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Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile
BACKGROUND: Dextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models. However, the microbial characteristics of DSS-triggered colitis require further clarification. To analyze the changes in gut microbiota associated with DSS-induced acute and chronic colitis. ME...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520286/ https://www.ncbi.nlm.nih.gov/pubmed/34654370 http://dx.doi.org/10.1186/s12866-021-02342-8 |
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author | Xu, Hao-Ming Huang, Hong-Li Liu, Yan-Di Zhu, Jia-Qi Zhou, You-Lian Chen, Hui-Ting Xu, Jing Zhao, Hai-Lan Guo, Xue Shi, Wei Nie, Yu-Qiang Zhou, Yong-Jian |
author_facet | Xu, Hao-Ming Huang, Hong-Li Liu, Yan-Di Zhu, Jia-Qi Zhou, You-Lian Chen, Hui-Ting Xu, Jing Zhao, Hai-Lan Guo, Xue Shi, Wei Nie, Yu-Qiang Zhou, Yong-Jian |
author_sort | Xu, Hao-Ming |
collection | PubMed |
description | BACKGROUND: Dextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models. However, the microbial characteristics of DSS-triggered colitis require further clarification. To analyze the changes in gut microbiota associated with DSS-induced acute and chronic colitis. METHODS: Acute colitis was induced in mice by administering 3% DSS for 1 week in the drinking water, and chronic colitis was induced by supplementing drinking water with 2.5% DSS every other week for 5 weeks. Control groups received the same drinking water without DSS supplementation. The histopathological score and length of the colons, and disease activity index (DAI) were evaluated to confirm the presence of experimental colitis. Intestinal microbiota was profiled by 16S rDNA sequencing of cecal content. RESULTS: Mice with both acute and chronic DSS-triggered colitis had significantly higher DAI and colon histopathological scores in contrast to the control groups (P < 0.0001, P < 0.0001), and the colon was remarkably shortened (P < 0.0001, P < 0.0001). The gut microbiota α-diversity was partly downregulated in both acute and chronic colitis groups in contrast to their respective control groups (Pielou index P = 0.0022, P = 0.0649; Shannon index P = 0.0022, P = 0.0931). The reduction in the Pielou and Shannon indices were more obvious in mice with acute colitis (P = 0.0022, P = 0.0043). The relative abundance of Bacteroides and Turicibacter was increased (all P < 0.05), while that of Lachnospiraceae, Ruminococcaceae, Ruminiclostridium, Rikenella, Alistipes, Alloprevotella, and Butyricicoccus was significantly decreased after acute DSS induction (all P < 0.05). The relative abundance of Bacteroides, Akkermansia, Helicobacter, Parabacteroides, Erysipelatoclostridium, Turicibacter and Romboutsia was also markedly increased (all P < 0.05), and that of Lachnospiraceae_NK4A136_group, Alistipes, Enterorhabdus, Prevotellaceae_UCG-001, Butyricicoccus, Ruminiclostridium_6, Muribaculum, Ruminococcaceae_NK4A214_group, Family_XIII_UCG-001 and Flavonifractor was significantly decreased after chronic DSS induction (all P < 0.05). CONCLUSION: DSS-induced acute and chronic colitis demonstrated similar symptoms and histopathological changes. The changes in the gut microbiota of the acute colitis model were closer to that observed in UC. The acute colitis model had greater abundance of SCFAs-producing bacteria and lower α-diversity compared to the chronic colitis model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02342-8. |
format | Online Article Text |
id | pubmed-8520286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85202862021-10-20 Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile Xu, Hao-Ming Huang, Hong-Li Liu, Yan-Di Zhu, Jia-Qi Zhou, You-Lian Chen, Hui-Ting Xu, Jing Zhao, Hai-Lan Guo, Xue Shi, Wei Nie, Yu-Qiang Zhou, Yong-Jian BMC Microbiol Research BACKGROUND: Dextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models. However, the microbial characteristics of DSS-triggered colitis require further clarification. To analyze the changes in gut microbiota associated with DSS-induced acute and chronic colitis. METHODS: Acute colitis was induced in mice by administering 3% DSS for 1 week in the drinking water, and chronic colitis was induced by supplementing drinking water with 2.5% DSS every other week for 5 weeks. Control groups received the same drinking water without DSS supplementation. The histopathological score and length of the colons, and disease activity index (DAI) were evaluated to confirm the presence of experimental colitis. Intestinal microbiota was profiled by 16S rDNA sequencing of cecal content. RESULTS: Mice with both acute and chronic DSS-triggered colitis had significantly higher DAI and colon histopathological scores in contrast to the control groups (P < 0.0001, P < 0.0001), and the colon was remarkably shortened (P < 0.0001, P < 0.0001). The gut microbiota α-diversity was partly downregulated in both acute and chronic colitis groups in contrast to their respective control groups (Pielou index P = 0.0022, P = 0.0649; Shannon index P = 0.0022, P = 0.0931). The reduction in the Pielou and Shannon indices were more obvious in mice with acute colitis (P = 0.0022, P = 0.0043). The relative abundance of Bacteroides and Turicibacter was increased (all P < 0.05), while that of Lachnospiraceae, Ruminococcaceae, Ruminiclostridium, Rikenella, Alistipes, Alloprevotella, and Butyricicoccus was significantly decreased after acute DSS induction (all P < 0.05). The relative abundance of Bacteroides, Akkermansia, Helicobacter, Parabacteroides, Erysipelatoclostridium, Turicibacter and Romboutsia was also markedly increased (all P < 0.05), and that of Lachnospiraceae_NK4A136_group, Alistipes, Enterorhabdus, Prevotellaceae_UCG-001, Butyricicoccus, Ruminiclostridium_6, Muribaculum, Ruminococcaceae_NK4A214_group, Family_XIII_UCG-001 and Flavonifractor was significantly decreased after chronic DSS induction (all P < 0.05). CONCLUSION: DSS-induced acute and chronic colitis demonstrated similar symptoms and histopathological changes. The changes in the gut microbiota of the acute colitis model were closer to that observed in UC. The acute colitis model had greater abundance of SCFAs-producing bacteria and lower α-diversity compared to the chronic colitis model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02342-8. BioMed Central 2021-10-16 /pmc/articles/PMC8520286/ /pubmed/34654370 http://dx.doi.org/10.1186/s12866-021-02342-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (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 Xu, Hao-Ming Huang, Hong-Li Liu, Yan-Di Zhu, Jia-Qi Zhou, You-Lian Chen, Hui-Ting Xu, Jing Zhao, Hai-Lan Guo, Xue Shi, Wei Nie, Yu-Qiang Zhou, Yong-Jian Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title | Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title_full | Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title_fullStr | Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title_full_unstemmed | Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title_short | Selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
title_sort | selection strategy of dextran sulfate sodium-induced acute or chronic colitis mouse models based on gut microbial profile |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520286/ https://www.ncbi.nlm.nih.gov/pubmed/34654370 http://dx.doi.org/10.1186/s12866-021-02342-8 |
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