Diet-conditioned microbiota enhances fecal microbiota transplantation efficacy in alcoholic liver disease through caproic acid-PPARα signaling
Nishu ChoudharyiD, Ashi MittaliD, Sandeep KumariD, Kavita Yadav, Anupama KumariiD, Deepanshu MaheshwariiD, Pragyan Parimita RathiD, Jaswinder Singh MarasiD, Asif MohmmediD, Anupam Kumar, Shiv Sarin, Shvetank SharmaiD
Abstract
Background and Aim: Fecal microbiota transplantation (FMT) in Alcohol-related liver disease (ALD) has shown therapeutic potential, with variable efficacy and unclear mechanism. Because dietary protein influences gut microbiota composition, we hypothesized that donor dietary preconditioning could enhance FMT efficacy. We therefore examined in a murine ALD model if high-protein donor diet improves FMT outcome. Methods: ALD was induced in C57BL/6N mice using a Lieber-DeCarli ethanol diet combined with thioacetamide administration for 12 weeks. FMT was performed using stool from diet-modulated donors, and recovery was assessed on day7 post-FMT. Multi-omics analysis using 16s rRNA and mass spectroscopy was performed for Gut microbiota composition, plasma- and stool-metabolome, and hepatic proteomes. Multi-omics outcomes were validated in ALD animal and Huh7 hepatocytes. Results: Both protein-based FMTs improved ALD recovery; Veg-FMT indicated superior efficacy, significantly reducing hepatic injury (AST 1.2FC, p=0.002; bilirubin 1.2FC, p=0.03; steatosis 1.7FC,p=0.01) and restoring gut barrier integrity (occludin 1.5FC,p=0.04; mucin 2 2.2FC, p=002; and plasma endotoxin 1.7FC, p=0.02). A significant 2FC increase was observed in Lachnospiraceae NK4A136, Coriobacteriaceae UCG-002, and short-chain fatty acids, particularly caproic acid. Functional validation confirmed that caproic acid promoted hepatic fatty acid {beta}-oxidation through PPAR-dependent mechanisms, reducing triglyceride accumulation and lipogenesis in both cellular and animal models. Conclusion: Donor preconditioning with a plant-protein enriched diet enhances FMT efficacy in ALD by gut microbiota modulation with increased metabolites like caproic acid. These findings highlight a microbiota-metabolite-host axis through which diet-modulated FMT improves hepatic lipid metabolism and injury, and identifies a pathway via which FMT imparts its effect.
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