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

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 population...

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Autores principales: Patterson, Adrian G., Jackson, Simon A., Taylor, Corinda, Evans, Gary B., Salmond, George P.C., Przybilski, Rita, Staals, Raymond H.J., Fineran, Peter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179492/
https://www.ncbi.nlm.nih.gov/pubmed/27867010
http://dx.doi.org/10.1016/j.molcel.2016.11.012
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author Patterson, Adrian G.
Jackson, Simon A.
Taylor, Corinda
Evans, Gary B.
Salmond, George P.C.
Przybilski, Rita
Staals, Raymond H.J.
Fineran, Peter C.
author_facet Patterson, Adrian G.
Jackson, Simon A.
Taylor, Corinda
Evans, Gary B.
Salmond, George P.C.
Przybilski, Rita
Staals, Raymond H.J.
Fineran, Peter C.
author_sort Patterson, Adrian G.
collection PubMed
description 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.
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spelling pubmed-51794922016-12-23 Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems Patterson, Adrian G. Jackson, Simon A. Taylor, Corinda Evans, Gary B. Salmond, George P.C. Przybilski, Rita Staals, Raymond H.J. Fineran, Peter C. Mol Cell Short Article 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. Cell Press 2016-12-15 /pmc/articles/PMC5179492/ /pubmed/27867010 http://dx.doi.org/10.1016/j.molcel.2016.11.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Short Article
Patterson, Adrian G.
Jackson, Simon A.
Taylor, Corinda
Evans, Gary B.
Salmond, George P.C.
Przybilski, Rita
Staals, Raymond H.J.
Fineran, Peter C.
Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title_full Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title_fullStr Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title_full_unstemmed Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title_short Quorum Sensing Controls Adaptive Immunity through the Regulation of Multiple CRISPR-Cas Systems
title_sort quorum sensing controls adaptive immunity through the regulation of multiple crispr-cas systems
topic Short Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179492/
https://www.ncbi.nlm.nih.gov/pubmed/27867010
http://dx.doi.org/10.1016/j.molcel.2016.11.012
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