Production of Shiga toxin by Shiga toxin-expressing Escherichia coli (STEC) in broth media: from divergence to definition

Lett Appl Microbiol. 2007 Oct;45(4):411-7. doi: 10.1111/j.1472-765X.2007.02214.x.

Abstract

Aims: To determine the suitability of eight different commercial broth media for Shiga toxin (Stx) production.

Methods and results: Shiga toxin-producing Escherichia coli (STEC) strains producing Stx1 or Stx2 were grown at 37 degrees C (250 rev min(-1)) for 24 h in brain heart infusion broth, E. coli broth, Evans medium, Luria-Bertani broth, Penassay broth, buffered-peptone water, syncase broth and trypticase soy broth. Toxin production was measured by enzyme-linked immunosorbent assay (ELISA) in polymyxin-treated cell pellets and/or supernatants of cultures, ELISA optical densities reached 1 when isolates were grown for 2-4 h in E. coli broth in the presence of antibiotic. Besides, a collection of STEC-expressing Stx strains was evaluated and the Stx production was assayed in the supernatants and in polymyxin-treated pellets of bacterial growth after 4 h of cultivation in E. coli broth in the presence of antibiotic.

Conclusions: The most suitable medium for Stx production was E. coli broth when the bacterial isolates were grown for 4 h in the presence of ciprofloxacin and the Stx production is detected in the supernatant.

Significance and impact of the study: This study presents the first comprehensive comparison of different broth media with regard to Stx production to establish optimal culture conditions for STEC detection in routine diagnostic laboratories.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Chlorocebus aethiops
  • Culture Media*
  • Enzyme-Linked Immunosorbent Assay
  • Escherichia coli / metabolism*
  • Escherichia coli / pathogenicity
  • Shiga Toxins / biosynthesis*
  • Vero Cells

Substances

  • Culture Media
  • Shiga Toxins