Pilicides regulate pili expression in E. coli without affecting the functional properties of the pilus rod

Mol Biosyst. 2007 Mar;3(3):214-8. doi: 10.1039/b613441f. Epub 2007 Jan 19.

Abstract

The infectious ability of uropathogenic Escherichia coli relies on adhesive fibers, termed pili or fimbriae, that are expressed on the bacterial surface. Pili are multi-protein structures that are formed via a highly preserved assembly and secretion system called the chaperone-usher pathway. We have earlier reported that small synthetic compounds, referred to as pilicides, disrupt both type 1 and P pilus biogenesis in E. coli. In this study, we show that the pilicides do not affect the structure, dynamics or function of the pilus rod. This was demonstrated by first suppressing the expression of P pili in E. coli by pilicide treatment and, next, measuring the biophysical properties of the pilus rod. The reduced abundance of pili was assessed with hemagglutination, atomic force microscopy and Western immunoblot analysis. The biodynamic properties of the pili fibers were determined by optical tweezers force measurements on individual pili and were found to be intact. The presented results establish a potential use of pilicides as chemical tools to study important biological processes e.g. adhesion, pilus biogenesis and the role of pili in infections and biofilm formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Blotting, Western
  • Dose-Response Relationship, Drug
  • Escherichia coli / drug effects*
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism
  • Escherichia coli Proteins / metabolism
  • Fimbriae Proteins / metabolism
  • Fimbriae, Bacterial / chemistry
  • Fimbriae, Bacterial / drug effects*
  • Fimbriae, Bacterial / physiology
  • Microscopy, Atomic Force
  • Models, Biological
  • Molecular Chaperones / metabolism
  • Molecular Structure
  • Naphthalenes / chemistry
  • Naphthalenes / pharmacology*
  • Optical Tweezers
  • Periplasmic Proteins / metabolism
  • Porins / metabolism
  • Thiazoles / chemistry
  • Thiazoles / pharmacology*

Substances

  • Anti-Bacterial Agents
  • AtpA protein, E coli
  • Escherichia coli Proteins
  • Molecular Chaperones
  • Naphthalenes
  • PapD protein, E coli
  • Periplasmic Proteins
  • Porins
  • Thiazoles
  • atpG protein, E coli
  • Fimbriae Proteins