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Time-programmable drug dosing allows the manipulation, suppression and reversal of antibiotic drug resistance in vitro

机译:时间可编程的药物剂量允许在体外操纵,抑制和逆转抗生素药物抗性

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摘要

Multi-drug strategies have been attempted to prolong the efficacy of existing antibiotics, but with limited success. Here we show that the evolution of multi-drug-resistant Escherichia coli can be manipulated in vitro by administering pairs of antibiotics and switching between them in ON/OFF manner. Using a multiplexed cell culture system, we find that switching between certain combinations of antibiotics completely suppresses the development of resistance to one of the antibiotics. Using this data, we develop a simple deterministic model, which allows us to predict the fate of multi-drug evolution in this system. Furthermore, we are able to reverse established drug resistance based on the model prediction by modulating antibiotic selection stresses. Our results support the idea that the development of antibiotic resistance may be potentially controlled via continuous switching of drugs.
机译:已经尝试了多种药物策略来延长现有抗生素的功效,但是成功有限。在这里,我们显示可以通过施用成对的抗生素并以ON / OFF方式在它们之间切换来在体外操纵耐多药大肠杆菌的进化。使用多重细胞培养系统,我们发现某些抗生素组合之间的切换完全抑制了对一种抗生素的耐药性的发展。利用这些数据,我们开发了一个简单的确定性模型,该模型使我们能够预测该系统中多种药物的发展命运。此外,我们能够通过调节抗生素选择应激逆转基于模型预测的既定耐药性。我们的结果支持这样的想法,即可以通过持续切换药物来控制抗生素耐药性的发展。

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