WITHDRAWN: Toxoplasma gondii virulence factor ROP18 inhibits the host NF-κB pathway by promoting p65 degradation

J Biol Chem. 2014 May 2;289(18):12578-92. doi: 10.1074/jbc.M113.544718. Epub 2014 Mar 19.

Abstract

The obligate intracellular parasite Toxoplasma gondii secretes effector molecules into the host cell to modulate host immunity. Previous studies have shown that T. gondii could interfere with host NF-κB signaling to promote their survival, but the effectors of type I strains remain unclear. The polymorphic rhoptry protein ROP18 is a key serine/threonine kinase that phosphorylates host proteins to modulate acute virulence. Our data demonstrated that the N-terminal portion of ROP18 is associated with the dimerization domain of p65. ROP18 phosphorylates p65 at Ser-468 and targets this protein to the ubiquitin-dependent degradation pathway. The kinase activity of ROP18 is required for p65 degradation and suppresses NF-κB activation. Consistently, compared with wild-type ROP18 strain, ROP18 kinase-deficient type I parasites displayed a severe inability to inhibit NF-κB, culminating in the enhanced production of IL-6, IL-12, and TNF-α in infected macrophages. In addition, studies have shown that transgenic parasites carrying kinase-deficient ROP18 induce M1-biased activation. These results demonstrate for the first time that the virulence factor ROP18 in T. gondii type I strains is responsible for inhibiting the host NF-κB pathway and for suppressing proinflammatory cytokine expression, thus providing a survival advantage to the infectious agent.

Keywords: Cell Biology; NF-kB Transcription Factor; NF-κB (NF-KB); Parasite; Parasitology; Pathogenesis; Signal Transduction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Female
  • HEK293 Cells
  • Host-Parasite Interactions
  • Humans
  • Interleukin-12 / metabolism
  • Interleukin-6 / metabolism
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Mutation
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Protein Binding
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proteolysis
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism*
  • Serine / metabolism
  • Signal Transduction*
  • Toxoplasma / genetics
  • Toxoplasma / metabolism*
  • Toxoplasma / physiology
  • Transcription Factor RelA / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism
  • Virulence Factors / genetics
  • Virulence Factors / metabolism

Substances

  • Interleukin-6
  • NF-kappa B
  • Protozoan Proteins
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • Virulence Factors
  • Interleukin-12
  • Serine
  • Protein Serine-Threonine Kinases
  • ROP18 protein, Toxoplasma gondii