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Narrative review on sepsis and the microbiome, highlighting unresolved causality and variability.

Narrative review on sepsis and the microbiome, highlighting unresolved causality and variability.
Photo by National Institute of Allergy and Infectious Diseases / Unsplash
Key Takeaway
Consider that microbiome-based sepsis approaches remain experimental due to unresolved causality and variability.

This is a narrative review focusing on the role of the microbiome in sepsis. The authors synthesize existing evidence, noting that causal relationships between the microbiome and sepsis outcomes remain unresolved. They emphasize that inter-individual variability and context-dependent responses complicate the interpretation of current findings.

The review does not report pooled effect sizes or specific trial data, as it is not a meta-analysis. Instead, it presents qualitative conclusions about the complexity of host–microbiome interactions in sepsis. The authors argue that current understanding is insufficient to support microbiome-based interventions.

Key limitations noted include unresolved causality, inter-individual variability, context-dependent responses, and safety concerns. The authors call for longitudinal multi-omic profiling, host–microbiome phenotyping, and mechanism-informed interventional trials to enable precision approaches.

Practice relevance is not specified in the review. The evidence is early and uncertain, so clinicians should interpret findings cautiously and await more robust data before considering microbiome-directed strategies in sepsis care.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Sepsis frequently involves early gastrointestinal dysfunction, in which intestinal barrier breakdown and microbiota dysbiosis amplify systemic inflammation and contribute to multi-organ failure. Emerging evidence indicates that the gut is not merely a bystander in sepsis but an active driver of pathogenic cascades through epithelial injury, mucosal immune dysregulation, ischemia–reperfusion stress, and impaired motility, collectively promoting microbial translocation and immune deviation. In parallel, sepsis is associated with profound remodeling of the gut microbiome, characterized by reduced commensal diversity, expansion of pathobionts, and functional shifts in key microbial metabolites, including short-chain fatty acids, bile acids, and tryptophan-derived products, which further compromise mucosal integrity and host immune tone. This narrative review synthesizes experimental, translational, and clinical findings to elucidate the bidirectional interaction gut barrier–microbiota interplay in sepsis and to summarize mechanistic links across epithelial, immune, and metabolic signaling pathways, including gut-liver and gut-brain axes relevant to sepsis-associated organ dysfunction. dysfunctional microbial community leads to systemic immune deviation, multi-organ dysfunction and sepsis-associated encephalopathy, a common and severe neurological complication of sepsis. We also discuss emerging therapeutic strategies targeting the gut–microbiota axis—such as early enteral nutrition, prebiotics/postbiotics, defined microbial consortia, fecal microbiota transplantation, and metabolite-based supplementation—and evaluate their potential and limitations in septic populations. Finally, we highlight key challenges, including unresolved causality, inter-individual variability, context-dependent responses, and safety concerns, underscoring the need for longitudinal multi-omic profiling, host–microbiome phenotyping, and mechanism-informed interventional trials to enable precision microbiome-based approaches for sepsis.
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