A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.

Different biomolecules have been identified in bacterial pathogens that sense changes in temperature and trigger expression of virulence programs upon host entry. However, the dynamics and quantitative outcome of this response in individual cells of a population, and how this influences pathogenicit...

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Main Authors: Aaron Mischa Nuss, Franziska Schuster, Louisa Roselius, Johannes Klein, René Bücker, Katharina Herbst, Ann Kathrin Heroven, Fabio Pisano, Christoph Wittmann, Richard Münch, Johannes Müller, Dieter Jahn, Petra Dersch
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-12-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1006091
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spelling doaj-3a285df91c224044b4d923e49bfd371f2021-04-21T16:59:11ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742016-12-011212e100609110.1371/journal.ppat.1006091A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.Aaron Mischa NussFranziska SchusterLouisa RoseliusJohannes KleinRené BückerKatharina HerbstAnn Kathrin HerovenFabio PisanoChristoph WittmannRichard MünchJohannes MüllerDieter JahnPetra DerschDifferent biomolecules have been identified in bacterial pathogens that sense changes in temperature and trigger expression of virulence programs upon host entry. However, the dynamics and quantitative outcome of this response in individual cells of a population, and how this influences pathogenicity are unknown. Here, we address these questions using a thermosensing virulence regulator of an intestinal pathogen (RovA of Yersinia pseudotuberculosis) as a model. We reveal that this regulator is part of a novel thermoresponsive bistable switch, which leads to high- and low-invasive subpopulations within a narrow temperature range. The temperature range in which bistability is observed is defined by the degradation and synthesis rate of the regulator, and is further adjustable via a nutrient-responsive regulator. The thermoresponsive switch is also characterized by a hysteretic behavior in which activation and deactivation occurred on vastly different time scales. Mathematical modeling accurately mirrored the experimental behavior and predicted that the thermoresponsiveness of this sophisticated bistable switch is mainly determined by the thermo-triggered increase of RovA proteolysis. We further observed RovA ON and OFF subpopulations of Y. pseudotuberculosis in the Peyer's patches and caecum of infected mice, and that changes in the RovA ON/OFF cell ratio reduce tissue colonization and overall virulence. This points to a bet-hedging strategy in which the thermoresponsive bistable switch plays a key role in adapting the bacteria to the fluctuating conditions encountered as they pass through the host's intestinal epithelium and suggests novel strategies for the development of antimicrobial therapies.https://doi.org/10.1371/journal.ppat.1006091
collection DOAJ
language English
format Article
sources DOAJ
author Aaron Mischa Nuss
Franziska Schuster
Louisa Roselius
Johannes Klein
René Bücker
Katharina Herbst
Ann Kathrin Heroven
Fabio Pisano
Christoph Wittmann
Richard Münch
Johannes Müller
Dieter Jahn
Petra Dersch
spellingShingle Aaron Mischa Nuss
Franziska Schuster
Louisa Roselius
Johannes Klein
René Bücker
Katharina Herbst
Ann Kathrin Heroven
Fabio Pisano
Christoph Wittmann
Richard Münch
Johannes Müller
Dieter Jahn
Petra Dersch
A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
PLoS Pathogens
author_facet Aaron Mischa Nuss
Franziska Schuster
Louisa Roselius
Johannes Klein
René Bücker
Katharina Herbst
Ann Kathrin Heroven
Fabio Pisano
Christoph Wittmann
Richard Münch
Johannes Müller
Dieter Jahn
Petra Dersch
author_sort Aaron Mischa Nuss
title A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
title_short A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
title_full A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
title_fullStr A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
title_full_unstemmed A Precise Temperature-Responsive Bistable Switch Controlling Yersinia Virulence.
title_sort precise temperature-responsive bistable switch controlling yersinia virulence.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2016-12-01
description Different biomolecules have been identified in bacterial pathogens that sense changes in temperature and trigger expression of virulence programs upon host entry. However, the dynamics and quantitative outcome of this response in individual cells of a population, and how this influences pathogenicity are unknown. Here, we address these questions using a thermosensing virulence regulator of an intestinal pathogen (RovA of Yersinia pseudotuberculosis) as a model. We reveal that this regulator is part of a novel thermoresponsive bistable switch, which leads to high- and low-invasive subpopulations within a narrow temperature range. The temperature range in which bistability is observed is defined by the degradation and synthesis rate of the regulator, and is further adjustable via a nutrient-responsive regulator. The thermoresponsive switch is also characterized by a hysteretic behavior in which activation and deactivation occurred on vastly different time scales. Mathematical modeling accurately mirrored the experimental behavior and predicted that the thermoresponsiveness of this sophisticated bistable switch is mainly determined by the thermo-triggered increase of RovA proteolysis. We further observed RovA ON and OFF subpopulations of Y. pseudotuberculosis in the Peyer's patches and caecum of infected mice, and that changes in the RovA ON/OFF cell ratio reduce tissue colonization and overall virulence. This points to a bet-hedging strategy in which the thermoresponsive bistable switch plays a key role in adapting the bacteria to the fluctuating conditions encountered as they pass through the host's intestinal epithelium and suggests novel strategies for the development of antimicrobial therapies.
url https://doi.org/10.1371/journal.ppat.1006091
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