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Cell cycle constraints on capsulation and bacteriophage susceptibility
Despite the crucial role of bacterial capsules in pathogenesis, it is still unknown if systemic cues such as the cell cycle can control capsule biogenesis. In this study, we show that the capsule of the synchronizable model bacterium Caulobacter crescentus is cell cycle regulated and we unearth a ba...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241560/ https://www.ncbi.nlm.nih.gov/pubmed/25421297 http://dx.doi.org/10.7554/eLife.03587 |
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author | Ardissone, Silvia Fumeaux, Coralie Bergé, Matthieu Beaussart, Audrey Théraulaz, Laurence Radhakrishnan, Sunish Kumar Dufrêne, Yves F Viollier, Patrick H |
author_facet | Ardissone, Silvia Fumeaux, Coralie Bergé, Matthieu Beaussart, Audrey Théraulaz, Laurence Radhakrishnan, Sunish Kumar Dufrêne, Yves F Viollier, Patrick H |
author_sort | Ardissone, Silvia |
collection | PubMed |
description | Despite the crucial role of bacterial capsules in pathogenesis, it is still unknown if systemic cues such as the cell cycle can control capsule biogenesis. In this study, we show that the capsule of the synchronizable model bacterium Caulobacter crescentus is cell cycle regulated and we unearth a bacterial transglutaminase homolog, HvyA, as restriction factor that prevents capsulation in G1-phase cells. This capsule protects cells from infection by a generalized transducing Caulobacter phage (φCr30), and the loss of HvyA confers insensitivity towards φCr30. Control of capsulation during the cell cycle could serve as a simple means to prevent steric hindrance of flagellar motility or to ensure that phage-mediated genetic exchange happens before the onset of DNA replication. Moreover, the multi-layered regulatory circuitry directing HvyA expression to G1-phase is conserved during evolution, and HvyA orthologues from related Sinorhizobia can prevent capsulation in Caulobacter, indicating that alpha-proteobacteria have retained HvyA activity. DOI: http://dx.doi.org/10.7554/eLife.03587.001 |
format | Online Article Text |
id | pubmed-4241560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42415602014-12-18 Cell cycle constraints on capsulation and bacteriophage susceptibility Ardissone, Silvia Fumeaux, Coralie Bergé, Matthieu Beaussart, Audrey Théraulaz, Laurence Radhakrishnan, Sunish Kumar Dufrêne, Yves F Viollier, Patrick H eLife Microbiology and Infectious Disease Despite the crucial role of bacterial capsules in pathogenesis, it is still unknown if systemic cues such as the cell cycle can control capsule biogenesis. In this study, we show that the capsule of the synchronizable model bacterium Caulobacter crescentus is cell cycle regulated and we unearth a bacterial transglutaminase homolog, HvyA, as restriction factor that prevents capsulation in G1-phase cells. This capsule protects cells from infection by a generalized transducing Caulobacter phage (φCr30), and the loss of HvyA confers insensitivity towards φCr30. Control of capsulation during the cell cycle could serve as a simple means to prevent steric hindrance of flagellar motility or to ensure that phage-mediated genetic exchange happens before the onset of DNA replication. Moreover, the multi-layered regulatory circuitry directing HvyA expression to G1-phase is conserved during evolution, and HvyA orthologues from related Sinorhizobia can prevent capsulation in Caulobacter, indicating that alpha-proteobacteria have retained HvyA activity. DOI: http://dx.doi.org/10.7554/eLife.03587.001 eLife Sciences Publications, Ltd 2014-11-25 /pmc/articles/PMC4241560/ /pubmed/25421297 http://dx.doi.org/10.7554/eLife.03587 Text en Copyright © 2014, Ardissone et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Ardissone, Silvia Fumeaux, Coralie Bergé, Matthieu Beaussart, Audrey Théraulaz, Laurence Radhakrishnan, Sunish Kumar Dufrêne, Yves F Viollier, Patrick H Cell cycle constraints on capsulation and bacteriophage susceptibility |
title | Cell cycle constraints on capsulation and bacteriophage susceptibility |
title_full | Cell cycle constraints on capsulation and bacteriophage susceptibility |
title_fullStr | Cell cycle constraints on capsulation and bacteriophage susceptibility |
title_full_unstemmed | Cell cycle constraints on capsulation and bacteriophage susceptibility |
title_short | Cell cycle constraints on capsulation and bacteriophage susceptibility |
title_sort | cell cycle constraints on capsulation and bacteriophage susceptibility |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241560/ https://www.ncbi.nlm.nih.gov/pubmed/25421297 http://dx.doi.org/10.7554/eLife.03587 |
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