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Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms

The evolutionary stability of temperate bacteriophages at low abundance of susceptible bacterial hosts lies in the trade-off between the maximization of phage replication, performed by the host-destructive lytic cycle, and the protection of the phage-host collective, enacted by lysogeny. Upon Bacill...

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Autores principales: Bernard, Charles, Li, Yanyan, Lopez, Philippe, Bapteste, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027211/
https://www.ncbi.nlm.nih.gov/pubmed/33028977
http://dx.doi.org/10.1038/s41396-020-00795-9
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author Bernard, Charles
Li, Yanyan
Lopez, Philippe
Bapteste, Eric
author_facet Bernard, Charles
Li, Yanyan
Lopez, Philippe
Bapteste, Eric
author_sort Bernard, Charles
collection PubMed
description The evolutionary stability of temperate bacteriophages at low abundance of susceptible bacterial hosts lies in the trade-off between the maximization of phage replication, performed by the host-destructive lytic cycle, and the protection of the phage-host collective, enacted by lysogeny. Upon Bacillus infection, Bacillus phages phi3T rely on the “arbitrium” quorum sensing (QS) system to communicate on their population density in order to orchestrate the lysis-to-lysogeny transition. At high phage densities, where there may be limited host cells to infect, lysogeny is induced to preserve chances of phage survival. Here, we report the presence of an additional, host-derived QS system in the phi3T genome, making it the first known virus with two communication systems. Specifically, this additional system, coined “Rapφ-Phrφ”, is predicted to downregulate host defense mechanisms during the viral infection, but only upon stress or high abundance of Bacillus cells and at low density of population of the phi3T phages. Post-lysogenization, Rapφ-Phrφ is also predicted to provide the lysogenized bacteria with an immediate fitness advantage: delaying the costly production of public goods while nonetheless benefiting from the public goods produced by other non-lysogenized Bacillus bacteria. The discovered “Rapφ-Phrφ” QS system hence provides novel mechanistic insights into how phage communication systems could contribute to the phage-host evolutionary stability.
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spelling pubmed-80272112021-04-21 Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms Bernard, Charles Li, Yanyan Lopez, Philippe Bapteste, Eric ISME J Article The evolutionary stability of temperate bacteriophages at low abundance of susceptible bacterial hosts lies in the trade-off between the maximization of phage replication, performed by the host-destructive lytic cycle, and the protection of the phage-host collective, enacted by lysogeny. Upon Bacillus infection, Bacillus phages phi3T rely on the “arbitrium” quorum sensing (QS) system to communicate on their population density in order to orchestrate the lysis-to-lysogeny transition. At high phage densities, where there may be limited host cells to infect, lysogeny is induced to preserve chances of phage survival. Here, we report the presence of an additional, host-derived QS system in the phi3T genome, making it the first known virus with two communication systems. Specifically, this additional system, coined “Rapφ-Phrφ”, is predicted to downregulate host defense mechanisms during the viral infection, but only upon stress or high abundance of Bacillus cells and at low density of population of the phi3T phages. Post-lysogenization, Rapφ-Phrφ is also predicted to provide the lysogenized bacteria with an immediate fitness advantage: delaying the costly production of public goods while nonetheless benefiting from the public goods produced by other non-lysogenized Bacillus bacteria. The discovered “Rapφ-Phrφ” QS system hence provides novel mechanistic insights into how phage communication systems could contribute to the phage-host evolutionary stability. Nature Publishing Group UK 2020-10-07 2021-02 /pmc/articles/PMC8027211/ /pubmed/33028977 http://dx.doi.org/10.1038/s41396-020-00795-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bernard, Charles
Li, Yanyan
Lopez, Philippe
Bapteste, Eric
Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title_full Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title_fullStr Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title_full_unstemmed Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title_short Beyond arbitrium: identification of a second communication system in Bacillus phage phi3T that may regulate host defense mechanisms
title_sort beyond arbitrium: identification of a second communication system in bacillus phage phi3t that may regulate host defense mechanisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027211/
https://www.ncbi.nlm.nih.gov/pubmed/33028977
http://dx.doi.org/10.1038/s41396-020-00795-9
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