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Antimicrobial Agents and Chemotherapy, March 2008, p. 980-990, Vol. 52, No. 3
0066-4804/08/$08.00+0     doi:10.1128/AAC.01121-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Transcriptional Profiling Reveals that Daptomycin Induces the Staphylococcus aureus Cell Wall Stress Stimulon and Genes Responsive to Membrane Depolarization{triangledown} ,{dagger}

Arunachalam Muthaiyan,1 Jared A. Silverman,2 Radheshyam K. Jayaswal,1 and Brian J. Wilkinson1*

Microbiology Group, Department of Biological Sciences, Illinois State University, Normal, Illinois 61790-4120,1 Cubist Pharmaceuticals, Inc., Lexington, Massachusetts 024212

Received 24 August 2007/ Returned for modification 21 October 2007/ Accepted 5 December 2007

Daptomycin is a lipopeptide antibiotic that has recently been approved for treatment of gram-positive bacterial infections. The mode of action of daptomycin is not yet entirely clear. To further understand the mechanism transcriptomic analysis of changes in gene expression in daptomycin-treated Staphylococcus aureus was carried out. The expression profile indicated that cell wall stress stimulon member genes (B. J. Wilkinson, A. Muthaiyan, and R. K. Jayaswal, Curr. Med. Chem. Anti-Infect. Agents 4:259-276, 2005) were significantly induced by daptomycin and by the cell wall-active antibiotics vancomycin and oxacillin. Comparison of the daptomycin response of a two-component cell wall stress stimulon regulator VraSR mutant, S. aureus KVR, to its parent N315 showed diminished expression of the cell wall stress stimulon in the mutant. Daptomycin has been proposed to cause membrane depolarization, and the transcriptional responses to carbonyl cyanide m-chlorophenylhydrazone (CCCP) and nisin were determined. Transcriptional profiles of the responses to these antimicrobial agents showed significantly different patterns compared to those of the cell wall-active antibiotics, including little or no induction of the cell wall stress stimulon. However, there were a significant number of genes induced by both CCCP and daptomycin that were not induced by oxacillin or vancomycin, so the daptomycin transcriptome probably reflected a membrane depolarizing activity of this antimicrobial also. The results indicate that inhibition of peptidoglycan biosynthesis, either directly or indirectly, and membrane depolarization are parts of the mode of action of daptomycin.

* Corresponding author. Mailing address: Department of Biological Sciences, Illinois State University, Normal, IL 61790-4120. Phone: (303) 438-7244. Fax: (309) 438-3722. E-mail: bjwilkin{at}ilstu.edu

{triangledown} Published ahead of print on 17 December 2007.

{dagger} Supplemental material for this article may be found at http://aac.asm.org/.

Antimicrobial Agents and Chemotherapy, March 2008, p. 980-990, Vol. 52, No. 3
0066-4804/08/$08.00+0     doi:10.1128/AAC.01121-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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