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Accounting for Space­Quantification of Cell-To-Cell Transmission Kinetics Using Virus Dynamics Models.
Kumberger, Peter; Durso-Cain, Karina; Uprichard, Susan L; Dahari, Harel; Graw, Frederik.
Afiliação
  • Kumberger P; Center for Modeling and Simulation in the Biosciences, BioQuant-Center, Heidelberg University, 69120 Heidelberg, Germany. peter.kumberger@bioquant.uni-heidelberg.de.
  • Durso-Cain K; Department of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA. kdurso@luc.edu.
  • Uprichard SL; The Program for Experimental and Theoretical Modeling, Division of Hepatology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA. kdurso@luc.edu.
  • Dahari H; Department of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA. suprichard@luc.edu.
  • Graw F; The Program for Experimental and Theoretical Modeling, Division of Hepatology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA. suprichard@luc.edu.
Viruses ; 10(4)2018 04 17.
Article em En | MEDLINE | ID: mdl-29673154
ABSTRACT
Mathematical models based on ordinary differential equations (ODE) that describe the population dynamics of viruses and infected cells have been an essential tool to characterize and quantify viral infection dynamics. Although an important aspect of viral infection is the dynamics of viral spread, which includes transmission by cell-free virions and direct cell-to-cell transmission, models used so far ignored cell-to-cell transmission completely, or accounted for this process by simple mass-action kinetics between infected and uninfected cells. In this study, we show that the simple mass-action approach falls short when describing viral spread in a spatially-defined environment. Using simulated data, we present a model extension that allows correct quantification of cell-to-cell transmission dynamics within a monolayer of cells. By considering the decreasing proportion of cells that can contribute to cell-to-cell spread with progressing infection, our extension accounts for the transmission dynamics on a single cell level while still remaining applicable to standard population-based experimental measurements. While the ability to infer the proportion of cells infected by either of the transmission modes depends on the viral diffusion rate, the improved estimates obtained using our novel approach emphasize the need to correctly account for spatial aspects when analyzing viral spread.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus / Células / Modelos Estatísticos Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus / Células / Modelos Estatísticos Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article