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Updated: May 23, 2026

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues
Published on: February 19, 2019
Transcriptional regulator PerA influences biofilm-associated, platelet binding, and metabolic gene expression in
Scott M Maddox1, Phillip S Coburn, Nathan Shankar
1Advanced Center for Genome Technology, University of Oklahoma, Norman, Oklahoma, United States of America.
Abstract:
Enterococcus faecalis is an opportunistic pathogen and a leading cause of nosocomial infections, traits facilitated by the ability to quickly acquire and transfer virulence determinants. A 150 kb pathogenicity island (PAI) comprised of genes contributing to virulence is found in many enterococcal isolates and is known to undergo horizontal transfer. We have shown that the PAI-encoded transcriptional regulator PerA contributes to pathogenicity in the mouse peritonitis infection model. In this study, we used whole-genome microarrays to determine the PerA regulon. The PerA regulon is extensive, as transcriptional analysis showed 151 differentially regulated genes. Our findings reveal that PerA coordinately regulates genes important for metabolism, amino acid degradation, and pathogenicity. Further transcriptional analysis revealed that PerA is influenced by bicarbonate. Additionally, PerA influences the ability of E. faecalis to bind to human platelets. Our results suggest that PerA is a global transcriptional regulator that coordinately regulates genes responsible for enterococcal pathogenicity.
Insights
PerA is a key regulator in Enterococcus faecalis, controlling numerous genes involved in metabolism and virulence. This finding deepens our understanding of how this opportunistic pathogen causes infections.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Enterococcus faecalis is a major cause of hospital-acquired infections.
- Virulence factors are often acquired via horizontal gene transfer on pathogenicity islands (PAIs).
- The PAI-encoded regulator PerA is known to contribute to E. faecalis pathogenicity.
Purpose of the Study:
- To identify the genes regulated by PerA (the PerA regulon) in E. faecalis.
- To understand the role of PerA in coordinating virulence and metabolic functions.
- To investigate potential environmental influences on PerA activity.
Main Methods:
- Whole-genome microarrays were employed to analyze gene expression.
- Transcriptional analysis was performed to identify differentially regulated genes.
- E. faecalis strains were assessed for platelet binding capabilities.
Main Results:
- The PerA regulon encompasses 151 differentially regulated genes.
- PerA coordinately controls genes involved in metabolism, amino acid degradation, and pathogenicity.
- PerA activity is influenced by bicarbonate and affects bacterial binding to human platelets.
Conclusions:
- PerA acts as a global transcriptional regulator in E. faecalis.
- PerA plays a central role in coordinating pathogenicity and metabolic processes.
- Understanding PerA regulation offers insights into controlling enterococcal infections.
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