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. 2020 Aug 14;2020(1):420. doi: 10.1186/s13662-020-02873-w

Dynamics of a fractional order mathematical model for COVID-19 epidemic

Zizhen Zhang 1, Anwar Zeb 2,, Oluwaseun Francis Egbelowo 3, Vedat Suat Erturk 4
PMCID: PMC7427275  PMID: 32834820

Abstract

In this work, we formulate and analyze a new mathematical model for COVID-19 epidemic with isolated class in fractional order. This model is described by a system of fractional-order differential equations model and includes five classes, namely, S (susceptible class), E (exposed class), I (infected class), Q (isolated class), and R (recovered class). Dynamics and numerical approximations for the proposed fractional-order model are studied. Firstly, positivity and boundedness of the model are established. Secondly, the basic reproduction number of the model is calculated by using the next generation matrix approach. Then, asymptotic stability of the model is investigated. Lastly, we apply the adaptive predictor–corrector algorithm and fourth-order Runge–Kutta (RK4) method to simulate the proposed model. Consequently, a set of numerical simulations are performed to support the validity of the theoretical results. The numerical simulations indicate that there is a good agreement between theoretical results and numerical ones.

Keywords: COVID-19 epidemic, Stability analysis, Adaptive predictor–corrector algorithm, Fractional differential equations, Numerical simulations

Introduction

Mathematical models describing infectious diseases have an important role both in theory and practice (see, for example, [68, 18, 34]). The construction and analysis of models of this type can help us understand the mechanism of the transmission as well as characteristics of diseases, and therefore, we can propose effective strategies to predict, prevent, and restrain diseases, as well as to protect population health. Up to now, many mathematical models for infectious diseases formulated by differential equations have been constructed and analyzed to study the spreading of viruses, for instance, [68, 18, 34]. Recently, mathematical models for COVID-19 epidemic have attracted the attention of many mathematicians, biologists, epidemiologists, pharmacists, chemists with many notable and important results (see, for instance, [1, 5, 9, 14, 15, 19, 23, 26, 2830, 33, 35, 36] and references therein). This can be considered an effective approach to study, simulate, and predict the mechanism and transmission of COVID-19.

Motivated by the above reason, in this work, we formulate and analyze a new mathematical model for COVID-19 epidemic. This model is described by a system of fractional-order differential equations model and includes five classes, namely, S (susceptible class), E (exposed class), I (infected class), Q (isolated class), and R (recovered class). This model is a generalization of a well-known ODE model formulated in [35]. In the proposed fractional-order model, we use the Caputo fractional derivative instead of the integer-order one because when modeling processes and phenomena arising in the real world, fractional-order models are more accurate than integer-order ones. In particular, fractional-order models provide more degrees of freedom in the model while an unlimited memory is also guaranteed in contrast to integer-models with limited memory [11, 24, 27].

Our main aim is to study the dynamics and numerical approximations for the proposed fractional-order model. Firstly, the positivity and boundedness of the model are investigated based on standard techniques of mathematical analysis. Secondly, the basic reproduction number of the model is calculated by using the next generation matrix approach. Then, asymptotic stability of the model is investigated based on the Lyapunov stability theorem for fractional dynamical systems. Lastly, we apply the adaptive predictor–corrector algorithm and fourth-order Runge–Kutta (RK4) method formulated in [20] to simulate the proposed model. Consequently, a set of numerical simulations is performed to support the validity of the theoretical results. The numerical simulations indicate that there is a good agreement between theoretical results and numerical ones.

This work is organized as follows. The fractional-order differential model is formulated in Sect. 2. Dynamics of the model is investigated in Sect. 3. Numerical simulations by the adaptive predictor–corrector algorithm are performed in Sect. 4. The last section present some remarks, conclusions, and discussions.

