Cyclic AMP-Independent Control of Twitching Motility in Pseudomonas aeruginosa
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- Ryan N. C. Buensuceso
- Department of Biochemistry and Biomedical Sciences and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada
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- Martin Daniel-Ivad
- Program in Molecular Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada
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- Sara L. N. Kilmury
- Department of Biochemistry and Biomedical Sciences and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada
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- Tiffany L. Leighton
- Department of Biochemistry and Biomedical Sciences and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada
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- Hanjeong Harvey
- Department of Biochemistry and Biomedical Sciences and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada
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- P. Lynne Howell
- Program in Molecular Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada
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- Lori L. Burrows
- Department of Biochemistry and Biomedical Sciences and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada
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- George O'Toole
- editor
Abstract
<jats:title>ABSTRACT</jats:title> <jats:p> FimV is a <jats:named-content content-type="genus-species">Pseudomonas aeruginosa</jats:named-content> inner membrane hub protein that modulates levels of the second messenger, cyclic AMP (cAMP), through the activation of adenylate cyclase CyaB. Although type IVa pilus (T4aP)-dependent twitching motility is modulated by cAMP levels, mutants lacking FimV are twitching impaired, even when exogenous cAMP is provided. Here we further define FimV's cAMP-dependent and -independent regulation of twitching. We confirmed that the response regulator of the T4aP-associated Chp chemotaxis system, PilG, requires both FimV and the CyaB regulator, FimL, to activate CyaB. However, in cAMP-replete backgrounds—lacking the cAMP phosphodiesterase CpdA or the CheY-like protein PilH or expressing constitutively active CyaB— <jats:italic>pilG</jats:italic> and <jats:italic>fimV</jats:italic> mutants failed to twitch. Both cytoplasmic and periplasmic domains of FimV were important for its cAMP-dependent and -independent roles, while its septal peptidoglycan-targeting LysM motif was required only for twitching motility. Polar localization of the sensor kinase PilS, a key regulator of transcription of the major pilin, was FimV dependent. However, unlike its homologues in other species that localize flagellar system components, FimV was not required for swimming motility. These data provide further evidence to support FimV's role as a key hub protein that coordinates the polar localization and function of multiple structural and regulatory proteins involved in <jats:named-content content-type="genus-species">P. aeruginosa</jats:named-content> twitching motility. </jats:p> <jats:p> <jats:bold>IMPORTANCE</jats:bold> <jats:named-content content-type="genus-species">Pseudomonas aeruginosa</jats:named-content> is a serious opportunistic pathogen. Type IVa pili (T4aP) are important for its virulence, because they mediate dissemination and invasion via twitching motility and are involved in surface sensing, which modulates pathogenicity via changes in cAMP levels. Here we show that the hub protein FimV and the response regulator of the Chp system, PilG, regulate twitching independently of their roles in the modulation of cAMP synthesis. These functions do not require the putative scaffold protein FimL, proposed to link PilG with FimV. PilG may regulate asymmetric functioning of the T4aP system to allow for directional movement, while FimV appears to localize both structural and regulatory elements—including the PilSR two-component system—to cell poles for optimal function. </jats:p>
Journal
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- Journal of Bacteriology
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Journal of Bacteriology 199 (16), 2017-08-15
American Society for Microbiology
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Details 詳細情報について
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- CRID
- 1360292618674556288
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- ISSN
- 10985530
- 00219193
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- Data Source
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- Crossref