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Unveiling ubiquitinome rearrangements induced by Salmonella infection

Ubiquitination plays a critical role in the activation of host immune responses to infection and serves as a signal for pathogen delivery to phagophores along the xenophagy pathway. We recently performed systematic ubiquitination site profiling of epithelial cells infected with Salmonella Typhimuriu...

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Autores principales: Bionda, Tihana, Behrends, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082772/
https://www.ncbi.nlm.nih.gov/pubmed/27467224
http://dx.doi.org/10.1080/15548627.2016.1203490
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author Bionda, Tihana
Behrends, Christian
author_facet Bionda, Tihana
Behrends, Christian
author_sort Bionda, Tihana
collection PubMed
description Ubiquitination plays a critical role in the activation of host immune responses to infection and serves as a signal for pathogen delivery to phagophores along the xenophagy pathway. We recently performed systematic ubiquitination site profiling of epithelial cells infected with Salmonella Typhimurium. Our findings specifically highlight components of the NFKB, membrane trafficking pathways and RHO GTPase systems as ubiquitination hubs during infection. In addition, a broad spectrum of bacterial effectors and several outer membrane proteins are ubiquitinated in infected cells. This comprehensive resource of ubiquitinome dynamics during Salmonella infection enables further understanding of the complex host-pathogen interplay and may reveal novel targets for the inhibition of Salmonella invasion and inflammation.
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spelling pubmed-50827722016-10-31 Unveiling ubiquitinome rearrangements induced by Salmonella infection Bionda, Tihana Behrends, Christian Autophagy Autophagic Puncta Ubiquitination plays a critical role in the activation of host immune responses to infection and serves as a signal for pathogen delivery to phagophores along the xenophagy pathway. We recently performed systematic ubiquitination site profiling of epithelial cells infected with Salmonella Typhimurium. Our findings specifically highlight components of the NFKB, membrane trafficking pathways and RHO GTPase systems as ubiquitination hubs during infection. In addition, a broad spectrum of bacterial effectors and several outer membrane proteins are ubiquitinated in infected cells. This comprehensive resource of ubiquitinome dynamics during Salmonella infection enables further understanding of the complex host-pathogen interplay and may reveal novel targets for the inhibition of Salmonella invasion and inflammation. Taylor & Francis 2016-07-28 /pmc/articles/PMC5082772/ /pubmed/27467224 http://dx.doi.org/10.1080/15548627.2016.1203490 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Autophagic Puncta
Bionda, Tihana
Behrends, Christian
Unveiling ubiquitinome rearrangements induced by Salmonella infection
title Unveiling ubiquitinome rearrangements induced by Salmonella infection
title_full Unveiling ubiquitinome rearrangements induced by Salmonella infection
title_fullStr Unveiling ubiquitinome rearrangements induced by Salmonella infection
title_full_unstemmed Unveiling ubiquitinome rearrangements induced by Salmonella infection
title_short Unveiling ubiquitinome rearrangements induced by Salmonella infection
title_sort unveiling ubiquitinome rearrangements induced by salmonella infection
topic Autophagic Puncta
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082772/
https://www.ncbi.nlm.nih.gov/pubmed/27467224
http://dx.doi.org/10.1080/15548627.2016.1203490
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