Cell ReportsMicrobiologyPeer-reviewed journal article
Integrative multi-omic analysis reveals oral microbiome-metabolome signatures of obesity
Ahmed A. ShibliD, Tsedenia W DenekewiD, Anique R. AhmadiD, Salah AbdelrazigiD, C. Leonor, Lina Utenova, Guihao Zhang, Mamoun AbdelBaqi, Yashaswi Malla, Muhammad Arshad, Marc ArnouxiD, Nizar DrouiD, Abdishakur M AbdulleiD, The UAE Healthy Future Study Investigators Group, Raghib AliiD, Shady A. AminiD, Youssef IdaghdouriD, Aashish R. JhaiD
Abstract
Obesity is a major global health challenge and a leading risk factor for cardiometabolic disorders. The global surge in obesity, driven by industrialization and the widespread consumption of low-fiber, ultra-processed food, highlights an urgent need for deeper biological insights. While the gut microbiome has been studied in the context of obesity, the contribution of the oral microbiome--the second largest microbial ecosystem in the human body-remains largely underexplored. Here, we report findings from a deeply-phenotyped prospective-cohort of 628 Emirati adults, leveraging amplicon sequencing of mouthwash samples and multi-omics profiling and functional and metabolic activity analysis of 97 obese individuals and 95 matched controls, making this the most comprehensive multi-omics analysis of the oral microbiome. We identified significant differences in oral microbial diversity, composition, functional pathways, and metabolic profiles between obese and non-obese groups. Integrated multi-omics analysis of the 192 matched metagenomes and metabolome samples uncovered significant metabolic reprogramming and altered energy regulation in obesity. Specifically, the oral microbiome of obese participants were enriched for the proinflammatory Streptococcus parasanguinis and Actinomyces oris, and the lactate-producing Oribacterium sinus. Many microbial pathways involved in dietary carbohydrate metabolism, histidine degradation, as well as the production of obesogenic biomolecules were also enriched in obese participants; however, B-vitamin and heme production pathways were depleted. Consequently, metabolites resulting from these pathways such as lactate, histidine derivatives, choline, uridine, and uracil were elevated in obesity. These consistent microbiome-metabolite shifts were strongly associated with prominent obesity-associated cardiometabolic markers, including serum triglycerides and alkaline phosphatases, establishing a robust link between oral microbiome and obesity. These findings provide the most comprehensive insights into how disrupted microbial-metabolic cross-talk in the oral cavity may contribute to obesity and related cardiometabolic disease risk, underscoring the potential of targeting of oral microbiome-host interactions as a novel avenue for obesity prevention and intervention.
- organism: human
- assay: metagenomics
- assay: metabolomics
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 5
- FWCI
- 34.19
- Field percentile
- top 1%
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