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Published on: January 22, 2013
Phase Variation of the mrp Fimbrial Promoter
1Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA. mpears@med.umich.edu.
Abstract:
Mannose-resistant Proteus-like (MR/P) fimbriae, produced by the uropathogen Proteus mirabilis, are major contributors to urinary tract infection. Expression of mrp genes is controlled by an invertible element in the mrp operon promoter, and promoter orientation is controlled by a single recombinase, MrpI, which determines whether the element is in the on or off orientation. Detailed here is a simple assay to determine the orientation of the invertible element in a population of P. mirabilis, a rapid screen to detect element-locked mrpI mutants, and quantification of mixtures of on and off bacteria.
Insights
Researchers developed a simple assay to determine the orientation of mannose-resistant Proteus-like (MR/P) fimbriae gene expression in Proteus mirabilis. This method aids in studying urinary tract infections and identifying mutants.
Area of Science:
- Microbiology
- Molecular Biology
- Urology
Background:
- Mannose-resistant Proteus-like (MR/P) fimbriae from Proteus mirabilis are key factors in urinary tract infections (UTIs).
- The expression of mrp genes, responsible for MR/P fimbriae, is regulated by an invertible genetic element within the mrp operon promoter.
- The orientation of this invertible element, controlled by the MrpI recombinase, dictates whether the mrp genes are expressed (on) or silenced (off).
Purpose of the Study:
- To develop a straightforward assay for determining the orientation of the invertible element in MR/P fimbriae gene expression.
- To establish a rapid screening method for identifying mutants with locked promoter orientations.
- To enable the quantification of bacterial populations with different promoter orientations.
Main Methods:
- Development of a simple assay to detect the orientation of the invertible element in P. mirabilis.
- Implementation of a rapid screening protocol to identify element-locked mrpI mutants.
- Methodology for quantifying mixtures of bacteria with 'on' and 'off' promoter orientations.
Main Results:
- A simple and effective assay was established to determine the orientation of the invertible element controlling MR/P fimbriae expression.
- A rapid screening method successfully identified P. mirabilis mutants with fixed promoter orientations.
- The assay allows for accurate quantification of mixed bacterial populations based on promoter orientation.
Conclusions:
- The developed assay provides a valuable tool for studying the regulation of MR/P fimbriae in Proteus mirabilis.
- This method facilitates research into the pathogenesis of UTIs caused by P. mirabilis.
- The ability to screen for and quantify promoter orientations aids in understanding gene regulation and identifying relevant mutants.
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