Use of Collateral Sensitivity Networks to Design Drug Cycling Protocols That Avoid Resistance Development

被引:342
作者
Imamovic, Lejla [1 ]
Sommer, Morten O. A. [1 ,2 ]
机构
[1] Tech Univ Denmark, Dept Syst Biol, DK-2800 Lyngby, Denmark
[2] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, DK-2970 Horsholm, Denmark
关键词
ANTIMICROBIAL STEWARDSHIP PROGRAMS; ESCHERICHIA-COLI; ANTIBIOTIC-RESISTANCE; INFECTIONS; AGENTS; COST; CHALLENGES; STRATEGIES; MUTATIONS; HOSPITALS;
D O I
10.1126/scitranslmed.3006609
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
New drug deployment strategies are imperative to address the problem of drug resistance, which is limiting the management of infectious diseases and cancers. We evolved resistance in Escherichia coli toward 23 drugs used clinically for treating bacterial infections and mapped the resulting collateral sensitivity and resistance profiles, revealing a complex collateral sensitivity network. On the basis of these data, we propose a new treatment framework-collateral sensitivity cycling-in which drugs with compatible collateral sensitivity profiles are used sequentially to treat infection and select against drug resistance development. We identified hundreds of such drug sets and demonstrated that the antibiotics gentamicin and cefuroxime can be deployed cyclically such that the treatment regimen selected against resistance to either drug. We then validated our findings with related bacterial pathogens. These results provide proof of principle for collateral sensitivity cycling as a sustainable treatment paradigm that may be generally applicable to infectious diseases and cancer.
引用
收藏
页数:10
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