Toll-like receptors participate in Naegleria fowleri recognition

Parasitol Res. 2018 Jan;117(1):75-87. doi: 10.1007/s00436-017-5666-9. Epub 2017 Nov 11.

Abstract

Naegleria fowleri is a protozoan that invades the central nervous system and causes primary amoebic meningoencephalitis. It has been reported that N. fowleri induces an important inflammatory response during the infection. In the present study, we evaluated the roles of Toll-like receptors in the recognition of N. fowleri trophozoites by human mucoepithelial cells, analyzing the expression and production of innate immune response mediators. After amoebic interactions with NCI-H292 cells, the expression and production levels of IL-8, TNF-α, IL-1β, and human beta defensin-2 were evaluated by RT-PCR, ELISA, immunofluorescence, and dot blot assays, respectively. To determine whether the canonical signaling pathways were engaged, we used different inhibitors, namely, IMG-2005 for MyD88 and BAY 11-7085 for the nuclear factor NFkB. Our results showed that the expression and production of the pro-inflammatory cytokines and beta defensin-2 were induced by N. fowleri mainly through the canonical TLR4 pathway in a time-dependent manner.

Keywords: Antimicrobial peptides; Mucoepithelial cells; Naegleria fowleri; Primary amoebic meningoencephalitis; Pro-inflammatory cytokines; Toll-like receptors.

MeSH terms

  • Amebiasis
  • Animals
  • Cell Line
  • Cytokines / metabolism
  • Defensins / metabolism
  • Epithelial Cells / immunology
  • Humans
  • Immunity, Innate
  • Interleukin-1beta / metabolism
  • NF-kappa B / metabolism
  • Naegleria fowleri / immunology*
  • Naegleria fowleri / metabolism*
  • Nitriles / pharmacology
  • Signal Transduction / drug effects
  • Sulfones / pharmacology
  • Toll-Like Receptors / metabolism*
  • Trophozoites / immunology
  • Trophozoites / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • BAY 11-7085
  • Cytokines
  • Defensins
  • Interleukin-1beta
  • NF-kappa B
  • Nitriles
  • Sulfones
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha

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