Papillation in Bacillus anthracis colonies: a tool for finding new mutators

Mol Microbiol. 2011 Mar;79(5):1276-93. doi: 10.1111/j.1365-2958.2011.07519.x. Epub 2011 Jan 11.

Abstract

Colonies of Bacillus anthracis Sterne allow the growth of papillation after 6 days of incubation at 30°C on Luria-Bertani medium. The papillae are due to mutations that allow the cells to overcome the barriers to continued growth. Cells isolated from papillae display two distinct gross phenotypes (group A and group B). We determined that group A mutants have mutations in the nprR gene including frameshifts, deletions, duplications and base substitutions. We used papillation as a tool for finding new mutators as the mutators generate elevated levels of papillation. We discovered that disruption of yycJ or recJ leads to a spontaneous mutator phenotype. We defined the nprR/papillation system as a new mutational analysis system for B. anthracis. The mutational specificity of the new mutator yycJ is similar to that of mismatch repair-deficient strains (MMR⁻) such as those with mutations in mutL or mutS. Deficiency in recJ results in a unique specificity, generating only tandem duplications.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus anthracis / genetics*
  • Bacillus anthracis / growth & development*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • DNA Mutational Analysis / methods*
  • Mutation*
  • Phenotype

Substances

  • Bacterial Proteins