The Ess-Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversityReportar como inadecuado


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


The Ess-Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Publication Date: 2016-03-11

Journal Title: BMC Genomics

Publisher: BioMed Central

Volume: 17

Number: 222

Language: English

Type: Article

Metadata: Show full item record

Citation: Warne, B., Harkins, C. P., Harris, S. R., Vatsiou, A., Stanley-Wall, N., Parkhill, J., Peacock, S. J., et al. (2016). The Ess/Type VII secretion system of Staphylococcus aureus shows unexpected genetic diversity. BMC Genomics, 17 (222)

Description: This is the final version of the article. It first appeared from BioMed Central via http://dx.doi.org/10.1186/s12864-016-2426-7

Abstract: 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.

Keywords: Staphylococcus aureus, secretion, Type VII

Sponsorship: We thank the core sequencing and informatics teams at the Sanger Institute for their assistance and The Wellcome Trust for its support of the Sanger Institute Pathogen Genomics and Biology groups. SRH, JP and MTGH were supported by Wellcome Trust grant 098051. Bioinformatics and Computational Biology analyses were supported by the University of St Andrews Bioinformatics Unit that is funded by a Wellcome Trust ISSF award (grant 105621/Z/14/Z). SP is funded by the UKCRC Translational Infection Research Initiative, and the NIHR Cambridge Biomedical Research Centre. CPH is supported by the Wellcome Trust (grant number 104241/z/14/z) TP is a Royal Society/Wolfson Merit Award Holder. We thank Drs James Chalmers and Holger Kneuper for helpful discussion, and acknowledge Dr Holger Kneuper’s assistance in preparing Fig. 2.

Identifiers:

This record's URL: http://dx.doi.org/10.1186/s12864-016-2426-7https://www.repository.cam.ac.uk/handle/1810/255081

Rights: Attribution 2.0 UK: England & Wales

Licence URL: http://creativecommons.org/licenses/by/2.0/uk/





Autor: Warne, BenHarkins, Catriona P.Harris, Simon R.Vatsiou, AlexandraStanley-Wall, NicolaParkhill, JulianPeacock, Sharon J.Palmer, Trac

Fuente: https://www.repository.cam.ac.uk/handle/1810/255081



DESCARGAR PDF




Documentos relacionados