Phosphorylation of immunity-related GTPases by a Toxoplasma gondii-secreted kinase promotes macrophage survival and virulence.

Published

Journal Article

Macrophages are specialized to detect and destroy intracellular microbes and yet a number of pathogens have evolved to exploit this hostile niche. Here we demonstrate that the obligate intracellular parasite Toxoplasma gondii disarms macrophage innate clearance mechanisms by secreting a serine threonine kinase called ROP18, which binds to and phosphorylates immunity-related GTPases (IRGs). Substrate profiling of ROP18 revealed a preference for a conserved motif within switch region I of the GTPase domain, a modification predicted to disrupt IRG function. Consistent with this, expression of ROP18 was both necessary and sufficient to block recruitment of Irgb6, which was in turn required for parasite destruction. ROP18 phosphorylation of IRGs prevented clearance within inflammatory monocytes and IFN-γ-activated macrophages, conferring parasite survival in vivo and promoting virulence. IRGs are implicated in clearance of a variety of intracellular pathogens, suggesting that other virulence factors may similarly thwart this innate cellular defense mechanism.

Full Text

Duke Authors

Cited Authors

  • Fentress, SJ; Behnke, MS; Dunay, IR; Mashayekhi, M; Rommereim, LM; Fox, BA; Bzik, DJ; Taylor, GA; Turk, BE; Lichti, CF; Townsend, RR; Qiu, W; Hui, R; Beatty, WL; Sibley, LD

Published Date

  • December 2010

Published In

Volume / Issue

  • 8 / 6

Start / End Page

  • 484 - 495

PubMed ID

  • 21147463

Pubmed Central ID

  • 21147463

Electronic International Standard Serial Number (EISSN)

  • 1934-6069

International Standard Serial Number (ISSN)

  • 1931-3128

Digital Object Identifier (DOI)

  • 10.1016/j.chom.2010.11.005

Language

  • eng