Abstract
The development of new approaches for the treatment of antimicrobial-resistant infections is an urgent public health priority. The Pseudomonas aeruginosa pathogen, in particular, is a leading source of infection in hospital settings, with few available treatment options. In the context of an effort to develop antivirulence strategies to combat bacterial infection, we identified a series of highly effective small molecules that inhibit the production of pyocyanin, a redox-active virulence factor produced by P. aeruginosa. Interestingly, these new antagonists appear to suppress P. aeruginosa virulence factor production through a pathway that is independent of LasR and RhlR.
Original language | English (US) |
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Pages (from-to) | 1298-1306 |
Number of pages | 9 |
Journal | Journal of Medicinal Chemistry |
Volume | 58 |
Issue number | 3 |
DOIs | |
State | Published - Feb 12 2015 |
All Science Journal Classification (ASJC) codes
- Drug Discovery
- Molecular Medicine