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.

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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