Chen Zhenhui, Tang Ziyu, Li Wendan, Deng Xiaoshi, Yu Lu, Yang Jixiang, Liu Jiaxin, Cheng Yunshui, Huang Wanwen, Guo Xiaotong, Shan Jiamin, Zhou Daixuan, Zeng Weisen, Bai Yang, Fan Hongying
Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical, Disease Research, School of Public Health, Southern Medical University, Guangzhou, China.
Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Gut Microbes. 2024 Jan-Dec;16(1):2313770. doi: 10.1080/19490976.2024.2313770. Epub 2024 Feb 9.
The widespread prevalence of 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 infection has potential in restoring gastric microbiota homeostasis. Five novel strains of human gastrogenic (BCF-01-05) were isolated from healthy gastric mucosa and characterized using 16S rDNA identification. Acid resistance, inhibition, and adherence to gastric epithelial cells were evaluated in experiments and the molecular mechanism explored in experiments. Among the gastric-derived strains, BCF-01 exhibited the strongest adhesion and inhibition, warranting further safety evaluation. Through 16S rRNA sequencing of a mouse model, BCF-01 was determined to significantly restore -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 infection. Specifically, treatment with BCF-01 effectively restored gastric microecology and improved -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 infections, offering minimal side effects with high suitability for high-risk individuals.
感染的广泛流行,尤其是在中国,促成了胃肠道疾病的发展。抗生素存在局限性,包括不良反应和抗生素耐药性增加。因此,鉴定能够在酸性胃环境中存活并有效对抗感染的新型胃源益生菌,对于恢复胃微生物群稳态具有潜力。从健康胃黏膜中分离出五株新型人源胃源菌(BCF-01-05),并使用16S rDNA鉴定进行表征。在体外实验中评估了耐酸性、幽门螺杆菌抑制以及对胃上皮细胞的黏附情况,并在体内实验中探索了分子机制。在源自胃的菌株中,BCF-01表现出最强的黏附力和幽门螺杆菌抑制作用,值得进一步进行体内安全性评估。通过对小鼠模型进行16S rRNA测序,确定BCF-01可显著恢复与幽门螺杆菌相关的胃生态失调,并增加潜在益生菌的丰度。此外,qRT-PCR和蛋白质印迹法表明,BCF-01增强了黏膜紧密连接蛋白的表达,并抑制了巨噬细胞中的TLR4-NFκB-焦亡信号通路。这些发现凸显了BCF-01在预防和控制幽门螺杆菌感染方面的潜力。具体而言,用BCF-01治疗可有效恢复胃微生态,改善幽门螺杆菌介导的黏膜屏障破坏,同时通过抑制巨噬细胞中的TLR4-NFκB-焦亡信号通路减轻炎症。BCF-01是幽门螺杆菌感染传统三联疗法的一种有前景的替代方案,副作用极小,对高危个体具有很高的适用性。