Skip to main content
Springer Nature - PMC COVID-19 Collection logoLink to Springer Nature - PMC COVID-19 Collection
. 2021 Jan 4;2021(1):2. doi: 10.1186/s13662-020-03192-w

Mathematical model of SIR epidemic system (COVID-19) with fractional derivative: stability and numerical analysis

Rubayyi T Alqahtani 1,
PMCID: PMC7779337  PMID: 33424955

Abstract

In this paper, we study and analyze the susceptible-infectious-removed (SIR) dynamics considering the effect of health system. We consider a general incidence rate function and the recovery rate as functions of the number of hospital beds. We prove the existence, uniqueness, and boundedness of the model. We investigate all possible steady-state solutions of the model and their stability. The analysis shows that the free steady state is locally stable when the basic reproduction number R0 is less than unity and unstable when R0>1. The analysis shows that the phenomenon of backward bifurcation occurs when R0<1. Then we investigate the model using the concept of fractional differential operator. Finally, we perform numerical simulations to illustrate the theoretical analysis and study the effect of the parameters on the model for various fractional orders.

Keywords: SIR model, Stability, Nonlinear recovery rate, Hospital bed, Backward bifurcation, Fractional model

Introduction

The spread of Covid-19 diseases is a very complex phenomenon carried out by many researchers. Many mathematical models were proposed including complex and simple mathematical models to understand the disease behavior. Faal et al. [1] proposed a model for the spread of the COVID-19 disease taking into account the superspreader, hospitalized, and fatality class. The authors analyzed the local stability of the steady-state solution and the model sensitivity. Mandal et al. [2] introduced a mathematical model taking into account a quarantine class and governmental intervention measures. In this study, the authors consider the basic reproduction number as an important parameter in analyzing the dynamics of the model. Recently, significant works were carried out to study the behavior of COVID-19 by means of mathematical models. Lin et al. [3] proposed SEIR models for the COVID-19 using data from China considering the impact of social isolation policies including governmental actions. The model successfully captures the course of the COVID-19 outbreak, whereas Wells et al. [4] and Gostic et al. [5] consider the impact of travel restrictions and border control on the global spread of the COVID-19.

The SIR model is commonly used for disease modeling, in particular, for the COVID-19 analysis [68]. The dynamic behavior of SIR model, including the stability, bifurcation, and chaos, has been studied over many decades [912]. In most studies the authors assume that the recovery rate is a constant. However, in reality the recovery rate depends on time of recovering process such as the health system, including the number of hospital beds and medicines.

In recent years, many researchers have studied the systems of differential equations with fractional operators [1315]. The epidemic models involving a fractional operator were also investigated by many authors because they deeply show biological and physical perspectives of the diseases [16, 17].

Rao et al. [18] studied an SIRS epidemic model assuming different death rates for each subclass, and the fraction of newborn children is represented by the parameter p. In this paper, we propose and analyze the extended SIRS epidemic model presented in [18] with the concept of fractional differential operator. In fact, we propose and study a model including three nonlinear differential equations with general incidence rate function and nonlinear recovery rate depending on the health system. The main focus of this study is analyzing the basic properties of model and demonstrating the stability properties of the model.

The rest of the paper is arranged as follows. We propose a dynamical model in Sect. 2. Then we formulate and establish the existence, uniqueness, positivity, and boundedness of solutions in Sect. 3. The steady-state solutions of the model and their stability are studied in Sects. 4 and 5, whereas numerical simulations of the steady-state solution brunches has is presented in Sect. 6. Section (7) contains a detailed dynamic behavior of the model with fractional derivative. We finish this study with conclusion in Sect. 8.

The dimensional model

In this section, we extend the model suggested in [18] to include a nonlinear incidence rate and recovery rate. The recovery rate is a function of both the hospital bed-population ratio b1>0 and the infected I. Thus the recovery rate α is given by [19]

α=α0+(α1α0)b1I+b1, 1

where the parameter α1 and α0 are the maximum and minimum per capita recovery rates, respectively. The nonlinear incidence rate is generalized by the function

f(S,I)=β1SIa1+a2S+a3I. 2

Thus the system of differential equations is given by

dSdt=(1p)bμ1Sf(S,I)+γR, 3
dIdt=f(S,I)(μ2+α)I, 4
dRdt=pb(μ3+γ)R+αI, 5

where the total population is split into three parts: S(t) is the susceptible population, I(t) is the infected population, and R(t) is the recovered population, so that N=S+I+R. The details and interpretation of the model can be found in [18]. We assume that all parameters are positive.

