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Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain

The highly virulent Escherichia coli O104:H4 that caused the large 2011 outbreak of diarrhoea and haemolytic uraemic syndrome secretes blended virulence factors of enterohaemorrhagic and enteroaggregative E. coli, but their secretion pathways are unknown. We demonstrate that the outbreak strain rele...

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Autores principales: Kunsmann, Lisa, Rüter, Christian, Bauwens, Andreas, Greune, Lilo, Glüder, Malte, Kemper, Björn, Fruth, Angelika, Wai, Sun Nyunt, He, Xiaohua, Lloubes, Roland, Schmidt, M. Alexander, Dobrindt, Ulrich, Mellmann, Alexander, Karch, Helge, Bielaszewska, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539607/
https://www.ncbi.nlm.nih.gov/pubmed/26283502
http://dx.doi.org/10.1038/srep13252
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author Kunsmann, Lisa
Rüter, Christian
Bauwens, Andreas
Greune, Lilo
Glüder, Malte
Kemper, Björn
Fruth, Angelika
Wai, Sun Nyunt
He, Xiaohua
Lloubes, Roland
Schmidt, M. Alexander
Dobrindt, Ulrich
Mellmann, Alexander
Karch, Helge
Bielaszewska, Martina
author_facet Kunsmann, Lisa
Rüter, Christian
Bauwens, Andreas
Greune, Lilo
Glüder, Malte
Kemper, Björn
Fruth, Angelika
Wai, Sun Nyunt
He, Xiaohua
Lloubes, Roland
Schmidt, M. Alexander
Dobrindt, Ulrich
Mellmann, Alexander
Karch, Helge
Bielaszewska, Martina
author_sort Kunsmann, Lisa
collection PubMed
description The highly virulent Escherichia coli O104:H4 that caused the large 2011 outbreak of diarrhoea and haemolytic uraemic syndrome secretes blended virulence factors of enterohaemorrhagic and enteroaggregative E. coli, but their secretion pathways are unknown. We demonstrate that the outbreak strain releases a cocktail of virulence factors via outer membrane vesicles (OMVs) shed during growth. The OMVs contain Shiga toxin (Stx) 2a, the major virulence factor of the strain, Shigella enterotoxin 1, H4 flagellin, and O104 lipopolysaccharide. The OMVs bind to and are internalised by human intestinal epithelial cells via dynamin-dependent and Stx2a-independent endocytosis, deliver the OMV-associated virulence factors intracellularly and induce caspase-9-mediated apoptosis and interleukin-8 secretion. Stx2a is the key OMV component responsible for the cytotoxicity, whereas flagellin and lipopolysaccharide are the major interleukin-8 inducers. The OMVs represent novel ways for the E. coli O104:H4 outbreak strain to deliver pathogenic cargoes and injure host cells.
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spelling pubmed-45396072015-08-26 Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain Kunsmann, Lisa Rüter, Christian Bauwens, Andreas Greune, Lilo Glüder, Malte Kemper, Björn Fruth, Angelika Wai, Sun Nyunt He, Xiaohua Lloubes, Roland Schmidt, M. Alexander Dobrindt, Ulrich Mellmann, Alexander Karch, Helge Bielaszewska, Martina Sci Rep Article The highly virulent Escherichia coli O104:H4 that caused the large 2011 outbreak of diarrhoea and haemolytic uraemic syndrome secretes blended virulence factors of enterohaemorrhagic and enteroaggregative E. coli, but their secretion pathways are unknown. We demonstrate that the outbreak strain releases a cocktail of virulence factors via outer membrane vesicles (OMVs) shed during growth. The OMVs contain Shiga toxin (Stx) 2a, the major virulence factor of the strain, Shigella enterotoxin 1, H4 flagellin, and O104 lipopolysaccharide. The OMVs bind to and are internalised by human intestinal epithelial cells via dynamin-dependent and Stx2a-independent endocytosis, deliver the OMV-associated virulence factors intracellularly and induce caspase-9-mediated apoptosis and interleukin-8 secretion. Stx2a is the key OMV component responsible for the cytotoxicity, whereas flagellin and lipopolysaccharide are the major interleukin-8 inducers. The OMVs represent novel ways for the E. coli O104:H4 outbreak strain to deliver pathogenic cargoes and injure host cells. Nature Publishing Group 2015-08-18 /pmc/articles/PMC4539607/ /pubmed/26283502 http://dx.doi.org/10.1038/srep13252 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kunsmann, Lisa
Rüter, Christian
Bauwens, Andreas
Greune, Lilo
Glüder, Malte
Kemper, Björn
Fruth, Angelika
Wai, Sun Nyunt
He, Xiaohua
Lloubes, Roland
Schmidt, M. Alexander
Dobrindt, Ulrich
Mellmann, Alexander
Karch, Helge
Bielaszewska, Martina
Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title_full Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title_fullStr Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title_full_unstemmed Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title_short Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain
title_sort virulence from vesicles: novel mechanisms of host cell injury by escherichia coli o104:h4 outbreak strain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539607/
https://www.ncbi.nlm.nih.gov/pubmed/26283502
http://dx.doi.org/10.1038/srep13252
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