The widespread prevalence of
Helicobacter pylori
infection, particularly in China, contributes to the development of gastrointestinal diseases. Antibiotics have limitations, including adverse reactions and increased antibiotic resistance. Therefore, identification of novel gastrogenic probiotics capable of surviving the acidic gastric environment and effectively combating
H. pylori
infection has potential in restoring gastric microbiota homeostasis. Five novel strains of human gastrogenic
Weizmannia coagulans
(BCF-01–05) were isolated from healthy gastric mucosa and characterized using 16S rDNA identification. Acid resistance,
H. pylori
inhibition, and adherence to gastric epithelial cells were evaluated in
in-vitro
experiments and the molecular mechanism explored in
in-vivo
experiments. Among the gastric-derived
W. coagulans
strains, BCF-01 exhibited the strongest adhesion and
H. pylori
inhibition, warranting further
in-vivo
safety evaluation. Through 16S rRNA sequencing of a mouse model, BCF-01 was determined to significantly restore
H. pylori
-associated gastric dysbiosis and increase the abundance of potential probiotic bacteria. Furthermore, BCF-01 enhanced mucosal tight junction protein expression and inhibited the TLR4-NFκB-pyroptosis signaling pathway in macrophages, as demonstrated by qRT-PCR and western blotting.
These findings highlight the potential of BCF-01 in the prevention and control of
H. pylori
infection. Specifically, treatment with BCF-01 effectively restored gastric microecology and improved
H. pylori
-mediated mucosal barrier destruction while reducing inflammation through inhibition of the TLR4-NFκB-pyroptosis signaling pathway in macrophages. BCF-01 is a promising alternative to traditional triple therapy for
H. pylori
infections, offering minimal side effects with high suitability for high-risk individuals.