Basic properties of model

Positivity of solution

In this section, we prove that under nonnegative conditions, the model solutions are positive.

Theorem 1

Let S0,I0,R00. The solution of (3)(5) with (S(0),I(0),R(0))=(S0,I0,R0) is nonnegative, that is, S(t),I(t),R(t)0 for t>0.

Proof

Let x(t)=(S(t),I(t),R(t)) be the solution of system under initial conditions x0=(S(0),I(0),R(0))=(S0,I0,R0)0.

By the continuity of solution, for all of S(t),I(t),R(t) that have positive initial values at t=0, we have the existence of an interval (0,t0) such that S(t),I(t),R(t)0 for 0<t<t0. We will prove that t0=.

If S(t1)=0 for t10 and other solutions stay positive at t=t1, then

dSdt(t=t1)=(1p)A+γR>0. 6

This ensures that at any time the solution reaches the axis, its derivative increases, and the function S(t) does not cross to negative part. We can show by similar analysis that

dIdt(t=t1)=0, 7
dRdt(t=t1)=pb+αI0. 8

So x(t) never crosses the axes S=0,I=0,R=0 when it touches them. Thus, for any positive initial conditions, all equation solutions are positive. □

Theorem 1

Let (S(t),I(t),R(t)) be the solution of system (3)(5) with initial conditions (S0,I0,R0), and let μ=min(μ1,μ2,μ3). The compact set

Ψ={(S(t),I(t),R(t))R+3,Wb/μ} 9

is positively invariant and attracts all solutions in R+3.

Proof

Let W(t)=S(t)+I(t)+R(t). Then from the system (3)–(5) we have

dWdtbmin(μ1,μ2,μ3)W=bμW.

This implies that

dWdt+μWb. 10

Solving (10), we obtain

0<Wbμ+(W(0)bμ)exp(μt), 11

where W(0) is the initial condition. Thus 0<W(t)<bμ as t reaches infinity, and hence Ψ is a positively invariant and attractive set. □

Basic reproduction number

We use the next-generation matrix method [24] to calculate the reproduction number R0 of model (3)–(5):

R0=(γ1+μ3[1p])bβ1a2(γ1+μ3[1p])(α1+μ2)b+a1μ1(μ3+γ1)(α1+μ2). 12

Equilibria

In this section, we consider the number of equilibrium solutions of model (3)–(5). It is clear that the model has a disease-free equilibrium given by

E0(S,I,R)=(b(γ1+μ3[1p])μ1(μ3+γ1),0,pbμ3+γ1). 13

The non-free steady state of model (3)–(5) can be obtained by setting the right sides to zero. From equations (3)–(5) we have

S=(α0+μ2)I2+((p1)b+b1[α1+μ2]γ1R)I+bb1(p1)γ1b1Rμ1(I+b1), 14
R=α0I2+(b1α1+pb)I+bb1p(I+b1)(μ3+γ1). 15

Substituting equations ((14) and (15)) into equation (3), we obtain

E1(I)=c3I3+c2I2+c1I+c0=0, 16

where c0, c1, c2, and c3 are defined by

c3=((α0+μ2)μ3+γ1μ2)β1+(α0+μ2)(a2α0+a2μ2a3μ1)μ3c3=+γ1(α0+μ2)(a2μ2a3μ1),c2=(γ1+μ3(1p))(a2α0+a2μ2β1)b+(c21+c22+c23)b1+c24,c1=(γ1+μ3(1p))(a2[α0+α1+2μ2]2β1)b1b+(c11+c12)b12+c13,c0=b12[R01],c21=((2γ1+2μ3)μ22+(γ1+2μ3)(α0+α1)μ2+2α0α1μ3)a2,c22=(2μ1μ2(μ3+γ1)+μ1(μ3+γ1)(α0+α1))a3,c23=(2μ2(γ1+μ3)+μ3(α0+α1))β1,c24=a1μ1(μ3+γ1)(α0+μ2),c11=(α1+μ2)(μ3α1+γ1μ2+μ2μ3)a2,c12=[(μ3+γ1)(α1+μ2)μ1a3+(μ3α1+γ1μ2+μ2μ3)β1],c13=(μ3+γ1)(α0+α1+2μ2)b1a1μ1. 17