Model formulation

The total population is divided into five compartments: susceptible (S), exposed (E), infected (I), isolated (Q), and recovered (R) from the disease. We assume that all the classes are normalized. This leads to the mathematical model formulation in which the interaction of the exposed population and infected population is linked to the susceptible population. In this model, we assume that the natural death rate includes the disease death rate. When there is no symptom of the disease, the exposed class moves with a certain rate to the isolated class, but in the case when symptoms are developed, it moves to the infected class. Keeping in mind the above assumptions, we obtain the following ODE model (see [35]):

dS(t)dt=ΛμS(t)βS(t)(E(t)+I(t)),dE(t)dt=βS(t)(E(t)+I(t))πE(t)(μ+γ)E(t),dI(t)dt=πE(t)σI(t)μI(t),dQ(t)dt=γE(t)+σI(t)θQ(t)μQ(t),dR(t)dt=θQ(t)μR(t), 1

where the parameters and variables used are described in Table 1.

Table 1.

Parameters in the model

Symbols Description
S Susceptible population
E Exposed population
I Infected Population
Q Isolated population
R Recovered population
Λ = μN Recruitment rate
β Rate at which susceptible move to infected and exposed class
π Rate at which exposed population moves to infected one
γ Rate at which exposed people become isolated
σ Rate at which infected people are added to isolated individuals
θ Rate at which isolated persons become recovered
μ Natural death rate plus disease related death rate

Let us introduce the notation

N=S+E+I+Q+R. 2

From the ODE system (1), we obtain

dNdt=ΛμN,

which implies that the total population in this case we take as constant because Λ=μN.

To include into the model (1) the past history or hereditary properties, we replace the first derivative by the Caputo fractional derivative. More precisely, we propose the following system of fractional differential equations:

Dtα0CS=ΛαμαSβαS(E+I),Dtα0CE=βαS(E+I)παE(μα+γα)E,Dtα0CI=παEσαIμαI,Dtα0CQ=γαE+σαIθαQμαQ,Dtα0CR=θαQ(t)μαR(t), 3

where 0<α<1, and Dtα0C denotes the fractional derivative in the Caputo sense. We refer the readers to [24, 10, 25] for the definition of the fractional Caputo derivative.

Dynamics of the fractional-order model

Positivity and boundedness

Let us denote

R+4={(S,E,I,Q)|S,E,I,Q0}.

The following theorem is proved by using a generalized mean value theorem [21, 22] and a fractional comparison principle [16, Lemma 10].

Theorem 1

(Positivity and boundedness)

Let (S0,E0,I0,Q0)be any initial data belonging to R+4and (S(t),E(t),I(t),Q(t))be the solution corresponding to the initial data. Then, the set R+4is a positively invariant set of the model (3). Furthermore, we have

lim suptS(t)S:=Λαμα,lim suptE(t)E:=Λαπα+μα+γα,lim suptI(t)I:=παEσα+μα,lim suptQ(t)Q:=γαE+σαIδα+μα,lim suptR(t)θαμα. 4

Proof

First, it is easy to prove the existence and unique of solutions of the model thanks to results proved in [17].

For the model (3), we have

Dtα0CS|S=0=Λα>0,Dtα0CE|E=0=βαSI0,Dtα0CI|I=0=παE0,Dtα0CQ|Q=0=γαE+σαI0. 5

By (5) and the generalized mean value theorem [21, 22], we deduce that S(t),E(t),I(t),Q(t)0 for all t0.

From the first equation of the system (3), we obtain

Dtα0CSΛαμαS.

By using the fractional comparison principle, we have the first estimate of (4).

From the second equation of the system (3), we have

Dtα0C(S+E)ΛαμαSπαE(μα+γα)E,

which implies that

lim supt(S(t)+E(t))E.

Consequently, we have the second estimate of (4).

From the third equation of the system (3), we get

Dtα0CIπαEσαIμαI

for t large enough. This implies the third estimate of (4).

From the fourth equation of the system (3), we have

Dtα0CQγαE+σαIθαQμαQ,

for t large enough. From this we get the fourth estimate of (4).

