scholarly journals Investigation of the Staphylococcus aureus GraSR Regulon Reveals Novel Links to Virulence, Stress Response and Cell Wall Signal Transduction Pathways

PLoS ONE ◽  
2011 ◽  
Vol 6 (7) ◽  
pp. e21323 ◽  
Author(s):  
Mélanie Falord ◽  
Ulrike Mäder ◽  
Aurélia Hiron ◽  
Michel Débarbouillé ◽  
Tarek Msadek
2006 ◽  
Vol 50 (10) ◽  
pp. 3424-3434 ◽  
Author(s):  
S. Gardete ◽  
S. W. Wu ◽  
S. Gill ◽  
A. Tomasz

ABSTRACT Exposure of Staphylococcus aureus to cell wall inhibitors induces massive overexpression of a number of genes, provided that the VraSR two-component sensory regulatory system is intact. Inactivation of vraS blocks this transcriptional response and also causes a drastic reduction in the levels of resistance to beta-lactam antibiotics and vancomycin. We used an experimental system in which the essential cell wall synthesis gene of S. aureus, pbpB, was put under the control of an isopropyl-β-d-thiogalactopyranoside-inducible promoter in order to induce reversible perturbations in cell wall synthesis without the use of any cell wall-active inhibitor. Changes in the level of transcription of pbpB were rapidly followed by parallel changes in the vraSR signal, and the abundance of the pbpB transcript was precisely mirrored by the abundance of the transcripts of vraSR and some additional genes that belong to the VraSR regulon. Beta-lactam resistance in S. aureus appears to involve a complex stress response in which VraSR performs the critical role of a sentinel system capable of sensing the perturbation of cell wall synthesis and allowing mobilization of genes that are essential for the generation of a highly resistant phenotype. One of the sites in cell wall synthesis “sensed” by the VraSR system appears to be a step catalyzed by PBP 2.


2008 ◽  
Vol 8 (1) ◽  
pp. 186 ◽  
Author(s):  
Peter Sass ◽  
Andrea Jansen ◽  
Christiane Szekat ◽  
Vera Sass ◽  
Hans-Georg Sahl ◽  
...  

2012 ◽  
Vol 333 (2) ◽  
pp. 109-120 ◽  
Author(s):  
Vanina Dengler ◽  
Patricia Stutzmann Meier ◽  
Ronald Heusser ◽  
Peter Kupferschmied ◽  
Judit Fazekas ◽  
...  

2001 ◽  
Vol 39 (1) ◽  
pp. 87-100 ◽  
Author(s):  
F. Navarro-García ◽  
B. Eisman ◽  
E. Román ◽  
C. Nombela ◽  
J. Pla

2004 ◽  
Vol 48 (8) ◽  
pp. 3057-3063 ◽  
Author(s):  
Roger Pechous ◽  
Nagender Ledala ◽  
Brian J. Wilkinson ◽  
Radheshyam K. Jayaswal

ABSTRACT Genome-wide transcriptional profiling studies of the response of Staphylococcus aureus to cell wall-active antibiotics have led to the discovery of a cell wall stress stimulon of genes induced by these agents. msrA1, encoding methionine sulfoxide reductase, is a highly induced member gene of this stimulon. In the present study we show that msrA1 induction by oxacillin is common to all methicillin-susceptible strains studied but did not occur in two homogeneous and two heterogeneous methicillin-resistant strains. However, msrA1 was induced by vancomycin and/or d-cycloserine in methicillin-resistant strains. Lysozyme and lysostaphin treatment did not induce msrA1 expression. Oxacillin-induced msrA1 expression was enhanced by ca. 30% in a SigB+ derivative (SH1000) of the SigB-defective RN450 (NCTC 8325-4) strain. msrA1 expression was not affected in mutants in the global regulatory systems agr and sar. Glycerol monolaurate, an inhibitor of signal transduction, inhibited the oxacillin-induced transcription of msrA1 and other cell wall stress stimulon member genes, vraS and dnaK. These observations suggest that the cell wall stress stimulon is induced by inhibition of the process of peptidoglycan biosynthesis, and the inhibitory effects of glycerol monolaurate indicate that gene expression is dependent on a signal transduction pathway.


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