Cargando…
Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection
BACKGROUND: Arcobacter (A.) butzleri has been described as causative agent for sporadic cases of human gastroenteritis with abdominal pain and acute or prolonged watery diarrhea. In vitro studies revealed distinct adhesive, invasive and cytotoxic properties of A. butzleri. Information about the unde...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610047/ https://www.ncbi.nlm.nih.gov/pubmed/26483849 http://dx.doi.org/10.1186/s13099-015-0075-z |
_version_ | 1782395891444875264 |
---|---|
author | Heimesaat, Markus M. Karadas, Gül Alutis, Marie Fischer, André Kühl, Anja A. Breithaupt, Angele Göbel, Ulf B. Alter, Thomas Bereswill, Stefan Gölz, Greta |
author_facet | Heimesaat, Markus M. Karadas, Gül Alutis, Marie Fischer, André Kühl, Anja A. Breithaupt, Angele Göbel, Ulf B. Alter, Thomas Bereswill, Stefan Gölz, Greta |
author_sort | Heimesaat, Markus M. |
collection | PubMed |
description | BACKGROUND: Arcobacter (A.) butzleri has been described as causative agent for sporadic cases of human gastroenteritis with abdominal pain and acute or prolonged watery diarrhea. In vitro studies revealed distinct adhesive, invasive and cytotoxic properties of A. butzleri. Information about the underlying immunopathological mechanisms of infection in vivo, however, are scarce. The aim of this study was to investigate the immunopathological properties of two different A.butzleri strains in a well-established murine infection model. RESULTS: Gnotobiotic IL-10(−/−) mice, in which the intestinal microbiota was depleted by broad-spectrum antibiotic treatment, were perorally infected with two different A. butzleri strains isolated from a diseased patient (CCUG 30485) or fresh chicken meat (C1), respectively. Eventhough bacteria of either strain could stably colonize the intestinal tract at day 6 and day 16 postinfection (p.i.), mice did not exert infection induced symptoms such as diarrhea or wasting. In small intestines of infected mice, however, increased numbers of apoptotic cells could be detected at day 16, but not day 6 following infection with either strain. A strain-dependent influx of distinct immune cell populations such as T and B cells as well as of regulatory T cells could be observed upon A. butzleri infection which was accompanied by increased small intestinal concentrations of pro-inflammatory cytokines such as TNF, IFN-γ, MCP-1 and IL-6. Remarkably, inflammatory responses following A. butzleri infection were not restricted to the intestinal tract, given that the CCUG 30485 strain induced systemic immune responses as indicated by increased IFN-γ concentrations in spleens at day 6, but not day 16 following infection. CONCLUSION: Upon peroral infection A. butzleri stably colonized the intestinal tract of gnotobiotic IL-10(−/−) mice. The dynamics of distinct local and systemic inflammatory responses could be observed in a strain-dependent fashion pointing towards an immunopathogenic potential of A. butzleri in vivo. These results indicate that gnotobiotic IL-10(−/−) mice are well suited to further investigate the molecular mechanisms underlying arcobacteriosis in vivo. |
format | Online Article Text |
id | pubmed-4610047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46100472015-10-20 Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection Heimesaat, Markus M. Karadas, Gül Alutis, Marie Fischer, André Kühl, Anja A. Breithaupt, Angele Göbel, Ulf B. Alter, Thomas Bereswill, Stefan Gölz, Greta Gut Pathog Research BACKGROUND: Arcobacter (A.) butzleri has been described as causative agent for sporadic cases of human gastroenteritis with abdominal pain and acute or prolonged watery diarrhea. In vitro studies revealed distinct adhesive, invasive and cytotoxic properties of A. butzleri. Information about the underlying immunopathological mechanisms of infection in vivo, however, are scarce. The aim of this study was to investigate the immunopathological properties of two different A.butzleri strains in a well-established murine infection model. RESULTS: Gnotobiotic IL-10(−/−) mice, in which the intestinal microbiota was depleted by broad-spectrum antibiotic treatment, were perorally infected with two different A. butzleri strains isolated from a diseased patient (CCUG 30485) or fresh chicken meat (C1), respectively. Eventhough bacteria of either strain could stably colonize the intestinal tract at day 6 and day 16 postinfection (p.i.), mice did not exert infection induced symptoms such as diarrhea or wasting. In small intestines of infected mice, however, increased numbers of apoptotic cells could be detected at day 16, but not day 6 following infection with either strain. A strain-dependent influx of distinct immune cell populations such as T and B cells as well as of regulatory T cells could be observed upon A. butzleri infection which was accompanied by increased small intestinal concentrations of pro-inflammatory cytokines such as TNF, IFN-γ, MCP-1 and IL-6. Remarkably, inflammatory responses following A. butzleri infection were not restricted to the intestinal tract, given that the CCUG 30485 strain induced systemic immune responses as indicated by increased IFN-γ concentrations in spleens at day 6, but not day 16 following infection. CONCLUSION: Upon peroral infection A. butzleri stably colonized the intestinal tract of gnotobiotic IL-10(−/−) mice. The dynamics of distinct local and systemic inflammatory responses could be observed in a strain-dependent fashion pointing towards an immunopathogenic potential of A. butzleri in vivo. These results indicate that gnotobiotic IL-10(−/−) mice are well suited to further investigate the molecular mechanisms underlying arcobacteriosis in vivo. BioMed Central 2015-10-19 /pmc/articles/PMC4610047/ /pubmed/26483849 http://dx.doi.org/10.1186/s13099-015-0075-z Text en © Heimesaat et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Heimesaat, Markus M. Karadas, Gül Alutis, Marie Fischer, André Kühl, Anja A. Breithaupt, Angele Göbel, Ulf B. Alter, Thomas Bereswill, Stefan Gölz, Greta Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title | Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title_full | Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title_fullStr | Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title_full_unstemmed | Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title_short | Survey of small intestinal and systemic immune responses following murine Arcobacter butzleri infection |
title_sort | survey of small intestinal and systemic immune responses following murine arcobacter butzleri infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610047/ https://www.ncbi.nlm.nih.gov/pubmed/26483849 http://dx.doi.org/10.1186/s13099-015-0075-z |
work_keys_str_mv | AT heimesaatmarkusm surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT karadasgul surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT alutismarie surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT fischerandre surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT kuhlanjaa surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT breithauptangele surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT gobelulfb surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT alterthomas surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT bereswillstefan surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection AT golzgreta surveyofsmallintestinalandsystemicimmuneresponsesfollowingmurinearcobacterbutzleriinfection |