Abstract

The Congo red derivative (E,E)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy) styrylbenzene (FSB) specifically stains the functional amyloid curli in Escherichia coli biofilms. FSB binds to curli with similar affinity as Congo red, yet exhibits much greater fluorescence upon binding to curli as compared to Congo red and does not exhibit undesired binding to the cellulosic component of the biofilm. Thus, FSB presents a powerful tool to identify and visualize curli in E. coli biofilms and also enables new biophysical investigations of curli.

Highlights

  • Bacteria are able to colonize an astonishing range of environments

  • Curli production is prevalent among uropathogenic E. coli (UPEC) clinical isolates, the major causative agent of urinary tract infections including acute and chronic and recurrent infections [14]

  • Congo red (CR) exhibits a red-shift in absorbance and fluorescence when bound to amyloid fibers

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Summary

Introduction

Bacteria tend to associate with surfaces which improves their access to nutritive, protective, or otherwise beneficial environments [1] To this end, bacteria employ a range of cellsurface fibers, adhesins, and receptors to interact with their environments [2,3,4,5,6,7]. Bacteria employ a range of cellsurface fibers, adhesins, and receptors to interact with their environments [2,3,4,5,6,7] As one of their adhesive strategies, many bacterial species can produce cell surface-associated amyloid fibers, which have a variety of functions including cell adhesion, biofilm formation, and virulence [2,6,7,8,9,10,11,12]. Curli and phosphoethanolamine-modified cellulose, compose the insoluble UTI89 extracellular matrix in an approximate 6:1 mass ratio [17,18]

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