Bhunyakarnjanarat T.Suksamai C.Wannigama D.L.Doi K.Chancharoenthana W.Leelahavanichkul A.Mahidol University2026-05-162026-05-162026-01-01Animal Models and Experimental Medicine (2026)20965451https://repository.li.mahidol.ac.th/handle/123456789/116759Background: Gut barrier integrity prevents microbial translocation and systemic infection. Chronic alcohol disrupts this barrier, but its role in infection susceptibility among immune-compromised hosts remains unclear. We investigated how chronic alcohol promotes gut barrier dysfunction, endotoxemia, and dysbiosis, predisposing to bacterial translocation and sepsis. Methods: Twenty-four-week-old female FcγRIIb^−/− and wild-type mice received oral gavage of 35% ethanol (4.2 g/kg/day) or water for 10 weeks. Gut barrier integrity was assessed by serum endotoxin, FITC-dextran permeability, ileal claudin-1, and intestinal IgG/neutrophil infiltration. Systemic inflammation was evaluated by serum TNF-α, IL-1β, and IL-6; gut microbiota by 16S rRNA sequencing. Bone marrow–derived macrophages and hepatocytes from both genotypes were stimulated with LPS or ethanol to assess inflammatory responses, mitochondrial damage, and cGAS-STING activation. Results: Chronic alcohol induced gut barrier dysfunction in both groups, with more severe effects in FcγRIIb^−/− mice, which showed marked increases in serum endotoxin and FITC-dextran permeability, reduced claudin-1, and enhanced intestinal IgG deposition with neutrophil accumulation. Serum TNF-α, IL-1β, and IL-6 were significantly elevated, reflecting a sepsis-like profile. Alcohol induced dysbiosis with an increased Firmicutes-to-Bacteroidota ratio, elevated Lachnospiraceae, and reduced Alistipes, Bacteroides, and Odoribacter. In vitro, LPS elicited stronger inflammation than ethanol in both cell types, with FcγRIIb^−/− cells producing greater cytokine levels. Both stimuli caused comparable mitochondrial damage and cGAS-STING activation. Conclusions: Alcohol-induced gut barrier dysfunction, endotoxemia, and dysbiosis predispose to bacterial translocation and early sepsis, particularly in hosts with impaired inhibitory Fcγ receptor signaling, supporting gut barrier preservation as a strategy for preventing alcohol-associated infections and sepsis.Biochemistry, Genetics and Molecular BiologyMedicineVeterinaryHealth ProfessionsArticleSCOPUS10.1002/ame2.702182-s2.0-10503836541525762095