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Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera

Although the evolution of tailed bacteriophages has increasingly been better understood through comparisons of their DNA sequences, the functional consequences of this evolution on phage infectious strategies have remained unresolved. In this study, we comprehensively compared the transcriptional st...

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Autores principales: Blasdel, Bob G, Chevallereau, Anne, Monot, Marc, Lavigne, Rob, Debarbieux, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563952/
https://www.ncbi.nlm.nih.gov/pubmed/28498372
http://dx.doi.org/10.1038/ismej.2017.63
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author Blasdel, Bob G
Chevallereau, Anne
Monot, Marc
Lavigne, Rob
Debarbieux, Laurent
author_facet Blasdel, Bob G
Chevallereau, Anne
Monot, Marc
Lavigne, Rob
Debarbieux, Laurent
author_sort Blasdel, Bob G
collection PubMed
description Although the evolution of tailed bacteriophages has increasingly been better understood through comparisons of their DNA sequences, the functional consequences of this evolution on phage infectious strategies have remained unresolved. In this study, we comprehensively compared the transcriptional strategies of two related myoviruses, PAK_P3 and PAK_P4, infecting the same Pseudomonas aeruginosa host strain. Outside of the conservation of their structural clusters, their highly syntenic genomes display only limited DNA similarity. Despite this apparent divergence, we found that both viruses follow a similar infection scheme, relying on a temporal regulation of their gene expression, likely involving the use of antisense transcripts, as well as a rapid degradation of 90% of the host non-ribosomal mRNA, as previously reported for PAK_P3. However, the kinetics of the mRNA degradation is remarkably faster during PAK_P4 infection. Moreover, we found that each virus has evolved specific adaptations, as exemplified by the distinct patterns of their core genes expression as well as the specific manipulation of the expression of iron-related host genes by PAK_P4. This study enhances our understanding of the evolutionary process of virulent phages, which relies on adjusting globally conserved ancestral infection mechanisms.
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spelling pubmed-55639522017-09-18 Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera Blasdel, Bob G Chevallereau, Anne Monot, Marc Lavigne, Rob Debarbieux, Laurent ISME J Original Article Although the evolution of tailed bacteriophages has increasingly been better understood through comparisons of their DNA sequences, the functional consequences of this evolution on phage infectious strategies have remained unresolved. In this study, we comprehensively compared the transcriptional strategies of two related myoviruses, PAK_P3 and PAK_P4, infecting the same Pseudomonas aeruginosa host strain. Outside of the conservation of their structural clusters, their highly syntenic genomes display only limited DNA similarity. Despite this apparent divergence, we found that both viruses follow a similar infection scheme, relying on a temporal regulation of their gene expression, likely involving the use of antisense transcripts, as well as a rapid degradation of 90% of the host non-ribosomal mRNA, as previously reported for PAK_P3. However, the kinetics of the mRNA degradation is remarkably faster during PAK_P4 infection. Moreover, we found that each virus has evolved specific adaptations, as exemplified by the distinct patterns of their core genes expression as well as the specific manipulation of the expression of iron-related host genes by PAK_P4. This study enhances our understanding of the evolutionary process of virulent phages, which relies on adjusting globally conserved ancestral infection mechanisms. Nature Publishing Group 2017-09 2017-05-12 /pmc/articles/PMC5563952/ /pubmed/28498372 http://dx.doi.org/10.1038/ismej.2017.63 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Blasdel, Bob G
Chevallereau, Anne
Monot, Marc
Lavigne, Rob
Debarbieux, Laurent
Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title_full Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title_fullStr Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title_full_unstemmed Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title_short Comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
title_sort comparative transcriptomics analyses reveal the conservation of an ancestral infectious strategy in two bacteriophage genera
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563952/
https://www.ncbi.nlm.nih.gov/pubmed/28498372
http://dx.doi.org/10.1038/ismej.2017.63
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