If R0=1, then c0=0, so equation (16) reduces to the equation

E1(I)=I[a3I2+a2I+a1]=0, 18

where I=0 is the disease-free equilibrium. By equation (16) the coefficient c0>0 when R0>1 and c0<0 when R0<1. Thus the number of possible positive real roots depends on the values of c3, c2, and c1. The possible roots analyzed by the Descartes rule of signs are shown in Table 1.

Table 1.

Number of possible positive real roots of equation (16). c4= basic reproduction number R0, c5= sign change number, c6= possible number of positive real roots

Case c3 c2 c1 c0 c4 c5 c6
1 + + + R0>1 1 1
2 + + R0<1 2 0, 2
3 + + R0>1 3 1, 3
4 + R0<1 2 0, 2
5 + + R0>1 1 1
6 + R0<1 2 0, 2
7 + R0>1 1 1
8 R0<1 0 0

Theorem 2

System (3)(5):

  1. has a one equilibrium if the basic reproduction number is greater than 1 and Cases 1, 5, and 7 are satisfied;

  2. can have more than one equilibrium if the basic reproduction number is greater than 1 and Case 3 is satisfied;

  3. can have two or more equilibria if the basic reproduction number is less than 1 and Cases 2, 4, and 6 are satisfied.

The existence of multiple steady state suggests the possibility of backward bifurcation where the phenomenon of three branches of steady-state equilibrium occurs at the same point.

Stability

In this section, we focus on analysis of the stability of the equilibrium of equations (3)–(5). We study the stabilities of two types of the disease equilibrium, that is, E0 and E1.

Local stability of the disease-free equilibrium

In this section, we study the stability of the free equilibrium E0. The Jacobian matrix of system (3)–(5) at E0 is

J(E0)=[μj12γ10j2200α1[μ3+γ1]], 19

where

J12=β1b(γ1+μ31[1p])μ1(μ3+γ1)(a2b(γ1+μ3[1p])μ1(μ3+γ1)+a1)1<0,J22=(γ1+μ3[1p])(a2α1+a2μ2β1)b+a1μ1(μ3+γ1)(α1+μ2)a2b(γ1+μ3[1p])+a1μ1(μ3+γ1).

The eigenvalues of matrix (19) are given by

λi=[μ1[μ3+γ1]J22]. 20

A simple calculation shows that J22=R01. So, we have the following result.

Lemma 1

The free steady-state solution E0 is locally asymptotically stable if R0<1 and is unstable if R0>1.

Stability of equilibria E1

In this section, we show that the nonfree steady-state solution E1 of system (3)–(5) is stable under specific condition. The Jacobian of the system can be written as

J(E1)=[J11J12γ1J21J2200J32[μ3+γ1]], 21

where

J11=[β1I(Ia3+a1)(Ia3+a2S+a1)2+μ1], 22
J12=[β1S(a2S+a1)(Ia3+a2S+a1)2],J21=β1I(Ia3+a1)(Ia3+a2S+a1)2,J22=(α1α0)b12(I+b1)2+α0β1S(a2S+a1)(Ia3+a2S+a1)2+μ2,J32=(α1α0)b12(I+b1)2+α0. 23

From equation (4) we get the following relations:

β1SIa1+a2S+a3I(μ2+α0+(α1α0)b1I+b1)I=0, 24
J22=β1SIa3(Ia3+a2S+a1)2+(α1α0)b1I(I+b1)2. 25

By simple analysis we get that the characteristics equation of J(E1) is

λ3+B1λ2+B2λ+B3, 26

where

B1=J22+J11+μ1+μ3+γ1,B2=(J12+J22+γ1+μ3)J11+(J22+γ1+μ3)μ1+(γ1+μ3)J22,B3=((J12+J22J32)γ1+μ3(J12+J22))J11+J22μ1[γ1+μ3].

