Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin

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作者
Nada M. Nass
Sannia Farooque
Charlotte Hind
Matthew E. Wand
Christopher P. Randall
J. Mark Sutton
Ryan F. Seipke
Christopher M. Rayner
Alex J. O’Neill
机构
[1] Antimicrobial Research Centre and School of Molecular and Cellular Biology,
[2] Faculty of Biological Sciences,undefined
[3] University of Leeds,undefined
[4] School of Chemistry,undefined
[5] University of Leeds,undefined
[6] Public Health England,undefined
[7] National Infection Service,undefined
[8] Porton Down,undefined
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Of the thousands of natural product antibiotics discovered to date, only a handful have been developed for the treatment of bacterial infection. The clinically unexploited majority likely include compounds with untapped potential as antibacterial drugs, and in view of the ever-growing unmet medical need for such agents, warrant systematic re-evaluation. Here we revisit the actinorhodins, a class that was first reported 70 years ago, but which remains poorly characterized. We show that γ-actinorhodin possesses many of the requisite properties of an antibacterial drug, displaying potent and selective bactericidal activity against key Gram-positive pathogens (including Staphylococcus aureus and enterococci), a mode of action distinct from that of other agents in clinical use, an extremely low potential for the development of resistance, and a degree of in vivo efficacy in an invertebrate model of infection. Our findings underscore the utility of revisiting unexploited antibiotics as a source of novel antibacterial drug candidates.
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