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ORIGINAL RESEARCH article

Front. Phys., 17 January 2020
Sec. Statistical and Computational Physics
This article is part of the Research Topic New Numerical and Analytical Methods for Nonlinear Partial Differential Equations with Applications in Quantum Physics View all 18 articles

Numerical Analysis of the Susceptible Exposed Infected Quarantined and Vaccinated (SEIQV) Reaction-Diffusion Epidemic Model

\nNauman Ahmed,Nauman Ahmed1,2Mehreen FatimaMehreen Fatima3Dumitru Baleanu,Dumitru Baleanu4,5Kottakkaran Sooppy NisarKottakkaran Sooppy Nisar6Ilyas Khan
Ilyas Khan2*Muhammad RafiqMuhammad Rafiq7Muhammad Aziz ur RehmanMuhammad Aziz ur Rehman1Muhammad Ozair AhmadMuhammad Ozair Ahmad8
  • 1Department of Mathematics, University of Management and Technology, Lahore, Pakistan
  • 2Department of Mathematics, College of Science Al-Zulfi, Majmaah University, Al-Majma'ah, Saudi Arabia
  • 3Department of Electrical Engineering, University of Lahore, Lahore, Pakistan
  • 4Department of Mathematics, Cankaya University, Ankara, Turkey
  • 5Institute of Space Sciences, Mǎgurele, Romania
  • 6Department of Mathematics, College of Arts and Sciences, Wadi Aldawaser, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia
  • 7Faculty of Engineering, University of Central Punjab, Lahore, Pakistan
  • 8Department of Mathematics and Statistics, University of Lahore, Lahore, Pakistan

In this paper, two structure-preserving nonstandard finite difference (NSFD) operator splitting schemes are designed for the solution of reaction diffusion epidemic models. The proposed schemes preserve all the essential properties possessed by the continuous systems. These schemes are applied on a diffusive SEIQV epidemic model with a saturated incidence rate to validate the results. Furthermore, the stability of the continuous system is proved, and the bifurcation value is evaluated. A comparison is also made with the existing operator splitting numerical scheme. Simulations are also performed for numerical experiments.

1. Introduction

Mathematical modeling has a prominent role in describing physical phenomena in various disciplines of mathematics, physical sciences, social sciences, engineering, life sciences, and many more [16]. The transmission of infectious diseases and the control of their spread can be studied effectively by constructing mathematical models for various strategies like vaccination and quarantine. The word quarantine denotes forced isolation or being cut off from interactions with others. Quarantine is an effective intervention process for restraining the spread of infection by isolating individuals who are affected by the disease. Such isolation has been adopted to decrease the communication of infectious diseases like dengue, measles, smallpox, cholera, leprosy, tuberculosis, and many more.

Epidemic models, that is, mathematical models of infectious diseases, are a simplified way to illustrate the transmission dynamics of the complicated nonlinear processes and complex behavior of an infectious disease in individuals within a population. These are deterministic models that are used to allocate the population to different subclasses or compartments, describing a particular stage of the epidemic. The incidence rate, which is proportional to the number of susceptible and infected persons, is an important parameter of compartment-based epidemic models. The mathematical models of infectious diseases are often based on bilinear incidence rate βSI, but a more concise approach to use the saturated incidence rate rather than the bilinear incidence rate. In the saturated incidence rate βSI1+αI, if number of infected individuals I becomes very large, βSI1+αI approaches the saturation level. The infection force is measured by βI, which describes the penetration of the disease into a fully susceptible population. 11+αI is used to measure the inhibition effect of behavioral change of susceptible persons. Liu and Yang [7] proposed the SEIQV epidemic model, which uses the saturated incidence rate. The model is expressed as:

dS(t)dt=b-βS(t)I(t)1+αI(t)-(ω+μ+q3)S(t)    (1)
dE(t)dt=βS(t)I(t)1+αI(t)-(μ+σ+q2)E(t)    (2)
dI(t)dt=σE(t)-(μ+ϵ+γ+q1)I(t)    (3)
dQ(t)dt=q3S(t)+q2E(t)+q1I(t)-(μ+ϕ)Q(t)    (4)
dV(t)dt=ωS(t)+ϕQ(t)+γI(t)-μV(t)    (5)

The variables and parameters of the model are defined as:

S(t) = Susceptible persons at time t,

E(t) = Exposed persons at time t,

I(t) = Infected persons at time t,

Q(t) = Quarantined persons at time t,

V(t) = Vaccinated persons at time t,

b = Rate of recruitment,

β = Rate of transmission,

μ = Rate of natural death,

ϵ = Rate of death due to disease in infected compartment,

α = Parameter that measures psychological or inhibitory effects,

γ = Rate at which infected individuals are being vaccinated infected persons,

σ = Rate at which exposed persons become infected,

ω = Rate at which infected individuals are being vaccinated susceptible persons,

ϕ = Rate at which infected individuals are being vaccinated quarantined persons,

q1, q2, q3 = Effective quarantine probabilities.