Finally, the fifth equation of (3) implies that

Dtα0CRθαQμαR,

which implies the fifth estimate of (4). The proof is complete. □

Equilibria and the reproduction number

Firstly, to find equilibria of the model (3), we consider the following algebraic system:

ΛαμαSβαS(E+I)=0,βαS(E+I)παE(μα+γα)E=0,παEσαIμαI=0,γαE+σαIθαQμαQ=0,θαQμαR=0. 6

By some algebraic manipulations, we obtain two solutions of the system (6) that are

S0=Λαμα,E0=0,I0=0,E0=0,R0=0, 7

and

S=Λα(πα+μα+γα)Eμα,I=πασα+μαE,Q=γαE+σαIθα+μα,E=βαΛα(πα+σα+μα)μα(μα+σα)(πα+μα+γα)βα(πα+μα+γα)(πα+σα+μα),R=θαQμα. 8

Note that S, E, I, Q and R are positive if and only if

βαΛα(πα+σα+μα)μα(μα+σα)(πα+μα+γα)>0.

We now compute the reproduction number of the model (3) by using the next generation matrix approach developed by van den Driessche and Watmough [31]. Let x=(E,I,Q,R,S). We rewrite the model (3) in the matrix form

Dtα0Cx=F(x)V(x), 9

where

F(x)=(βαS(E+I)0000),V(x)=(παE+(μα+γα)EπαE+σαI+μαIγαEσαI+θαQ+μαQθαQ+μαRΛα+μαS+βαS(E+I)). 10

Hence, the reproduction number of the model (3) can be determined by

R0=ρ(FV1)=βαΛα(πα+σα+μα)μα(σα+μα)(πα+μα+γα). 11

It is easy to verify that S, E, I, Q, and R>0 if and only if R0>1.

Theorem 2

(Equilibria)

The model (3) always possesses a disease-free equilibrium (DFE) point F0=(S0,E0,I0,Q0,R0)given by (8) for all values of the parameters. Moreover, the model has a unique disease endemic equilibrium point F=(S,E,I,Q,R)given by (9) if and only if R0>1.

Stability analysis

Theorem 3

The DFE point of the model (3) is locally asymptotically stable if R0<1.

Proof

The Jacobian matrix of the model (3) at the DFE point is

J(F0)=(μαβαS0βαS0000βαS0(πα+μα+γα)βαS0000πα(σα+μα)000γασα(θα+μα)0000θαμα). 12

The characteristic polynomial of J is

PJ(x)=(λ+μα)[λ+(θα+μα)](λ+μα)(λ2+τ1λ+τ2),

where

τ1=[βS0(πα+μα+γα)(σα+μα)],τ2=(πα+μα+γα)(σα+μα)βαS0(πα+σα+μα). 13

It is easy to verify that if R0<1, then τ1>0 and τ2>0. This implies that two roots of the polynomial λ2+τ1λ+τ2 have negative real parts. Consequently, the real parts of five eigenvalues of the matrix J(F0) are all negative, or equivalently, F0 is locally stable. The proof is complete. □

We now prove the uniform asymptotical stability of the DFE point of the model (3) by using the Lyapunov stability theorem [12, Theorem 3.1].

Theorem 4

If R0<1, then the DFE point of the model (3) is not only locally asymptotically stable but also uniformly asymptotically stable.

Proof

Since the first three equations of the model (3) do not depend on the states Q and R, we need only consider the following subsystem:

Dtα0CS=ΛαμαSβαS(E+I),Dtα0CE=βαS(E+I)παE(μα+γα)E,Dtα0CI=παEσαIμαI. 14

From (4), it is sufficient to consider the model (3) in its feasible set defined by

Ω={(S,E,I)|S,E,I0,SΛαμα}.

Consider a Lyapunov function V:ΩR+ given by

V(S,E,I)=(SS0lnSS0S0)+E+πα+μα+γαπα+σα+μαI. 15

By using the linearity property of the Caputo derivative and [32, Lemma 3.1] and some algebraic manipulations, we obtain

Dtα0CV(SS0)2+τ1I+τ2E,

where

τ1=βαΛαμα(πα+μα+γα)+παπα+μα+γαπα+σα+μα,τ2=βαΛαμαπα+σα+γαπα+σα+μα.

