Pseudomonas aeruginosa LasR·DNA Binding Is Directly Inhibited by Quorum Sensing Antagonists

• Published in: ACS infectious diseases Vol. 3; no. 3; pp. 183 - 189
• Main Authors: Suneby, Emma G, Herndon, Leslie R, Schneider, Tanya L
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 10.03.2017
• Subjects: Anti-Bacterial Agents - chemistry; Anti-Bacterial Agents - pharmacology; Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; DNA - metabolism; Gene Expression Regulation, Bacterial - drug effects; Protein Binding - drug effects; Pseudomonas aeruginosa - drug effects; Pseudomonas aeruginosa - metabolism; Quorum Sensing - drug effects; Small Molecule Libraries - chemistry; Small Molecule Libraries - pharmacology; Structure-Activity Relationship; Trans-Activators - chemistry; Trans-Activators - metabolism; Virulence - drug effects; LasR; transcription factor; Pseudomonas aeruginosa; quorum sensing; antivirulence
• ISSN: 2373-8227; 2373-8227
• DOI: 10.1021/acsinfecdis.6b00163

Inhibition of quorum sensing in Pseudomonas aeruginosa is of interest as a possible antivirulence strategy for this pathogenic bacterium. The LasR regulator protein is important in coordinating gene expression in response to quorum sensing signaling molecules. One predominant strategy for LasR inhibition is the development of small-molecule antagonists that mimic the native autoinducer, though the mechanism by which they inactivate LasR is not known. This work reveals that multiple antagonists function by binding to and stabilizing LasR in a conformation that renders it unable to bind DNA. Further analysis of purified LasR complexed with known antagonists indicates that DNA binding can be recovered with the addition of native autoinducer, providing insights into the reversibility of ligand binding for this transcription factor. This in vitro assay could be used to assess future promising antagonists and complements existing cell-based reporter assays.