The above model (1)–(5) assumes a homogeneous population, where the population mixes in such a way that there is no difference between person in one place and person in another place. However, in actual scenarios, the disease may spread faster in one place than in another because of different circumstances like different weather conditions, etc. Hence, it is essential for the variables to depend on space also. Therefore, we extend system (1)–(5) to make it a reaction-diffusion system by adding a diffusion term.

S(x,t)t=b-βS(x,t)I(x,t)1+αI(x,t)-(ω+μ+q3)S(x,t)                 +d12S(x,t)x2    (6)
E(x,t)t=βS(x,t)I(x,t)1+αI(x,t)-(μ+σ+q2)E(x,t)+d22E(x,t)x2    (7)
I(x,t)t=σE(x,t)-(μ+ϵ+γ+q1)I(x,t)+d32I(x,t)x2    (8)
Q(x,t)t=q3S(x,t)+q2E(x,t)+q1I(x,t)-(μ+ϕ)Q(x,t)                     +  d42Q(x,t)x2    (9)
V(x,t)t=ωS(x,t)+ϕQ(x,t)+γI(x,t)-μV(x,t)                     +  d52V(x,t)x2    (10)

with the initial conditions:

S(x,0)=g1(x)   0xL    (11)
E(x,0)=g2(x)   0xL    (12)
I(x,0)=g3(x)   0xL    (13)
Q(x,0)=g4(x)   0xL    (14)
V(x,0)=g5(x)   0xL    (15)

The boundary conditions are no flux,

Sx(0,t)=Sx(L,t)=0    (16)
Ex(0,t)=Ex(L,t)=0    (17)
Ix(0,t)=Ix(L,t)=0    (18)
Qx(0,t)=Qx(L,t)=0    (19)
Vx(0,t)=Vx(L,t)=0    (20)

Epidemic models always demonstrate two equilibrium points: the disease-free equilibrium (DFE) point and the endemic equilibrium (EE) point. The DFE point exists if R0 < 1, where R0 is the reproductive number, which basically measures the occurrence of disease. The EE point exists if R0 > 1. This implies that the SEIQV reaction-diffusion system (6–10) always converges to the DFE point or EE point if R0 < 1 or R0 > 1, respectively. Analytical solution of the SEIQV epidemic system is not possible, so we have to use numerical techniques to find its solution. Note that the numerical technique must show the same behavior as is possessed by the continuous SEIQV reaction-diffusion epidemic system.

In this work, we propose two operator-splitting NSFD methods, one explicit and one implicit. These methods are used to solve the SEIQV epidemic model with diffusion. As S, E, I, Q, and V are population sizes and evaluated in absolute scale, we propose NSFD methods because they give a positive solution. Also, the convergence of the proposed NSFD operator splitting methods toward the equilibrium points is the same as the convergence of continuous an SEIQV reaction-diffusion epidemic system. The proposed splitting methods are designed with the aid of rules given by Mickens [8]. In the recent era, positivity preserving FD methods have gained importance, as many physical dynamical systems possess the positivity property [911]. The NSFD method presented by Mickens [8, 12, 13] has becomes an effective and important structure-preserving FD method for solving differential equations. In epidemic models, population dynamics and population size cannot be negative, so the numerical technique must be a positivity-preserving technique. Various authors have used different positivity-preserving numerical techniques for the approximate solution of epidemic models: see, for example [1422].

In this work, we also show the numerical stability of the SEIQV epidemic model with diffusion and evaluate the bifurcation value of the vaccination parameter ω with the aid of the Routh-Hurwitz method.

