Pseudomonas evades immune recognition of flagellin in both mammals and plants.

The building blocks of bacterial flagella, flagellin monomers, are potent stimulators of host innate immune systems. Recognition of flagellin monomers occurs by flagellin-specific pattern-recognition receptors, such as Toll-like receptor 5 (TLR5) in mammals and flagellin-sensitive 2 (FLS2) in plants...

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Main Authors: Bart W Bardoel, Sjoerd van der Ent, Michiel J C Pel, Jan Tommassen, Corné M J Pieterse, Kok P M van Kessel, Jos A G van Strijp
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-08-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3161968?pdf=render
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spelling doaj-b675527be2c74d91abd8bd11a79c91602020-11-25T01:08:22ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-08-0178e100220610.1371/journal.ppat.1002206Pseudomonas evades immune recognition of flagellin in both mammals and plants.Bart W BardoelSjoerd van der EntMichiel J C PelJan TommassenCorné M J PieterseKok P M van KesselJos A G van StrijpThe building blocks of bacterial flagella, flagellin monomers, are potent stimulators of host innate immune systems. Recognition of flagellin monomers occurs by flagellin-specific pattern-recognition receptors, such as Toll-like receptor 5 (TLR5) in mammals and flagellin-sensitive 2 (FLS2) in plants. Activation of these immune systems via flagellin leads eventually to elimination of the bacterium from the host. In order to prevent immune activation and thus favor survival in the host, bacteria secrete many proteins that hamper such recognition. In our search for Toll like receptor (TLR) antagonists, we screened bacterial supernatants and identified alkaline protease (AprA) of Pseudomonas aeruginosa as a TLR5 signaling inhibitor as evidenced by a marked reduction in IL-8 production and NF-κB activation. AprA effectively degrades the TLR5 ligand monomeric flagellin, while polymeric flagellin (involved in bacterial motility) and TLR5 itself resist degradation. The natural occurring alkaline protease inhibitor AprI of P. aeruginosa blocked flagellin degradation by AprA. P. aeruginosa aprA mutants induced an over 100-fold enhanced activation of TLR5 signaling, because they fail to degrade excess monomeric flagellin in their environment. Interestingly, AprA also prevents flagellin-mediated immune responses (such as growth inhibition and callose deposition) in Arabidopsis thaliana plants. This was due to decreased activation of the receptor FLS2 and clearly demonstrated by delayed stomatal closure with live bacteria in plants. Thus, by degrading the ligand for TLR5 and FLS2, P. aeruginosa escapes recognition by the innate immune systems of both mammals and plants.http://europepmc.org/articles/PMC3161968?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Bart W Bardoel
Sjoerd van der Ent
Michiel J C Pel
Jan Tommassen
Corné M J Pieterse
Kok P M van Kessel
Jos A G van Strijp
spellingShingle Bart W Bardoel
Sjoerd van der Ent
Michiel J C Pel
Jan Tommassen
Corné M J Pieterse
Kok P M van Kessel
Jos A G van Strijp
Pseudomonas evades immune recognition of flagellin in both mammals and plants.
PLoS Pathogens
author_facet Bart W Bardoel
Sjoerd van der Ent
Michiel J C Pel
Jan Tommassen
Corné M J Pieterse
Kok P M van Kessel
Jos A G van Strijp
author_sort Bart W Bardoel
title Pseudomonas evades immune recognition of flagellin in both mammals and plants.
title_short Pseudomonas evades immune recognition of flagellin in both mammals and plants.
title_full Pseudomonas evades immune recognition of flagellin in both mammals and plants.
title_fullStr Pseudomonas evades immune recognition of flagellin in both mammals and plants.
title_full_unstemmed Pseudomonas evades immune recognition of flagellin in both mammals and plants.
title_sort pseudomonas evades immune recognition of flagellin in both mammals and plants.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2011-08-01
description The building blocks of bacterial flagella, flagellin monomers, are potent stimulators of host innate immune systems. Recognition of flagellin monomers occurs by flagellin-specific pattern-recognition receptors, such as Toll-like receptor 5 (TLR5) in mammals and flagellin-sensitive 2 (FLS2) in plants. Activation of these immune systems via flagellin leads eventually to elimination of the bacterium from the host. In order to prevent immune activation and thus favor survival in the host, bacteria secrete many proteins that hamper such recognition. In our search for Toll like receptor (TLR) antagonists, we screened bacterial supernatants and identified alkaline protease (AprA) of Pseudomonas aeruginosa as a TLR5 signaling inhibitor as evidenced by a marked reduction in IL-8 production and NF-κB activation. AprA effectively degrades the TLR5 ligand monomeric flagellin, while polymeric flagellin (involved in bacterial motility) and TLR5 itself resist degradation. The natural occurring alkaline protease inhibitor AprI of P. aeruginosa blocked flagellin degradation by AprA. P. aeruginosa aprA mutants induced an over 100-fold enhanced activation of TLR5 signaling, because they fail to degrade excess monomeric flagellin in their environment. Interestingly, AprA also prevents flagellin-mediated immune responses (such as growth inhibition and callose deposition) in Arabidopsis thaliana plants. This was due to decreased activation of the receptor FLS2 and clearly demonstrated by delayed stomatal closure with live bacteria in plants. Thus, by degrading the ligand for TLR5 and FLS2, P. aeruginosa escapes recognition by the innate immune systems of both mammals and plants.
url http://europepmc.org/articles/PMC3161968?pdf=render
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