Glycophorin A-knockout mice, which lost sialoglycoproteins from the red blood cell membrane, are resistant to lethal infection of Babesia rodhaini

Vet Parasitol. 2007 Sep 1;148(2):93-101. doi: 10.1016/j.vetpar.2007.06.011. Epub 2007 Jul 24.

Abstract

Recent in vitro-based studies using several Babesia spp. have suggested that sialic acids and/or sialoglycoproteins on host red blood cells (RBCs) play an important role in their invasion of RBCs. In the present study, we analyzed the RBC characteristics of glycophorin A (GPA)-knockout mice and studied their in vivo susceptibility to lethal infection of Babesia rodhaini for the first time. In immunoblot and lectin blot analyses, glycoproteins containing O-linked oligosaccharides terminated with alpha2-3-linked sialic acids disappeared from the RBCs of GPA homozygous ((-/-)) mice. Flow cytometric analysis showed a remarkable reduction of Maackia amurensis lectin II binding to the surface of GPA(-/-) RBCs relative to control RBCs, indicating an appreciable loss of alpha2-3-linked sialic acids on the RBC surface of GPA(-/-) mice. Importantly, while B. rodhaini caused lethal infection in wild-type mice, the infected GPA(-/-) mice showed inhibition of parasite growth and eventually survived. These results indicate that RBC sialoglycoproteins lost in GPA(-/-) mice are involved in the in vivo growth of B. rodhaini, probably functioning as essential molecule(s) for the parasite invasion of host RBCs in the blood circulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens
  • Babesia / pathogenicity*
  • Babesiosis / immunology
  • Babesiosis / veterinary*
  • Disease Susceptibility / veterinary
  • Erythrocyte Membrane / metabolism
  • Female
  • Flow Cytometry / methods
  • Flow Cytometry / veterinary
  • Fluorescent Antibody Technique / veterinary
  • Glycophorins / immunology*
  • Glycophorins / metabolism*
  • Mice
  • Mice, Knockout
  • Oligosaccharides / analysis
  • Oligosaccharides / chemistry
  • Time Factors

Substances

  • Antigens
  • Glycophorins
  • Oligosaccharides