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多组学分析揭示肥胖症患者肠道微生物硫胺素生成发生改变。

Multi-omics analyses reveal altered gut microbial thiamine production in obesity.

作者信息

Xia Yu, Lu Longya, Wang Lulu, Qiu Yanyan, Liu Xingyin, Ge Weihong

机构信息

Department of Pharmacy, China Pharmaceutical University Nanjing Drum Tower Hospital, Nanjing, China.

School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, China.

出版信息

Front Microbiol. 2025 Jun 17;16:1516393. doi: 10.3389/fmicb.2025.1516393. eCollection 2025.

Abstract

OBJECTIVE

Accumulating evidence highlights the important role of B vitamins in maintaining the balance of gut microbial ecology and metabolism, however, few studies have focused on changes in B vitamins homeostasis in the gut and their associations with disease. This study aims to investigate the potential interplay between B vitamins, gut microbiota, and obesity.

METHODS

We conducted an integrated analysis of fecal shotgun metagenomics, fecal metabolome concerning B vitamins and short chain fatty acids (SCFAs), and obese phenotypes in a cohort of 63 participants, including 31 healthy controls and 32 individuals with obesity.

RESULTS

Metabolomic analysis identified significantly lower levels of fecal thiamine in individuals with obesity ( < 0.001). Fecal thiamine levels exhibited a positive correlation with HDL-C and a negative correlation with BMI, DBP, fasting serum insulin, HOMA-IR, triglycerides, and propionic acid. Binary logistics regression suggested that fecal thiamine deficiency may be a potential contributor to the onset of obesity (Odds ratio: 0.295). Metagenomic analysis indicated that the microbial composition in individuals with obesity was characterized by a predominance of potential opportunistic pathogens, a loss of complexity, and a decrease in thiamine-producing bacteria. Integrated analysis indicated that thiamine deficiency was positively associated with the depletion of thiamine auxotrophic bacteria in the obese microbiome. Functional analysis revealed that KOs content for enzymes involved in the microbial production of thiamine were significantly lower in obesity, including tRNA uracil 4-sulfurtransferase (ThiI, = 0.001) and nucleoside-triphosphatase (NTPCR, = 0.006), both of which were positively associated with fecal thiamine.

CONCLUSION

Our study highlights the impairment of microbial thiamine production and its broad associations with gut microbiota dysbiosis and obesity-related phenotypes. Our findings provide a rationale for developing treatments that utilize thiamine to prevent obesity by modulating gut microbiota.

摘要

目的

越来越多的证据表明B族维生素在维持肠道微生物生态和代谢平衡中起重要作用,然而,很少有研究关注肠道中B族维生素稳态的变化及其与疾病的关联。本研究旨在探讨B族维生素、肠道微生物群和肥胖之间的潜在相互作用。

方法

我们对63名参与者(包括31名健康对照者和32名肥胖个体)的粪便鸟枪法宏基因组学、与B族维生素和短链脂肪酸(SCFAs)有关的粪便代谢组以及肥胖表型进行了综合分析。

结果

代谢组学分析发现肥胖个体粪便中的硫胺素水平显著降低(<0.001)。粪便硫胺素水平与高密度脂蛋白胆固醇呈正相关,与体重指数、舒张压、空腹血清胰岛素、胰岛素抵抗指数、甘油三酯和丙酸呈负相关。二元逻辑回归表明,粪便硫胺素缺乏可能是肥胖发病的一个潜在因素(比值比:0.295)。宏基因组学分析表明,肥胖个体的微生物组成以潜在的机会性病原体占优势、复杂性丧失和产硫胺素细菌减少为特征。综合分析表明,硫胺素缺乏与肥胖微生物群中硫胺素营养缺陷型细菌的消耗呈正相关。功能分析显示,肥胖人群中参与微生物硫胺素产生的酶的KO含量显著降低,包括tRNA尿嘧啶4-硫转移酶(ThiI,=0.001)和核苷三磷酸酶(NTPCR,=0.006),两者均与粪便硫胺素呈正相关。

结论

我们的研究强调了微生物硫胺素产生的损害及其与肠道微生物群失调和肥胖相关表型的广泛关联。我们的研究结果为开发利用硫胺素通过调节肠道微生物群来预防肥胖的治疗方法提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8430/12209360/81d165fa17b8/fmicb-16-1516393-g0001.jpg

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