Disentangling competence for genetic transformation and virulence in Streptococcus pneumoniae

Curr Genet. 2016 Feb;62(1):97-103. doi: 10.1007/s00294-015-0520-z. Epub 2015 Sep 24.

Abstract

Horizontal gene transfer mediated by the competence regulon is a major driver of genome plasticity in Streptococcus pneumoniae. When pneumococcal cells enter the competent state, about 6% of the genes in the genome are up-regulated. Among these, some genes are essential for genetic transformation while others are dispensable for the process. Exhaustive deletion analyses show that some up-regulated genes dispensable for genetic transformation contribute to pneumococcal-mediated pneumonia and bacteremia infections. Interestingly, virulence functions of such genes are either dependent or independent of the competent state. Among the competent-state-dependent genes are those mediating allolysis, a process where small fraction of non-competent cells within the pneumococcal population are lysed by their competent counterparts, releasing DNA presumably for transformation. Inadvertently, the pore-forming toxin pneumolysin is also released during allolysis, contributing to virulence. In this review, we discuss recent advances in our understanding of pneumococcal virulence processes mediated by the competence regulon. We proposed that coupling of competence induction and bacterial fitness drives the natural selection to favor an intact competence regulon, which in turn, provides the long-term benefits of genetic plasticity.

Keywords: Allolysis; Competence; Pneumolysin; Streptococcus pneumoniae; Virulence.

Publication types

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

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Gene Transfer, Horizontal*
  • Genes, Bacterial
  • Humans
  • Mutation
  • Operon
  • Recombination, Genetic
  • Streptococcus pneumoniae / pathogenicity
  • Streptococcus pneumoniae / physiology*
  • Streptolysins / genetics
  • Streptolysins / metabolism
  • Transformation, Bacterial*
  • Virulence / genetics

Substances

  • Bacterial Proteins
  • Streptolysins
  • plY protein, Streptococcus pneumoniae