Assessment of lipopolysaccharide-binding activity of Bifidobacterium and its relationship with cell surface hydrophobicity, autoaggregation, and inhibition of interleukin-8 production

J Microbiol Biotechnol. 2007 Jul;17(7):1120-6.

Abstract

This study was performed to screen probiotic bifidobacteria for their ability to bind and neutralize lipopolysaccharides (LPS) from Escherichia coli and to verify the relationship between LPS-binding ability, cell surface hydrophobicity (CSH), and inhibition of LPS-induced interleukin-8 (IL-8) secretion by HT-29 cells of the various bifidobacterial strains. Ninety bifidobacteria isolates from human feces were assessed for their ability to bind fluorescein isothiocyanate (FITC)-labeled LPS from E. coli. Isolates showing 30-60% binding were designated LPS-high binding (LPS-H) and those with less than 15% binding were designated LPS-low binding (LPS-L). The CSH, autoaggregation (AA), and inhibition of LPS-induced IL-8 release from HT-29 cells of the LPS-H and LPS-L groups were evaluated. Five bifidobacteria strains showed high levels of LPS binding, CSH, AA, and inhibition of IL-8 release. However, statistically significant correlations between LPS binding, CSH, AA, and reduction of IL-8 release were not found. Although we could isolate bifidobacteria with high LPS-binding ability, CSH, AA, and inhibition of IL-8 release, each characteristic should be considered as strain dependent. Bifidobacteria with high LPS binding and inhibition of IL-8 release may be good agents for preventing inflammation by neutralizing Gram-negative endotoxins and improving intestinal health.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bifidobacterium / classification
  • Bifidobacterium / isolation & purification
  • Bifidobacterium / metabolism*
  • Bifidobacterium / physiology*
  • Escherichia coli / chemistry
  • Escherichia coli / classification
  • Feces / microbiology
  • Fluorescein-5-isothiocyanate / metabolism
  • Fluorescent Dyes / metabolism
  • HT29 Cells
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Interleukin-8 / antagonists & inhibitors*
  • Lipopolysaccharides / metabolism*
  • Membrane Proteins / physiology
  • Probiotics / pharmacology
  • Serotyping
  • Surface Properties

Substances

  • Fluorescent Dyes
  • Interleukin-8
  • Lipopolysaccharides
  • Membrane Proteins
  • Fluorescein-5-isothiocyanate