HeLa cell invasion by a strain of enteropathogenic Escherichia coli that lacks the O-antigenic polysaccharide

Mol Microbiol. 1990 Oct;4(10):1661-6. doi: 10.1111/j.1365-2958.1990.tb00543.x.

Abstract

The interaction with HeLa cells of an enteropathogenic Escherichia coli (EPEC) strain and its plasmid-cured derivative strain was examined. An O111:NM EPEC strain B171 harbours a 54 megadalton plasmid (pYR111) necessary for the expression of both localized adherence (LA) to HeLa cells and the O-repeating side chain of the lipopolysaccharide. Under light microscopy, the plasmid-cured derivative strain B171-4 was observed to interact with HeLa cells in a pattern distinct from LA. Transmission electron microscopy showed that the bacteria were internalized by HeLa cells. In contrast, strain B171 induced pedestal-like projections and invaginations of the plasma membrane, but was never completely internalized. A quantitative assay to determine the number of internalized bacteria revealed that strain B171-4 was internalized at levels 30-70-fold higher than those of avirulent E. coli strains. Cytochalasin B reduced the levels of internalization of both strain B171-4 and an enteroinvasive E. coli strain (E11), but did not affect LA by strain B171. These results suggest that EPEC strain B171 may carry a specific chromosomally determined surface factor needed to initiate internalization by HeLa cells. However, a plasmid-determined factor alters the nature of this interaction; the combined effects of the chromosomal and plasmid determinants lead to the characteristic attachment of the bacteria in clusters on the surface of the eukaryotic cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Bacterial / genetics*
  • Bacterial Adhesion / drug effects
  • Cell Adhesion / drug effects
  • Cytochalasin B / pharmacology
  • Escherichia coli / genetics
  • Escherichia coli / immunology
  • Escherichia coli / pathogenicity*
  • Genes, Bacterial
  • HeLa Cells / microbiology
  • HeLa Cells / ultrastructure
  • Humans
  • Microscopy, Electron
  • O Antigens
  • Plasmids
  • Polysaccharides, Bacterial / metabolism*

Substances

  • Antigens, Bacterial
  • O Antigens
  • Polysaccharides, Bacterial
  • Cytochalasin B