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. 2020 Mar 24;64(4):e02070-19. doi: 10.1128/AAC.02070-19

TABLE 1.

Overview of parameters in the final model with values estimated on all data (including both static and dynamic cefuroxime concentrations)a

Parameter (unit) Parameter description Estimate (RSE [%])
kgrowth (h−1) Bacterial growth rate 1.45 (5.1)
kdeath (h−1) Bacterial natural death rate 0.179 (fix)
Bmax (CFU/ml) Bacterial system capacity 1.42 × 108 (19)
TSR (CFU/ml) Threshold for transition from S state to R state 7.01 × 107 (14)

Emax (h−1)
Maximum antibiotic-induced killing rate 3.26 (3.8)
EC50 (mg/liter) Potency for drug effect (MIC dependent)
MIC = 2 mg/liter 2.93 (2.7)
MIC = 4 mg/liter 4.88 (11)
γ Sigmoidal Hill coefficient 3.37 (25)
kdeg (h−1) Degradation rate of antibiotic (both systems) 0.026 (fix)
kel (h−1) Elimination rate (dynamic system) 0.462 (fix)
Mix Fraction of experiments with typical elimination 0.574 (24)
Offset Proportional change for atypical elimination 1.36 (4.7)
kG,ETX (EU/CFU) LPS/endotoxin from bacterial growth (S) 0.000292 (11)
kK,ETX (EU/CFU) LPS/endotoxin from antibiotic-killed bacteria (S) 0.00636 (25)
kFK,ETX (EU/CFU) LPS/endotoxin from antibiotic-killed filaments (F) 0.295 (43)
ktr,ETX (h−1) Transit rate for LPS/endotoxin release (S + F) 0.131 (27)
θMIC,F Concentration × MIC for filament formation 5.90 (8.2)
ω2 CFU unexplained residual variance 0.409 (12)
ωrepl2 CFU replication error (plate spread) variance 0.0363 (16)
ω2 LPS/endotoxin unexplained residual variance 0.164 (13)
a

EU, endotoxin units; F, filament biomass state; R, resting state; RSE, relative standard error; S, susceptible state.