2. Equilibrium Points

The model (6–10) has two equilibrium points [7], the DFE point and EE point. The DFE point is:

DFE=(S0,E0,I0,Q0,V0)         =(bω+μ+q3,0,0,q3S0μ+ϕ,ωS0+ϕQ0μ)    (21)

and the EE point is:

EE=(S*,E*,I*,Q*,V*)    (22)

where,

S*=(μ+σ+q2)(μ+ϵ+γ+q1)(1+αI)γβE*=(μ+ϵ+γ+q1)IσQ*=q3S+q2E+q1Iμ+ϕV*=ωS+ϕQ+γIμI*=σβb-(ω+μ+q3)(μ+σ+q2)(μ+ϵ+γ+q1)(μ+σ+q2)(μ+ϵ+γ+q1)(β+α(ω+μ+q3))

Reproductive number R0 is given as:

R0=σβb(ω+μ+q3)(μ+σ+q2)(μ+ϵ+γ+q1),            when,d1=d2=d3=d4=d5=0

R0 is the reproductive value. Now, if R0 < 1, the model acquires a DFE point, and if R0 > 1, the model acquires an EE point.

3. Numerical Stability of the SEIQV Model at Equilibrium Point

We evaluated the small perturbation S1(x, t), E1(x, t), I1(x, t), Q1(x, t), and V1(x, t) so that (6)–(10) is linearized at the EE point (S*, E*, I*, Q*, V*), as discussed in Chakrabrty et al. [23].

S1t=a11S1+a12E1+a13I1+a14Q1+a15V1+d12S1x2    (23)
E1t=a21S1+a22E1+a23I1+a24Q1+a25V1+d22E1x2    (24)
I1t=a31S1+a32E1+a33I1+a34Q1+a35V1+d32I1x2    (25)
Q1t=a41S1+a42E1+a43I1+a44Q1+a45V1+d42Q1x2    (26)
V1t=a51S1+a52E1+a53I1+a54Q1+a55V1+d52V1x2    (27)

Suppose a Fourier series solution is demonstrated for Equations (23)–(27) of the form:

S1(x,t)=kSkeλtcos(kx)    (28)
E1(x,t)=kEkeλtcos(kx)    (29)
I1(x,t)=kIkeλtcos(kx)    (30)
Q1(x,t)=kQkeλtcos(kx)    (31)
V1(x,t)=kVkeλtcos(kx)    (32)

Here, k = /2, (n = 1, 2, 3,…) exhibits the value of the wave number for the node n. Substituting Equations (28)–(32) in the system (23)–(27), the system is converted into:

k(a11-d1k2-λ)Sk+ka12Ek+ka13Ik+ka14Qk                                                    +ka15Vk=0    (33)
                               ka21Sk+k(a22-d2k2-λ)Ek+ka23Ik                                                    +ka24Qk+ka25Vk=0    (34)
                               ka31Sk+ka32Ek+k(a33-d3k2-λ)Ik                                                    +ka34Qk+ka35Vk=0    (35)
                                ka41Sk+ka42Ek+ka43Ik                                                     +k(a44-d4k2-λ)Qk+ka45Vk=0    (36)
                                ka51Sk+ka52Ek+ka53Ik+ka54Qk                                                     +k(a55-d5k2-λ)Vk=0    (37)

The variational matrix V for the system (33)–(37) is:

V=(a11-d1k2a12a13a14a15a21a22-d2k2a23a24a25a31a32a33-d3k2a34a35a41a42a43a44-d4k2a45a51a52a53a54a55-d5k2)    (38)

where,

a11=-βI*(1+αI*)-(ω+μ+q3),a12=0,a13=-βS*(1+αI*)2a14=0,a15=0,a21=βI*(1+αI*),a22=-(σ+μ+q2)a23=βS*(1+αI*)2,a24=0,a25=0,a31=0,a32=σa33=-(μ+ϵ+γ+q1),a34=0,a35=0,a41=q3,a42=q2,a43=q1a44=-(μ+ϕ),a45=0,a51=ω,a52=0,a53=γ,a54=ϕ,a55=-μ

The characteristics equation for matrix V is:

λ5+ξ1λ4+ξ2λ3+ξ3λ2+ξ4λ+ξ5=0

The expressions for ξ1, ξ2, ξ3, ξ4, and ξ5 with diffusion and without diffusion are mentioned in Islam and Haider [24].

