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The gastrointestinal and oral microbiota comprise the complex communities of bacteria, archaea, fungi, and viruses inhabiting the human digestive tract and oral cavity. These microbial ecosystems function as a collective metabolic organ, essential for digesting complex polysaccharides, synthesizing vitamins such as K and B12, and training the host immune system to distinguish between commensals and pathogens [1, 4]. Dysbiosis, characterized by a loss of microbial diversity or an overgrowth of opportunistic pathogens, is implicated in numerous local and systemic diseases, including Clostridioides difficile infection (CDI), inflammatory bowel disease (IBD), and periodontitis [3, 4]. Therapeutic interventions targeting the microbiota range from broad-spectrum antibiotics to precision live biotherapeutic products (LBPs) and fecal microbiota transplantation (FMT), which aim to restore a healthy ecological state [2]. While traditionally viewed as a collection of organisms, the microbiota is increasingly treated as a unified therapeutic target for modulating host physiology and treating chronic inflammatory and metabolic conditions [1, 2]. The oral microbiota specifically serves as a reservoir for pathogens that can enter the systemic circulation, contributing to cardiovascular and neurodegenerative pathologies [3]. As a therapeutic target, the microbiota offers a unique opportunity to modulate host health through the manipulation of complex biological networks rather than single molecular pathways [1].
Restoration of microbial diversity and ecological balance, competitive inhibition of pathogenic colonization, and modulation of host metabolic and inflammatory pathways through microbial metabolites.
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