Cargando…
miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis
BACKGROUND: Zoonotic microorganisms are increasingly impacting human health worldwide. Due to the development of the global population, humans and animals live in shared and progressively crowded ecosystems, which enhances the risk of zoonoses. Although Campylobacter species are among the most impor...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583435/ https://www.ncbi.nlm.nih.gov/pubmed/37848994 http://dx.doi.org/10.1186/s13099-023-00577-6 |
_version_ | 1785122551792402432 |
---|---|
author | Kraski, Angelina Mousavi, Soraya Heimesaat, Markus M. Bereswill, Stefan Einspanier, Ralf Alter, Thomas Gölz, Greta Sharbati, Soroush |
author_facet | Kraski, Angelina Mousavi, Soraya Heimesaat, Markus M. Bereswill, Stefan Einspanier, Ralf Alter, Thomas Gölz, Greta Sharbati, Soroush |
author_sort | Kraski, Angelina |
collection | PubMed |
description | BACKGROUND: Zoonotic microorganisms are increasingly impacting human health worldwide. Due to the development of the global population, humans and animals live in shared and progressively crowded ecosystems, which enhances the risk of zoonoses. Although Campylobacter species are among the most important bacterial zoonotic agents worldwide, the molecular mechanisms of many host and pathogen factors involved in colonisation and infection are poorly understood. Campylobacter jejuni colonises the crypts of the human colon and causes acute inflammatory processes. The mucus and associated proteins play a central host-protective role in this process. The aim of this study was to explore the regulation of specific glycosyltransferase genes relevant to differential mucin-type O-glycosylation that could influence host colonisation and infection by C. jejuni. RESULTS: Since microRNAs are known to be important regulators of the mammalian host cell response to bacterial infections, we focussed on the role of miR-125a-5p in C. jejuni infection. Combining in vitro and in vivo approaches, we show that miR-125a-5p regulates the expression of the sialyltransferase ST3GAL1 in an infection-dependent manner. The protein ST3GAL1 shows markedly increased intestinal levels in infected mice, with enhanced distribution in the mucosal epithelial layer in contrast to naïve mice. CONCLUSION: From our previous studies and the data presented here, we conclude that miR-125a-5p and the previously reported miR-615-3p are involved in regulating the glycosylation patterns of relevant host cell response proteins during C. jejuni infection. The miRNA-dependent modulation of mucin-type O-glycosylation could be part of the mucosal immune response, but also a pathogen-driven modification that allows colonisation and infection of the mammalian host. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00577-6. |
format | Online Article Text |
id | pubmed-10583435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105834352023-10-19 miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis Kraski, Angelina Mousavi, Soraya Heimesaat, Markus M. Bereswill, Stefan Einspanier, Ralf Alter, Thomas Gölz, Greta Sharbati, Soroush Gut Pathog Research BACKGROUND: Zoonotic microorganisms are increasingly impacting human health worldwide. Due to the development of the global population, humans and animals live in shared and progressively crowded ecosystems, which enhances the risk of zoonoses. Although Campylobacter species are among the most important bacterial zoonotic agents worldwide, the molecular mechanisms of many host and pathogen factors involved in colonisation and infection are poorly understood. Campylobacter jejuni colonises the crypts of the human colon and causes acute inflammatory processes. The mucus and associated proteins play a central host-protective role in this process. The aim of this study was to explore the regulation of specific glycosyltransferase genes relevant to differential mucin-type O-glycosylation that could influence host colonisation and infection by C. jejuni. RESULTS: Since microRNAs are known to be important regulators of the mammalian host cell response to bacterial infections, we focussed on the role of miR-125a-5p in C. jejuni infection. Combining in vitro and in vivo approaches, we show that miR-125a-5p regulates the expression of the sialyltransferase ST3GAL1 in an infection-dependent manner. The protein ST3GAL1 shows markedly increased intestinal levels in infected mice, with enhanced distribution in the mucosal epithelial layer in contrast to naïve mice. CONCLUSION: From our previous studies and the data presented here, we conclude that miR-125a-5p and the previously reported miR-615-3p are involved in regulating the glycosylation patterns of relevant host cell response proteins during C. jejuni infection. The miRNA-dependent modulation of mucin-type O-glycosylation could be part of the mucosal immune response, but also a pathogen-driven modification that allows colonisation and infection of the mammalian host. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00577-6. BioMed Central 2023-10-17 /pmc/articles/PMC10583435/ /pubmed/37848994 http://dx.doi.org/10.1186/s13099-023-00577-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Kraski, Angelina Mousavi, Soraya Heimesaat, Markus M. Bereswill, Stefan Einspanier, Ralf Alter, Thomas Gölz, Greta Sharbati, Soroush miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title | miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title_full | miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title_fullStr | miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title_full_unstemmed | miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title_short | miR-125a-5p regulates the sialyltransferase ST3GAL1 in murine model of human intestinal campylobacteriosis |
title_sort | mir-125a-5p regulates the sialyltransferase st3gal1 in murine model of human intestinal campylobacteriosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583435/ https://www.ncbi.nlm.nih.gov/pubmed/37848994 http://dx.doi.org/10.1186/s13099-023-00577-6 |
work_keys_str_mv | AT kraskiangelina mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT mousavisoraya mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT heimesaatmarkusm mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT bereswillstefan mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT einspanierralf mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT alterthomas mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT golzgreta mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis AT sharbatisoroush mir125a5pregulatesthesialyltransferasest3gal1inmurinemodelofhumanintestinalcampylobacteriosis |