Sex-dependent effects on the gut microbiota and host metabolome in type 1 diabetic mice

被引:10
作者
Zhang, Xi [1 ,2 ]
Wang, Die [2 ]
Zheng, Yafei [2 ]
Tu, Yingxin [2 ]
Xu, Qingqing [2 ]
Jiang, Haowei [2 ]
Li, Chen [2 ]
Zhao, Liangcai [2 ]
Li, Yuping [1 ]
Zheng, Hong [1 ,2 ]
Gao, Hongchang [1 ,2 ]
机构
[1] Wenzhou Med Univ, Dept Pulm & Crit Care Med, Affiliated Hosp 1, Wenzhou 325015, Peoples R China
[2] Wenzhou Med Univ, Inst Metabon & Med NMR, Sch Pharmaceut Sci, Wenzhou 325035, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2021年 / 1867卷 / 12期
基金
中国国家自然科学基金;
关键词
Correlation network; Diabetes; Sex difference; Microbiome; Metabolomics; AMINO-ACID-METABOLISM; AUTOIMMUNITY; DATABASE;
D O I
10.1016/j.bbadis.2021.166266
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sexual dimorphism exists in the onset and development of type 1 diabetes (T1D), but its potential pathological mechanism is poorly understood. In the present study, we examined sex-specific changes in the gut microbiome and host metabolome of T1D mice via 16S rRNA gene sequencing and nuclear magnetic resonance (NMR)-based metabolomics approach, and aimed to investigate potential mechanism of the gut microbiota-host metabolic interaction in the sexual dimorphism of T1D. Our results demonstrate that female mice had a greater shift in the gut microbiota than male mice during the development of T1D; however, host metabolome was more susceptible to T1D in male mice. The correlation network analysis indicates that T1D-induced host metabolic changes may be regulated by the gut microbiota in a sex-specific manner, mainly involving short-chain fatty acids (SCFAs) metabolism, energy metabolism, amino acid metabolism, and choline metabolism. Therefore, our study suggests that sex-dependent "gut microbiota-host metabolism axis" may be implicated in the sexual dimorphism of T1D, and the link between microbes and metabolites might contribute to the prevention and treatment of T1D.
引用
收藏
页数:12
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