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Global analysis of transcriptional regulators in Staphylococcus aureus

BACKGROUND: Staphylococcus aureus is a widely distributed human pathogen capable of infecting almost every ecological niche of the host. As a result, it is responsible for causing many different diseases. S. aureus has a vast array of virulence determinants whose expression is modulated by an intric...

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Autores principales: Ibarra, Jose Antonio, Pérez-Rueda, Ernesto, Carroll, Ronan K, Shaw, Lindsey N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616918/
https://www.ncbi.nlm.nih.gov/pubmed/23442205
http://dx.doi.org/10.1186/1471-2164-14-126
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author Ibarra, Jose Antonio
Pérez-Rueda, Ernesto
Carroll, Ronan K
Shaw, Lindsey N
author_facet Ibarra, Jose Antonio
Pérez-Rueda, Ernesto
Carroll, Ronan K
Shaw, Lindsey N
author_sort Ibarra, Jose Antonio
collection PubMed
description BACKGROUND: Staphylococcus aureus is a widely distributed human pathogen capable of infecting almost every ecological niche of the host. As a result, it is responsible for causing many different diseases. S. aureus has a vast array of virulence determinants whose expression is modulated by an intricate regulatory network, where transcriptional factors (TFs) are the primary elements. In this work, using diverse sequence analysis, we evaluated the repertoire of TFs and sigma factors in the community-associated methicillin resistant S. aureus (CA-MRSA) strain USA300-FPR3757. RESULTS: A total of 135 TFs and sigma factors were identified and classified into 36 regulatory families. From these around 43% have been experimentally characterized to date, which demonstrates the significant work still at hand to unravel the regulatory network in place for this important pathogen. A comparison of the TF repertoire of S. aureus against 1209 sequenced bacterial genomes was carried out allowing us to identify a core set of orthologous TFs for the Staphylococacceae, and also allowing us to assign potential functions to previously uncharacterized TFs. Finally, the USA300 TFs were compared to those in eleven other S. aureus strains including: Newman, COL, JH1, JH9, MW2, Mu3, Mu50, N315, RF122, MRSA252 and MSSA476. We identify conserved TFs among these strains and suggest possible regulatory interactions. CONCLUSIONS: The analysis presented herein highlights the complexity of regulatory networks in S. aureus strains, identifies key conserved TFs among the Staphylococacceae, and offers unique insights into several as yet uncharacterized TFs.
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spelling pubmed-36169182013-04-05 Global analysis of transcriptional regulators in Staphylococcus aureus Ibarra, Jose Antonio Pérez-Rueda, Ernesto Carroll, Ronan K Shaw, Lindsey N BMC Genomics Research Article BACKGROUND: Staphylococcus aureus is a widely distributed human pathogen capable of infecting almost every ecological niche of the host. As a result, it is responsible for causing many different diseases. S. aureus has a vast array of virulence determinants whose expression is modulated by an intricate regulatory network, where transcriptional factors (TFs) are the primary elements. In this work, using diverse sequence analysis, we evaluated the repertoire of TFs and sigma factors in the community-associated methicillin resistant S. aureus (CA-MRSA) strain USA300-FPR3757. RESULTS: A total of 135 TFs and sigma factors were identified and classified into 36 regulatory families. From these around 43% have been experimentally characterized to date, which demonstrates the significant work still at hand to unravel the regulatory network in place for this important pathogen. A comparison of the TF repertoire of S. aureus against 1209 sequenced bacterial genomes was carried out allowing us to identify a core set of orthologous TFs for the Staphylococacceae, and also allowing us to assign potential functions to previously uncharacterized TFs. Finally, the USA300 TFs were compared to those in eleven other S. aureus strains including: Newman, COL, JH1, JH9, MW2, Mu3, Mu50, N315, RF122, MRSA252 and MSSA476. We identify conserved TFs among these strains and suggest possible regulatory interactions. CONCLUSIONS: The analysis presented herein highlights the complexity of regulatory networks in S. aureus strains, identifies key conserved TFs among the Staphylococacceae, and offers unique insights into several as yet uncharacterized TFs. BioMed Central 2013-02-26 /pmc/articles/PMC3616918/ /pubmed/23442205 http://dx.doi.org/10.1186/1471-2164-14-126 Text en Copyright © 2013 Ibarra et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ibarra, Jose Antonio
Pérez-Rueda, Ernesto
Carroll, Ronan K
Shaw, Lindsey N
Global analysis of transcriptional regulators in Staphylococcus aureus
title Global analysis of transcriptional regulators in Staphylococcus aureus
title_full Global analysis of transcriptional regulators in Staphylococcus aureus
title_fullStr Global analysis of transcriptional regulators in Staphylococcus aureus
title_full_unstemmed Global analysis of transcriptional regulators in Staphylococcus aureus
title_short Global analysis of transcriptional regulators in Staphylococcus aureus
title_sort global analysis of transcriptional regulators in staphylococcus aureus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616918/
https://www.ncbi.nlm.nih.gov/pubmed/23442205
http://dx.doi.org/10.1186/1471-2164-14-126
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