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DOI 10.1371/journal.pcbi.1008106

Медицинская библиотека · PLoS computational biology · 2020

Drug-target binding quantitatively predicts optimal antibiotic dose levels in quinolones.

Clarelli Fabrizio, Palmer Adam, Singh Bhupender, Storflor Merete, Lauksund Silje, Cohen Ted, Abel Sören, Abel Zur Wiesch Pia

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Antibiotic resistance is rising and we urgently need to gain a better quantitative understanding of how antibiotics act, which in turn would also speed up the development of new antibiotics. Here, we describe a computational model (COMBAT-COmputational Model of Bacterial Antibiotic Target-binding) that can quantitatively predict antibiotic dose-response relationships. Our goal is dual: We address a fundamental biological question and investigate how drug-target binding shapes antibiotic action. We also create a tool that can predict antibiotic efficacy a priori. COMBAT requires measurable biochemical parameters of drug-target interaction and can be directly fitted to time-kill curves. As a proof-of-concept, we first investigate the utility of COMBAT with antibiotics belonging to the widely used quinolone class. COMBAT can predict antibiotic efficacy in clinical isolates for quinolones from drug affinity (R2>0.9). To further challenge our approach, we also do the reverse: estimate the magnitude of changes in drug-target binding based on antibiotic dose-response curves. We overexpress target molecules to infer changes in antibiotic-target binding from changes in antimicrobial efficacy of ciprofloxacin with 92-94% accuracy. To test the generality of our approach, we use the beta-lactam ampicillin to predict target molecule occupancy at MIC from antimicrobial action with 90% accuracy. Finally, we apply COMBAT to predict antibiotic concentrations that can select for resistance due to novel resistance mutations. Using ciprofloxacin and ampicillin as well defined test cases, our work demonstrates that drug-target binding is a major predictor of bacterial responses to antibiotics. This is surprising because antibiotic action involves many additional effects downstream of drug-target binding. In addition, COMBAT provides a framework to inform optimal antibiotic dose levels that maximize efficacy and minimize the rise of resistant mutants.

Для цитирования: Clarelli Fabrizio, Palmer Adam, Singh Bhupender, Storflor Merete, Lauksund Silje, Cohen Ted, Abel Sören, Abel Zur Wiesch Pia. Drug-target binding quantitatively predicts optimal antibiotic dose levels in quinolones.. PLoS computational biology. 2020. DOI: 10.1371/journal.pcbi.1008106.

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