Cargando…
Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation
Pelvic radiotherapy is known to evoke intestinal mucositis and dysbiosis. Currently, there are no effective therapies available to mitigate these injuries, which is partly due to a lack of insight into the events causing mucositis and dysbiosis. Here, the complex interplay between the murine host an...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723693/ https://www.ncbi.nlm.nih.gov/pubmed/36737646 http://dx.doi.org/10.1038/s43705-021-00024-0 |
_version_ | 1784844242046156800 |
---|---|
author | Segers, Charlotte Mysara, Mohamed Claesen, Jürgen Baatout, Sarah Leys, Natalie Lebeer, Sarah Verslegers, Mieke Mastroleo, Felice |
author_facet | Segers, Charlotte Mysara, Mohamed Claesen, Jürgen Baatout, Sarah Leys, Natalie Lebeer, Sarah Verslegers, Mieke Mastroleo, Felice |
author_sort | Segers, Charlotte |
collection | PubMed |
description | Pelvic radiotherapy is known to evoke intestinal mucositis and dysbiosis. Currently, there are no effective therapies available to mitigate these injuries, which is partly due to a lack of insight into the events causing mucositis and dysbiosis. Here, the complex interplay between the murine host and its microbiome following pelvic irradiation was mapped by characterizing intestinal mucositis along with extensive 16S microbial profiling. We demonstrated important morphological and inflammatory implications within one day after exposure, thereby impairing intestinal functionality and inducing translocation of intraluminal bacteria into mesenteric lymph nodes as innovatively quantified by flow cytometry. Concurrent 16S microbial profiling revealed a delayed impact of pelvic irradiation on beta diversity. Analysis of composition of microbiomes identified biomarkers for pelvic irradiation. Among them, members of the families Ruminococcaceae, Lachnospiraceae and Porphyromonadaceae were differentially affected. Altogether, our unprecedented findings showed how pelvic irradiation evoked structural and functional changes in the intestine, which secondarily resulted in a microbiome shift. Therefore, the presented in vivo irradiation-gut-microbiome platform allows further research into the pathobiology of pelvic irradiation-induced intestinal mucositis and resultant dysbiosis, as well as the exploration of mitigating treatments including drugs and food supplements. |
format | Online Article Text |
id | pubmed-9723693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97236932023-01-04 Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation Segers, Charlotte Mysara, Mohamed Claesen, Jürgen Baatout, Sarah Leys, Natalie Lebeer, Sarah Verslegers, Mieke Mastroleo, Felice ISME Commun Article Pelvic radiotherapy is known to evoke intestinal mucositis and dysbiosis. Currently, there are no effective therapies available to mitigate these injuries, which is partly due to a lack of insight into the events causing mucositis and dysbiosis. Here, the complex interplay between the murine host and its microbiome following pelvic irradiation was mapped by characterizing intestinal mucositis along with extensive 16S microbial profiling. We demonstrated important morphological and inflammatory implications within one day after exposure, thereby impairing intestinal functionality and inducing translocation of intraluminal bacteria into mesenteric lymph nodes as innovatively quantified by flow cytometry. Concurrent 16S microbial profiling revealed a delayed impact of pelvic irradiation on beta diversity. Analysis of composition of microbiomes identified biomarkers for pelvic irradiation. Among them, members of the families Ruminococcaceae, Lachnospiraceae and Porphyromonadaceae were differentially affected. Altogether, our unprecedented findings showed how pelvic irradiation evoked structural and functional changes in the intestine, which secondarily resulted in a microbiome shift. Therefore, the presented in vivo irradiation-gut-microbiome platform allows further research into the pathobiology of pelvic irradiation-induced intestinal mucositis and resultant dysbiosis, as well as the exploration of mitigating treatments including drugs and food supplements. Nature Publishing Group UK 2021-06-10 /pmc/articles/PMC9723693/ /pubmed/36737646 http://dx.doi.org/10.1038/s43705-021-00024-0 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Segers, Charlotte Mysara, Mohamed Claesen, Jürgen Baatout, Sarah Leys, Natalie Lebeer, Sarah Verslegers, Mieke Mastroleo, Felice Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title | Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title_full | Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title_fullStr | Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title_full_unstemmed | Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title_short | Intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
title_sort | intestinal mucositis precedes dysbiosis in a mouse model for pelvic irradiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723693/ https://www.ncbi.nlm.nih.gov/pubmed/36737646 http://dx.doi.org/10.1038/s43705-021-00024-0 |
work_keys_str_mv | AT segerscharlotte intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT mysaramohamed intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT claesenjurgen intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT baatoutsarah intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT leysnatalie intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT lebeersarah intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT verslegersmieke intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation AT mastroleofelice intestinalmucositisprecedesdysbiosisinamousemodelforpelvicirradiation |