Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems

Mol Cell. 2016 Dec 15;64(6):1102-1108. doi: 10.1016/j.molcel.2016.11.012. Epub 2016 Nov 17.

Abstract

Bacteria commonly exist in high cell density populations, making them prone to viral predation and horizontal gene transfer (HGT) through transformation and conjugation. To combat these invaders, bacteria possess an arsenal of defenses, such as CRISPR-Cas adaptive immunity. Many bacterial populations coordinate their behavior as cell density increases, using quorum sensing (QS) signaling. In this study, we demonstrate that QS regulation results in increased expression of the type I-E, I-F, and III-A CRISPR-Cas systems in Serratia cells in high-density populations. Strains unable to communicate via QS were less effective at defending against invaders targeted by any of the three CRISPR-Cas systems. Additionally, the acquisition of immunity by the type I-E and I-F systems was impaired in the absence of QS signaling. We propose that bacteria can use chemical communication to modulate the balance between community-level defense requirements in high cell density populations and host fitness costs of basal CRISPR-Cas activity.

Keywords: CRISPR-Cas; bacterial communication; horizontal gene transfer; phage resistance; quorum sensing; regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives
  • 4-Butyrolactone / pharmacology
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / immunology
  • CRISPR-Associated Proteins / genetics
  • CRISPR-Associated Proteins / immunology
  • CRISPR-Cas Systems / immunology*
  • Clustered Regularly Interspaced Short Palindromic Repeats
  • Endodeoxyribonucleases / genetics*
  • Endodeoxyribonucleases / immunology
  • Gene Expression Regulation, Bacterial / immunology*
  • Quorum Sensing / drug effects
  • Quorum Sensing / genetics*
  • Quorum Sensing / immunology
  • Repressor Proteins / genetics
  • Repressor Proteins / immunology
  • Serratia / drug effects
  • Serratia / genetics*
  • Serratia / immunology

Substances

  • Bacterial Proteins
  • CRISPR-Associated Proteins
  • N-butyrylhomoserine lactone
  • Repressor Proteins
  • Endodeoxyribonucleases
  • 4-Butyrolactone