Use of single nucleotide polymorphisms in the plcR gene for specific identification of Bacillus anthracis

J Clin Microbiol. 2005 Apr;43(4):1995-7. doi: 10.1128/JCM.43.4.1995-1997.2005.

Abstract

A TaqMan-minor groove binding assay designed around a nonsense mutation in the plcR gene was used to genotype Bacillus anthracis, B. cereus, and B. thuringiensis isolates. The assay differentiated B. anthracis from these genetic near-neighbors and determined that the nonsense mutation is ubiquitous across 89 globally and genetically diverse B. anthracis strains.

Publication types

  • Evaluation Study
  • 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

  • Anthrax / diagnosis*
  • Anthrax / microbiology
  • Bacillus anthracis / classification*
  • Bacillus anthracis / genetics
  • Bacillus anthracis / isolation & purification
  • Bacterial Proteins / genetics*
  • Bacterial Typing Techniques*
  • Base Sequence
  • Codon, Nonsense
  • DNA, Bacterial / analysis
  • Humans
  • Molecular Sequence Data
  • Polymorphism, Single Nucleotide / genetics*
  • Sequence Analysis, DNA
  • Taq Polymerase / metabolism
  • Trans-Activators / genetics*

Substances

  • Bacterial Proteins
  • Codon, Nonsense
  • DNA, Bacterial
  • PlcR protein, Bacillus
  • Trans-Activators
  • Taq Polymerase