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Updated: Aug 8, 2026

Bile Salt-induced Biofilm Formation in Enteric Pathogens: Techniques for Identification and Quantification
Published on: May 6, 2018
Bundle-forming pili and EspA are involved in biofilm formation by enteropathogenic Escherichia coli
Cristiano G Moreira1, Kelli Palmer, Marvin Whiteley
1Department of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9048, USA.
Abstract:
Microcolony formation is one of the initial steps in biofilm development, and in enteropathogenic Escherichia coli (EPEC) it is mediated by several adhesins, including the bundle-forming pilus (BFP) and the EspA filament. Here we report that EPEC forms biofilms on plastic under static conditions and a flowthrough continuous culture system. The abilities of several EPEC isogenic mutants to form biofilms were assessed. Adhesins such as BFP and EspA, important in microcolony formation on epithelial cells, are also involved in bacterial aggregation during biofilm formation on abiotic surfaces. Mutants that do not express BFP or EspA form more-diffuse biofilms than does the wild type. We also determined, using gfp transcriptional fusions, that, consistent with the role of these adhesins in biofilms, the genes encoding BFP and EspA are expressed during biofilm formation. Finally, expression of espA is controlled by a quorum-sensing (QS) regulatory mechanism, and the EPEC qseA QS mutant also forms altered biofilms, suggesting that this signaling mechanism plays an important role in EPEC biofilm development. Taken together, these studies allowed us to propose a model of EPEC biofilm formation.
Insights
Enteropathogenic Escherichia coli (EPEC) forms biofilms using adhesins like bundle-forming pilus (BFP) and EspA. Quorum-sensing regulation also impacts EPEC biofilm development, influencing bacterial aggregation and structure.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Biofilm Formation
Background:
- Biofilm development is a crucial step in bacterial pathogenesis.
- Enteropathogenic Escherichia coli (EPEC) utilizes adhesins for initial microcolony formation.
Purpose of the Study:
- To investigate the role of adhesins (BFP, EspA) and quorum-sensing (QS) in EPEC biofilm formation on abiotic surfaces.
- To characterize EPEC biofilm formation under static and continuous culture conditions.
- To propose a model for EPEC biofilm development.
Main Methods:
- Assessment of biofilm formation in EPEC isogenic mutants.
- Utilized gfp transcriptional fusions to monitor gene expression during biofilm formation.
- Investigated the impact of quorum-sensing (QS) regulation on biofilm development.
Main Results:
- EPEC forms biofilms on plastic surfaces under static and flowthrough conditions.
- Bundle-forming pilus (BFP) and EspA are involved in bacterial aggregation during EPEC biofilm formation.
- Mutants lacking BFP or EspA exhibited altered, more-diffuse biofilm structures.
- Genes encoding BFP and EspA are expressed during biofilm formation.
- Quorum-sensing (QS) regulates espA expression and influences EPEC biofilm architecture.
Conclusions:
- Adhesins BFP and EspA play significant roles in EPEC biofilm formation on abiotic surfaces.
- Quorum-sensing (QS) is an important regulatory mechanism controlling EPEC biofilm development.
- A model for EPEC biofilm formation incorporating adhesins and QS has been proposed.
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