Sialoglycoconjugates in Herpetomonas megaseliae: role in the adhesion to insect host epithelial cells

FEMS Microbiol Lett. 2009 Jun;295(2):274-80. doi: 10.1111/j.1574-6968.2009.01606.x. Epub 2009 May 1.

Abstract

Herpetomonas megaseliae is a monoxenic trypanosomatid isolated from the phorid fly Megaselia scalaris. In the present report, the expression of cell surface sialoglycoconjugates in this parasite was analyzed by Western blotting, flow cytometry and fluorescence microscopy analyses using lectins that specifically recognize sialic acid residues. A strong reaction was detected when parasites were treated with Limax flavus, Maackia amurensis and Sambucus nigra lectins. Analysis of crude protein extracts by Western blotting revealed that bands with molecular masses ranging from 19 to 80 kDa were reactive to these lectins, which showed a sugar-inhibited recognition with the parasite extract. These results indicated that molecules containing alpha2,3- and alpha2,6-sialylgalactosyl sequences are present in this protozoan. The role of the surface sialomolecules in the interaction with explanted guts from Aedes aegypti was assessed. The interaction of H. megaseliae with the insect gut was strongly inhibited in the presence of mucin (71%), fetuin (68%) and sialyllactose (68%). Collectively, our results suggest a possible involvement of sialomolecules in the interaction between this insect trypanosomatid and the invertebrate host.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes / cytology
  • Aedes / parasitology*
  • Animals
  • Blotting, Western
  • Cell Adhesion
  • Culture Media
  • Epithelial Cells / parasitology*
  • Female
  • Flow Cytometry
  • Glycoconjugates / metabolism*
  • Host-Parasite Interactions*
  • Lectins / metabolism
  • Microscopy, Fluorescence
  • N-Acetylneuraminic Acid / metabolism*
  • Plant Lectins
  • Ribosome Inactivating Proteins
  • Trypanosomatina / chemistry
  • Trypanosomatina / metabolism
  • Trypanosomatina / physiology*

Substances

  • Culture Media
  • Glycoconjugates
  • Lectins
  • Plant Lectins
  • Sambucus nigra lectins
  • Ribosome Inactivating Proteins
  • N-Acetylneuraminic Acid