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Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583

Small RNA molecules (sRNAs) are key mediators of virulence and stress inducible gene expressions in some pathogens. In this work we identify sRNAs in the Gram positive opportunistic pathogen Enterococcus faecalis. We characterized 11 sRNAs by tiling microarray analysis, 5′ and 3′ RACE-PCR, and North...

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Autores principales: Shioya, Kouki, Michaux, Charlotte, Kuenne, Carsten, Hain, Torsten, Verneuil, Nicolas, Budin-Verneuil, Aurélie, Hartsch, Thomas, Hartke, Axel, Giard, Jean-Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166299/
https://www.ncbi.nlm.nih.gov/pubmed/21912655
http://dx.doi.org/10.1371/journal.pone.0023948
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author Shioya, Kouki
Michaux, Charlotte
Kuenne, Carsten
Hain, Torsten
Verneuil, Nicolas
Budin-Verneuil, Aurélie
Hartsch, Thomas
Hartke, Axel
Giard, Jean-Christophe
author_facet Shioya, Kouki
Michaux, Charlotte
Kuenne, Carsten
Hain, Torsten
Verneuil, Nicolas
Budin-Verneuil, Aurélie
Hartsch, Thomas
Hartke, Axel
Giard, Jean-Christophe
author_sort Shioya, Kouki
collection PubMed
description Small RNA molecules (sRNAs) are key mediators of virulence and stress inducible gene expressions in some pathogens. In this work we identify sRNAs in the Gram positive opportunistic pathogen Enterococcus faecalis. We characterized 11 sRNAs by tiling microarray analysis, 5′ and 3′ RACE-PCR, and Northern blot analysis. Six sRNAs were specifically expressed at exponential phase, two sRNAs were observed at stationary phase, and three were detected during both phases. Searches of putative functions revealed that three of them (EFA0080_EFA0081 and EFB0062_EFB0063 on pTF1 and pTF2 plasmids, respectively, and EF0408_EF04092 located on the chromosome) are similar to antisense RNA involved in plasmid addiction modules. Moreover, EF1097_EF1098 shares strong homologies with tmRNA (bi-functional RNA acting as both a tRNA and an mRNA) and EF2205_EF2206 appears homologous to 4.5S RNA member of the Signal Recognition Particle (SRP) ribonucleoprotein complex. In addition, proteomic analysis of the ΔEF3314_EF3315 sRNA mutant suggests that it may be involved in the turnover of some abundant proteins. The expression patterns of these transcripts were evaluated by tiling array hybridizations performed with samples from cells grown under eleven different conditions some of which may be encountered during infection. Finally, distribution of these sRNAs among genome sequences of 54 E. faecalis strains was assessed. This is the first experimental genome-wide identification of sRNAs in E. faecalis and provides impetus to the understanding of gene regulation in this important human pathogen.
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spelling pubmed-31662992011-09-12 Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583 Shioya, Kouki Michaux, Charlotte Kuenne, Carsten Hain, Torsten Verneuil, Nicolas Budin-Verneuil, Aurélie Hartsch, Thomas Hartke, Axel Giard, Jean-Christophe PLoS One Research Article Small RNA molecules (sRNAs) are key mediators of virulence and stress inducible gene expressions in some pathogens. In this work we identify sRNAs in the Gram positive opportunistic pathogen Enterococcus faecalis. We characterized 11 sRNAs by tiling microarray analysis, 5′ and 3′ RACE-PCR, and Northern blot analysis. Six sRNAs were specifically expressed at exponential phase, two sRNAs were observed at stationary phase, and three were detected during both phases. Searches of putative functions revealed that three of them (EFA0080_EFA0081 and EFB0062_EFB0063 on pTF1 and pTF2 plasmids, respectively, and EF0408_EF04092 located on the chromosome) are similar to antisense RNA involved in plasmid addiction modules. Moreover, EF1097_EF1098 shares strong homologies with tmRNA (bi-functional RNA acting as both a tRNA and an mRNA) and EF2205_EF2206 appears homologous to 4.5S RNA member of the Signal Recognition Particle (SRP) ribonucleoprotein complex. In addition, proteomic analysis of the ΔEF3314_EF3315 sRNA mutant suggests that it may be involved in the turnover of some abundant proteins. The expression patterns of these transcripts were evaluated by tiling array hybridizations performed with samples from cells grown under eleven different conditions some of which may be encountered during infection. Finally, distribution of these sRNAs among genome sequences of 54 E. faecalis strains was assessed. This is the first experimental genome-wide identification of sRNAs in E. faecalis and provides impetus to the understanding of gene regulation in this important human pathogen. Public Library of Science 2011-09-02 /pmc/articles/PMC3166299/ /pubmed/21912655 http://dx.doi.org/10.1371/journal.pone.0023948 Text en Shioya 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shioya, Kouki
Michaux, Charlotte
Kuenne, Carsten
Hain, Torsten
Verneuil, Nicolas
Budin-Verneuil, Aurélie
Hartsch, Thomas
Hartke, Axel
Giard, Jean-Christophe
Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title_full Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title_fullStr Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title_full_unstemmed Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title_short Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
title_sort genome-wide identification of small rnas in the opportunistic pathogen enterococcus faecalis v583
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166299/
https://www.ncbi.nlm.nih.gov/pubmed/21912655
http://dx.doi.org/10.1371/journal.pone.0023948
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