TY - JOUR T1 - Dynamical Model of Drug Accumulation in Bacteria: Sensitivity Analysis and Experimentally Testable Predictions JF - bioRxiv DO - 10.1101/030908 SP - 030908 AU - Neda Vesselinova AU - Boian S. Alexandrov AU - Michael E. Wall Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/10/20/030908.abstract N2 - We present a dynamical model of drug accumulation in bacteria. The model captures key features in experimental time courses on ofloxacin accumulation: initial uptake; two-phase response; and long-term acclimation. In combination with experimental data, the model provides estimates of import and export rates in each phase, the time of entry into the second phase, and the decrease of internal drug during acclimation. Global sensitivity analysis, local sensitivity analysis, and Bayesian sensitivity analysis of the model provide information about the robustness of these estimates, and about the relative importance of different parameters in determining the features of the accumulation time courses in three different bacterial species: Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. The results lead to experimentally testable predictions of the effects of membrane permeability, drug efflux and trapping (e.g., by DNA binding) on drug accumulation. A key prediction is that a sudden increase in ofloxacin accumulation in both E. coli and S. aureus is accompanied by a decrease in membrane permeability.Author Summary Bacteria live or die depending on how much antibiotic gets inside them. Using a simple mathematical model, detailed information about drug import and export can be teased out of time courses of internal drug levels after a sudden exposure. The results suggest that membrane permeability can suddenly decrease during exposure to drug, accompanied by an increase, rather than a decrease, in the internal drug level. ER -