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The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process
BACKGROUND: Dairy cows are susceptible to postpartum systemic oxidative stress (OS), which leads to significant production loss and metabolic disorders. The gut microbiota has been linked to host health and stress levels. However, to what extent the gut microbiota is associated with postpartum OS re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122372/ https://www.ncbi.nlm.nih.gov/pubmed/37087457 http://dx.doi.org/10.1186/s40168-023-01535-9 |
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author | Gu, Fengfei Zhu, Senlin Hou, Jinxiu Tang, Yifan Liu, Jian-Xin Xu, Qingbiao Sun, Hui-Zeng |
author_facet | Gu, Fengfei Zhu, Senlin Hou, Jinxiu Tang, Yifan Liu, Jian-Xin Xu, Qingbiao Sun, Hui-Zeng |
author_sort | Gu, Fengfei |
collection | PubMed |
description | BACKGROUND: Dairy cows are susceptible to postpartum systemic oxidative stress (OS), which leads to significant production loss and metabolic disorders. The gut microbiota has been linked to host health and stress levels. However, to what extent the gut microbiota is associated with postpartum OS remains unknown. In this study, the contribution of the fecal microbiota to postpartum systemic OS and its underlying mechanisms were investigated by integrating 16S rRNA gene sequencing, metagenomics, and metabolomics in postpartum dairy cattle and by transplanting fecal microbiota from cattle to mice. RESULTS: A strong link was found between fecal microbial composition and postpartum OS, with an explainability of 43.1%. A total of 17 significantly differential bacterial genera and 19 species were identified between cows with high (HOS) and low OS (LOS). Among them, 9 genera and 16 species showed significant negative correlations with OS, and Marasmitruncus and Ruminococcus_sp._CAG:724 had the strongest correlations. The microbial functional analysis showed that the fecal microbial metabolism of glutamine, glutamate, glycine, and cysteine involved in glutathione synthesis was lower in HOS cows. Moreover, 58 significantly different metabolites were identified between HOS and LOS cows, and of these metabolites, 19 were produced from microbiota or cometabolism of microbiota and host. Furthermore, these microbial metabolites were enriched in the metabolism of glutamine, glutamate, glycine, and cysteine. The mice gavaged with HOS fecal microbiota had significantly higher OS and lower plasma glutathione peroxidase and glutathione content than those orally administered saline or LOS fecal microbiota. CONCLUSIONS: Integrated results suggest that the fecal microbiota is responsible for OS and that lower glutathione production plays a causative role in HOS. These findings provide novel insights into the mechanisms of postpartum OS and potential regulatory strategies to alleviate OS in dairy cows. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01535-9. |
format | Online Article Text |
id | pubmed-10122372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101223722023-04-23 The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process Gu, Fengfei Zhu, Senlin Hou, Jinxiu Tang, Yifan Liu, Jian-Xin Xu, Qingbiao Sun, Hui-Zeng Microbiome Research BACKGROUND: Dairy cows are susceptible to postpartum systemic oxidative stress (OS), which leads to significant production loss and metabolic disorders. The gut microbiota has been linked to host health and stress levels. However, to what extent the gut microbiota is associated with postpartum OS remains unknown. In this study, the contribution of the fecal microbiota to postpartum systemic OS and its underlying mechanisms were investigated by integrating 16S rRNA gene sequencing, metagenomics, and metabolomics in postpartum dairy cattle and by transplanting fecal microbiota from cattle to mice. RESULTS: A strong link was found between fecal microbial composition and postpartum OS, with an explainability of 43.1%. A total of 17 significantly differential bacterial genera and 19 species were identified between cows with high (HOS) and low OS (LOS). Among them, 9 genera and 16 species showed significant negative correlations with OS, and Marasmitruncus and Ruminococcus_sp._CAG:724 had the strongest correlations. The microbial functional analysis showed that the fecal microbial metabolism of glutamine, glutamate, glycine, and cysteine involved in glutathione synthesis was lower in HOS cows. Moreover, 58 significantly different metabolites were identified between HOS and LOS cows, and of these metabolites, 19 were produced from microbiota or cometabolism of microbiota and host. Furthermore, these microbial metabolites were enriched in the metabolism of glutamine, glutamate, glycine, and cysteine. The mice gavaged with HOS fecal microbiota had significantly higher OS and lower plasma glutathione peroxidase and glutathione content than those orally administered saline or LOS fecal microbiota. CONCLUSIONS: Integrated results suggest that the fecal microbiota is responsible for OS and that lower glutathione production plays a causative role in HOS. These findings provide novel insights into the mechanisms of postpartum OS and potential regulatory strategies to alleviate OS in dairy cows. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01535-9. BioMed Central 2023-04-22 /pmc/articles/PMC10122372/ /pubmed/37087457 http://dx.doi.org/10.1186/s40168-023-01535-9 Text en © The Author(s) 2023 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 Gu, Fengfei Zhu, Senlin Hou, Jinxiu Tang, Yifan Liu, Jian-Xin Xu, Qingbiao Sun, Hui-Zeng The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title | The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title_full | The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title_fullStr | The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title_full_unstemmed | The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title_short | The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
title_sort | hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122372/ https://www.ncbi.nlm.nih.gov/pubmed/37087457 http://dx.doi.org/10.1186/s40168-023-01535-9 |
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