It is easy to check that if R0<1, then τ1,τ2<0. Consequently, by the Lyapunov stability theorem for fractional dynamical systems, we deduce that F0 is uniformly asymptotically stable. The proof is complete. □

Remark 1

The analysis of stability of F is an interesting mathematical problem, but in this work, we mainly focus on the case R0<1 to find an effective strategy to prevent the disease.

R0 sensitivity analysis

Theorem 3 suggests that we should control the parameters such that R0<1. This provides a good strategy to prevent and restrain the disease. More precisely, when R0<1, then

limtS(t)=Λαμα,limtE(t)=limtI(t)=limtQ(t)=limtR(t)=0,

which means that the disease will be completely controlled and prevented. Motivated by this, we now perform an R0 sensitivity analysis to find ways to choose suitable parameters.

It is easy to verify that

R0β=αβα1Λα(πα+σα+μα)μα(σα+μα)(πα+μα+γα)>0,R0π=βαΛαμα(σα+μα)απα1(γαμα)(πα+μα+γα)2,R0σ=βαΛαμα(μα+μα+γα)ασα1πα(σα+μα)2<0,R0γ=βαΛα(πα+σα+μα)μα(σα+μα)αγα1(πα+μα+γα)<0. 16

Equation (16) suggests some ways to choose the parameters such that R0<1. Hence, based on this, we can propose suitable strategies to control and prevent the disease.

Numerical simulations by the adaptive predictor–corrector algorithm

The adaptive predictor–corrector algorithm

In this section we review the method that is proposed by [20]. The proposed algorithm is given as follows. Consider the initial value problem (IVP) governed by:

{Da+α,ρy(t)=f(t,y(t)),t[0,T],yk(a)=y0k,k=0,1,2,,[α]1, 17

where Da+α,ρ is the proposed generalized Caputo-type fractional derivative operator given [20, Definition 4]. Initially, for m1<αm, a0, ρ>0 and yCm([a,T]), the IVP (17) is equivalent, using [20, Theorem 3], to the Volterra integral equation:

y(t)=u(t)+ρ1αΓ(α)at(s)ρ1(tρsρ)α1f(s,y(s))ds, 18

where

u(t)=n=0m11ρnn!(tρaρ)n[(x1ρddx)ny(x)]|x=a. 19

The first step of our algorithm, under the assumption that the function f is such that a unique solution exists on some interval [a,T], consists of dividing the interval [a,T] into N unequal subintervals [tk,tk+1], k=0,1,,N1 using the mesh points

{t0=a,tk+1=(tkρ+h)1ρk=0,1,2,,N1, 20

where h=(Tρaρ)N. Now, we are going to generate the approximations yk, k=0,1,,N, to solve numerically the IVP (17). The basic step, assuming that we have already evaluated the approximations yiy(tj) (j=1,2,,k), is that we want to get the approximation yky(tk+1) by means of the integral equation

y(tk+1)=u(tk+1)+ραΓ(α)atk+1sρ1(tk+1ρsρ)α1f(s,y(s))ds. 21

Making the substitution

z=(s)ρ, 22

we get

y(tk+1)=u(tk+1)+ραΓ(α)atk+1ρ(tk+1ρz)α1f(z1ρ,y(z1ρ)dz, 23

that is,

y(tk+1)=u(tk+1)+ραΓ(α)j=0ktjρtj+1ρ(tk+1ρz)α1f(z1ρ,y(z1ρ)dz. 24

Next, if we use the trapezoidal quadrature rule with respect to the weight function (tk+1ρz)α1 to approximate the integrals appear in the right-hand side of Eq. (24), replacing the function f(z1ρ,y(z1ρ)) by its piecewise linear interpolant with nodes chosen at the tjρ (j=0,1,,k+1), then we obtain

tjρtj+1ρ(tk+1ρz)α1f(z1ρ,y(z1ρ)dzhαα(α+1)[((kj)α+1(kjα+)(kj+1)α)f(tj,y(tj))+((kj+1)α+1(kj+α+1)(kj)α)f(tj+1,y(tj+1))]. 25

