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Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1

Our innate immune system distinguishes microbes from self by detecting conserved pathogen-associated molecular patterns (PAMPs) (1). However, all microbes produce PAMPs, regardless of their pathogenic potential. To distinguish virulent microbes from ones with lower disease-causing potential the inna...

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Autores principales: Keestra, A. Marijke, Winter, Maria G., Auburger, Josef J., Fräßle, Simon P., Xavier, Mariana N., Winter, Sebastian E., Kim, Anita, Poon, Victor, Ravesloot, Mariëtta M., Waldenmaier, Julian, Tsolis, Renée M., Eigenheer, Richard A., Bäumler, Andreas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625479/
https://www.ncbi.nlm.nih.gov/pubmed/23542589
http://dx.doi.org/10.1038/nature12025
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author Keestra, A. Marijke
Winter, Maria G.
Auburger, Josef J.
Fräßle, Simon P.
Xavier, Mariana N.
Winter, Sebastian E.
Kim, Anita
Poon, Victor
Ravesloot, Mariëtta M.
Waldenmaier, Julian
Tsolis, Renée M.
Eigenheer, Richard A.
Bäumler, Andreas J.
author_facet Keestra, A. Marijke
Winter, Maria G.
Auburger, Josef J.
Fräßle, Simon P.
Xavier, Mariana N.
Winter, Sebastian E.
Kim, Anita
Poon, Victor
Ravesloot, Mariëtta M.
Waldenmaier, Julian
Tsolis, Renée M.
Eigenheer, Richard A.
Bäumler, Andreas J.
author_sort Keestra, A. Marijke
collection PubMed
description Our innate immune system distinguishes microbes from self by detecting conserved pathogen-associated molecular patterns (PAMPs) (1). However, all microbes produce PAMPs, regardless of their pathogenic potential. To distinguish virulent microbes from ones with lower disease-causing potential the innate immune system detects conserved pathogen-induced processes (2), such as the presence of microbial products in the host cytosol, by mechanisms that are not fully resolved. Here we show that Nod1 senses cytosolic microbial products by monitoring the activation state of small Rho GTPases. Activation of Rac1 and Cdc42 by bacterial delivery or ectopic expression of a Salmonella virulence factor, SopE, triggered the Nod1 signaling pathway with consequent Rip2-mediated induction of NF-κB-dependent inflammatory responses. Similarly, activation of the Nod1 signaling pathway by peptidoglycan required Rac1 activity. Furthermore, constitutively active forms of Rac1, Cdc42 and RhoA activated the Nod1 signaling pathway. Our data identify activation of small Rho GTPases as a pathogen-induced process sensed through the Nod1 signaling pathway (Fig. S1).
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spelling pubmed-36254792013-10-11 Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1 Keestra, A. Marijke Winter, Maria G. Auburger, Josef J. Fräßle, Simon P. Xavier, Mariana N. Winter, Sebastian E. Kim, Anita Poon, Victor Ravesloot, Mariëtta M. Waldenmaier, Julian Tsolis, Renée M. Eigenheer, Richard A. Bäumler, Andreas J. Nature Article Our innate immune system distinguishes microbes from self by detecting conserved pathogen-associated molecular patterns (PAMPs) (1). However, all microbes produce PAMPs, regardless of their pathogenic potential. To distinguish virulent microbes from ones with lower disease-causing potential the innate immune system detects conserved pathogen-induced processes (2), such as the presence of microbial products in the host cytosol, by mechanisms that are not fully resolved. Here we show that Nod1 senses cytosolic microbial products by monitoring the activation state of small Rho GTPases. Activation of Rac1 and Cdc42 by bacterial delivery or ectopic expression of a Salmonella virulence factor, SopE, triggered the Nod1 signaling pathway with consequent Rip2-mediated induction of NF-κB-dependent inflammatory responses. Similarly, activation of the Nod1 signaling pathway by peptidoglycan required Rac1 activity. Furthermore, constitutively active forms of Rac1, Cdc42 and RhoA activated the Nod1 signaling pathway. Our data identify activation of small Rho GTPases as a pathogen-induced process sensed through the Nod1 signaling pathway (Fig. S1). 2013-03-31 2013-04-11 /pmc/articles/PMC3625479/ /pubmed/23542589 http://dx.doi.org/10.1038/nature12025 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Keestra, A. Marijke
Winter, Maria G.
Auburger, Josef J.
Fräßle, Simon P.
Xavier, Mariana N.
Winter, Sebastian E.
Kim, Anita
Poon, Victor
Ravesloot, Mariëtta M.
Waldenmaier, Julian
Tsolis, Renée M.
Eigenheer, Richard A.
Bäumler, Andreas J.
Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title_full Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title_fullStr Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title_full_unstemmed Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title_short Manipulation of small Rho GTPases is a pathogen-induced process detected by Nod1
title_sort manipulation of small rho gtpases is a pathogen-induced process detected by nod1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625479/
https://www.ncbi.nlm.nih.gov/pubmed/23542589
http://dx.doi.org/10.1038/nature12025
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