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Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation
This study was conducted to explore the therapeutic effect of the probiotic Bifidobacterium animalis subsp. lactis BLa80 on inflammatory bowel disease. A model of ulcerative colitis (UC) was induced in C57BL/6 mice by administering of 2.5% dextran sulphate sodium (DSS) for 8 days. After developing U...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174416/ https://www.ncbi.nlm.nih.gov/pubmed/35670877 http://dx.doi.org/10.1186/s13568-022-01411-z |
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author | Dong, Yao Liao, Wenyan Tang, Jing Fei, Teng Gai, Zhonghui Han, Mei |
author_facet | Dong, Yao Liao, Wenyan Tang, Jing Fei, Teng Gai, Zhonghui Han, Mei |
author_sort | Dong, Yao |
collection | PubMed |
description | This study was conducted to explore the therapeutic effect of the probiotic Bifidobacterium animalis subsp. lactis BLa80 on inflammatory bowel disease. A model of ulcerative colitis (UC) was induced in C57BL/6 mice by administering of 2.5% dextran sulphate sodium (DSS) for 8 days. After developing UC, some mice were treated via intragastric administration of BLa80 at a dose of 10(9) colony-forming units to assess the preventive effects of BLa80 on DSS-induced UC. Compared with non-treated UC model mice, BLa80-treated mice had reduced colon shortening and improvements in colonic tissue structure. Treatment with BLa80 also decreased the serum concentrations of the proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), interleukin (IL) 6 and IL-17 in mice. 16S rRNA gene sequencing revealed that BLa80 increased gut microbial diversity in mice and modulated UC-associated imbalances in the gut microbiota. BLa80 selectively promoted the growth of beneficial bacteria, including Romboutsia and Adlercreutzia, the abundances of which were negatively correlated with concentration of cellular inflammatory factors. In summary, the study results demonstrated that pretreatment with B. lactis BLa80 reduced intestinal inflammation and altered the gut microbiota, implying that BLa80 is a promising probiotic strain with potential therapeutic function in UC. |
format | Online Article Text |
id | pubmed-9174416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91744162022-06-09 Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation Dong, Yao Liao, Wenyan Tang, Jing Fei, Teng Gai, Zhonghui Han, Mei AMB Express Original Article This study was conducted to explore the therapeutic effect of the probiotic Bifidobacterium animalis subsp. lactis BLa80 on inflammatory bowel disease. A model of ulcerative colitis (UC) was induced in C57BL/6 mice by administering of 2.5% dextran sulphate sodium (DSS) for 8 days. After developing UC, some mice were treated via intragastric administration of BLa80 at a dose of 10(9) colony-forming units to assess the preventive effects of BLa80 on DSS-induced UC. Compared with non-treated UC model mice, BLa80-treated mice had reduced colon shortening and improvements in colonic tissue structure. Treatment with BLa80 also decreased the serum concentrations of the proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), interleukin (IL) 6 and IL-17 in mice. 16S rRNA gene sequencing revealed that BLa80 increased gut microbial diversity in mice and modulated UC-associated imbalances in the gut microbiota. BLa80 selectively promoted the growth of beneficial bacteria, including Romboutsia and Adlercreutzia, the abundances of which were negatively correlated with concentration of cellular inflammatory factors. In summary, the study results demonstrated that pretreatment with B. lactis BLa80 reduced intestinal inflammation and altered the gut microbiota, implying that BLa80 is a promising probiotic strain with potential therapeutic function in UC. Springer Berlin Heidelberg 2022-06-07 /pmc/articles/PMC9174416/ /pubmed/35670877 http://dx.doi.org/10.1186/s13568-022-01411-z Text en © The Author(s) 2022 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/) . |
spellingShingle | Original Article Dong, Yao Liao, Wenyan Tang, Jing Fei, Teng Gai, Zhonghui Han, Mei Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title | Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title_full | Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title_fullStr | Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title_full_unstemmed | Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title_short | Bifidobacterium BLa80 mitigates colitis by altering gut microbiota and alleviating inflammation |
title_sort | bifidobacterium bla80 mitigates colitis by altering gut microbiota and alleviating inflammation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174416/ https://www.ncbi.nlm.nih.gov/pubmed/35670877 http://dx.doi.org/10.1186/s13568-022-01411-z |
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