Zou Zhen-Ping, Wang Xin-Ge, Shi Xuan-Ren, Sun Shu-Ting, Mi Jing, Zhang Xiao-Peng, Yin Bin-Cheng, Zhou Ying, Ye Bang-Ce
Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Institute of Engineering Biology and Health, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Adv Sci (Weinh). 2025 Aug;12(31):e06486. doi: 10.1002/advs.202406486. Epub 2025 May 28.
Engineered bacteria have demonstrated great potential for treating a broad array of tumors. However, the precision and safety of controlling the performance of engineered bacteria in vivo remains a central challenge. Here, genetic circuit programming strategy is utilized to construct an engineered Escherichia coli Nissle 1917 with accurate targeted colonizing and on-demand payloads releasing ability. The engineered probiotic survives only in the presence of more than 5 mM L-lactate by employing an improved lactate-sensing system, which leads to preventing the growth outside the permissive environments in mice. Meanwhile an expressing α-hemolysin (SAH) circuit based on quorum-sensing system is introduced to augment anti-tumor effect. Furthermore, coagulase (Coa) induced by high-level lactate creates the closure to deprive tumor of nutrients and oxygen and may help prevent the leakage of bacteria and SAH, which enhances the therapeutic effectiveness and biosafety. This self-adjusting living biotherapeutics significantly inhibits tumor proliferation and prolongs the survival time of colorectal tumor-bearing mice. Together, this work takes a step toward safer and more effective application of living bacteria for tumor treatment in practice.
工程菌已显示出在治疗多种肿瘤方面的巨大潜力。然而,在体内控制工程菌性能的精确性和安全性仍然是一个核心挑战。在此,利用基因回路编程策略构建了一种具有精确靶向定殖和按需释放载荷能力的工程化大肠杆菌Nissle 1917。通过采用改进的乳酸感应系统,工程益生菌仅在存在超过5 mM L-乳酸的情况下存活,这导致其在小鼠体内的允许环境之外无法生长。同时,引入基于群体感应系统的表达α-溶血素(SAH)回路以增强抗肿瘤效果。此外,由高水平乳酸诱导的凝固酶形成封闭,剥夺肿瘤的营养和氧气,并可能有助于防止细菌和SAH泄漏,从而提高治疗效果和生物安全性。这种自我调节的活体生物疗法显著抑制肿瘤增殖并延长结直肠癌荷瘤小鼠的存活时间。总之,这项工作朝着在实践中更安全、更有效地应用活菌进行肿瘤治疗迈出了一步。