| Literature DB >> 18719281 |
David A Rasko1, Cristiano G Moreira, De Run Li, Nicola C Reading, Jennifer M Ritchie, Matthew K Waldor, Noelle Williams, Ron Taussig, Shuguang Wei, Michael Roth, David T Hughes, Jason F Huntley, Maggy W Fina, John R Falck, Vanessa Sperandio.
Abstract
Many bacterial pathogens rely on a conserved membrane histidine sensor kinase, QseC, to respond to host adrenergic signaling molecules and bacterial signals in order to promote the expression of virulence factors. Using a high-throughput screen, we identified a small molecule, LED209, that inhibits the binding of signals to QseC, preventing its autophosphorylation and consequently inhibiting QseC-mediated activation of virulence gene expression. LED209 is not toxic and does not inhibit pathogen growth; however, this compound markedly inhibits the virulence of several pathogens in vitro and in vivo in animals. Inhibition of signaling offers a strategy for the development of broad-spectrum antimicrobial drugs.Entities:
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Year: 2008 PMID: 18719281 PMCID: PMC2605406 DOI: 10.1126/science.1160354
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728