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Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model
Clostridioides difficile infection (CDI) as of recent has become a great concern to the impact on human health due to its high hazardous risk and rate of recurrence. Live bacterial therapeutics is a promising method to treat or prevent CDI. Here, a synthetic microbial consortia (SMC) B10 was constru...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10527189/ https://www.ncbi.nlm.nih.gov/pubmed/37602713 http://dx.doi.org/10.1111/1751-7915.14333 |
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author | Liu, Jinqiu Zhu, Wei Lessing, Duncan James Chu, Weihua |
author_facet | Liu, Jinqiu Zhu, Wei Lessing, Duncan James Chu, Weihua |
author_sort | Liu, Jinqiu |
collection | PubMed |
description | Clostridioides difficile infection (CDI) as of recent has become a great concern to the impact on human health due to its high hazardous risk and rate of recurrence. Live bacterial therapeutics is a promising method to treat or prevent CDI. Here, a synthetic microbial consortia (SMC) B10 was constructed using probiotic strains with antibacterial and anti‐quorum sensing activities, and the therapeutic effect of SMC B10 against C. difficile infection was evaluated in vitro. Compared to the model group, the treatment of SMC B10 significantly increased the survival rate. The clinical signs of mice were significantly ameliorated, especially the cecum injury, while the secretion of pro‐inflammatory associated cytokines such as IL‐1α, IL‐6, IL‐17A and TNF‐α was reduced, the expression of TLR4 was inhibited, which alleviated the inflammatory response, and the expression of the tight junction protein Claudin‐1 was increased, ultimately promoting the recovery of host health. The treatment of B10 restored gut microbiota dysbiosis and led to a healthy intestinal microbiota structure, significantly improved alpha diversity, suppressing potentially harmful bacteria and restoring other core bacterial species. In conclusion, SMC B10 can effectively treat CDI through modulate gut microbiota and attenuate the inflammatory response. |
format | Online Article Text |
id | pubmed-10527189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105271892023-09-28 Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model Liu, Jinqiu Zhu, Wei Lessing, Duncan James Chu, Weihua Microb Biotechnol Research Articles Clostridioides difficile infection (CDI) as of recent has become a great concern to the impact on human health due to its high hazardous risk and rate of recurrence. Live bacterial therapeutics is a promising method to treat or prevent CDI. Here, a synthetic microbial consortia (SMC) B10 was constructed using probiotic strains with antibacterial and anti‐quorum sensing activities, and the therapeutic effect of SMC B10 against C. difficile infection was evaluated in vitro. Compared to the model group, the treatment of SMC B10 significantly increased the survival rate. The clinical signs of mice were significantly ameliorated, especially the cecum injury, while the secretion of pro‐inflammatory associated cytokines such as IL‐1α, IL‐6, IL‐17A and TNF‐α was reduced, the expression of TLR4 was inhibited, which alleviated the inflammatory response, and the expression of the tight junction protein Claudin‐1 was increased, ultimately promoting the recovery of host health. The treatment of B10 restored gut microbiota dysbiosis and led to a healthy intestinal microbiota structure, significantly improved alpha diversity, suppressing potentially harmful bacteria and restoring other core bacterial species. In conclusion, SMC B10 can effectively treat CDI through modulate gut microbiota and attenuate the inflammatory response. John Wiley and Sons Inc. 2023-08-21 /pmc/articles/PMC10527189/ /pubmed/37602713 http://dx.doi.org/10.1111/1751-7915.14333 Text en © 2023 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Liu, Jinqiu Zhu, Wei Lessing, Duncan James Chu, Weihua Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title | Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title_full | Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title_fullStr | Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title_full_unstemmed | Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title_short | Synthetic microbial consortia for the treatment of Clostridioides difficile infection in mice model |
title_sort | synthetic microbial consortia for the treatment of clostridioides difficile infection in mice model |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10527189/ https://www.ncbi.nlm.nih.gov/pubmed/37602713 http://dx.doi.org/10.1111/1751-7915.14333 |
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