Drug intelligence / Profile preview

Bacteroides fragilis strain ZY-312

Development stage
Preclinical
Lead developer
Zhiyi Pharmaceutics
Modality
Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics
Administration
Oral
01

Overview

Bacteroides fragilis strain ZY-312 is a live, non-pathogenic, anaerobic probiotic bacterial strain isolated from the feces of a healthy, breast-fed infant. It exhibits high resistance to bile and moderate resistance to acidic conditions, allowing it to survive in the gastrointestinal tract. The strain enhances macrophage phagocytic function, modulates inflammatory signaling, and polarizes macrophages toward the M1 phenotype by upregulating IL-12, IL-1β, and inducible nitric oxide synthase. As a probiotic, ZY-312 has demonstrated efficacy in animal models of necrotizing enterocolitis (NEC), radiation-induced intestinal injury, and colitis. Its mechanisms of action include direct suppression of pathogenic bacteria (Cronobacter sakazakii), modulation of the host immune response (notably via the IL-22/STAT3 pathway), promotion of intestinal epithelial cell proliferation, stem cell regeneration, goblet cell (mucus-secreting cell) generation, and maintenance of tight junction integrity. These properties highlight its therapeutic potential in gastrointestinal disorders and suggest possible clinical applications as a next-generation probiotic, particularly in intestinal inflammation and injury[1][2][3][4][5][6][7].

Other names
B. fragilis ZY-312
02

Targets

IL12 (Interleukin-12)NOS2 (Nitric Oxide Synthase 2)IL22 (Interleukin 22)NLRP3 (Nod-like receptor family pyrin domain-containing protein 3)IL1B (Interleukin-1 beta)

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