Cargando…

Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model

BACKGROUND: The prevalence of human infections with the zoonotic pathogen Campylobacter jejuni is rising worldwide. Therefore, the identification of compounds with potent anti-pathogenic and anti-inflammatory properties for future therapeutic and/or preventive application to combat campylobacteriosi...

Descripción completa

Detalles Bibliográficos
Autores principales: Mousavi, Soraya, Schmidt, Anna-Maria, Escher, Ulrike, Kittler, Sophie, Kehrenberg, Corinna, Thunhorst, Elisa, Bereswill, Stefan, Heimesaat, Markus M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947993/
https://www.ncbi.nlm.nih.gov/pubmed/31921356
http://dx.doi.org/10.1186/s13099-019-0343-4
_version_ 1783485670069633024
author Mousavi, Soraya
Schmidt, Anna-Maria
Escher, Ulrike
Kittler, Sophie
Kehrenberg, Corinna
Thunhorst, Elisa
Bereswill, Stefan
Heimesaat, Markus M.
author_facet Mousavi, Soraya
Schmidt, Anna-Maria
Escher, Ulrike
Kittler, Sophie
Kehrenberg, Corinna
Thunhorst, Elisa
Bereswill, Stefan
Heimesaat, Markus M.
author_sort Mousavi, Soraya
collection PubMed
description BACKGROUND: The prevalence of human infections with the zoonotic pathogen Campylobacter jejuni is rising worldwide. Therefore, the identification of compounds with potent anti-pathogenic and anti-inflammatory properties for future therapeutic and/or preventive application to combat campylobacteriosis is of importance for global health. Results of recent studies suggested carvacrol (4-isopropyl-2-methylphenol) as potential candidate molecule for the treatment of campylobacteriosis in humans and for the prevention of Campylobacter colonization in farm animals. RESULTS: To address this in a clinical murine infection model of acute campylobacteriosis, secondary abiotic IL-10(−/−) mice were subjected to synthetic carvacrol via the drinking water starting 4 days before peroral C. jejuni challenge. Whereas at day 6 post-infection placebo treated mice suffered from acute enterocolitis, mice from the carvacrol cohort not only harbored two log orders of magnitude lower pathogen loads in their intestines, but also displayed significantly reduced disease symptoms. Alleviated campylobacteriosis following carvacrol application was accompanied by less distinct intestinal apoptosis and pro-inflammatory immune responses as well as by higher numbers of proliferating colonic epithelial cells. Remarkably, the inflammation-ameliorating effects of carvacrol treatment were not restricted to the intestinal tract, but could also be observed in extra-intestinal organs such as liver, kidneys and lungs and, strikingly, systemically as indicated by lower IFN-γ, TNF, MCP-1 and IL-6 serum concentrations in carvacrol versus placebo treated mice. Furthermore, carvacrol treatment was associated with less frequent translocation of viable C. jejuni originating from the intestines to extra-intestinal compartments. CONCLUSION: The lowered C. jejuni loads and alleviated symptoms observed in the here applied clinical murine model for human campylobacteriosis highlight the application of carvacrol as a promising novel option for both, the treatment of campylobacteriosis and hence, for prevention of post-infectious sequelae in humans, and for the reduction of C. jejuni colonization in the intestines of vertebrate lifestock animals.
format Online
Article
Text
id pubmed-6947993
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69479932020-01-09 Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model Mousavi, Soraya Schmidt, Anna-Maria Escher, Ulrike Kittler, Sophie Kehrenberg, Corinna Thunhorst, Elisa Bereswill, Stefan Heimesaat, Markus M. Gut Pathog Research BACKGROUND: The prevalence of human infections with the zoonotic pathogen Campylobacter jejuni is rising worldwide. Therefore, the identification of compounds with potent anti-pathogenic and anti-inflammatory properties for future therapeutic and/or preventive application to combat campylobacteriosis is of importance for global health. Results of recent studies suggested carvacrol (4-isopropyl-2-methylphenol) as potential candidate molecule for the treatment of campylobacteriosis in humans and for the prevention of Campylobacter colonization in farm animals. RESULTS: To address this in a clinical murine infection model of acute campylobacteriosis, secondary abiotic IL-10(−/−) mice were subjected to synthetic carvacrol via the drinking water starting 4 days before peroral C. jejuni challenge. Whereas at day 6 post-infection placebo treated mice suffered from acute enterocolitis, mice from the carvacrol cohort not only harbored two log orders of magnitude lower pathogen loads in their intestines, but also displayed significantly reduced disease symptoms. Alleviated campylobacteriosis following carvacrol application was accompanied by less distinct intestinal apoptosis and pro-inflammatory immune responses as well as by higher numbers of proliferating colonic epithelial cells. Remarkably, the inflammation-ameliorating effects of carvacrol treatment were not restricted to the intestinal tract, but could also be observed in extra-intestinal organs such as liver, kidneys and lungs and, strikingly, systemically as indicated by lower IFN-γ, TNF, MCP-1 and IL-6 serum concentrations in carvacrol versus placebo treated mice. Furthermore, carvacrol treatment was associated with less frequent translocation of viable C. jejuni originating from the intestines to extra-intestinal compartments. CONCLUSION: The lowered C. jejuni loads and alleviated symptoms observed in the here applied clinical murine model for human campylobacteriosis highlight the application of carvacrol as a promising novel option for both, the treatment of campylobacteriosis and hence, for prevention of post-infectious sequelae in humans, and for the reduction of C. jejuni colonization in the intestines of vertebrate lifestock animals. BioMed Central 2020-01-08 /pmc/articles/PMC6947993/ /pubmed/31921356 http://dx.doi.org/10.1186/s13099-019-0343-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Mousavi, Soraya
Schmidt, Anna-Maria
Escher, Ulrike
Kittler, Sophie
Kehrenberg, Corinna
Thunhorst, Elisa
Bereswill, Stefan
Heimesaat, Markus M.
Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title_full Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title_fullStr Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title_full_unstemmed Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title_short Carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
title_sort carvacrol ameliorates acute campylobacteriosis in a clinical murine infection model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947993/
https://www.ncbi.nlm.nih.gov/pubmed/31921356
http://dx.doi.org/10.1186/s13099-019-0343-4
work_keys_str_mv AT mousavisoraya carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT schmidtannamaria carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT escherulrike carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT kittlersophie carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT kehrenbergcorinna carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT thunhorstelisa carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT bereswillstefan carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel
AT heimesaatmarkusm carvacrolamelioratesacutecampylobacteriosisinaclinicalmurineinfectionmodel