We further use the Rough–Hurtwiz criterion to show the stability of the steady state E1. We have

B1B2B3=B11J112+B22J11+B33,B11=(J22+J12+μ3+γ1),B22=(J222+(J12+2[μ3+μ1+γ1])J22+γ12+(J32+2[μ3+μ1])γ1B22=+μ1[J12+2μ3]+μ32),B33=(μ3+μ1+γ1)J222+(μ3+μ1+γ1)2J22+μ1(μ3+μ1+γ1)(μ3+γ1). 27

By the Routh–Hurwitz theorem E1 is locally asymptotically stable when B1>0, B3>0, and B1B2B3>0. Theses conditions are satisfied when the following condition holds:

S(Ia3+a2S+a1)2<μ2β1. 28

Thus we have following results.

Lemma 2

The steady-state solution E1 of model (3)(5) is locally asymptotically if

S(Ia3+a2S+a1)2<μ2β1. 29

Theorem 3

The backward bifurcation occurs if b1<bcr, and no backward bifurcation otherwise.

Proof

We show the conditions for the existence of backward bifurcation for system (3)–(5) using the center manifold approach.

First, making a transformation of variables, we have x1=S,x2=I,x3=R. Then model (3)–(5) can be written in the form dXdt=F(X), where F=(f1,f2,f3). Hence

dSdt=f1=(1p)bμ1Sf(S,I)+γR, 30
dIdt=f2=f(S)(μ2+α)I, 31
dRdt=f3=pb(μ3+γ)R+αI,α=α0+(α1α0)b1I+b1,f(S,I)=β1SIa1+a2S+a3I. 32

Now let β1=β1 be the bifurcation parameter. When R0=1, we have the following relation:

β1=S0a2[α1+μ2]+a1[α1+μ2]S0, 33

and the model equation has one zero eigenvalue, and the other eigenvalues are negative. The behavior of the system near β1=β1 can be studied by applied the center manifold theory. The Jacobian matrix at free steady state E0 is

J(E0)=[μ1β1S0S0a2+a1γ10β1S0S0a2+a1α1μ200α1[μ3+γ1]]. 34

The right eigenvectors can be obtained as W=(w1,w2,w3)T, where (w1,w2,w3)T=(α1μ3+μ2[γ1+μ3]α1μ1,μ3+γ1α1,1). The left eigenvectors can be obtained as V=(v1,v2,v3)=(0,1,0). The existence of backward bifurcation depends on the coefficients a and b in [25, Theorem 4.1]. The nonzero partial derivatives of system (30)–(32) at disease-free equilibrium E0 are

f1x1x2(E0)=(α1+μ2)a1S0(a2S0+a1), 35
f1x2x1(E0)=(α1+μ2)a1S0(a2S0+a1), 36
f1x2x2(E0)=2a3(α1+μ2)a2S0+a1, 37
f2x1x2(E0)=(α1+μ2)a1S0(a2S0+a1), 38
f2x2x1(E0)=(α1+μ2)a1S0(a2S0+a1), 39
f2x2x2(E0)=2((α1+μ2)a3a2S0+a1+α0α1b1), 40
f3x2x2(E0)=2(α0α1b1). 41

The coefficient a is obtained as

a=k,i,j=13vkwiwjfkxixj=w1w2f2x1x2(E0)+w2w1f2x2x1(E0)+w2w2f2x2x2(E0)=2(a3(μ3+γ1)2(α1+μ2)α12(a2S0+a1)+(α0α1)(μ3+γ1)2b1α12)2(α1μ3+μ2[γ1+μ3])(μ3+γ1)(α1+μ2)a1α12μ1S0(a2S0+a1). 42

The bifurcation parameter b at E0 is given by

f2x2β1(E0)=S0S0a2+a1

and can be obtained as

b=k,i=13vkwifkxiβ1=v2w2f2x2β1(E0)=(μ3+γ1)S0α1(S0a2+a1)>0. 43

Clearly, b is always positive. According to [25, Theorem 4.1], the backward bifurcation phenomenon exists when the coefficient a is positive. Thus the condition for backward bifurcation is given by

b1<b1,cr=μ1S0[a2(μ3+γ1)(α1α0)S0+a1(μ3+γ1)(α1α0)][α1+μ2][S0a3μ1(μ3+γ1)+a1(α1μ3+μ2[γ1+μ3])]. 44

 □

The existence of the backward bifurcation at R0=1 requires condition (44) to be satisfied. When the number of hospital beds b1 is below the critical point b1,cr, the number of hospital beds open to the public is below demand, and as a result, some patients fail to access to healthcare. In this situation, there remains a high infection leading to a backward bifurcation.

