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The host gut microbiota community is a vast and diverse ecosystem of trillions of microorganisms, primarily bacteria, residing in the human gastrointestinal tract that functions as a critical metabolic organ (Thursby & Juge, 2017). It plays a fundamental role in host physiology by fermenting non-digestible dietary fibers into short-chain fatty acids (SCFAs), synthesizing essential vitamins such as B12 and K, and regulating the development and activity of the host immune system (Fan & Pedersen, 2021). Beyond local digestion, the microbiota influences systemic health through the gut-brain axis and the production of metabolites that enter the systemic circulation (Cryan et al., 2019). Dysbiosis, or a pathological imbalance in this community, is strongly implicated in the pathogenesis of numerous diseases, including Clostridioides difficile infection, inflammatory bowel disease (IBD), and metabolic syndromes (Guinane & Cotter, 2013). Therapeutic interventions targeting the gut microbiota include the use of probiotics, prebiotics, and fecal microbiota transplantation (FMT), as well as newly FDA-approved defined microbial consortia like SER-109 designed to restore ecological balance (Khanna et al., 2022). This target represents a paradigm shift in pharmacology from single-molecule inhibition to the ecological restoration of a complex biological community.
Restoration of microbial diversity and ecological balance, competitive exclusion of pathogenic species, and modulation of host metabolic and immune pathways through the production of metabolites like short-chain fatty acids (Thursby & Juge, 2017; Khanna et al., 2022).
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