The Routh-Hurwitz stability criterion gives:

ξ1>0,ξ2>0,ξ3>0,ξ4>0,ξ5>0
t1=ξ1ξ2ξ3-ξ32-ξ12ξ4>0

and

t2=(ξ1ξ4-ξ5)(ξ1ξ2ξ3-ξ32-ξ12ξ4)-ξ5(ξ1ξ2-ξ3)2          -ξ1ξ52>0.

The Table 2 reflects the numerical stability of the equilibrium point against the various cases, as discussed in Table 1.

TABLE 1
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Table 1. Values of parameters.

TABLE 2
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Table 2. Stability of equilibrium point.

4. Bifurcation Value of Vaccination Parameter ω Independent of Diffusion

Considering the vaccination parameter ω, to find its bifurcation value, a11, a12, are used instead of S*, E*, I*, Q*, and V*.

a11=-0.6893640968ω-0.2309369724,a13=-1.1198107335ω-0.3751365957a21=0.0709369724-0.3106359032ω,a22=-0.96a23=1.1198107335ω+0.3751365957,a32=0.7,a33=-0.46,a41=0.1,a42=0.2a43=0.2,a44=-0.46,a51=ω,a53=0.15,a54=0.4,a55=-0.06a12=a14=a15=a24=a25=a31=a34=a35=a45=a52=0

The Routh-Hurwitz criterion for stability gives:

                                      ξ1=0.6893640968ω+2.1709369724=f1(ω)                                      ξ2=0.5534988343ω+1.3930221095=f2(ω)                                      ξ3=-0.7838675135ω2+0.0368505571ω                                                 +0.3691384683=f3(ω)                                      ξ4=-0.4076111070ω2-0.0380846274ω                                                 +0.0451739663=f4(ω)                                      ξ5=-0.0216347434ω2-0.0023071181ω                                                 +0.00165507=f5(ω)ξ1ξ2ξ3-ξ32-ξ12ξ4=-0.7198363952ω4-0.3846861900ω3                                                  +0.4409094061ω2+0.9265604777ω                                                  +0.7671683354=f6(ω)
(ξ1ξ4ξ5)(ξ1ξ2ξ3ξ32ξ12ξ4)ξ5(ξ1ξ2ξ3)2ξ1ξ52            =0.2022686014ω7+0.7777858386ω6+0.3637035355ω5            0.4633365077ω40.8380985505ω30.5245415951ω2            +0.0491674986ω+0.0622935244=f7(ω)

where the values of ξ1, ξ2, ξ3, ξ4, and ξ5 are obtained from the expression of the characteristic equation (without diffusion) given in paper [24].

f5(ω) = 0 gives the value of bifurcation for ω. This value transfers the stability of a continuous model from stable to unstable. f5(ω) = 0 provides the bifurcation value ω = 0.228360507. The EE point is stable for ω less than ω = 0.228360507.

5. Bifurcation Value of Vaccination Parameter ω With Diffusion

For the bifurcation value of vaccination parameter ω, the values of S*, E*, I*, Q*, and V* are replaced into a11, a12, to

a11=-0.6893640968ω-0.2309369724,a13=-1.1198107335ω-0.3751365957a21=0.0709369724-0.3106359032ω,a22=-0.96a23=1.1198107335ω+0.3751365957,a32=0.7,a33=-0.46,a41=0.1a42=0.2,a43=0.2,a44=-0.46,a51=ω,a53=0.15,a54=0.4,a55=-0.06a14=a12=a15=a24=a25=a31=a34=a35       =a45=a52=0

The Routh-Hurwitz criterion for stability gives:

                                      ξ1=0.6893640968ω+2.3707964615=f1(ω)                                      ξ2=0.60622790397ω+1.7722067841=f2(ω)                                      ξ3=-0.7838675135ω2-0.0208144715ω                                                 +0.5625469972=f3(ω)                                      ξ4=-0.4462934183ω2-0.0884716755ω                                                 +0.0784487226=f4(ω)                                      ξ5=-0.0321693682ω2-0.0070094221ω                                                 +0.0035676470=f5(ω)ξ1ξ2ξ3-ξ32-ξ12ξ4=-0.7299468904ω4-0.6247499708ω3                                                +0.5281660018ω2+1.6725898825ω                                                +1.6061706299=f6(ω)
(ξ1  ξ4ξ5)(ξ1ξ2ξ3ξ32ξ12ξ4)ξ5(ξ1ξ2ξ3)2ξ1ξ52  =0.2245744816ω7+1.0320435772ω6+0.8416645931ω5        0.5793147772ω41.7894315920ω31.3916904163ω2        +0.0896889602ω+0.2457209648=f7(ω)

f5(ω) = 0 gives ω = 0.24144152. The EE point is stable therefore for any value less than ω = 0.24144152.

