Abstract
Bacterial populations display extraordinary resilience to antibiotic stress, driven by diverse physiological states that allow some cells to persist and later repopulate. This phenotypic heterogeneity, amplified by environmental fluctuations, undermines the effectiveness of conventional fixed-dose treatment regimens. To address this challenge, we introduce a reinforcement learning (RL) framework that discovers adaptive treatment strategies using only experimentally accessible, population-level measurements. The RL agent learns to infer the hidden physiological state of the population and leverages this knowledge to maintain control even under conditions not encountered during training. Moreover, when granted control over nutrient availability, an important driver of physiological change often overlooked in antibiotic treatment protocols, the agent consistently drives population extinction, surpassing adaptive protocols based solely on drug dynamics. This computational framework offers a powerful, data-driven approach for designing adaptive treatment strategies to counter the growing threat of antimicrobial resistance.
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Abstract
Bacterial populations display extraordinary resilience to antibiotic stress, driven by diverse physiological states that allow some cells to persist and later repopulate. This phenotypic heterogeneity, amplified by environmental fluctuations, undermines the effectiveness of conventional fixed-dose treatment regimens. To address this challenge, we introduce a reinforcement learning (RL) framework that discovers adaptive treatment strategies using only experimentally accessible, population-level measurements. The RL agent learns to infer the hidden physiological state of the population and leverages this knowledge to maintain control even under conditions not encountered during training. Moreover, when granted control over nutrient availability, an important driver of physiological change often overlooked in antibiotic treatment protocols, the agent consistently drives population extinction, surpassing adaptive protocols based solely on drug dynamics. This computational framework offers a powerful, data-driven approach for designing adaptive treatment strategies to counter the growing threat of antimicrobial resistance.
Competing Interest Statement
The authors have declared no competing interest.
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