Thus, substituting the above approximations into Eq. (24), we obtain the corrector formula for y(tk+1), k=0,1,,N1,

y(tk+1)u(tk+1)+ραΓ(α+2)j=0kaj,k+1f(tj,y(tj))+ραhαΓ(α+2)f(tk+1,y(tk+1)), 26

where

aj,k+1={kα+1(kα)(k+1)αif j=0,(kj+2)α+1+(kj)α+12(kj+1)α+1if 1j<k. 27

The last step of our algorithm is to replace the quantity y(tk+1) shown on the right-hand side of formula (26) with the predictor value yp(tk+1) that can be obtained by applying the one-step Adams–Bashforth method to the integral equation (23). In this case, by replacing the function f(z1ρ,y(z1ρ)) with the quantity f(tj,y(tj)) at each integral in Eq. (24), we get

yp(tk+1)u(tk+1)+ραΓ(α)j=0ktjρtj+1ρ(tk+1ρz)α1f(tj,y(tj))dz=u(tk+1)+ραhαΓ(α+1)j=0k[(k+1j)α(kj)α]f(tj,y(tj)). 28

Therefore, the present adaptive predictor–corrector algorithm, for evaluating the approximation yk+1y(tk+1), is completely described by the formula

yk+1u(tk+1)+ραhαΓ(α+2)j=0kaj,k+1f(tj,yj)+ραhαΓ(α+2)f(tk+1,yk+1p), 29

where yjy(tj), j=0,1,,k, and the predicted value yk+1pyp(tk+1) can be determined as described in Eq. (28) with the weights aj,k+1 being defined according to (27). It is easily observed that when ρ=1, the present adaptive predictor–corrector algorithm will be reduced to the predictor–corrector approach presented in [13].

Implementation with numerical simulation

In this section, we solve numerically Eq. (3) using the method given in the former section. In view of the above algorithm, following the rule (27), the approximations Sk+1, Ek+1, Ik+1, Qk+1, and Rk+1 can be simply evaluated using the iterative formulas, for NN and T>0,

Sk+1S0+ραhαΓ(α+2)j=0kaj,k+1[ΛαμαSjβαSj(Ej+Ij)]Sk+1+ραhαΓ(α+2)[AαμαSk+1p)βαSk+1p(Ek+1p+Ik+1p)],Ek+1E0+ραhαΓ(α+2)j=0kaj,k+1[βαSj(Ej+Ij)(πα+μα+γα)Ej]Ek+1+ραhαΓ(α+2)[βαSk+1p(Ek+1p+Ik+1p)(πα+μα+γα)Ek+1p],Ik+1I0+ραhαΓ(α+2)j=0kaj,k+1[παEj(σα+μα)Ij]Ik+1+ραhαΓ(α+2)[παEk+1p(σα+μα)Ik+1p],Qk+1Q0+ραhαΓ(α+2)j=0kaj,k+1[γαEj+σαIj(θα+μα)Qj]Qk+1+ραhαΓ(α+2)[γαEk+1p+σαIk+1p(θα+μα)Qk+1p],Rk+1R0+ραhαΓ(α+2)j=0kaj,k+1[θαQjμαRj]Rk+1+ραhαΓ(α+2)[θαQk+1pμαRk+1p],

where h=TρN and

Sk+1pS0+ραhαΓ(α+1)j=0k((k+1j)α(kj)α)[ΛαμαSjβαSj(Ej+Ij)],Ek+1pE0+ραhαΓ(α+2)j=0k((k+1j)α(kj)α)[βαSj(Ej+Ij)(πα+μα+γα)Ej],Ik+1pI0+ραhαΓ(α+2)j=0k((k+1j)α(kj)α)[παEj(σα+μα)Ij],Qk+1pQ0+ραhαΓ(α+2)j=0k((k+1j)α(kj)α)[γαEj+σαIj(θα+μα)Qj],Rk+1pR0+ραhαΓ(α+2)j=0k((k+1j)α(kj)α)[θαQjμαRj].

