Abstract
Novel antimicrobials and new approaches to developing them are urgently needed. Repurposing already-approved drugs with well-characterized toxicology and pharmacology is a novel way to reduce the time, cost, and risk associated with antibiotic innovation. Ebselen, an organoselenium compound, is known to be clinically safe and has a well-known pharmacology profile. It has shown potent bactericidal activity against multidrug-resistant clinical isolates of staphylococcus aureus, including methicillin- and vancomycin-resistant S. aureus (MRSA and VRSA). We demonstrated that ebselen acts through inhibition of protein synthesis and subsequently inhibited toxin production in MRSA. Additionally, ebselen was remarkably active and significantly reduced established staphylococcal biofilms. The therapeutic efficacy of ebselen was evaluated in a mouse model of staphylococcal skin infections. Ebselen 1% and 2% significantly reduced the bacterial load and the levels of the pro-inflammatory cytokines tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1 beta (IL-1β), and monocyte chemo attractant protein-1 (MCP-1) in MRSA USA300 skin lesions. Furthermore, it acts synergistically with traditional antimicrobials. This study provides evidence that ebselen has great potential for topical treatment of MRSA skin infections and lays the foundation for further analysis and development of ebselen as a potential treatment for multidrug-resistant staphylococcal infections.
Keywords
pathogens, drug development
Date of this Version
6-26-2015
DOI
10.1038/srep11596
Recommended Citation
Thangamani, Shankar; Younis, Waleed; and Seleem, Mohamed N., "Repurposing ebselen for Treatment of Multidrug-Resistant Staphylococcal Infections" (2015). Department of Comparative Pathobiology Faculty Publications. Paper 28.
http://dx.doi.org/10.1038/srep11596
Comments
This is the published PDF version of Thangamani, S., Younis, W., Seleem, M.N. (2015). Repurposing ebselen for Treatment of Multidrug-Resistant Staphylococcal Infections. Scientific Reports, 5, 1-13.http://dx.doi.org/10.1371/journal.pone.0130385.
CC-BY 4.0 International http://creativecommons.org/licenses/by/4.0/