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Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa

As interest in the therapeutic and biotechnological potentials of bacteriophages has grown, so has value in understanding their basic biology. However, detailed knowledge of infection cycles has been limited to a small number of model bacteriophages, mostly infecting Escherichia coli. We present her...

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Autores principales: Chevallereau, Anne, Blasdel, Bob G., De Smet, Jeroen, Monot, Marc, Zimmermann, Michael, Kogadeeva, Maria, Sauer, Uwe, Jorth, Peter, Whiteley, Marvin, Debarbieux, Laurent, Lavigne, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933390/
https://www.ncbi.nlm.nih.gov/pubmed/27380413
http://dx.doi.org/10.1371/journal.pgen.1006134
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author Chevallereau, Anne
Blasdel, Bob G.
De Smet, Jeroen
Monot, Marc
Zimmermann, Michael
Kogadeeva, Maria
Sauer, Uwe
Jorth, Peter
Whiteley, Marvin
Debarbieux, Laurent
Lavigne, Rob
author_facet Chevallereau, Anne
Blasdel, Bob G.
De Smet, Jeroen
Monot, Marc
Zimmermann, Michael
Kogadeeva, Maria
Sauer, Uwe
Jorth, Peter
Whiteley, Marvin
Debarbieux, Laurent
Lavigne, Rob
author_sort Chevallereau, Anne
collection PubMed
description As interest in the therapeutic and biotechnological potentials of bacteriophages has grown, so has value in understanding their basic biology. However, detailed knowledge of infection cycles has been limited to a small number of model bacteriophages, mostly infecting Escherichia coli. We present here the first analysis coupling data obtained from global next-generation approaches, RNA-Sequencing and metabolomics, to characterize interactions between the virulent bacteriophage PAK_P3 and its host Pseudomonas aeruginosa. We detected a dramatic global depletion of bacterial transcripts coupled with their replacement by viral RNAs over the course of infection, eventually leading to drastic changes in pyrimidine metabolism. This process relies on host machinery hijacking as suggested by the strong up-regulation of one bacterial operon involved in RNA processing. Moreover, we found that RNA-based regulation plays a central role in PAK_P3 lifecycle as antisense transcripts are produced mainly during the early stage of infection and viral small non coding RNAs are massively expressed at the end of infection. This work highlights the prominent role of RNA metabolism in the infection strategy of a bacteriophage belonging to a new characterized sub-family of viruses with promising therapeutic potential.
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spelling pubmed-49333902016-07-18 Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa Chevallereau, Anne Blasdel, Bob G. De Smet, Jeroen Monot, Marc Zimmermann, Michael Kogadeeva, Maria Sauer, Uwe Jorth, Peter Whiteley, Marvin Debarbieux, Laurent Lavigne, Rob PLoS Genet Research Article As interest in the therapeutic and biotechnological potentials of bacteriophages has grown, so has value in understanding their basic biology. However, detailed knowledge of infection cycles has been limited to a small number of model bacteriophages, mostly infecting Escherichia coli. We present here the first analysis coupling data obtained from global next-generation approaches, RNA-Sequencing and metabolomics, to characterize interactions between the virulent bacteriophage PAK_P3 and its host Pseudomonas aeruginosa. We detected a dramatic global depletion of bacterial transcripts coupled with their replacement by viral RNAs over the course of infection, eventually leading to drastic changes in pyrimidine metabolism. This process relies on host machinery hijacking as suggested by the strong up-regulation of one bacterial operon involved in RNA processing. Moreover, we found that RNA-based regulation plays a central role in PAK_P3 lifecycle as antisense transcripts are produced mainly during the early stage of infection and viral small non coding RNAs are massively expressed at the end of infection. This work highlights the prominent role of RNA metabolism in the infection strategy of a bacteriophage belonging to a new characterized sub-family of viruses with promising therapeutic potential. Public Library of Science 2016-07-05 /pmc/articles/PMC4933390/ /pubmed/27380413 http://dx.doi.org/10.1371/journal.pgen.1006134 Text en © 2016 Chevallereau et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chevallereau, Anne
Blasdel, Bob G.
De Smet, Jeroen
Monot, Marc
Zimmermann, Michael
Kogadeeva, Maria
Sauer, Uwe
Jorth, Peter
Whiteley, Marvin
Debarbieux, Laurent
Lavigne, Rob
Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title_full Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title_fullStr Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title_full_unstemmed Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title_short Next-Generation “-omics” Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa
title_sort next-generation “-omics” approaches reveal a massive alteration of host rna metabolism during bacteriophage infection of pseudomonas aeruginosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933390/
https://www.ncbi.nlm.nih.gov/pubmed/27380413
http://dx.doi.org/10.1371/journal.pgen.1006134
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