Han Ziyi, Zhao Lingyang, Hu Qilin, Hung Ifen, Liu Chunxue, Liu Shijie, Mei Xuehua, Zeng Xiu, Bin Peng, Wang Junhong
State Key Laboratory of Livestock and Poultry Breeding, College of Animal Science, South China Agricultural University, Guangzhou, China.
Anyou Biotechnology Group Co, LTD, Taicang, China.
Gut Microbes. 2025 Dec;17(1):2552345. doi: 10.1080/19490976.2025.2552345. Epub 2025 Aug 28.
The gut microbiota plays a crucial role in regulating host amino acid availability and metabolism through complex interactions with the host metabolic processes. This review summarizes three main mechanisms through which the microbiota influences host amino acid homeostasis. Firstly, gut microbiota actively competes for luminal amino acids derived from the diet and concurrently contributes to the host's amino acid pool through biosynthesis. Secondly, they modulate host intestinal hydrolases and amino acid transporters, thereby fine-tuning amino acid absorption and systemic bioavailability. Thirdly, microbially secreted factors, including diverse metabolites and extracellular vesicles, reprogram host amino acid metabolic pathways. The inherent inter-individual variations in microbial composition and metabolic capacity highlight the necessity of personalized therapeutic strategies targeting the microbiota. By summarizing current findings, this review aims to provide a deeper understanding of this dynamic interplay and to identify promising avenues for future investigations in the field.
肠道微生物群通过与宿主代谢过程的复杂相互作用,在调节宿主氨基酸可用性和代谢方面发挥着关键作用。本综述总结了微生物群影响宿主氨基酸稳态的三种主要机制。首先,肠道微生物群积极竞争饮食来源的管腔氨基酸,并通过生物合成同时为宿主的氨基酸库做出贡献。其次,它们调节宿主肠道水解酶和氨基酸转运体,从而微调氨基酸吸收和全身生物利用度。第三,微生物分泌的因子,包括各种代谢物和细胞外囊泡,重新编程宿主氨基酸代谢途径。微生物组成和代谢能力的个体间固有差异突出了针对微生物群的个性化治疗策略的必要性。通过总结当前的研究结果,本综述旨在更深入地理解这种动态相互作用,并确定该领域未来研究的有希望的途径。
Gut Microbes. 2025-12
Microbiol Spectr. 2025-7
Cell Metab. 2025-4-1
Cell Insight. 2025-1-10
Cell Host Microbe. 2025-1-8
Proc Natl Acad Sci U S A. 2024-11-19