Leishmania donovani requires functional Cdc42 and Rac1 to prevent phagosomal maturation

Infect Immun. 2006 May;74(5):2613-8. doi: 10.1128/IAI.74.5.2613-2618.2006.

Abstract

Leishmania donovani promastigotes survive inside macrophage phagosomes by inhibiting phagosomal maturation. The main surface glycoconjugate on promastigotes, lipophosphoglycan (LPG), is crucial for survival and mediates the formation of a protective shell of F-actin around the phagosome. Previous studies have demonstrated that this effect involves inhibition of protein kinase C alpha. The present study shows that functional Cdc42 and Rac1 are required for the formation of F-actin around L. donovani phagosomes. Moreover, we present data showing that phagosomes containing LPG-defective L. donovani, which is unable to induce F-actin accumulation, display both elevated levels of periphagosomal F-actin and impaired phagosomal maturation in macrophages with permanently active forms of Cdc42 and Rac1. We conclude that L. donovani engages Cdc42 and Rac1 to build up a protective coat of F-actin around its phagosome to prevent phagosomal maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / analysis
  • Actins / physiology
  • Animals
  • Cell Line
  • Glycosphingolipids / physiology
  • Leishmania donovani / physiology*
  • Lysosomal-Associated Membrane Protein 1 / metabolism
  • Mice
  • Phagosomes / physiology*
  • Protein Kinase C-alpha / physiology
  • Protein Transport
  • cdc42 GTP-Binding Protein / physiology*
  • rac1 GTP-Binding Protein / physiology*

Substances

  • Actins
  • Glycosphingolipids
  • Lysosomal-Associated Membrane Protein 1
  • lipophosphonoglycan
  • Protein Kinase C-alpha
  • cdc42 GTP-Binding Protein
  • rac1 GTP-Binding Protein