Numerical simulations

In this section, we carry out some numerical calculations to support our theoretical results. The values of parameters used for numerical simulations are indicated in Table 2. We study the branch of steady state with respect to the model parameters. Figure 1 shows the curves of the infected population I for different values of b1, donated by the number of hospital beds and a specific value of general incidence rate (a1=a2=a3=1). It shows that there is a forward bifurcation at R0=1.

Table 2.

Parameters values

Parameters Values Reference
b 1 [20]
p 0.8 [0,1] [21]
α0 0.0714 Assumed.
α1 0.0857 Assumed.
β1 0.5 [20]
γ 0.25 [20]
μ1 0.2 [22]
μ2 0.2 [22]
μ3 0.2 [22]
b1 [0,20] 1.9 [23]
a1 1 Assumed.
a2 1 Assumed.
a3 1 Assumed.

Figure 1.

Figure 1

The figure showing a backward bifurcation varying the parameter b1 for R0. The values of the parameters are stated in Table 2

If we decrease the value of b1 from 2 to 1.6, then the backward bifurcation does not occur. These values are higher than the critical value of b1,cr=1.64. If we decrease the value of b1 to 0.1, less than the critical value b1,cr=1.64, then we can observe from Fig. 1(a) that the backward bifurcation occurs. Note that in Fig. 1(a) the above line of the curve is a stable state and the below line of the curve is an unstable state. This result indicates that in managing an infectious disease the number of hospital beds plays a significant role. Figure 2 shows the effect of the value of b1 on the curve when the backward bifurcation occurs. We observe that as the value of b1 decreases, the area of the curve increases.

Figure 2.

Figure 2

The figure showing a backward bifurcation varying the parameter b1 for R0<1. The values of the parameters are stated in Table 2

Figure 2 shows the infected population size I as a function of reproduction number R0 when the parameter b1 is varied for the case R0<1. It illustrates that as the value of b1 increases, the infected population size I decreases. It also shows the existence of a backward bifurcation, and the area of backward bifurcation curve decreases as the value b1 increases.

The model with fractional derivative

We consider the model with the Caputo–Fabrizio fractional derivatives

Dtα3S(t)=(1p)bμ1Sf(S,I)+γR,Dtα3I(t)=f(S)(μ2+α)I,Dtα3R(t)=pb(μ3+γ)R+αI,α=α0+(α1α0)b1I+b1,f(S,I)=β1SIa1+a2S+a3I.

Here we have 0<α3<1 and

Dtα3=1Γ(1α3)0tf(τ)(tτ)α3dτ. 45

We present the existence of positive solution of the system,

Dtα3S(t)=(1p)bμ1Sf(S,I)+γRμ1Sf(S,I)μ1S. 46

Then

S(t)S(0)exp(μ1tα3)for all t[0,t].

We can similarly show that

I(t)I(0)exp((μ2+a0)tα3)for all t[0,t].R(t)R(0)exp((μ3+γ)tα3)for all t[0,t].

Thus for all t[0,t], we have that S(t),I(t), and R(t) are positive.

Existence and uniqueness

Here we present the condition under which the system of equations has a unique solution. To achieve this, we have

S(t)S(0)=1Γ(α3)0tf1(S,I,R,τ)1(tτ)α31dτ. 47
I(t)I(0)=1Γ(α3)0tf2(S,I,R,τ)2(tτ)α31dτ. 48
R(t)R(0)=1Γ(α3)0tf3(S,I,R,τ)3(tτ)α31dτ. 49

