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


ABSTRACT: 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.

SUBMITTER: Yoshida M 

PROVIDER: S-EPMC5472167 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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

Yoshida Mari M   Reyes Sabrina Galiñanes SG   Tsuda Soichiro S   Horinouchi Takaaki T   Furusawa Chikara C   Cronin Leroy L  

Nature communications 20170608


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 d  ...[more]

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