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Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice
Clostridioides difficile infection (CDI) is the leading cause of hospital-acquired diarrhea, and emerging evidence has linked dietary components with CDI pathogenesis, suggesting that dietary modulation may be an effective strategy for prevention. Here, we show that mice fed a high-fat/low-fiber “We...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975876/ https://www.ncbi.nlm.nih.gov/pubmed/35365681 http://dx.doi.org/10.1038/s41522-022-00276-1 |
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author | Hazleton, Keith Z. Martin, Casey G. Orlicky, David J. Arnolds, Kathleen L. Nusbacher, Nichole M. Moreno-Huizar, Nancy Armstrong, Michael Reisdorph, Nichole Lozupone, Catherine A. |
author_facet | Hazleton, Keith Z. Martin, Casey G. Orlicky, David J. Arnolds, Kathleen L. Nusbacher, Nichole M. Moreno-Huizar, Nancy Armstrong, Michael Reisdorph, Nichole Lozupone, Catherine A. |
author_sort | Hazleton, Keith Z. |
collection | PubMed |
description | Clostridioides difficile infection (CDI) is the leading cause of hospital-acquired diarrhea, and emerging evidence has linked dietary components with CDI pathogenesis, suggesting that dietary modulation may be an effective strategy for prevention. Here, we show that mice fed a high-fat/low-fiber “Western-type” diet (WD) had dramatically increased mortality in a murine model of antibiotic-induced CDI compared to a low-fat/low-fiber (LF/LF) diet and standard mouse chow controls. We found that the WD had a pro- C. difficile bile acid composition that was driven in part by higher levels of primary bile acids that are produced to digest fat, and a lower level of secondary bile acids that are produced by the gut microbiome. This lack of secondary bile acids was associated with a greater disturbance to the gut microbiome with antibiotics in both the WD and LF/LF diet compared to mouse chow. Mice fed the WD also had the highest level of toxin TcdA just prior to the onset of mortality, but not of TcdB or increased inflammation. These findings indicate that dietary intervention to decrease fat may complement previously proposed dietary intervention strategies to prevent CDI in high-risk individuals. |
format | Online Article Text |
id | pubmed-8975876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89758762022-04-20 Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice Hazleton, Keith Z. Martin, Casey G. Orlicky, David J. Arnolds, Kathleen L. Nusbacher, Nichole M. Moreno-Huizar, Nancy Armstrong, Michael Reisdorph, Nichole Lozupone, Catherine A. NPJ Biofilms Microbiomes Article Clostridioides difficile infection (CDI) is the leading cause of hospital-acquired diarrhea, and emerging evidence has linked dietary components with CDI pathogenesis, suggesting that dietary modulation may be an effective strategy for prevention. Here, we show that mice fed a high-fat/low-fiber “Western-type” diet (WD) had dramatically increased mortality in a murine model of antibiotic-induced CDI compared to a low-fat/low-fiber (LF/LF) diet and standard mouse chow controls. We found that the WD had a pro- C. difficile bile acid composition that was driven in part by higher levels of primary bile acids that are produced to digest fat, and a lower level of secondary bile acids that are produced by the gut microbiome. This lack of secondary bile acids was associated with a greater disturbance to the gut microbiome with antibiotics in both the WD and LF/LF diet compared to mouse chow. Mice fed the WD also had the highest level of toxin TcdA just prior to the onset of mortality, but not of TcdB or increased inflammation. These findings indicate that dietary intervention to decrease fat may complement previously proposed dietary intervention strategies to prevent CDI in high-risk individuals. Nature Publishing Group UK 2022-04-01 /pmc/articles/PMC8975876/ /pubmed/35365681 http://dx.doi.org/10.1038/s41522-022-00276-1 Text en © The Author(s) 2022 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 Hazleton, Keith Z. Martin, Casey G. Orlicky, David J. Arnolds, Kathleen L. Nusbacher, Nichole M. Moreno-Huizar, Nancy Armstrong, Michael Reisdorph, Nichole Lozupone, Catherine A. Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title | Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title_full | Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title_fullStr | Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title_full_unstemmed | Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title_short | Dietary fat promotes antibiotic-induced Clostridioides difficile mortality in mice |
title_sort | dietary fat promotes antibiotic-induced clostridioides difficile mortality in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975876/ https://www.ncbi.nlm.nih.gov/pubmed/35365681 http://dx.doi.org/10.1038/s41522-022-00276-1 |
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