It can be seen that the value of bifurcation of ω for the system with diffusion is greater than value of bifurcation of ω for the system without diffusion.

6. Numerical Methods

In this section, we apply two proposed and classical splitting methods to the SEIQV reaction-diffusion epidemic model with diffusion. Operator-splitting techniques very effectively handle the nonlinearity and complexity of reaction-diffusion equations. Therefore, these techniques are used frequently by several researchers for the solution of nonlinear differential equations [23, 2533]. The SEIQV epidemic model with diffusion is split in two ways. The nonlinear reaction equations are split in the first step as,

12St=b-βSI1+αI-(ω+μ+q3)S    (39)
12Et=βSI1+αI-(μ+σ+q2)E    (40)
12It=σE-(μ+ϵ+γ+q1)I    (41)
12Qt=q3S+q2E+q1I-(μ+ϕ)Q    (42)
12Vt=ωS+ϕQ+γI-μV    (43)

and the diffusion equations are split in the second step as:

12St=d12Sx2    (44)
12Et=d22Ex2    (45)
12It=d32Ix2    (46)
12Qt=d42Qx2    (47)
12Vt=d52Vx2    (48)

Now, we apply forward and backward Euler methods with operator splitting on the system (6)–(7).

S¯im+12=Sim+τ(b-βSimIim1+αIim-(ω+μ+q3)Sim)    (49)
E¯im+12=Eim+τ(βSimIim1+αIim-(μ+σ+q2)Eim)    (50)
I¯im+12=Iim+τ(σEim-(μ+ϵ+γ+q1)Iim)    (51)
Q¯im+12=Qim+τ(q3Sim+q2Eim+q1Iim-(μ+ϕ)Qim)    (52)
V¯im+12=Vim+τ(ωSim+ϕQim+γIim-μVim)    (53)

where Sim,Eim,Iim,Qim and Vim at mτ, m = 0, 1, … and 0 + ih, i = 0, 1, … reflects difference approximations of S, E, I, Q, and V. The values of S¯im+12, E¯im+12, I¯im+12, Q¯im+12, and V¯im+12 are the values at the half time step. Both forward and backward Euler methods have same process at first step, but, at the second half step of time, they have different procedures. Since the forward Euler operator splitting method is explicit, we use:

Sim+1=S¯im+12+λ1(S¯i-1m+12-2S¯im+12+S¯i+1m+12)    (54)
Eim+1=E¯im+12+λ2(E¯i-1m+12-2E¯im+12+E¯i+1m+12)    (55)
Iim+1=I¯im+12+λ3(I¯i-1m+12-2I¯im+12+I¯i+1m+12)    (56)
Qim+1=Q¯im+12+λ4(Q¯i-1m+12-2Q¯im+12+Q¯i+1m+12)    (57)
Vim+1=V¯im+12+λ5(V¯i-1m+12-2V¯im+12+V¯i+1m+12)    (58)

For the backward Euler method, we use:

-λ1Si-1m+1+(1+2λ1)Sim+1-λ1Si-1m+1=S¯im+12    (59)
-λ2Ei-1m+1+(1+2λ2)Eim+1-λ2Ei-1m+1=E¯im+12    (60)
-λ3Ii-1m+1+(1+2λ3)Iim+1-λ3Ii-1m+1=I¯im+12    (61)
-λ4Qi-1m+1+(1+2λ4)Qim+1-λ4Qi-1m+1=Q¯im+12    (62)
-λ5Vi-1m+1+(1+2λ5)Vim+1-λ5Vi-1m+1=V¯im+12    (63)

For the proposed NSFD operator splitting methods, we implement the rules constructed by Mickens [8]. The technique for both explicit and implicit schemes is similar at the first half time step:

S¯im+12=Sim+τb1+τβIim1+αIim+τ(ω+μ+q3)    (64)
E¯im+12=Eim+τβSimIim1+αIim1+τ(μ+σ+q2)    (65)
I¯im+12=Iim+τσEim1+τ(μ+ϵ+γ+q1)    (66)
Q¯im+12=Qim+τ(q3Sim+q2Eim+q1Iim)1+τ(μ+ϕ)    (67)
V¯im+12=Vim+τ(ωSim+ϕQim+γIim)1+τμ    (68)

