Abstract

Curli amyloid fibers are the major protein component of the extracellular matrix produced by Enterobacteriaceae during biofilm formation. Curli are required for proper biofilm development and environmental persistence by Escherichia coli. Here, we present a complete and vetted genetic analysis of functional amyloid fiber biogenesis. The Keio collection of single gene deletions was screened on Congo red indicator plates to identify E. coli mutants that had defective amyloid production. We discovered that more than three hundred gene products modulated curli production. These genes were involved in fundamental cellular processes such as regulation, environmental sensing, respiration, metabolism, cell envelope biogenesis, transport, and protein turnover. The alternative sigma factors, σS and σE, had opposing roles in curli production. Mutations that induced the σE or Cpx stress response systems had reduced curli production, while mutant strains with increased σS levels had increased curli production. Mutations in metabolic pathways, including gluconeogenesis and the biosynthesis of lipopolysaccharide (LPS), produced less curli. Regulation of the master biofilm regulator, CsgD, was diverse, and the screen revealed several proteins and small RNAs (sRNA) that regulate csgD messenger RNA (mRNA) levels. Using previously published studies, we found minimal overlap between the genes affecting curli biogenesis and genes known to impact swimming or swarming motility, underlying the distinction between motile and sessile lifestyles. Collectively, the diversity and number of elements required suggest curli production is part of a highly regulated and complex developmental pathway in E. coli.

Highlights

  • Curli are thin aggregative fimbriae produced by many Enterobacteriaceae including Escherichia coli and Salmonella typhimurium [1,2]

  • The Keio collection consists of 3985 nonessential gene mutants comprising more than 90% of the 4390 open reading frames of E. coli K-12 [40]

  • Following growth in conditions that favor curli production (26 ◦ C for 48 h), strains with changes in Congo red (CR) phenotypes were isolated and scored according to their color, which varied from the white color of csgA to the darker red of cpxR (Figure 1B)

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Summary

Introduction

Curli are thin aggregative fimbriae produced by many Enterobacteriaceae including Escherichia coli and Salmonella typhimurium [1,2]. As the major protein component of the extracellular matrix, curli are associated with biofilm development [3]. Curli fibers have been implicated in pathogenesis and aid in host cell adhesion, invasion, and immune system activation [12,13,14]. Curli fibers are the product of a dedicated and highly regulated assembly system encoded by curli specific genes (csg), which are arranged on two divergent operons csgDEFG and csgBAC [15,16,17]. Found primarily in the genomes of Enterobacteriaceae, csg genes are present in other

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