The hindgut microbiome contributes to host oxidative stress in postpartum dairy cows by affecting glutathione synthesis process

被引:25
|
作者
Gu, Fengfei [1 ,2 ]
Zhu, Senlin [1 ,2 ]
Hou, Jinxiu [3 ]
Tang, Yifan [1 ,2 ]
Liu, Jian-Xin [1 ,2 ,4 ]
Xu, Qingbiao [3 ]
Sun, Hui-Zeng [1 ,2 ,4 ]
机构
[1] Zhejiang Univ, Coll Anim Sci, Inst Dairy Sci, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Minist Educ, Key Lab Mol Anim Nutr, Hangzhou 310058, Peoples R China
[3] Huazhong Agr Univ, Coll Anim Sci & Technol, Wuhan 430070, Peoples R China
[4] Zhejiang Univ, Minist Educ, Innovat Team Dev & Funct Anim Digest Syst, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
Dairy cows; Fecal microbiota transplantation; Glutathione synthesis; Multiomics; Oxidative stress; Transition period; GUT MICROBIOTA; INTESTINAL MICROBIOME; TRANSITION COW; DIET; INFLAMMATION; ENVIRONMENT; CIRRHOSIS; TOOL;
D O I
10.1186/s40168-023-01535-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:16
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