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Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7

Infection with Escherichia coli O157:H7 may develop into hemorrhagic colitis, or hemolytic uremic syndrome (HUS), which usually causes kidney failure or even death. The adhesion and toxins are the important virulent factors. In this study, a novel vaccine candidate rSOBGs was constructed based on th...

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Autores principales: Cai, Kun, Tu, Wei, Liu, Yuenan, Li, Tao, Wang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667225/
https://www.ncbi.nlm.nih.gov/pubmed/26626573
http://dx.doi.org/10.1038/srep17479
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author Cai, Kun
Tu, Wei
Liu, Yuenan
Li, Tao
Wang, Hui
author_facet Cai, Kun
Tu, Wei
Liu, Yuenan
Li, Tao
Wang, Hui
author_sort Cai, Kun
collection PubMed
description Infection with Escherichia coli O157:H7 may develop into hemorrhagic colitis, or hemolytic uremic syndrome (HUS), which usually causes kidney failure or even death. The adhesion and toxins are the important virulent factors. In this study, a novel vaccine candidate rSOBGs was constructed based on the bacterial ghost (BG). rSOBGs maintained the integrity of cellular morphology and displayed the linear Stx2Am-Stx1B antigen on the surface of outer membrane. rSOBGs induced Stxs-specific IgA/IgG antibodies and stronger intimin-specific IgA/IgG antibodies effectively in sera in this study. In vivo, the rSOBGs provided the higher protection rate (52%) than native bacterial ghost-OBGs (12%) when challenged intragastricly with high dose (500 LD50) viable E. coli O157:H7. Meanwhile, the rSOBGs provided higher protection rate (73.33%) than OBGs when challenged with 2 LD50 even to 5 LD50 lysed E. coli O157:H7. In vitro, the rSOBGs-immunized sera possessed neutralizing activity to lysed pathogenic bacteria. Furthermore, the results of histopathology also displayed that the administration of rSOBGs have the ability to reduce or inhibit the adhesion lesions and toxins damages of organs. The novel vaccine candidate rSOBGs induced both anti-toxin and anti-adhesion immune protection, suggesting the possibility to prevent the infectious diseases caused by Escherichia coli O157:H7.
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spelling pubmed-46672252015-12-08 Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7 Cai, Kun Tu, Wei Liu, Yuenan Li, Tao Wang, Hui Sci Rep Article Infection with Escherichia coli O157:H7 may develop into hemorrhagic colitis, or hemolytic uremic syndrome (HUS), which usually causes kidney failure or even death. The adhesion and toxins are the important virulent factors. In this study, a novel vaccine candidate rSOBGs was constructed based on the bacterial ghost (BG). rSOBGs maintained the integrity of cellular morphology and displayed the linear Stx2Am-Stx1B antigen on the surface of outer membrane. rSOBGs induced Stxs-specific IgA/IgG antibodies and stronger intimin-specific IgA/IgG antibodies effectively in sera in this study. In vivo, the rSOBGs provided the higher protection rate (52%) than native bacterial ghost-OBGs (12%) when challenged intragastricly with high dose (500 LD50) viable E. coli O157:H7. Meanwhile, the rSOBGs provided higher protection rate (73.33%) than OBGs when challenged with 2 LD50 even to 5 LD50 lysed E. coli O157:H7. In vitro, the rSOBGs-immunized sera possessed neutralizing activity to lysed pathogenic bacteria. Furthermore, the results of histopathology also displayed that the administration of rSOBGs have the ability to reduce or inhibit the adhesion lesions and toxins damages of organs. The novel vaccine candidate rSOBGs induced both anti-toxin and anti-adhesion immune protection, suggesting the possibility to prevent the infectious diseases caused by Escherichia coli O157:H7. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667225/ /pubmed/26626573 http://dx.doi.org/10.1038/srep17479 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
Cai, Kun
Tu, Wei
Liu, Yuenan
Li, Tao
Wang, Hui
Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title_full Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title_fullStr Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title_full_unstemmed Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title_short Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7
title_sort novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of escherichia coli o157:h7
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667225/
https://www.ncbi.nlm.nih.gov/pubmed/26626573
http://dx.doi.org/10.1038/srep17479
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