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An SIR model with viral load-dependent transmission
The viral load is known to be a chief predictor of the risk of transmission of infectious diseases. In this work, we investigate the role of the individuals’ viral load in the disease transmission by proposing a new susceptible-infectious-recovered epidemic model for the densities and mean viral loa...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042434/ https://www.ncbi.nlm.nih.gov/pubmed/36973464 http://dx.doi.org/10.1007/s00285-023-01901-z |
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author | Della Marca, Rossella Loy, Nadia Tosin, Andrea |
author_facet | Della Marca, Rossella Loy, Nadia Tosin, Andrea |
author_sort | Della Marca, Rossella |
collection | PubMed |
description | The viral load is known to be a chief predictor of the risk of transmission of infectious diseases. In this work, we investigate the role of the individuals’ viral load in the disease transmission by proposing a new susceptible-infectious-recovered epidemic model for the densities and mean viral loads of each compartment. To this aim, we formally derive the compartmental model from an appropriate microscopic one. Firstly, we consider a multi-agent system in which individuals are identified by the epidemiological compartment to which they belong and by their viral load. Microscopic rules describe both the switch of compartment and the evolution of the viral load. In particular, in the binary interactions between susceptible and infectious individuals, the probability for the susceptible individual to get infected depends on the viral load of the infectious individual. Then, we implement the prescribed microscopic dynamics in appropriate kinetic equations, from which the macroscopic equations for the densities and viral load momentum of the compartments are eventually derived. In the macroscopic model, the rate of disease transmission turns out to be a function of the mean viral load of the infectious population. We analytically and numerically investigate the case that the transmission rate linearly depends on the viral load, which is compared to the classical case of constant transmission rate. A qualitative analysis is performed based on stability and bifurcation theory. Finally, numerical investigations concerning the model reproduction number and the epidemic dynamics are presented. |
format | Online Article Text |
id | pubmed-10042434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100424342023-03-28 An SIR model with viral load-dependent transmission Della Marca, Rossella Loy, Nadia Tosin, Andrea J Math Biol Article The viral load is known to be a chief predictor of the risk of transmission of infectious diseases. In this work, we investigate the role of the individuals’ viral load in the disease transmission by proposing a new susceptible-infectious-recovered epidemic model for the densities and mean viral loads of each compartment. To this aim, we formally derive the compartmental model from an appropriate microscopic one. Firstly, we consider a multi-agent system in which individuals are identified by the epidemiological compartment to which they belong and by their viral load. Microscopic rules describe both the switch of compartment and the evolution of the viral load. In particular, in the binary interactions between susceptible and infectious individuals, the probability for the susceptible individual to get infected depends on the viral load of the infectious individual. Then, we implement the prescribed microscopic dynamics in appropriate kinetic equations, from which the macroscopic equations for the densities and viral load momentum of the compartments are eventually derived. In the macroscopic model, the rate of disease transmission turns out to be a function of the mean viral load of the infectious population. We analytically and numerically investigate the case that the transmission rate linearly depends on the viral load, which is compared to the classical case of constant transmission rate. A qualitative analysis is performed based on stability and bifurcation theory. Finally, numerical investigations concerning the model reproduction number and the epidemic dynamics are presented. Springer Berlin Heidelberg 2023-03-27 2023 /pmc/articles/PMC10042434/ /pubmed/36973464 http://dx.doi.org/10.1007/s00285-023-01901-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Della Marca, Rossella Loy, Nadia Tosin, Andrea An SIR model with viral load-dependent transmission |
title | An SIR model with viral load-dependent transmission |
title_full | An SIR model with viral load-dependent transmission |
title_fullStr | An SIR model with viral load-dependent transmission |
title_full_unstemmed | An SIR model with viral load-dependent transmission |
title_short | An SIR model with viral load-dependent transmission |
title_sort | sir model with viral load-dependent transmission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042434/ https://www.ncbi.nlm.nih.gov/pubmed/36973464 http://dx.doi.org/10.1007/s00285-023-01901-z |
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