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Updated: Mar 21, 2026

Intratracheal Inoculation of Fischer 344 Rats with Francisella tularensis
Published on: September 30, 2017
A response regulator promotes Francisella tularensis intramacrophage growth by repressing an anti-virulence factor
Kathryn M Ramsey1, Simon L Dove1
1Division of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Abstract:
The orphan response regulator PmrA is essential for the intramacrophage growth and survival of Francisella tularensis. PmrA was thought to promote intramacrophage growth by binding directly to promoters on the Francisella Pathogenicity Island (FPI) and positively regulating the expression of FPI genes, which encode a Type VI secretion system required for intramacrophage growth. Using both ChIP-Seq and RNA-Seq we identify those regions of the F. tularensis chromosome occupied by PmrA and those genes that are regulated by PmrA. We find that PmrA associates with 252 distinct regions of the F. tularensis chromosome, but exerts regulatory effects at only a few of these locations. Rather than by functioning directly as an activator of FPI gene expression we present evidence that PmrA promotes intramacrophage growth by repressing the expression of a single target gene we refer to as priM (PmrA-repressed inhibitor of intramacrophage growth). Our findings thus indicate that the role of PmrA in facilitating intracellular growth is to repress a previously unknown anti-virulence factor. PriM is the first bacterially encoded factor to be described that can interfere with the intramacrophage growth and survival of F. tularensis.
Insights
The response regulator PmrA is crucial for Francisella tularensis survival within macrophages. Instead of activating virulence genes, PmrA represses priM, an anti-virulence factor, to promote intramacrophage growth.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- The orphan response regulator PmrA is essential for intramacrophage growth of Francisella tularensis.
- PmrA was previously thought to directly activate Francisella Pathogenicity Island (FPI) genes for Type VI secretion system (T6SS) expression.
Purpose of the Study:
- To elucidate the precise regulatory role of PmrA in Francisella tularensis intramacrophage survival.
- To identify direct PmrA binding sites and PmrA-regulated genes using genome-wide approaches.
Main Methods:
- Chromatin immunoprecipitation followed by sequencing (ChIP-Seq) to map PmrA binding sites.
- RNA sequencing (RNA-Seq) to identify PmrA-regulated gene expression.
Main Results:
- PmrA binds to 252 distinct chromosomal regions in F. tularensis.
- PmrA's regulatory impact is localized to a few binding sites, primarily through repression.
- PmrA represses the expression of a novel gene, priM (PmrA-repressed inhibitor of intramacrophage growth).
Conclusions:
- PmrA promotes intramacrophage growth by repressing priM, a previously unrecognized anti-virulence factor.
- This study redefines PmrA's function from a direct activator to a repressor of an anti-virulence gene, crucial for intracellular survival.
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