TgCDPK3 were required during ionophore‐induced egress, but only TgCDPK1 was required during invasion. Similarly, microneme secretion, which is necessary for motility during both invasion and egress, universally depended on TgCDPK1, but only exhibited TgCDPK3 dependence when triggered by certain stimuli. We also demonstrate that egress likely comes under a further level of control by cyclic GMP‐dependent protein kinase and that its activation can induce egress and partially compensate for the inhibition of TgCDPK3. These results demonstrate that separate signalling pathways are integrated to regulate motility in response to the different signals that promote invasion or egress during infection by Toxoplasma gondii . Toxoplasma gondii invasion into and egress from host cells are thought to depend upon similar pathways. Here, the TgCDPK3 signalling pathway is shown to be required for egress, while TgCDPK1 signalling governs both parasite egress and invasion.