Cysteine proteinase activity is required for survival of the parasite in experimental acute amoebic liver abscesses in hamsters

Parasitology. 2004 Jul;129(Pt 1):19-25. doi: 10.1017/s0031182004005116.

Abstract

Axenic trophozoites of Entamoeba histolytica strain HM1-IMSS grown in vitro in the presence of E-64, a potent irreversible inhibitor of cysteine proteinases, preserved their viability, their rate of replication, their resistance to complement, their haemolytic capacity and their ability to destroy target cells, despite complete inhibition of total cysteine proteinase activity. On the other hand, their erythrophagocytic capacity and their ability to decrease TER of MDCK cells was partially decreased. The same trophozoites injected into the portal vein of hamsters receiving a maintaining dose of E-64 failed to cause tissue damage and were rapidly eliminated. Our results suggest that amoebic cysteine proteinase activity is not required for amoebic functions in in vitro conditions, but that it becomes necessary for survival of trophozoites in in vivo conditions, whatever other role (if any) it may play in the parasite's virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Complement System Proteins / metabolism
  • Cricetinae
  • Cysteine Endopeptidases / metabolism*
  • Cysteine Proteinase Inhibitors / pharmacology
  • Electric Impedance
  • Entamoeba histolytica / enzymology*
  • Entamoeba histolytica / growth & development
  • Entamoeba histolytica / physiology
  • Erythrocytes / parasitology
  • Female
  • Histocytochemistry
  • Leucine / analogs & derivatives*
  • Leucine / pharmacology
  • Liver Abscess, Amebic / drug therapy
  • Liver Abscess, Amebic / parasitology*
  • Male
  • Phagocytosis

Substances

  • Cysteine Proteinase Inhibitors
  • Complement System Proteins
  • Cysteine Endopeptidases
  • Leucine
  • E 64