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恒河猴自发性糖尿病及糖尿病前期相关的微生物群和代谢物的改变。

Alterations in Microbiota and Metabolites Related to Spontaneous Diabetes and Pre-Diabetes in Rhesus Macaques.

机构信息

Key Laboratory of Bio-Resources and Eco-Environment (Ministry of Education), College of Life Sciences, Sichuan University, No. 24 South Section 1, Yihuan Road, Chengdu 610065, China.

SCU-SGHB Joint Laboratory on Non-Human Primates Research, Sichuan Green-House Biotech Co., Ltd., Meishan 620000, China.

出版信息

Genes (Basel). 2022 Aug 24;13(9):1513. doi: 10.3390/genes13091513.

DOI:10.3390/genes13091513
PMID:36140683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9498908/
Abstract

Spontaneous type 2 diabetes mellitus (T2DM) macaques are valuable resources for our understanding the pathological mechanism of T2DM. Based on one month's fasting blood glucose survey, we identified seven spontaneous T2DM macaques and five impaired glucose regulation (IGR) macaques from 1408 captive individuals. FPG, HbA1c, FPI and IR values were significant higher in T2DM and IGR than in controls. 16S rRNA sequencing of fecal microbes showed the significantly greater abundance of , bacteria inhibiting the production of secondary bile acids, and , bacteria producing short-chain fatty acids was significantly lower in T2DM macaques. In addition, several opportunistic pathogens, such as and were significantly more abundant in both T2DM and IGR macaques. Fecal metabolites analysis based on UHPLC-MS identified 50 differential metabolites (DMs) between T2DM and controls, and 26 DMs between IGR and controls. The DMs were significantly enriched in the bile acids metabolism, fatty acids metabolism and amino acids metabolism pathways. Combining results from physiochemical parameters, microbiota and metabolomics, we demonstrate that the imbalance of gut microbial community leading to the dysfunction of glucose, bile acids, fatty acids and amino acids metabolism may contribute to the hyperglycaemia in macaques, and suggest several microbes and metabolites are potential biomarkers for T2DM and IGR macaques.

摘要

自发性 2 型糖尿病(T2DM)猕猴是我们理解 T2DM 病理机制的宝贵资源。基于一个月的空腹血糖调查,我们从 1408 只圈养个体中鉴定出 7 只自发性 T2DM 猕猴和 5 只糖调节受损(IGR)猕猴。与对照组相比,T2DM 和 IGR 猕猴的 FPG、HbA1c、FPI 和 IR 值显著更高。粪便微生物的 16S rRNA 测序显示,T2DM 猕猴中抑制次级胆汁酸生成的细菌和产生短链脂肪酸的细菌的丰度显著降低。此外,几种机会性病原体,如 和 ,在 T2DM 和 IGR 猕猴中也明显更为丰富。基于 UHPLC-MS 的粪便代谢物分析在 T2DM 与对照组之间鉴定出 50 个差异代谢物(DMs),在 IGR 与对照组之间鉴定出 26 个 DMs。DMs 在胆汁酸代谢、脂肪酸代谢和氨基酸代谢途径中显著富集。综合生理化学参数、微生物组和代谢组学的结果,我们证明肠道微生物群落的失衡导致葡萄糖、胆汁酸、脂肪酸和氨基酸代谢功能障碍可能导致猕猴的高血糖,并且提示了一些微生物和代谢物可能是 T2DM 和 IGR 猕猴的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/6443f6965a36/genes-13-01513-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/ce2507806a15/genes-13-01513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/3aae0ad8799d/genes-13-01513-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/7688f190fd1f/genes-13-01513-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/8f9cbca29627/genes-13-01513-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/e012a01b8e1e/genes-13-01513-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/6443f6965a36/genes-13-01513-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/ce2507806a15/genes-13-01513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/3aae0ad8799d/genes-13-01513-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/7688f190fd1f/genes-13-01513-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/8f9cbca29627/genes-13-01513-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/e012a01b8e1e/genes-13-01513-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013b/9498908/6443f6965a36/genes-13-01513-g006.jpg

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