We will show that, for all i=1,2,3,

  1. |fi(xi,t)|2ki(|xi|2+1) and

  2. |fi(xi,t)fi(xi,t)|2ki(|xixi|2):

|f1(S,I,R,τ)|2=|(1p)bμ1SβSIa1+a2S+a3I+γR| 50
4((1p)b)2+4μ1|S|2+4γ2|R|2+4β2|S|2|I|2|a1+a2S+a3I|2 51
4(1p)2b2+4μ12|S|2+4γ2|R|2+4β2sup(|S|2|I|2)min|a1+a2S+a3I|2 52
4(1p)2b2+4μ12|S|2+4γ2R2+4μ12+4β2I2M|S|2 53
(4(1p)2b2+4μ12|S|2+4γ2R2)×(1+4μ12+4β2I2M|S|24(1p)2b2+4μ12|S|2+4γ2R2) 54
(4(1p)2b2+4μ12|S|2+4γ2R2)(1+|S|2) 55
k1(1+|S|2)if 4μ12+4β2I2M4(1p)2b2+4γ2R2<1, 56
|f1(S,I,R,τ)f(S1,I,R,τ)|2=|μ1(SS1)β(SS1)Ia1+a2S+a3I|2 57
2μ1SS1|2+2β2|Ia1+a2S+a3I|2|SS1|2 58
2μ1|SS1|2+2β2|supIa1+a2S+a3I|2|SS1|2 59
2μ1|SS1|2+2β2M|SS1|2k2|SS1|2, 60
|f2(S,I,R,τ)|2=|f(S,I)(μ2+α)I|2 61
sup|f(S)(μ2+α)|2|I|2k3(1+|I|2), 62

where

k3=sup|f(S)(μ2+α)|2, 63
|f2(S,I,R,τ)f(S,I1,R,τ)2|2k3|II1|2, 64
|f3(S,I,R,τ)|2=|pb(μ3+γ)R+αI|2 65
3(pb)2+3(μ3+γ)2|R|2+3|α|2|I|2 66
3(pb)2+3(μ3+γ)2|R|2+3sup|α|2|I|2 67
3(pb)2+3(μ3+γ)2|R|2+M1 68
3((pb)2+M1)(1+(μ3+γ)2(pb)2+M1|R|2 69
3((pb)2+M1)(1+|R|2)if (μ3+γ)2(pb)2+M1<1, 70
|f3(S,I,R,τ)f3(S,I,R3,τ)2|2=(μ3+γ)2|RR1|2k4|RR1|2. 71

Therefore, under the condition

max(4μ12+4β2I2M4(1p)2b2+4γ2R2,(μ3+γ)2(pb)2+M1)<1, 72

the system admits a unique solution.

Numerical solution

In this section, we present the numerical solution of the equations. We use the numerical scheme of Atangan and Toufiq [26]. To use their scheme, we have

DtαS(t)=f1(S,I,R,τ),DtαI(t)=f2(S,I,R,τ),DtαR(t)=f3(S,I,R,τ).

The next step is converting the above to

S(t)=S(0)+1Γ(α3)0tf1(S,I,R,τ)(tτ)α3dτ, 73
I(t)=I(0)+1Γ(α3)0tf2(S,I,R,τ)(tτ)α3dτ, 74
R(t)=R(0)+1Γ(α3)0tf3(S,I,R,τ)(tτ)α3dτ. 75

Following their scheme, we have

S(tn+1)=S(0)+(t)α3Γ(α3+2)j=0n(f1(Sj,Ij,Rj,τj))(n+1j)α3(nj+2+α3)(nj)α3(nj+1+α3))(f1(Sj1,Ij1,Rj1,τj1))(n+1j)α3+1(nj)α3(nj+1+α3)),I(tn+1)=I(0)+(t)α3Γ(α3+2)j=0n(f2(Sj,Ij,Rj,τj))(n+1j)α3(nj+2+α3)(nj)α3(nj+1+α3))(f2(Sj1,Ij1,Rj1,τj1))(n+1j)α3+1(nj)α3(nj+1+α3)),R(tn+1)=R(0)+(t)α3Γ(α3+2)j=0n(f3(Sj,Ij,Rj,τj))(n+1j)α3(nj+2+α3)(nj)α3(nj+1+α3))(f3(Sj1,Ij1,Rj1,τj1))(n+1j)α3+1(nj)α3(nj+1+α3)).

Figure 3 shows numerical simulations for different values of fractional order. We observe a slight change in the behavior of curves as the values of fractional order increase.

Figure 3.

Figure 3

Numerical simulation of the susceptible population S(t), the infected population I(t), and the recovered population R(t) for different values of fractional order. The values of the parameters are stated in Table 2

Conclusion

In this paper, we considered the SIR model with general incidence rate function and nonlinear recovery rate to model the spread of disease. The nonlinear recovery rate depends on the influence of health system.

