Literature DB >> 29158241

Polyphosphate Kinase Antagonizes Virulence Gene Expression in Francisella tularensis.

Amy E Rohlfing1, Kathryn M Ramsey1, Simon L Dove2.   

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.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  MglA; SspA; gene regulation; ppGpp

Mesh:

Substances:

Year:  2018        PMID: 29158241      PMCID: PMC5763045          DOI: 10.1128/JB.00460-17

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  66 in total

1.  DksA: a critical component of the transcription initiation machinery that potentiates the regulation of rRNA promoters by ppGpp and the initiating NTP.

Authors:  Brian J Paul; Melanie M Barker; Wilma Ross; David A Schneider; Cathy Webb; John W Foster; Richard L Gourse
Journal:  Cell       Date:  2004-08-06       Impact factor: 41.582

2.  Residual guanosine 3',5'-bispyrophosphate synthetic activity of relA null mutants can be eliminated by spoT null mutations.

Authors:  H Xiao; M Kalman; K Ikehara; S Zemel; G Glaser; M Cashel
Journal:  J Biol Chem       Date:  1991-03-25       Impact factor: 5.157

Review 3.  (p)ppGpp: still magical?

Authors:  Katarzyna Potrykus; Michael Cashel
Journal:  Annu Rev Microbiol       Date:  2008       Impact factor: 15.500

4.  The Protease Locus of Francisella tularensis LVS Is Required for Stress Tolerance and Infection in the Mammalian Host.

Authors:  Lihong He; Manoj Kumar Mohan Nair; Yuling Chen; Xue Liu; Mengyun Zhang; Karsten R O Hazlett; Haiteng Deng; Jing-Ren Zhang
Journal:  Infect Immun       Date:  2016-04-22       Impact factor: 3.441

5.  ppGpp Binding to a Site at the RNAP-DksA Interface Accounts for Its Dramatic Effects on Transcription Initiation during the Stringent Response.

Authors:  Wilma Ross; Patricia Sanchez-Vazquez; Albert Y Chen; Jeong-Hyun Lee; Hector L Burgos; Richard L Gourse
Journal:  Mol Cell       Date:  2016-05-26       Impact factor: 17.970

6.  Repression of phase-variable cup gene expression by H-NS-like proteins in Pseudomonas aeruginosa.

Authors:  Isabelle Vallet-Gely; Katherine E Donovan; Rui Fang; J Keith Joung; Simon L Dove
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-25       Impact factor: 11.205

7.  Guanosine pentaphosphate phosphohydrolase of Escherichia coli is a long-chain exopolyphosphatase.

Authors:  J D Keasling; L Bertsch; A Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

8.  A Francisella tularensis pathogenicity island required for intramacrophage growth.

Authors:  Francis E Nano; Na Zhang; Siobhán C Cowley; Karl E Klose; Karen K M Cheung; Michael J Roberts; Jagjit S Ludu; Gregg W Letendre; Anda I Meierovics; Gwen Stephens; Karen L Elkins
Journal:  J Bacteriol       Date:  2004-10       Impact factor: 3.490

9.  Coordinate control of virulence gene expression in Francisella tularensis involves direct interaction between key regulators.

Authors:  Amy E Rohlfing; Simon L Dove
Journal:  J Bacteriol       Date:  2014-07-28       Impact factor: 3.490

10.  Ubiquitous promoter-localization of essential virulence regulators in Francisella tularensis.

Authors:  Kathryn M Ramsey; Melisa L Osborne; Irina O Vvedenskaya; Cathy Su; Bryce E Nickels; Simon L Dove
Journal:  PLoS Pathog       Date:  2015-04-01       Impact factor: 6.823

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  3 in total

1.  [A fluorometric method for direct detection of inorganic polyphosphate in enterohemorrhagic Escherichia coli O157:H7].

Authors:  Yanli Du; Zongli Han; Xiangyu Wang; Chengsong Wan
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2019-03-30

Review 2.  Inorganic polyphosphate in host and microbe biology.

Authors:  Marvin Q Bowlin; Michael J Gray
Journal:  Trends Microbiol       Date:  2021-02-22       Impact factor: 17.079

Review 3.  Survival of the Fittest: The Relationship of (p)ppGpp With Bacterial Virulence.

Authors:  Shivani Kundra; Cristina Colomer-Winter; José A Lemos
Journal:  Front Microbiol       Date:  2020-12-03       Impact factor: 5.640

  3 in total

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