Biocontrol of Escherichia coli O157 with O157-specific bacteriophages

Appl Environ Microbiol. 1999 Sep;65(9):3767-73. doi: 10.1128/AEM.65.9.3767-3773.1999.

Abstract

Escherichia coli O157 antigen-specific bacteriophages were isolated and tested to determine their ability to lyse laboratory cultures of Escherichia coli O157:H7. A total of 53 bovine or ovine fecal samples were enriched for phage, and 5 of these samples were found to contain lytic phages that grow on E. coli O157:H7. Three bacteriophages, designated KH1, KH4, and KH5, were evaluated. At 37 or 4 degrees C, a mixture of these three O157-specific phages lysed all of the E. coli O157 cultures tested and none of the non-O157 E. coli or non-E. coli cultures tested. These results required culture aeration and a high multiplicity of infection. Without aeration, complete lysis of the bacterial cells occurred only after 5 days of incubation and only at 4 degrees C. Phage infection and plaque formation were influenced by the nature of the host cell O157 lipopolysaccharide (LPS). Strains that did not express the O157 antigen or expressed a truncated LPS were not susceptible to plaque formation or lysis by phage. In addition, strains that expressed abundant mid-range-molecular-weight LPS did not support plaque formation but were lysed in liquid culture. Virulent O157 antigen-specific phages could play a role in biocontrol of E. coli O157:H7 in animals and fresh foods without compromising the viability of other normal flora or food quality.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bacteriolysis
  • Cattle
  • Coliphages / isolation & purification
  • Coliphages / physiology*
  • Escherichia coli O157 / immunology
  • Escherichia coli O157 / physiology*
  • Escherichia coli O157 / virology*
  • Immunoblotting
  • Lipopolysaccharides / biosynthesis
  • Lipopolysaccharides / immunology
  • Lysogeny
  • O Antigens / immunology
  • Sheep
  • Species Specificity
  • Viral Plaque Assay

Substances

  • Lipopolysaccharides
  • O Antigens