PCR detection of cytK gene in Bacillus cereus group strains isolated from food samples

J Microbiol Methods. 2013 Nov;95(2):295-301. doi: 10.1016/j.mimet.2013.09.012. Epub 2013 Sep 20.

Abstract

A method for detection of the cytotoxin K cytK structural gene and its active promoter preceded by the PlcR-binding box, controlling the expression level of this enterotoxin, was developed. The method was applied for the purpose of the analysis of 47 bacterial strains belonging to the Bacillus cereus group isolated from different food products. It was found that the majority of the analyzed strains carried the fully functional cytK gene with its PlcR regulated promoter. The cytK gene was not detected in four emetic strains of Bacillus cereus carrying the cesB gene and potentially producing an emetic toxin - cereulide. The cytotoxin K gene was detected in 4 isolates classified as Bacillus mycoides and one reference strain B. mycoides PCM 2024. The promoter region and the N-terminal part of the cytK gene from two strains of B. mycoides (5D and 19E) showed similarities to the corresponding sequences of Bacillus cereus W23 and Bacillus thuringiensis HD-789, respectively. It was shown for the first time that the cytK gene promoter region from strains 5D and 19E of Bacillus mycoides had a similar arrangement to the corresponding sequence of Bacillus cereus ATCC 14579. The presence of the cytK gene in Bacillus mycoides shows that this species, widely recognized as nonpathogenic, may pose potential biohazard to human beings.

Keywords: Bacillus cereus group; Cytotoxin K; PCR; PlcR regulator.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus cereus / genetics*
  • Bacillus cereus / isolation & purification
  • Base Composition
  • Cytotoxins / genetics
  • Cytotoxins / isolation & purification*
  • DNA Primers / genetics
  • DNA, Bacterial / isolation & purification
  • Food Contamination / analysis*
  • Food Microbiology*
  • Genes, Bacterial
  • Molecular Sequence Data
  • Polymerase Chain Reaction / methods*
  • Polymorphism, Restriction Fragment Length
  • Promoter Regions, Genetic
  • Sequence Analysis, DNA

Substances

  • Cytotoxins
  • DNA Primers
  • DNA, Bacterial