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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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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. |
format | Online Article Text |
id | pubmed-5179492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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