Tao Shiyu, Fan Jinping, Li Jingjing, Wu Zhifeng, Yao Yong, Wang Zhenyu, Wu Yujun, Liu Xiangdong, Xiao Yingping, Wei Hong
College of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, China.
State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University, No. 2 Yuanmingyuan West Road, Beijing 100193, China.
J Adv Res. 2025 Mar;69:545-563. doi: 10.1016/j.jare.2024.03.011. Epub 2024 Mar 18.
Diarrheic disease is a common intestinal health problem worldwide, causing great suffering to humans and animals. Precise manipulation strategies based on probiotics to combat diarrheic diseases have not been fully developed.
The aim of this study was to investigate the molecular mechanisms by which probiotics manipulate macrophage against diarrheic disease.
Metagenome reveals gut microbiome profiles of healthy and diarrheic piglets. Fecal microbial transplantation (FMT) was employed to explore the causal relationship between gut microbes and diarrhea. The protective role of probiotics and their derived extracellular vesicles (EVs) was investigated in ETEC K88-infected mice. Macrophage depletion was performed to assess the role of macrophages in EVs against diarrhea. Execution of in vitro cell co-culture and transcriptome analyses elucidated the molecular mechanisms by which EVs modulate the macrophage and intestinal epithelial barrier.
Escherichia coli was enriched in weaned diarrheic piglets, while Lactobacillus johnsonii (L. john) showed a negative correlation with Escherichia coli. The transmission of diarrheic illness symptoms was achieved by transferring fecal microbiota, but not metabolites, from diarrheic pigs to germ-free (GF) mice. L. john's intervention prevented the transmission of disease phenotypes from diarrheic piglets to GF mice. L. john also reduces the gut inflammation induced by ETEC K88. The EVs secreted by L. john demonstrated enhanced efficacy in mitigating the adverse impacts induced by ETEC K88 through the modulation of macrophage phenotype. In vitro experiments have revealed that EVs activate M2 macrophages in a manner that shuts down ERK, thereby inhibiting NLRP3 activation in intestinal epithelial cells.
Our results reveal that intestinal microbiota drives the onset of diarrheic disease and that probiotic-derived EVs ameliorate diarrheic disease symptoms by modulating macrophage phenotypes. These findings can enhance the advancement of innovative therapeutic approaches for diarrheic conditions based on probiotic-derived EVs.
腹泻病是全球常见的肠道健康问题,给人类和动物带来巨大痛苦。基于益生菌对抗腹泻病的精确操纵策略尚未完全开发出来。
本研究旨在探讨益生菌操纵巨噬细胞对抗腹泻病的分子机制。
宏基因组揭示健康和腹泻仔猪的肠道微生物群概况。采用粪便微生物移植(FMT)来探索肠道微生物与腹泻之间的因果关系。在感染产肠毒素大肠杆菌K88(ETEC K88)的小鼠中研究了益生菌及其衍生的细胞外囊泡(EVs)的保护作用。进行巨噬细胞清除以评估巨噬细胞在EVs对抗腹泻中的作用。体外细胞共培养和转录组分析的实施阐明了EVs调节巨噬细胞和肠道上皮屏障的分子机制。
断奶腹泻仔猪中大肠杆菌富集,而约氏乳杆菌(L. john)与大肠杆菌呈负相关。通过将腹泻猪的粪便微生物群而非代谢产物转移到无菌(GF)小鼠中,实现了腹泻病症状的传播。L. john的干预阻止了疾病表型从腹泻仔猪向GF小鼠的传播。L. john还减轻了ETEC K88诱导的肠道炎症。L. john分泌的EVs通过调节巨噬细胞表型,在减轻ETEC K88诱导的不利影响方面显示出增强的功效。体外实验表明,EVs以关闭ERK的方式激活M2巨噬细胞,从而抑制肠道上皮细胞中的NLRP3激活。
我们的结果表明,肠道微生物群驱动腹泻病的发生,益生菌衍生的EVs通过调节巨噬细胞表型改善腹泻病症状。这些发现可以促进基于益生菌衍生的EVs的腹泻病创新治疗方法的发展。