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The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity

BACKGROUND: Type VII protein secretion (T7SS) is a specialised system for excreting extracellular proteins across bacterial cell membranes and has been associated with virulence in Staphylococcus aureus. The genetic diversity of the ess locus, which encodes the T7SS, and the functions of proteins en...

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Autores principales: Warne, Ben, Harkins, Catriona P., Harris, Simon R., Vatsiou, Alexandra, Stanley-Wall, Nicola, Parkhill, Julian, Peacock, Sharon J., Palmer, Tracy, Holden, Matthew T. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4788903/
https://www.ncbi.nlm.nih.gov/pubmed/26969225
http://dx.doi.org/10.1186/s12864-016-2426-7
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author Warne, Ben
Harkins, Catriona P.
Harris, Simon R.
Vatsiou, Alexandra
Stanley-Wall, Nicola
Parkhill, Julian
Peacock, Sharon J.
Palmer, Tracy
Holden, Matthew T. G.
author_facet Warne, Ben
Harkins, Catriona P.
Harris, Simon R.
Vatsiou, Alexandra
Stanley-Wall, Nicola
Parkhill, Julian
Peacock, Sharon J.
Palmer, Tracy
Holden, Matthew T. G.
author_sort Warne, Ben
collection PubMed
description BACKGROUND: Type VII protein secretion (T7SS) is a specialised system for excreting extracellular proteins across bacterial cell membranes and has been associated with virulence in Staphylococcus aureus. The genetic diversity of the ess locus, which encodes the T7SS, and the functions of proteins encoded within it are poorly understood. RESULTS: We used whole genome sequence data from 153 isolates representative of the diversity of the species to investigate the genetic variability of T7SS across S. aureus. The ess loci were found to comprise of four distinct modules based on gene content and relative conservation. Modules 1 and 4, comprising of the 5’ and 3’ modules of the ess locus, contained the most conserved clusters of genes across the species. Module 1 contained genes encoding the secreted protein EsxA, and the EsaAB and EssAB components of the T7SS machinery, and Module 4 contained two functionally uncharacterized conserved membrane proteins. Across the species four variants of Module 2 were identified containing the essC gene, each of which was associated with a specific group of downstream genes. The most diverse module of the ess locus was Module 3 comprising a highly variable arrangement of hypothetical proteins. RNA-Seq was performed on representatives of the four Module 2 variants and demonstrated strain-specific differences in the levels of transcription in the conserved Module 1 components and transcriptional linkage Module 2, and provided evidence of the expression of genes the variable regions of the ess loci. CONCLUSIONS: The ess locus of S. aureus exhibits modularity and organisational variation across the species and transcriptional variation. In silico analysis of ess loci encoded hypothetical proteins identified potential novel secreted substrates for the T7SS. The considerable variety in operon arrangement between otherwise closely related isolates provides strong evidence for recombination at this locus. Comparison of these recombination regions with each other, and with the genomes of other Staphylococcal species, failed to identify evidence of intra- and inter-species recombination, however the analysis identified a novel T7SS in another pathogenic staphylococci, Staphylococcus lugdunensis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2426-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-47889032016-03-13 The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity Warne, Ben Harkins, Catriona P. Harris, Simon R. Vatsiou, Alexandra Stanley-Wall, Nicola Parkhill, Julian Peacock, Sharon J. Palmer, Tracy Holden, Matthew T. G. BMC Genomics Research Article BACKGROUND: Type VII protein secretion (T7SS) is a specialised system for excreting extracellular proteins across bacterial cell membranes and has been associated with virulence in Staphylococcus aureus. The genetic diversity of the ess locus, which encodes the T7SS, and the functions of proteins encoded within it are poorly understood. RESULTS: We used whole genome sequence data from 153 isolates representative of the diversity of the species to investigate the genetic variability of T7SS across S. aureus. The ess loci were found to comprise of four distinct modules based on gene content and relative conservation. Modules 1 and 4, comprising of the 5’ and 3’ modules of the ess locus, contained the most conserved clusters of genes across the species. Module 1 contained genes encoding the secreted protein EsxA, and the EsaAB and EssAB components of the T7SS machinery, and Module 4 contained two functionally uncharacterized conserved membrane proteins. Across the species four variants of Module 2 were identified containing the essC gene, each of which was associated with a specific group of downstream genes. The most diverse module of the ess locus was Module 3 comprising a highly variable arrangement of hypothetical proteins. RNA-Seq was performed on representatives of the four Module 2 variants and demonstrated strain-specific differences in the levels of transcription in the conserved Module 1 components and transcriptional linkage Module 2, and provided evidence of the expression of genes the variable regions of the ess loci. CONCLUSIONS: The ess locus of S. aureus exhibits modularity and organisational variation across the species and transcriptional variation. In silico analysis of ess loci encoded hypothetical proteins identified potential novel secreted substrates for the T7SS. The considerable variety in operon arrangement between otherwise closely related isolates provides strong evidence for recombination at this locus. Comparison of these recombination regions with each other, and with the genomes of other Staphylococcal species, failed to identify evidence of intra- and inter-species recombination, however the analysis identified a novel T7SS in another pathogenic staphylococci, Staphylococcus lugdunensis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2426-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-11 /pmc/articles/PMC4788903/ /pubmed/26969225 http://dx.doi.org/10.1186/s12864-016-2426-7 Text en © Warne et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Warne, Ben
Harkins, Catriona P.
Harris, Simon R.
Vatsiou, Alexandra
Stanley-Wall, Nicola
Parkhill, Julian
Peacock, Sharon J.
Palmer, Tracy
Holden, Matthew T. G.
The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title_full The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title_fullStr The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title_full_unstemmed The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title_short The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity
title_sort ess/type vii secretion system of staphylococcus aureus shows unexpected genetic diversity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4788903/
https://www.ncbi.nlm.nih.gov/pubmed/26969225
http://dx.doi.org/10.1186/s12864-016-2426-7
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