Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, Institute of Engineering Biology and Health, East China University of Science and Technology, Shanghai, China.
Gut Microbes. 2024 Jan-Dec;16(1):2399213. doi: 10.1080/19490976.2024.2399213. Epub 2024 Sep 17.
Hyperuricemia, a prevalent metabolic disorder, poses a susceptibility to various complications. The conventional pharmacotherapeutic approaches for hyperuricemia often entail notable adverse effects, posing substantial clinical challenges. Hence, the imperative lies in the development of novel, safe and effective strategies for preventing and treating hyperuricemia. Here, we developed a probiotic Nissle 1917 strain, designated as YES301, which contains a rationally designed xanthine importer XanQ, enabling efficient uptake of xanthine and hypoxanthine, consequently leading to reduced serum uric acid concentrations and amelioration of renal impairments in a murine model of hyperuricemia. Importantly, YES301 exhibited a therapeutic efficacy comparable to allopurinol, a conventional uric acid-lowering agent, and manifesting fewer adverse effects and enhanced biosafety. These findings highlight the promising potential of engineered probiotics in the management of hyperuricemia through reducing intestinal purine levels.
高尿酸血症是一种常见的代谢紊乱,易引发多种并发症。传统的高尿酸血症药物治疗方法往往存在显著的不良反应,这给临床带来了巨大挑战。因此,迫切需要开发新型、安全有效的高尿酸血症预防和治疗策略。在这里,我们开发了一种益生菌菌株 Nissle 1917,命名为 YES301,它含有一个经过合理设计的黄嘌呤转运蛋白 XanQ,能够有效摄取黄嘌呤和次黄嘌呤,从而降低血清尿酸浓度,并改善高尿酸血症小鼠模型的肾脏损伤。重要的是,YES301 的治疗效果可与传统的尿酸降低剂别嘌呤醇相媲美,且不良反应更少,生物安全性更高。这些发现突出了工程益生菌通过降低肠道嘌呤水平来管理高尿酸血症的巨大潜力。