ORIGINAL RESEARCH article
Front. Microbiol.
Sec. Microorganisms in Vertebrate Digestive Systems
Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1516393
Multi-omics analyses reveal the alteration of gut microbial thiamine production in obesity
Provisionally accepted- 1China Pharmaceutical University, Nanjing, Jiangsu Province, China
- 2Nanjing Medical University, Nanjing, Jiangsu Province, China
- 3First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, Guangxi Zhuang Region, China
- 4Nanjing Drum Tower Hospital, Nanjing, Jiangsu Province, China
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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.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 (PWilcoxon < 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 thiamineproducing 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, PWilcoxon = 0.001) and nucleoside-triphosphatase (NTPCR, PWilcoxon = 0.006), both of which were positively associated with fecal thiamine.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.
Keywords: microbiota, fecal metabolomics, Thiamine, Short Chain Fatty Acids, Obesity
Received: 24 Oct 2024; Accepted: 09 May 2025.
Copyright: © 2025 XIA, Lu, Qiu, Wang, Liu and GE. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Xingyin Liu, Nanjing Medical University, Nanjing, 210029, Jiangsu Province, China
Weihong GE, Nanjing Drum Tower Hospital, Nanjing, 210008, Jiangsu Province, China
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