Specificity of binding of a strain of uropathogenic Escherichia coli to Gal alpha 1----4Gal-containing glycosphingolipids

J Biol Chem. 1985 Jul 15;260(14):8545-51.

Abstract

A strain of Escherichia coli originally isolated from urine of a patient with acute pyelonephritis was studied in detail for binding to glycosphingolipids. Bacteria labeled metabolically with [14C]glucose were layered over a glycolipid chromatogram and bound bacteria were detected by autoradiography. The detection was down to a few ng of glycolipid (pmol level) under these assay conditions. At a test level of 500 ng all glycolipids (more than a dozen molecular species analyzed) with Gal alpha 1----4Gal as an internal or terminal part bound the bacteria strongly while glycolipids known to lack this sequence were negative. Conformational analysis using hard sphere calculations including the exo-anomeric effect showed a bend in the saccharide chain at this disaccharide with a largely hydrophobic surface of the convex side, probably being part of the binding epitope. Mixtures of glycolipids isolated from a human ureter scraping and from urinary sediments bound bacteria in the 2- to 7-sugar interval. Thus, this infectious strain of E. coli recognizes glycolipids being present in epithelial cells lining the urinary tract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System
  • Animals
  • Carbohydrate Sequence
  • Cattle
  • Chromatography, Thin Layer
  • Dogs
  • Escherichia coli / metabolism*
  • Escherichia coli Infections / microbiology
  • Galactose / metabolism*
  • Glycosphingolipids / metabolism*
  • Humans
  • Kidney / metabolism
  • Mice
  • Models, Molecular
  • Pyelonephritis / microbiology
  • Rabbits
  • Rats
  • Substrate Specificity

Substances

  • ABO Blood-Group System
  • Glycosphingolipids
  • Galactose