Epithelial nitration by a peroxidase/NOX5 system mediates mosquito antiplasmodial immunity

Science. 2012 Feb 17;335(6070):856-9. doi: 10.1126/science.1209678. Epub 2012 Jan 26.

Abstract

Plasmodium ookinetes traverse midgut epithelial cells before they encounter the complement system in the mosquito hemolymph. We identified a heme peroxidase (HPX2) and NADPH oxidase 5 (NOX5) as critical mediators of midgut epithelial nitration and antiplasmodial immunity that enhance nitric oxide toxicity in Anopheles gambiae. We show that the two immune mechanisms that target ookinetes-epithelial nitration and thioester-containing protein 1 (TEP1)-mediated lysis-work sequentially, and we propose that epithelial nitration works as an opsonization-like system that promotes activation of the mosquito complement cascade.

Publication types

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

MeSH terms

  • Animals
  • Anopheles / genetics
  • Anopheles / immunology*
  • Anopheles / physiology
  • Complement System Proteins / metabolism
  • Female
  • Gene Silencing
  • Intestinal Mucosa / immunology
  • Malaria / immunology
  • Mice
  • Mice, Inbred BALB C
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism*
  • Nitrogen / metabolism*
  • Peroxidases / genetics
  • Peroxidases / metabolism*
  • Plasmodium berghei / immunology*
  • Plasmodium berghei / physiology

Substances

  • Complement System Proteins
  • Peroxidases
  • NADPH Oxidases
  • Nitrogen