Cargando…

A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria

The beneficial contribution of commensal bacteria to host health and homeostasis led to the concept that exogenous non-pathogenic bacteria called probiotics could be used to limit disease caused by pathogens. However, despite recent progress using gnotobiotic mammal and invertebrate models, mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales: Rendueles, Olaya, Ferrières, Lionel, Frétaud, Maxence, Bégaud, Evelyne, Herbomel, Philippe, Levraud, Jean-Pierre, Ghigo, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406073/
https://www.ncbi.nlm.nih.gov/pubmed/22911651
http://dx.doi.org/10.1371/journal.ppat.1002815
_version_ 1782239201213808640
author Rendueles, Olaya
Ferrières, Lionel
Frétaud, Maxence
Bégaud, Evelyne
Herbomel, Philippe
Levraud, Jean-Pierre
Ghigo, Jean-Marc
author_facet Rendueles, Olaya
Ferrières, Lionel
Frétaud, Maxence
Bégaud, Evelyne
Herbomel, Philippe
Levraud, Jean-Pierre
Ghigo, Jean-Marc
author_sort Rendueles, Olaya
collection PubMed
description The beneficial contribution of commensal bacteria to host health and homeostasis led to the concept that exogenous non-pathogenic bacteria called probiotics could be used to limit disease caused by pathogens. However, despite recent progress using gnotobiotic mammal and invertebrate models, mechanisms underlying protection afforded by commensal and probiotic bacteria against pathogens remain poorly understood. Here we developed a zebrafish model of controlled co-infection in which germ-free zebrafish raised on axenic living protozoa enabled the study of interactions between host and commensal and pathogenic bacteria. We screened enteric fish pathogens and identified Edwardsiella ictaluri as a virulent strain inducing a strong inflammatory response and rapid mortality in zebrafish larvae infected by the natural oro-intestinal route. Using mortality induced by infection as a phenotypic read-out, we pre-colonized zebrafish larvae with 37 potential probiotic bacterial strains and screened for survival upon E. ictaluri infection. We identified 3 robustly protective strains, including Vibrio parahaemolyticus and 2 Escherichia coli strains. We showed that the observed protective effect of E. coli was not correlated with a reduced host inflammatory response, nor with the release of biocidal molecules by protective bacteria, but rather with the presence of specific adhesion factors such as F pili that promote the emergence of probiotic bacteria in zebrafish larvae. Our study therefore provides new insights into the molecular events underlying the probiotic effect and constitutes a potentially high-throughput in vivo approach to the study of the molecular basis of pathogen exclusion in a relevant model of vertebrate oro-intestinal infection.
format Online
Article
Text
id pubmed-3406073
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34060732012-07-30 A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria Rendueles, Olaya Ferrières, Lionel Frétaud, Maxence Bégaud, Evelyne Herbomel, Philippe Levraud, Jean-Pierre Ghigo, Jean-Marc PLoS Pathog Research Article The beneficial contribution of commensal bacteria to host health and homeostasis led to the concept that exogenous non-pathogenic bacteria called probiotics could be used to limit disease caused by pathogens. However, despite recent progress using gnotobiotic mammal and invertebrate models, mechanisms underlying protection afforded by commensal and probiotic bacteria against pathogens remain poorly understood. Here we developed a zebrafish model of controlled co-infection in which germ-free zebrafish raised on axenic living protozoa enabled the study of interactions between host and commensal and pathogenic bacteria. We screened enteric fish pathogens and identified Edwardsiella ictaluri as a virulent strain inducing a strong inflammatory response and rapid mortality in zebrafish larvae infected by the natural oro-intestinal route. Using mortality induced by infection as a phenotypic read-out, we pre-colonized zebrafish larvae with 37 potential probiotic bacterial strains and screened for survival upon E. ictaluri infection. We identified 3 robustly protective strains, including Vibrio parahaemolyticus and 2 Escherichia coli strains. We showed that the observed protective effect of E. coli was not correlated with a reduced host inflammatory response, nor with the release of biocidal molecules by protective bacteria, but rather with the presence of specific adhesion factors such as F pili that promote the emergence of probiotic bacteria in zebrafish larvae. Our study therefore provides new insights into the molecular events underlying the probiotic effect and constitutes a potentially high-throughput in vivo approach to the study of the molecular basis of pathogen exclusion in a relevant model of vertebrate oro-intestinal infection. Public Library of Science 2012-07-26 /pmc/articles/PMC3406073/ /pubmed/22911651 http://dx.doi.org/10.1371/journal.ppat.1002815 Text en Rendueles et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rendueles, Olaya
Ferrières, Lionel
Frétaud, Maxence
Bégaud, Evelyne
Herbomel, Philippe
Levraud, Jean-Pierre
Ghigo, Jean-Marc
A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title_full A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title_fullStr A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title_full_unstemmed A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title_short A New Zebrafish Model of Oro-Intestinal Pathogen Colonization Reveals a Key Role for Adhesion in Protection by Probiotic Bacteria
title_sort new zebrafish model of oro-intestinal pathogen colonization reveals a key role for adhesion in protection by probiotic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406073/
https://www.ncbi.nlm.nih.gov/pubmed/22911651
http://dx.doi.org/10.1371/journal.ppat.1002815
work_keys_str_mv AT renduelesolaya anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT ferriereslionel anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT fretaudmaxence anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT begaudevelyne anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT herbomelphilippe anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT levraudjeanpierre anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT ghigojeanmarc anewzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT renduelesolaya newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT ferriereslionel newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT fretaudmaxence newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT begaudevelyne newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT herbomelphilippe newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT levraudjeanpierre newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria
AT ghigojeanmarc newzebrafishmodeloforointestinalpathogencolonizationrevealsakeyroleforadhesioninprotectionbyprobioticbacteria