Stochastic modeling of in vitro bactericidal potency
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Publication:2060039
Abstract: We provide a Galton--Watson model for the growth of a bacterial population in the presence of antibiotics. We assume that bacterial cells either die or duplicate, and the corresponding probabilities depend on the concentration of the antibiotic. Assuming that the mean offspring number is given by for some , where stands for the antibiotic concentration we obtain weakly consistent, asymptotically normal estimator both for and for the minimal inhibitory concentration (MIC), a relevant parameter in pharmacology. We apply our method to real data, where emph{Chlamydia trachomatis} bacteria was treated by azithromycin and ciprofloxacin. For the measurements of emph{Chlamydia} growth quantitative PCR technique was used. The 2-parameter model fits remarkably well to the biological data.
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- Branching Processes
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- Limit theorems for decomposable multi-dimensional Galton-Watson processes
- Optimal proliferation and differentiation of Chlamydia Trachomatis
- Stochastic chlamydia dynamics and optimal spread
Cited in
(13)- A model of the complex response of \textit{Staphylococcus aureus} to methicillin
- Modelling conjugation with stochastic differential equations
- Deterministic and stochastic modelling of endosome escape by staphylococcus aureus: ``quorum sensing by a single bacterium
- Application of growth rate from kinetic model to calculate stochastic growth of a bacteria population at low contamination level
- Modelling the stability of Stx lysogens
- A Bayesian approach to the semiparametric estimation of a minimum inhibitory concentration distribution
- Stochastic modeling of pseudomonas syringae growth in the phyllosphere
- scientific article; zbMATH DE number 888923 (Why is no real title available?)
- Multitype branching processes in random environment
- A stochastic formulation of the Gompertzian growth model for \textit{in vitro} bactericidal kinetics: parameter estimation and extinction probability
- Using stochastic cell division and death to probe minimal units of cellular replication
- Branching model with state dependent offspring distribution for chlamydia spread
- A stochastic model of bacterial spore germination
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