Analysis of Ca2+ mediated signaling regulating Toxoplasma infectivity reveals complex relationships between key molecules

• Published in: Cellular microbiology Vol. 19; no. 4
• Main Authors: Stewart, Rebecca J., Whitehead, Lachlan, Nijagal, Brunda, Sleebs, Brad E., Lessene, Guillaume, McConville, Malcolm J., Rogers, Kelly L., Tonkin, Christopher J.
• Format: Journal Article
• Language: English
• Published: Oxford Hindawi Limited 01.04.2017
• Subjects: Biosensors; Calcium (intracellular); Calcium ions; Calcium signalling; Calcium-binding protein; Calmodulin; Cyclic GMP; Egress; Fluxes; Genetic code; Infectivity; Intracellular; Intracellular signalling; Kinases; Motility; Parasites; Pathogenesis; Protein kinase; Signal transduction; Signaling
• ISSN: 1462-5814; 1462-5822
• DOI: 10.1111/cmi.12685

Host cell invasion, exit and parasite dissemination is critical to the pathogenesis of apicomplexan parasites such as Toxoplasma gondii and Plasmodium spp. These processes are regulated by intracellular Ca2+ signaling although the temporal dynamics of Ca2+ fluxes and down‐stream second messenger pathways are poorly understood. Here, we use a genetically encoded biosensor, GFP‐Calmodulin‐M13–6 (GCaMP6), to capture Ca2+ flux in live Toxoplasma and investigate the role of Ca2+ signaling in egress and motility. Our analysis determines how environmental cues and signal activation influence intracellular Ca2+ flux, allowing placement of effector molecules within this pathway. Importantly, we have identified key interrelationships between cGMP and Ca2+ signaling that are required for activation of egress and motility. Furthermore, we extend this analysis to show that the Ca2+ Dependent Protein Kinases–TgCDPK1 and TgCDPK3—play a role in signal quenching before egress. This work highlights the interrelationships of second messenger pathways of Toxoplasma in space and time, which is likely required for pathogenesis of all apicomplexan species.