Physica A 389 (2010) 1151–1157
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Physica A
journal homepage: www.elsevier.com/locate/physa
Modal series solution for an epidemic model
L. Acedo
a
, Gilberto González-Parra
a,b,∗
, Abraham J. Arenas
a,c
a
Instituto de Matemática Multidisciplinar, Universidad Politécnica de Valencia Edif. 8G, 2
o
, 46022 Valencia, Spain
b
Departamento Cálculo, Universidad de los Andes, Mérida, Venezuela
c
Departamento de Matemáticas y Estadística, Universidad de Córdoba, Montería, Colombia
article info
Article history:
Received 6 July 2009
Received in revised form 1 November 2009
Available online 13 November 2009
Keywords:
SIRS epidemic model
Exact solution
Modal expansion infinite series
abstract
In this article, we generalize a recently proposed method to obtain an exact general
solution for the classical Susceptible, Infected, Recovered and Susceptible (SIRS ) epidemic
mathematical model. This generalization is based upon the nonlinear coupling of two
frequencies in an infinite modal series solution. It is shown that these series provide a
nonstandard approach in order to obtain an accurate analytical solution for the classical
SIRS epidemic model. Numerical results of the SIRS epidemic model for real and complex
frequencies are included in order to test the validity and reliability of the method. This
method could be applied to a wide class of models in physics, chemistry or engineering.
© 2009 Elsevier B.V. All rights reserved.
1. Introduction
At the beginning of the second quarter of the past century, Kermack and McKendrick [1] proposed a system of ordinary
differential equations to determine the time evolution of the susceptible, infected and recovered populations of individuals
exposed to an infectious disease. This model is generally known by the acronym SIR and similar names have been given to
other compartmental models such as SIS , SIRS , SEIR, etc., by disposing the different populations considered in the models
in the same order as the flow from one compartment to another takes place. The importance acquired throughout the past
and present centuries by this simple model cannot be underestimated. This is probably the most widely used model in
Mathematical Epidemiology with applications to many epidemics such as: the bubonic plague [2], measles [3], cholera [4],
rubella [5], respiratory syncytial virus [6,7], hepatitis [8], influenza [9] and many other. Random perturbations has also been
added to these models [10].
From another point of view, this model has also been used to illustrate Fokker-Planck relaxation to an equilibrium point
in Statistical Physics [11]. A connection with the kinetic of reactions can also be easily developed, if we consider S and I as
two different chemical species which react as follows: S + I → I + I . Thus, relaxation towards chemical equilibrium can
also be described by very similar models which incorporate the binary reaction term SI into the dynamics. In order to make
reliable predictions, numerical integration methods such as Runge–Kutta can be efficiently implemented virtually in any
computer language. Nevertheless, exact solutions play a very important role in any nonlinear theory: Onsager’s solution of
2D Ising model [12], the Schwarzschild and Kerr solutions of Einstein’s Field Equations [13] exemplify the creation of new
concepts such as criticality or Black Holes which were disclosed more easily; thanks to these solutions.
Closed-form expressions for infected and susceptible individuals are known time ago for the SI epidemic model [14].
Recently, some authors have also found special solutions of the SIR model by means of modal series [15,16]. We used
modal series in terms of a single frequency to obtain a solution for a particular set of initial conditions [16]. The homotopy
perturbation method provides a similar approach, but oscillations in the transient regime are never observed because a
single real time scale is taken into account [15]. On the other hand, many numerical methods have been presented for
solving epidemics models [17].
∗
Corresponding author at: Departamento Cálculo, Universidad de los Andes, Mérida, Venezuela.
E-mail addresses: luiacrod@imm.upv.es (L. Acedo), gcarlos@ula.ve (G. González-Parra), aarenas@sinu.unicordoba.edu.co (A.J. Arenas).
0378-4371/$ – see front matter © 2009 Elsevier B.V. All rights reserved.
doi:10.1016/j.physa.2009.11.003