We proved the existence, uniqueness, and boundedness of the model solution. We studied all possible steady-state solutions of the model and details of stability and also derived the reproductive number. The analysis shows that the free steady state is locally stable when the reproductive number is less than unity and unstable otherwise. The model shows the phenomenon of backward bifurcation when R0<0 and the parameter b1 is less than the critical value given by

b1<b1,cr=μ1S0[a2(μ3+γ1)(α1α0)S0+a1(μ3+γ1)(α1α0)][α1+μ2][S0a3μ1(μ3+γ1)+a1(α1μ3+μ2[γ1+μ3])]. 76

When the parameter b1 is sufficiently greater that the critical value b1,cr, the disease infection decreases because the number of hospital beds increases. Therefore, to treat the disease in a community, the hospital resources must be improved.

Finally, we applied the theory of fractional derivatives to the model for different values of fractional orders. We used the numerical technique of Atangan and Toufiq, which is very accurate for solving fractional differential equations.

Acknowledgements

The author would like to thank the anonymous referees for their valuable suggestions, which have greatly helped in improving the presentation of this paper.

Authors’ contributions

The author worked in the derivation of the mathematical results and read and approved the final manuscript.

Funding

No funding available.

Availability of data and materials

Not applicable.

Competing interests

The author declares that they have no competing interests.