Parameter values which are calculated for basic time of coronavirus used in numerical example are Λ=0.145; μ=0.000411; β=0.00038; π=0.00211; γ=0.0021; σ=0.0169; θ=0.0181, with total population N=355 and initial data (S0,E0,I0,Q0,R0)=(153,55,79,68,20).

In Figs. 15, we plot numerical solutions of the model (3) with T=30 obtained using the proposed algorithm and the RK4 method when N=355 and (S0,E0,I0,Q0,R0)=(153,55,79,68,20) for α=1. From the graphical results in Figs. 15, it can be seen that the results obtained using the proposed algorithm match the results of the RK4 method very well, which implies that the presented method can predict the behavior of these variables accurately in the region under consideration.

Figure 2.

Figure 2

E(t) versus t: solid line presents the proposed approximation, dotted line stands for RK4 method

Figure 3.

Figure 3

I(t) against t: solid line presents the proposed approximation, dotted line stands for RK4 method

Figure 4.

Figure 4

Q(t) against t: solid line presents the proposed approximation, dotted line stands for RK4 method

Figure 1.

Figure 1

S(t) against t: solid line presents the proposed approximation, dotted line stands for RK4 method

Figure 5.

Figure 5

R(t) against t: solid line presents the proposed approximation, dotted line stands for RK4 method

Figures 610 show the approximate solutions for S(t), E(t), I(t), Q(t), and R(t) obtained for different values of α using the proposed algorithm. From the graphical results given in Figs. 610, it is clear that the approximate solutions depend continuously on the time-fractional derivative α. It is evident that the efficiency of this approach can be dramatically enhanced by decreasing the step size.

Figure 7.

Figure 7

E(t) against t: (solid line) a=1.0, (dot-dashed line) a=0.85, (dashed line) a=0.75

Figure 8.

Figure 8

I(t) against t: (solid line) a=1.0, (dot-dashed line) a=0.85, (dashed line) a=0.75

Figure 9.

Figure 9

Q(t) against t: (solid line) a=1.0, (dot-dashed line) a=0.85, (dashed line) a=0.75

Figure 6.

Figure 6

S(t) against t: (solid line) a=1.0, (dot-dashed line) a=0.85, (dashed line) a=0.75

Figure 10.

Figure 10

R(t) against t: (solid line) a=1.0, (dot-dashed line) a=0.85, (dashed line) a=0.75

Remarks and conclusions

In this paper, we have formulated and analyzed a new mathematical model for COVID-19 epidemic. The model is described by a system of fractional-order differential equations and includes five classes, namely, S (susceptible class), E (exposed class), I (infected class), Q (isolated class), and R (recovered class). It should be emphasized that the model is a generalization of our recent work proposed in [35].

Firstly, the positivity, boundedness, and stability of the model have been established. Furthermore, the basic reproduction number of the model has been calculated by using the next generation matrix approach. Lastly, we have applied the adaptive predictor–corrector algorithm and fourth-order Runge–Kutta (RK4) method to simulate the proposed model. A set of numerical simulations has been performed to support the validity of the theoretical results. The numerical simulations indicate that there is a good agreement between theoretical results and numerical ones.

In the near future, we will extend the results in this work to propose new mathematical models for COVID-19 epidemic. Especially, effective strategies to control and prevent the disease will be investigated.

Acknowledgments

Acknowledgements

The authors thank the editor and anonymous referees for useful comments that led to a great improvement of the paper.

Availability of data and materials

The authors confirm that the data supporting the findings of this study are available within the article cited herein.

Authors’ contributions

Authors have equally contributed in preparing this manuscript. All authors read and approved the final manuscript.

Funding

This paper was supported by the Natural Science Foundation of the Higher Education Institutions of Anhui Province (No. KJ2020A0002).

Competing interests

The authors declare that there is no conflict of interest regarding the publication of this paper.

Contributor Information

Zizhen Zhang, Email: zzzhaida@163.com.

Anwar Zeb, Email: anwar@cuiatd.edu.pk.

Oluwaseun Francis Egbelowo, Email: oluwaseun@aims.edu.gh.

Vedat Suat Erturk, Email: vserturk@omu.edu.tr.

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