copri Prevotella 可减轻小鼠的高血糖症状并调节肠道微生物群和代谢状况。

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-07-23 Epub Date: 2024-06-27 DOI:10.1128/msystems.00532-24
Caixin Yang, Ruiting Lan, Lijun Zhao, Ji Pu, Dalong Hu, Jing Yang, Huimin Zhou, Lichao Han, Lin Ye, Dong Jin, Jianguo Xu, Liyun Liu
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引用次数: 0

摘要

copri 普雷沃特氏菌是肠道普雷沃特氏菌属中的主要菌种,其基因组异质性强,分离困难,因此对该菌种的研究很少。本研究旨在探讨 P. copri 对高血糖的影响。研究人员从健康人体内分离出 39 株菌株,并选择葡萄糖消耗量最高的 3 株菌株(HF2123、HF1478 和 HF2130)来评估补充 copri 真菌对高血糖的影响。微生物组学和非目标代谢组学被用来揭示潜在的机制。糖尿病 db/db 小鼠口服 P. copri 可增加胰高血糖素样肽-1(GLP-1)的表达和分泌,显著改善高血糖、胰岛素抵抗和脂质积累,并减轻胰腺、肝脏和结肠的病理形态。P. copri 改变了糖尿病 db/db 小鼠肠道微生物群的组成,其特点是增加了类杆菌属与固醇菌属的比例,提高了 Bacteroides、Akkermansia 和 Faecalibacterium 属的相对丰度。使用 P. copri 进行干预后,粪便代谢分析表明富马酸和同型半胱氨酸含量下降,谷氨酰胺含量上升。此外,氨基酸代谢和 cAMP/PKA 信号通路也得到了丰富。我们的研究结果表明,P. copri 能改善糖尿病 db/db 小鼠的糖代谢异常。特别是其中的一个 P. copri 菌株 HF2130 在改善高血糖方面表现优异,可能具有作为抗高血糖益生菌的潜力:作为人类肠道生态系统的核心成员,Prevotelal copri 在以往的研究中与葡萄糖代谢平衡有关。然而,这些结果往往来自于元基因组研究,而且实验研究仅基于 DSM 18205T 型菌株。因此,需要从更多的分离菌株中获得更多的实验证据,以便根据其高度的基因组异质性来验证这些结果。在本研究中,我们分离了不同的菌株分支,并证明了 P. copri 可通过调节微生物活性来改善高血糖小鼠的代谢状况。这一发现支持了 P. copri 在宿主葡萄糖代谢中的作用。
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Prevotella copri alleviates hyperglycemia and regulates gut microbiota and metabolic profiles in mice.

Prevotella copri is the dominant species of the Prevotella genus in the gut, which is genomically heterogeneous and difficult to isolate; hence, scarce research was carried out for this species. This study aimed to investigate the effect of P. copri on hyperglycemia. Thirty-nine strains were isolated from healthy individuals, and three strains (HF2123, HF1478, and HF2130) that had the highest glucose consumption were selected to evaluate the effects of P. copri supplementation on hyperglycemia. Microbiomics and non-target metabolomics were used to uncover the underlying mechanisms. Oral administration of P. copri in diabetic db/db mice increased the expression and secretion of glucagon-like peptide-1 (GLP-1), significantly improved hyperglycemia, insulin resistance, and lipid accumulation, and alleviated the pathological morphology in the pancreas, liver, and colon. P. copri changed the composition of the gut microbiota of diabetic db/db mice, which was characterized by increasing the ratio of Bacteroidetes to Firmicutes and increasing the relative abundance of genera Bacteroides, Akkermansia, and Faecalibacterium. After intervention with P. copri, fecal metabolic profiling showed that fumaric acid and homocysteine contents decreased, and glutamine contents increased. Furthermore, amino acid metabolism and cAMP/PKA signaling pathways were enriched. Our findings indicate that P. copri improved glucose metabolism abnormalities in diabetic db/db mice. Especially, one of the P. copri strains, HF2130, has shown superior performance in improving hyperglycemia, which may have the potential as a probiotic against hyperglycemia.

Importance: As a core member of the human intestinal ecosystem, Prevotelal copri has been associated with glucose metabolic homeostasis in previous studies. However, these results have often been derived from metagenomic studies, and the experimental studies have been based solely on the type of strain DSM 18205T. Therefore, more experimental evidence from additional isolates is needed to validate the results according to their high genomic heterogeneity. In this study, we isolated different branches of strains and demonstrated that P. copri could improve the metabolic profile of hyperglycemic mice by modulating microbial activity. This finding supports the causal contribution of P. copri in host glucose metabolism.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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