TY - JOUR
T1 - Reaction-diffusion spatial modeling of COVID-19
T2 - Greece and Andalusia as case examples
AU - Kevrekidis, P. G.
AU - Cuevas-Maraver, J.
AU - Drossinos, Y.
AU - Rapti, Z.
AU - Kevrekidis, G. A.
N1 - Funding Information:
The authors are indebted to Dr. Maksym Bondarenko for his substantial help with the WorldPop maps and setup, and also thank Dr. Jinlan Huang for assistance in setting the relevant computation up in COMSOL. In addition, we thank Francisco Rodríguez Sánchez for providing the data and R code used to generate the map with the spatial distribution of the epidemic in Andalusia, Fig. . P.G.K. gratefully acknowledges discussions and input from Andy Ludu including regarding the layout of Fig. . This material is based upon work supported by the US National Science Foundation under Grants No. DMS-1815764 (Z.R.), PHY-1602994, and DMS-1809074 (P.G.K.). J.C-M. also thanks the Regional Government of Andalusia under the project P18-RT-3480 and MICINN, AEI, and EU (FEDER program) under the project PID2019-110430GB-C21. Z.R. and P.G.K. also acknowledge support through the C3.ai Digital Transformation Institute. P.G.K. also acknowledges support from the Leverhulme Trust via a Visiting Fellowship and thanks the Mathematical Institute of the University of Oxford for its hospitality during this work. The views expressed in this manuscript are purely those of the authors and may not, under any circumstances, be regarded as an official position of the European Commission.
Publisher Copyright:
© 2021 American Physical Society.
PY - 2021/8
Y1 - 2021/8
N2 - We examine the spatial modeling of the outbreak of COVID-19 in two regions: the autonomous community of Andalusia in Spain and the mainland of Greece. We start with a zero-dimensional (0D; ordinary-differential-equation-level) compartmental epidemiological model consisting of Susceptible, Exposed, Asymptomatic, (symptomatically) Infected, Hospitalized, Recovered, and deceased populations (SEAIHR model). We emphasize the importance of the viral latent period (reflected in the exposed population) and the key role of an asymptomatic population. We optimize model parameters for both regions by comparing predictions to the cumulative number of infected and total number of deaths, the reported data we found to be most reliable, via minimizing the 2 norm of the difference between predictions and observed data. We consider the sensitivity of model predictions on reasonable variations of model parameters and initial conditions, and we address issues of parameter identifiability. We model both the prequarantine and postquarantine evolution of the epidemic by a time-dependent change of the viral transmission rates that arises in response to containment measures. Subsequently, a spatially distributed version of the 0D model in the form of reaction-diffusion equations is developed. We consider that, after an initial localized seeding of the infection, its spread is governed by the diffusion (and 0D model "reactions") of the asymptomatic and symptomatically infected populations, which decrease with the imposed restrictive measures. We inserted the maps of the two regions, and we imported population-density data into the finite-element software package COMSOL Multiphysics®, which was subsequently used to numerically solve the model partial differential equations. Upon discussing how to adapt the 0D model to this spatial setting, we show that these models bear significant potential towards capturing both the well-mixed, zero-dimensional description and the spatial expansion of the pandemic in the two regions. Veins of potential refinement of the model assumptions towards future work are also explored.
AB - We examine the spatial modeling of the outbreak of COVID-19 in two regions: the autonomous community of Andalusia in Spain and the mainland of Greece. We start with a zero-dimensional (0D; ordinary-differential-equation-level) compartmental epidemiological model consisting of Susceptible, Exposed, Asymptomatic, (symptomatically) Infected, Hospitalized, Recovered, and deceased populations (SEAIHR model). We emphasize the importance of the viral latent period (reflected in the exposed population) and the key role of an asymptomatic population. We optimize model parameters for both regions by comparing predictions to the cumulative number of infected and total number of deaths, the reported data we found to be most reliable, via minimizing the 2 norm of the difference between predictions and observed data. We consider the sensitivity of model predictions on reasonable variations of model parameters and initial conditions, and we address issues of parameter identifiability. We model both the prequarantine and postquarantine evolution of the epidemic by a time-dependent change of the viral transmission rates that arises in response to containment measures. Subsequently, a spatially distributed version of the 0D model in the form of reaction-diffusion equations is developed. We consider that, after an initial localized seeding of the infection, its spread is governed by the diffusion (and 0D model "reactions") of the asymptomatic and symptomatically infected populations, which decrease with the imposed restrictive measures. We inserted the maps of the two regions, and we imported population-density data into the finite-element software package COMSOL Multiphysics®, which was subsequently used to numerically solve the model partial differential equations. Upon discussing how to adapt the 0D model to this spatial setting, we show that these models bear significant potential towards capturing both the well-mixed, zero-dimensional description and the spatial expansion of the pandemic in the two regions. Veins of potential refinement of the model assumptions towards future work are also explored.
UR - http://www.scopus.com/inward/record.url?scp=85113463408&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85113463408&partnerID=8YFLogxK
U2 - 10.1103/PhysRevE.104.024412
DO - 10.1103/PhysRevE.104.024412
M3 - Article
C2 - 34525669
AN - SCOPUS:85113463408
SN - 2470-0045
VL - 104
JO - Physical Review E
JF - Physical Review E
IS - 2
M1 - 024412
ER -