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Method for the Isolation of Francisella tularensis Outer Membranes
Published on: June 29, 2010
Polyphosphate Kinase Antagonizes Virulence Gene Expression in Francisella tularensis
Amy E Rohlfing1, Kathryn M Ramsey1, Simon L Dove2
1Division of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Abstract:
The alarmone ppGpp is a critical regulator of virulence gene expression in Francisella tularensis In this intracellular pathogen, ppGpp is thought to work in concert with the putative DNA-binding protein PigR and the SspA protein family members MglA and SspA to control a common set of genes. MglA and SspA form a complex that interacts with RNA polymerase (RNAP), and PigR functions by interacting with the RNAP-associated MglA-SspA complex. Prior work suggested that ppGpp indirectly exerts its regulatory effects in F. tularensis by promoting the accumulation of polyphosphate in the cell, which in turn was required for formation of the MglA-SspA complex. Here we show that in Escherichia coli, neither polyphosphate nor ppGpp is required for formation of the MglA-SspA complex but that ppGpp promotes the interaction between PigR and the MglA-SspA complex. Moreover, we show that polyphosphate kinase, the enzyme responsible for the synthesis of polyphosphate, antagonizes virulence gene expression in F. tularensis, a finding that is inconsistent with the notion that polyphosphate accumulation promotes virulence gene expression in this organism. Our findings identify polyphosphate kinase as a novel negative regulator of virulence gene expression in F. tularensis and support a model in which ppGpp exerts its positive regulatory effects by promoting the interaction between PigR and the MglA-SspA complex.IMPORTANCE In Francisella tularensis, MglA and SspA form a complex that associates with RNA polymerase to positively control the expression of key virulence genes. The MglA-SspA complex works together with the putative DNA-binding protein PigR and the alarmone ppGpp. PigR functions by interacting directly with the MglA-SspA complex, but how ppGpp exerts its effects was unclear. Prior work indicated that ppGpp acts by promoting the accumulation of polyphosphate, which is required for MglA and SspA to interact. Here we show that formation of the MglA-SspA complex does not require polyphosphate. Furthermore, we find that polyphosphate antagonizes the expression of virulence genes in F. tularensis Thus, ppGpp does not promote virulence gene expression in this organism through an effect on polyphosphate.
Insights
The alarmone guanosine tetraphosphate (ppGpp) positively regulates virulence in Francisella tularensis by enhancing the interaction between PigR and the MglA-SspA complex. Polyphosphate kinase, however, negatively impacts virulence gene expression.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Pathogenesis
Background:
- The alarmone guanosine tetraphosphate (ppGpp) is a key regulator of virulence gene expression in *Francisella tularensis*.
- ppGpp is believed to function with PigR, MglA, and SspA to control virulence genes, with MglA-SspA forming a complex with RNA polymerase (RNAP).
- Previous studies suggested ppGpp indirectly regulates virulence by increasing intracellular polyphosphate, essential for MglA-SspA complex formation.
Purpose of the Study:
- To investigate the precise role of ppGpp and polyphosphate in the regulation of virulence gene expression in *Francisella tularensis*.
- To elucidate the mechanism by which ppGpp influences the interaction between PigR and the MglA-SspA complex.
- To determine the effect of polyphosphate kinase on virulence gene expression in *F. tularensis*.
Main Methods:
- Investigated the requirement of polyphosphate and ppGpp for MglA-SspA complex formation in *Escherichia coli*.
- Assessed the effect of ppGpp on the interaction between PigR and the MglA-SspA complex.
- Examined the role of polyphosphate kinase in regulating virulence gene expression in *F. tularensis*.
Main Results:
- Neither polyphosphate nor ppGpp is necessary for the formation of the MglA-SspA complex in *E. coli*.
- ppGpp was shown to promote the interaction between PigR and the MglA-SspA complex.
- Polyphosphate kinase was identified as a novel negative regulator of virulence gene expression in *F. tularensis*, contradicting prior hypotheses.
Conclusions:
- The findings challenge the previous model where polyphosphate accumulation mediates ppGpp's regulatory effects on virulence.
- ppGpp positively regulates virulence in *F. tularensis* by facilitating the interaction between PigR and the MglA-SspA complex.
- Polyphosphate kinase acts as a direct antagonist of virulence gene expression in *F. tularensis*.
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