Department of Biosystems Science and Engineering, ETH Zürich , Mattenstrasse 26, CH-4058 Basel, Switzerland.
Focal Area of Infection Biology, Biozentrum, University of Basel , Klingelbergstrasse 46, CH-4056 Basel, Switzerland.
Nano Lett. 2017 Aug 9;17(8):5043-5050. doi: 10.1021/acs.nanolett.7b02270. Epub 2017 Jul 13.
Current antibiotics gradually lose their efficacy against chronic Pseudomonas aeruginosa infections due to development of increased resistance mediated by biofilm formation, as well as the large arsenal of microbial virulence factors that are coordinated by the cell density-dependent phenomenon of quorum sensing. Here, we address this issue by using synthetic biology principles to rationally engineer quorum-quencher cells with closed-loop control to autonomously dampen virulence and interfere with biofilm integrity. Pathogen-derived signals dynamically activate a synthetic mammalian autoinducer sensor driving downstream expression of next-generation anti-infectives. Engineered cells were able to sensitively score autoinducer levels from P. aeruginosa clinical isolates and mount a 2-fold defense consisting of an autoinducer-inactivating enzyme to silence bacterial quorum sensing and a bipartite antibiofilm effector to dissolve the biofilm matrix. The self-guided cellular device fully cleared autoinducers, potentiated bacterial antibiotic susceptibility, substantially reduced biofilms, and alleviated cytotoxicity to lung epithelial cells. We believe this strategy of dividing otherwise coordinated pathogens and breaking up their shielded stronghold represents a blueprint for cellular anti-infectives in the postantibiotic era.
由于生物膜形成介导的耐药性增加以及群体感应依赖性细胞密度现象协调的大量微生物毒力因子,当前的抗生素逐渐失去了对抗慢性铜绿假单胞菌感染的功效。在这里,我们使用合成生物学原理通过合理设计具有闭环控制的群体淬灭细胞来自主抑制毒力并干扰生物膜完整性来解决这个问题。病原体衍生的信号动态激活合成哺乳动物自动诱导传感器,驱动下一代抗感染药物的表达。工程细胞能够从铜绿假单胞菌临床分离株中灵敏地检测到自动诱导物水平,并构建一个由自动诱导物失活酶组成的 2 倍防御系统,以沉默细菌群体感应,以及一个双功能抗生物膜效应物来溶解生物膜基质。自我引导的细胞装置完全清除了自动诱导物,增强了细菌对抗生素的敏感性,大大减少了生物膜,并减轻了对肺上皮细胞的细胞毒性。我们相信,这种将原本协调一致的病原体分开并打破其保护据点的策略代表了后抗生素时代细胞抗感染药物的蓝图。