Mapping pilicide anti-virulence effect in Escherichia coli, a comprehensive structure-activity study

Erik Chorell, Jerome S. Pinkner, Christoffer Bengtsson, Thomas Sainte Luce Banchelin, Sofie Edvinsson, Anna Linusson, Scott J. Hultgren, Fredrik Almqvist

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Pilicides prevent pili formation and thereby the development of bacterial biofilms in Escherichia coli. We have performed a comprehensive structure activity relationship (SAR) study of the dihydrothiazolo ring-fused 2-pyridone pilicide central fragment by varying all open positions. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to distinguish active from inactive compounds in which polarity proved to be the most important factor for discrimination. A quantitative SAR (QSAR) partial least squares (PLS) model was calculated on the active compounds for prediction of biofilm inhibition activity. In this model, compounds with high inhibitory activity were generally larger, more lipophilic, more flexible and had a lower HOMO. Overall, this resulted in both highly valuable SAR information and potent inhibitors of type 1 pili dependent biofilm formation. The most potent biofilm inhibitor had an EC 50 of 400 nM.

Original languageEnglish
Pages (from-to)3128-3142
Number of pages15
JournalBioorganic and Medicinal Chemistry
Volume20
Issue number9
DOIs
StatePublished - May 1 2012

Keywords

  • 2-Pyridone
  • Antivirulence
  • Biofilm inhibitor
  • Peptidomimetic
  • Pilicide
  • Structure-activity

Fingerprint

Dive into the research topics of 'Mapping pilicide anti-virulence effect in Escherichia coli, a comprehensive structure-activity study'. Together they form a unique fingerprint.

Cite this