References

  • 1.Ndaïrow F., Area I., Nieto J.J., Torres D.F.M. Mathematical modeling of COVID-19 transmission dynamics with a case study of Wuhan. Chaos Solitons Fractals. 2020;135:109846. doi: 10.1016/j.chaos.2020.109846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Mandal M., Jana S., Nandi S.K., Khatua A., Adak S., Kar T.K. A model based study on the dynamics of COVID-19: prediction and control. Chaos Solitons Fractals. 2020;136:109889. doi: 10.1016/j.chaos.2020.109889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Lin Q., Zhao S., Gao D., Lou Y., Yang S., Musa S.S., Wang M.H., Cai Y., Wang W., Yang L., He D. A conceptual model for the coronavirus disease 2019 (COVID-19) outbreak in Wuhan, China with individual reaction and governmental action. Int. J. Infect. Dis. 2020;93:211–216. doi: 10.1016/j.ijid.2020.02.058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Wells C.R., Sah P., Moghadas S.M., Pandey A., Shoukat A., Wang Y., Wang Z., Meyers L.A., Singer B.H., Galvani A.P. Impact of international travel and border control measures on the global spread of the novel 2019 coronavirus outbreak. Proc. Natl. Acad. Sci. USA. 2020;117:7504–7509. doi: 10.1073/pnas.2002616117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Gostic K., Gomez A.C.R., Mummah R.O., Kucharski A.J., Lloyd-Smith J.O. Estimated effectiveness of symptom and risk screening to prevent the spread of COVID-19. eLife. 2020;9:e55570. doi: 10.7554/eLife.55570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Chen, Y.-C., Lu, P.-E., Chang, C.-S., Liu, T.-H.: A time-dependent SIR model for Covid-19 with undetectable infected persons (2020). arXiv:2003.00122 [DOI] [PMC free article] [PubMed]
  • 7.Anand N., Sabarinath A., Geetha S., et al. Predicting the spread of COVID-19 using SIR model augmented to incorporate quarantine and testing. Trans Indian Natl. Acad. Eng. 2020;5:141–148. doi: 10.1007/s41403-020-00151-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Nguemdjo U., Meno F., Dongfack A., Ventelou B. Simulating the progression of the COVID-19 disease in Cameroon using SIR models. PLoS ONE. 2020;15:8. doi: 10.1371/journal.pone.0237832. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Greenhalgh D., Khan Q., Lewis F. Hopf bifurcation in two SIRS density dependent epidemic models. Math. Comput. Model. 2004;39:11. doi: 10.1016/j.mcm.2004.06.007. [DOI] [Google Scholar]
  • 10.Tang Y., Huang Y., Ruan S., Zhang W. Coexistence of limit cycles and homoclinic loops in a SIRS model with a nonlinear incidence rate. SIAM J. Appl. Math. 2008;69:2. doi: 10.1137/070700966. [DOI] [Google Scholar]
  • 11.Yakui X., Tiantian L. Stability and Hopf bifurcation for a delayed SIR epidemic model with logistic growth. Abstr. Appl. Anal. 2013;2013:916130. [Google Scholar]
  • 12.Tailei Z., Junli L., Zhidong T. Stability of Hopf bifurcation of a delayed SIRS epidemic model with stage structure. Nonlinear Anal., Real World Appl. 2010;11:293–306. doi: 10.1016/j.nonrwa.2008.10.059. [DOI] [Google Scholar]
  • 13.Sonal J. Numerical analysis for the fractional diffusion and fractional Buckmaster’s equation by two step Adam–Bashforth method. Eur. Phys. J. Plus. 2018;133:19. doi: 10.1140/epjp/i2018-11854-x. [DOI] [Google Scholar]
  • 14.Abdon A., Sonal J. A new numerical approximation of the fractal ordinary differential equation. Eur. Phys. J. Plus. 2018;133:37. doi: 10.1140/epjp/i2018-11895-1. [DOI] [Google Scholar]
  • 15. Sania, Q., Mokhi, C., Asif Ali, S.: Analysis of series RL and RC circuits with time-invariant source using truncated M, atangana beta and conformable derivatives. J. Ocean Eng. Sci. (2020)
  • 16.Zizhen Z., Sonal J. Mathematical model of Ebola and Covid 19 with fractional differential operators: non-Markovian process and class for virus pathogen in the environment. Chaos Solitons Fractals. 2020;140:110175. doi: 10.1016/j.chaos.2020.110175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ernestine A., Abdon A. Facemasks simple but powerful weapons to protect against COVID-19 spread: can they have sides effects? Results Phys. 2020;19:103425. doi: 10.1016/j.rinp.2020.103425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Rao F., Mandal P.S., Kang Y. Complicated endemics of an SIRS model with a generalized incidence under preventive vaccination and treatment controls. Appl. Math. Model. 2019;67:38–61. doi: 10.1016/j.apm.2018.10.016. [DOI] [Google Scholar]
  • 19.Shan C., Zhu H. Bifurcations and complex dynamics of an SIR model with the impact of the number of hospital beds. J. Differ. Equ. 2014;257:1662–1688. doi: 10.1016/j.jde.2014.05.030. [DOI] [Google Scholar]
  • 20.Cai Y., Kang Y., Banerjee M., Wang W. A stochastic SIRS epidemic model with infectious force under intervention strategies. J. Differ. Equ. 2015;259:7463–7502. doi: 10.1016/j.jde.2015.08.024. [DOI] [Google Scholar]
  • 21.Lahrouz A., Omari L., Kiouach D., Belmaâti A. Complete global stability for an SIRS epidemic model with generalized non-linear incidence and vaccination. Appl. Math. Comput. 2012;218:6519–6525. [Google Scholar]
  • 22.Xiao D., Ruan S. Global analysis of an epidemic model with nonmonotone incidence rate. Math. Biosci. 2007;208:419–429. doi: 10.1016/j.mbs.2006.09.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Abdelrazec A., Belair J., Shan C., Zhu H. Modeling the spread and control of Dengue with limited public health resources. Math. Biosci. 2016;271:136–145. doi: 10.1016/j.mbs.2015.11.004. [DOI] [PubMed] [Google Scholar]
  • 24.Driessche P., Watmough J. Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission. Math. Biosci. 2002;180:29–48. doi: 10.1016/S0025-5564(02)00108-6. [DOI] [PubMed] [Google Scholar]
  • 25.Castillo-Chavez C., Song B. Dynamical models of tuberculosis and their applications. Math. Biosci. Eng. 2004;1:361–404. doi: 10.3934/mbe.2004.1.361. [DOI] [PubMed] [Google Scholar]
  • 26.Mekkaoui T., Abdon A. New numerical approximation of fractional derivative with non-local and non-singular kernel: application to chaotic models. Eur. Phys. J. Plus. 2017;132:444. doi: 10.1140/epjp/i2017-11717-0. [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Not applicable.


Articles from Advances in Difference Equations are provided here courtesy of Nature Publishing Group

RESOURCES