The trypanosome lytic factor of human serum and the molecular basis of sleeping sickness

Int J Parasitol. 2004 Jul;34(8):887-98. doi: 10.1016/j.ijpara.2004.04.008.

Abstract

Trypanosoma brucei brucei infects a wide range of mammals but is unable to infect humans because this subspecies is lysed by normal human serum (NHS). The trypanosome lytic factor is associated with High Density Lipoproteins (HDLs). Several HDL-associated components have been proposed as candidate lytic factors, and contradictory hypotheses concerning the mechanism of lysis have been suggested. Elucidation of the process by which Trypanosoma brucei rhodesiense resists lysis and causes human sleeping sickness has indicated that the HDL-bound apolipoprotein L-I (apoL-I) could be the long-sought after lytic component of NHS. This research also allowed the identification of a specific diagnostic DNA probe for T. b. rhodesiense, and may lead to the development of novel anti-trypanosome strategies for use in the field.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apolipoproteins / genetics
  • Apolipoproteins / metabolism
  • Endocytosis / physiology
  • Genes, Protozoan / genetics
  • Haptoglobins / genetics
  • Haptoglobins / metabolism
  • Humans
  • Lipoproteins, HDL / genetics*
  • Lipoproteins, HDL / metabolism
  • Lysosomes / genetics
  • Lysosomes / metabolism
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism
  • Toxins, Biological / genetics
  • Toxins, Biological / metabolism
  • Trypanosoma brucei brucei / genetics
  • Trypanosoma brucei brucei / metabolism
  • Trypanosoma brucei rhodesiense / genetics*
  • Trypanosoma brucei rhodesiense / metabolism
  • Trypanosomiasis, African / genetics*
  • Trypanosomiasis, African / metabolism
  • Trypanosomiasis, African / parasitology

Substances

  • Apolipoproteins
  • Haptoglobins
  • Lipoproteins, HDL
  • Protozoan Proteins
  • TLF1 protein, human
  • Toxins, Biological