Cargando…
Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus
The WalKR two-component system, controlling cell wall metabolism, is highly conserved among Bacilli and essential for cell viability. In Staphylococcus aureus, walR and walK are followed by three genes of unknown function: walH, walI and walJ. Sequence analysis and transcript mapping revealed a uniq...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4801191/ https://www.ncbi.nlm.nih.gov/pubmed/26999783 http://dx.doi.org/10.1371/journal.pone.0151449 |
_version_ | 1782422556899278848 |
---|---|
author | Poupel, Olivier Moyat, Mati Groizeleau, Julie Antunes, Luísa C. S. Gribaldo, Simonetta Msadek, Tarek Dubrac, Sarah |
author_facet | Poupel, Olivier Moyat, Mati Groizeleau, Julie Antunes, Luísa C. S. Gribaldo, Simonetta Msadek, Tarek Dubrac, Sarah |
author_sort | Poupel, Olivier |
collection | PubMed |
description | The WalKR two-component system, controlling cell wall metabolism, is highly conserved among Bacilli and essential for cell viability. In Staphylococcus aureus, walR and walK are followed by three genes of unknown function: walH, walI and walJ. Sequence analysis and transcript mapping revealed a unique genetic structure for this locus in S. aureus: the last gene of the locus, walJ, is transcribed independently, whereas transcription of the tetra-cistronic walRKHI operon occurred from two independent promoters located upstream from walR. Protein topology analysis and protein-protein interactions in E. coli as well as subcellular localization in S. aureus allowed us to show that WalH and WalI are membrane-bound proteins, which associate with WalK to form a complex at the cell division septum. While these interactions suggest that WalH and WalI play a role in activity of the WalKR regulatory pathway, deletion of walH and/or walI did not have a major effect on genes whose expression is strongly dependent on WalKR or on associated phenotypes. No effect of WalH or WalI was seen on tightly controlled WalKR regulon genes such as sle1 or saouhsc_00773, which encodes a CHAP-domain amidase. Of the genes encoding the two major S. aureus autolysins, AtlA and Sle1, only transcription of atlA was increased in the ΔwalH or ΔwalI mutants. Likewise, bacterial autolysis was not increased in the absence of WalH and/or WalI and biofilm formation was lowered rather than increased. Our results suggest that contrary to their major role as WalK inhibitors in B. subtilis, the WalH and WalI proteins have evolved a different function in S. aureus, where they are more accessory. A phylogenomic analysis shows a striking conservation of the 5 gene wal cluster along the evolutionary history of Bacilli, supporting the key importance of this signal transduction system, and indicating that the walH and walI genes were lost in the ancestor of Streptococcaceae, leading to their atypical 3 wal gene cluster, walRKJ. |
format | Online Article Text |
id | pubmed-4801191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48011912016-03-23 Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus Poupel, Olivier Moyat, Mati Groizeleau, Julie Antunes, Luísa C. S. Gribaldo, Simonetta Msadek, Tarek Dubrac, Sarah PLoS One Research Article The WalKR two-component system, controlling cell wall metabolism, is highly conserved among Bacilli and essential for cell viability. In Staphylococcus aureus, walR and walK are followed by three genes of unknown function: walH, walI and walJ. Sequence analysis and transcript mapping revealed a unique genetic structure for this locus in S. aureus: the last gene of the locus, walJ, is transcribed independently, whereas transcription of the tetra-cistronic walRKHI operon occurred from two independent promoters located upstream from walR. Protein topology analysis and protein-protein interactions in E. coli as well as subcellular localization in S. aureus allowed us to show that WalH and WalI are membrane-bound proteins, which associate with WalK to form a complex at the cell division septum. While these interactions suggest that WalH and WalI play a role in activity of the WalKR regulatory pathway, deletion of walH and/or walI did not have a major effect on genes whose expression is strongly dependent on WalKR or on associated phenotypes. No effect of WalH or WalI was seen on tightly controlled WalKR regulon genes such as sle1 or saouhsc_00773, which encodes a CHAP-domain amidase. Of the genes encoding the two major S. aureus autolysins, AtlA and Sle1, only transcription of atlA was increased in the ΔwalH or ΔwalI mutants. Likewise, bacterial autolysis was not increased in the absence of WalH and/or WalI and biofilm formation was lowered rather than increased. Our results suggest that contrary to their major role as WalK inhibitors in B. subtilis, the WalH and WalI proteins have evolved a different function in S. aureus, where they are more accessory. A phylogenomic analysis shows a striking conservation of the 5 gene wal cluster along the evolutionary history of Bacilli, supporting the key importance of this signal transduction system, and indicating that the walH and walI genes were lost in the ancestor of Streptococcaceae, leading to their atypical 3 wal gene cluster, walRKJ. Public Library of Science 2016-03-21 /pmc/articles/PMC4801191/ /pubmed/26999783 http://dx.doi.org/10.1371/journal.pone.0151449 Text en © 2016 Poupel 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Poupel, Olivier Moyat, Mati Groizeleau, Julie Antunes, Luísa C. S. Gribaldo, Simonetta Msadek, Tarek Dubrac, Sarah Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title | Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title_full | Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title_fullStr | Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title_full_unstemmed | Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title_short | Transcriptional Analysis and Subcellular Protein Localization Reveal Specific Features of the Essential WalKR System in Staphylococcus aureus |
title_sort | transcriptional analysis and subcellular protein localization reveal specific features of the essential walkr system in staphylococcus aureus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4801191/ https://www.ncbi.nlm.nih.gov/pubmed/26999783 http://dx.doi.org/10.1371/journal.pone.0151449 |
work_keys_str_mv | AT poupelolivier transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT moyatmati transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT groizeleaujulie transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT antunesluisacs transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT gribaldosimonetta transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT msadektarek transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus AT dubracsarah transcriptionalanalysisandsubcellularproteinlocalizationrevealspecificfeaturesoftheessentialwalkrsysteminstaphylococcusaureus |