RTP4 inhibits IFN-I response and enhances experimental cerebral malaria and neuropathology

Proc Natl Acad Sci U S A. 2020 Aug 11;117(32):19465-19474. doi: 10.1073/pnas.2006492117. Epub 2020 Jul 24.

Abstract

Infection by malaria parasites triggers dynamic immune responses leading to diverse symptoms and pathologies; however, the molecular mechanisms responsible for these reactions are largely unknown. We performed Trans-species Expression Quantitative Trait Locus analysis to identify a large number of host genes that respond to malaria parasite infections. Here we functionally characterize one of the host genes called receptor transporter protein 4 (RTP4) in responses to malaria parasite and virus infections. RTP4 is induced by type I IFN (IFN-I) and binds to the TANK-binding kinase (TBK1) complex where it negatively regulates TBK1 signaling by interfering with expression and phosphorylation of both TBK1 and IFN regulatory factor 3. Rtp4-/- mice were generated and infected with malaria parasite Plasmodiun berghei ANKA. Significantly higher levels of IFN-I response in microglia, lower parasitemia, fewer neurologic symptoms, and better survival rates were observed in Rtp4-/- than in wild-type mice. Similarly, RTP4 deficiency significantly reduced West Nile virus titers in the brain, but not in the heart and the spleen, of infected mice, suggesting a specific role for RTP4 in brain infection and pathology. This study reveals functions of RTP4 in IFN-I response and a potential target for therapy in diseases with neuropathology.

Keywords: Plasmodium berghei; Plasmodium yoelii; gene knockout; interferon; signaling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Brain / parasitology
  • Brain / pathology*
  • Brain / virology
  • HEK293 Cells
  • Host-Pathogen Interactions
  • Humans
  • Interferon Regulatory Factor-3
  • Interferon Type I / metabolism*
  • Malaria, Cerebral / metabolism
  • Malaria, Cerebral / parasitology
  • Malaria, Cerebral / pathology*
  • Membrane Proteins
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / metabolism
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism*
  • Phosphorylation
  • Plasmodium berghei / physiology
  • Plasmodium yoelii / physiology
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism
  • Signal Transduction
  • West Nile Fever / metabolism
  • West Nile Fever / pathology
  • West Nile Fever / virology
  • West Nile virus / physiology

Substances

  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • Interferon Type I
  • Membrane Proteins
  • Molecular Chaperones
  • Rtp4 protein, mouse
  • STING1 protein, human
  • Protein Serine-Threonine Kinases
  • TBK1 protein, human