Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.

Clostridium difficile is an emergent pathogen, and the most common cause of nosocomial diarrhea. In an effort to understand the role of small noncoding RNAs (sRNAs) in C. difficile physiology and pathogenesis, we used an in silico approach to identify 511 sRNA candidates in both intergenic and codin...

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Main Authors: Olga A Soutourina, Marc Monot, Pierre Boudry, Laure Saujet, Christophe Pichon, Odile Sismeiro, Ekaterina Semenova, Konstantin Severinov, Chantal Le Bouguenec, Jean-Yves Coppée, Bruno Dupuy, Isabelle Martin-Verstraete
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-05-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3649979?pdf=render
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spelling doaj-3f27bf2d17064afd9ec7a0971bce56142020-11-25T00:02:54ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-05-0195e100349310.1371/journal.pgen.1003493Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.Olga A SoutourinaMarc MonotPierre BoudryLaure SaujetChristophe PichonOdile SismeiroEkaterina SemenovaKonstantin SeverinovChantal Le BouguenecJean-Yves CoppéeBruno DupuyIsabelle Martin-VerstraeteClostridium difficile is an emergent pathogen, and the most common cause of nosocomial diarrhea. In an effort to understand the role of small noncoding RNAs (sRNAs) in C. difficile physiology and pathogenesis, we used an in silico approach to identify 511 sRNA candidates in both intergenic and coding regions. In parallel, RNA-seq and differential 5'-end RNA-seq were used for global identification of C. difficile sRNAs and their transcriptional start sites at three different growth conditions (exponential growth phase, stationary phase, and starvation). This global experimental approach identified 251 putative regulatory sRNAs including 94 potential trans riboregulators located in intergenic regions, 91 cis-antisense RNAs, and 66 riboswitches. Expression of 35 sRNAs was confirmed by gene-specific experimental approaches. Some sRNAs, including an antisense RNA that may be involved in control of C. difficile autolytic activity, showed growth phase-dependent expression profiles. Expression of each of 16 predicted c-di-GMP-responsive riboswitches was observed, and experimental evidence for their regulatory role in coordinated control of motility and biofilm formation was obtained. Finally, we detected abundant sRNAs encoded by multiple C. difficile CRISPR loci. These RNAs may be important for C. difficile survival in bacteriophage-rich gut communities. Altogether, this first experimental genome-wide identification of C. difficile sRNAs provides a firm basis for future RNome characterization and identification of molecular mechanisms of sRNA-based regulation of gene expression in this emergent enteropathogen.http://europepmc.org/articles/PMC3649979?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Olga A Soutourina
Marc Monot
Pierre Boudry
Laure Saujet
Christophe Pichon
Odile Sismeiro
Ekaterina Semenova
Konstantin Severinov
Chantal Le Bouguenec
Jean-Yves Coppée
Bruno Dupuy
Isabelle Martin-Verstraete
spellingShingle Olga A Soutourina
Marc Monot
Pierre Boudry
Laure Saujet
Christophe Pichon
Odile Sismeiro
Ekaterina Semenova
Konstantin Severinov
Chantal Le Bouguenec
Jean-Yves Coppée
Bruno Dupuy
Isabelle Martin-Verstraete
Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
PLoS Genetics
author_facet Olga A Soutourina
Marc Monot
Pierre Boudry
Laure Saujet
Christophe Pichon
Odile Sismeiro
Ekaterina Semenova
Konstantin Severinov
Chantal Le Bouguenec
Jean-Yves Coppée
Bruno Dupuy
Isabelle Martin-Verstraete
author_sort Olga A Soutourina
title Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
title_short Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
title_full Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
title_fullStr Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
title_full_unstemmed Genome-wide identification of regulatory RNAs in the human pathogen Clostridium difficile.
title_sort genome-wide identification of regulatory rnas in the human pathogen clostridium difficile.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2013-05-01
description Clostridium difficile is an emergent pathogen, and the most common cause of nosocomial diarrhea. In an effort to understand the role of small noncoding RNAs (sRNAs) in C. difficile physiology and pathogenesis, we used an in silico approach to identify 511 sRNA candidates in both intergenic and coding regions. In parallel, RNA-seq and differential 5'-end RNA-seq were used for global identification of C. difficile sRNAs and their transcriptional start sites at three different growth conditions (exponential growth phase, stationary phase, and starvation). This global experimental approach identified 251 putative regulatory sRNAs including 94 potential trans riboregulators located in intergenic regions, 91 cis-antisense RNAs, and 66 riboswitches. Expression of 35 sRNAs was confirmed by gene-specific experimental approaches. Some sRNAs, including an antisense RNA that may be involved in control of C. difficile autolytic activity, showed growth phase-dependent expression profiles. Expression of each of 16 predicted c-di-GMP-responsive riboswitches was observed, and experimental evidence for their regulatory role in coordinated control of motility and biofilm formation was obtained. Finally, we detected abundant sRNAs encoded by multiple C. difficile CRISPR loci. These RNAs may be important for C. difficile survival in bacteriophage-rich gut communities. Altogether, this first experimental genome-wide identification of C. difficile sRNAs provides a firm basis for future RNome characterization and identification of molecular mechanisms of sRNA-based regulation of gene expression in this emergent enteropathogen.
url http://europepmc.org/articles/PMC3649979?pdf=render
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