We are developing chemical tools that attenuate cell-cell communication pathways in bacteria. Many bacteria communicate using small organic molecules and peptides to monitor their population densities in a process called 'quorum sensing.' At high cell densities, bacteria use this signaling network to switch from an isolated, nomadic existence to that of a multicellular community. This lifestyle switch is significant; only in groups will pathogenic bacteria turn on virulence pathways and grow into drug-impervious communities called biofilms that are the basis of myriad chronic infections. In turn, certain symbiotic bacteria will only colonize their hosts and initiate beneficial behaviors at high population densities. The molecular mechanisms of these processes are only now being delineated. Our research is broadly focused on the design of non-native ligands that can intercept quorum sensing and provide new insights into its role in host/microbe interactions. We have developed a series of efficient synthetic methods that provide us straightforward access to these ligands. In addition, we have applied both quorum sensing antagonists and agonists in vitro and in vivo to investigate quorum sensing as an anti-infective target. This talk will introduce our research approach and highlight recent results

Synthetic ligands for the interception of quorum sensing in bacterial pathogens and symbionts

247th National Meeting (2014)

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