Cargando…

Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a

The small intestinal epithelium of Vibrio cholerae infected patients expresses the immunomodulatory microRNAs miR-146a and miR-155 at acute stage of disease. V. cholerae release outer membrane vesicles (OMVs) that serve as vehicles for translocation of virulence factors including V. cholerae cytolys...

Descripción completa

Detalles Bibliográficos
Autores principales: Bitar, Aziz, Aung, Kyaw Min, Wai, Sun Nyunt, Hammarström, Marie-Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510749/
https://www.ncbi.nlm.nih.gov/pubmed/31076615
http://dx.doi.org/10.1038/s41598-019-43691-9
_version_ 1783417458704515072
author Bitar, Aziz
Aung, Kyaw Min
Wai, Sun Nyunt
Hammarström, Marie-Louise
author_facet Bitar, Aziz
Aung, Kyaw Min
Wai, Sun Nyunt
Hammarström, Marie-Louise
author_sort Bitar, Aziz
collection PubMed
description The small intestinal epithelium of Vibrio cholerae infected patients expresses the immunomodulatory microRNAs miR-146a and miR-155 at acute stage of disease. V. cholerae release outer membrane vesicles (OMVs) that serve as vehicles for translocation of virulence factors including V. cholerae cytolysin (VCC). The aim was to investigate whether OMVs, with and/or without VCC-cargo could be responsible for induction of microRNAs in intestinal epithelial cells and thereby contribute to immunomodulation. Polarized tight monolayers of T84 cells were challenged with OMVs of wildtype and a VCC deletion mutant of the non-O1/non-O139 (NOVC) V. cholerae strain V:5/04 and with soluble VCC. OMVs, with and without VCC-cargo, caused significantly increased levels of miR-146a. Increase was seen already after 2 hours challenge with OMVs and persisted after 12 hours. Challenge with soluble VCC caused significant increases in interleukin-8 (IL-8), tumour necrosis factor-α (TNF-α), CCL20, IL-1β, and IRAK2 mRNA levels while challenge with OMVs did not cause increases in expression levels of any of these mRNAs. These results suggest that V. cholerae bacteria release OMVs that induce miR-146a in order to pave the way for colonization by reducing the strength of an epithelial innate immune defence reaction and also preventing inflammation in the mucosa that factors like VCC can evoke.
format Online
Article
Text
id pubmed-6510749
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-65107492019-05-23 Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a Bitar, Aziz Aung, Kyaw Min Wai, Sun Nyunt Hammarström, Marie-Louise Sci Rep Article The small intestinal epithelium of Vibrio cholerae infected patients expresses the immunomodulatory microRNAs miR-146a and miR-155 at acute stage of disease. V. cholerae release outer membrane vesicles (OMVs) that serve as vehicles for translocation of virulence factors including V. cholerae cytolysin (VCC). The aim was to investigate whether OMVs, with and/or without VCC-cargo could be responsible for induction of microRNAs in intestinal epithelial cells and thereby contribute to immunomodulation. Polarized tight monolayers of T84 cells were challenged with OMVs of wildtype and a VCC deletion mutant of the non-O1/non-O139 (NOVC) V. cholerae strain V:5/04 and with soluble VCC. OMVs, with and without VCC-cargo, caused significantly increased levels of miR-146a. Increase was seen already after 2 hours challenge with OMVs and persisted after 12 hours. Challenge with soluble VCC caused significant increases in interleukin-8 (IL-8), tumour necrosis factor-α (TNF-α), CCL20, IL-1β, and IRAK2 mRNA levels while challenge with OMVs did not cause increases in expression levels of any of these mRNAs. These results suggest that V. cholerae bacteria release OMVs that induce miR-146a in order to pave the way for colonization by reducing the strength of an epithelial innate immune defence reaction and also preventing inflammation in the mucosa that factors like VCC can evoke. Nature Publishing Group UK 2019-05-10 /pmc/articles/PMC6510749/ /pubmed/31076615 http://dx.doi.org/10.1038/s41598-019-43691-9 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bitar, Aziz
Aung, Kyaw Min
Wai, Sun Nyunt
Hammarström, Marie-Louise
Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title_full Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title_fullStr Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title_full_unstemmed Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title_short Vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microRNA-146a
title_sort vibrio cholerae derived outer membrane vesicles modulate the inflammatory response of human intestinal epithelial cells by inducing microrna-146a
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510749/
https://www.ncbi.nlm.nih.gov/pubmed/31076615
http://dx.doi.org/10.1038/s41598-019-43691-9
work_keys_str_mv AT bitaraziz vibriocholeraederivedoutermembranevesiclesmodulatetheinflammatoryresponseofhumanintestinalepithelialcellsbyinducingmicrorna146a
AT aungkyawmin vibriocholeraederivedoutermembranevesiclesmodulatetheinflammatoryresponseofhumanintestinalepithelialcellsbyinducingmicrorna146a
AT waisunnyunt vibriocholeraederivedoutermembranevesiclesmodulatetheinflammatoryresponseofhumanintestinalepithelialcellsbyinducingmicrorna146a
AT hammarstrommarielouise vibriocholeraederivedoutermembranevesiclesmodulatetheinflammatoryresponseofhumanintestinalepithelialcellsbyinducingmicrorna146a