A positive solution desires that if:

       Sim0,Eim0,Iim0,Qim0,Vim0S¯im+120,E¯im+120,I¯im+120,Q¯im+120,V¯im+120    (69)

The techniques for the implicit and explicit NSFD schemes are not similar for the second half of the time step. The procedure for the explicit NSFD scheme is as follows:

Sim+1=(1-2λ1)S¯im+12+λ1(S¯i-1m+12+S¯i+1m+12)    (70)
Eim+1=(1-2λ2)E¯im+12+λ2(E¯i-1m+12+E¯i+1m+12)    (71)
Iim+1=(1-2λ3)I¯im+12+λ3(I¯i-1m+12+I¯i+1m+12)    (72)
Qim+1=(1-2λ4)Q¯im+12+λ4(Q¯i-1m+12+Q¯i+1m+12)    (73)
Vim+1=(1-2λ5)V¯im+12+λ5(V¯i-1m+12+V¯i+1m+12)    (74)

We use an implicit procedure for the second NSFD method at the second half of the time step:

-λ1Si-1m+1+(1+2λ1)Sim+1-λ1Si-1m+1=S¯im+12    (75)
-λ2Ei-1m+1+(1+2λ2)Eim+1-λ2Ei-1m+1=E¯im+12    (76)
-λ3Ii-1m+1+(1+2λ3)Iim+1-λ3Ii-1m+1=I¯im+12    (77)
-λ4Qi-1m+1+(1+2λ4)Qim+1-λ4Ii-1m+1=Q¯im+12    (78)
-λ5Vi-1m+1+(1+2λ5)Vim+1-λ5Vi-1m+1=V¯im+12    (79)

where,

λ1=d1τh2,λ2=d2τh2,λ3=d3τh2,λ4=d4τh2,λ5=d5τh2

6.1. Stability and Accuracy of Splitting Schemes

In finite difference operator splitting techniques, the step involving the reaction term is unconditionally stable because it is solved exactly [25, 26]. On the other hand, the step involving the diffusion term has different stability in different techniques. The explicit procedure has conditional stability in the region:

λi12,(i=1,2,3,4,5).    (80)

while the implicit procedure has unconditionally stability [25, 26]. The accuracy of both schemes is O(τ) and O(h2) for all the methods under study.

6.2. Positivity of Proposed Schemes

Equations (64)–(65) in the reaction step of both proposed methods preserve the property of positivity depicted by the continuous SEIQV model, as there is no negative term involved in (64)–(65).

As far as the diffusion step is concerned, the proposed explicit scheme (70)–(74) demonstrates the positivity of the solution if:

1-2λi0,i=1,2,3,4,5

so,

λi12,(i=1,2,3,4,5)

which is the condition of stability for the explicit operator-splitting NSFD scheme (70)–(74). This verifies that the explicit NSFD scheme retains the positive solution in the region of stability. M matrix theory has been used for the verification of the positivity of the implicit NSFD method (75)–(79). For more details [34] is referred.

6.2.1. Theorem [21, 22]

For any positive τ and h, the system described by (75)–(79) is also positive, i.e., Sm > 0, Em > 0, Qm > 0 and Vm > 0, ∀m = 0, 1, 2…

Proof

Equations (75)–(79) can be written as:

ASm+1=Sm    (81)
BEm+1=Em    (82)
CIm+1=Im    (83)
DQm+1=Qm    (84)
GVm+1=Vm    (85)

In Equations (81)–(85), the letters A, B, C, D, and G represent the square matrices. Where,

A=(a3a100a2a3a2   0a2a3a2      a2a3a20   a2a3a200a1a3)    (86)
B=(b3b100b2b3b2   0b2b3b2      b2b3b20   b2b3b200b1b3)    (87)
C=(c3c100c2c3c2   0c2c3c2      c2c3c20   c2c3c200c1c3)    (88)
D=(d3d100d2d3d2   0d2d3d2      d2d3d20   d2d3d200d1d3)    (89)
G=(g3g100g2g3g2   0g2g3g2      g2g3g20   g2g3g200g1g3)    (90)

The off-diagonal entries of A are a1 = −2λ1, a2 = −λ1, and the diagonal entries are a3 = 1 + 2λ1. The entries of B in the off-diagonal are b1 = −2λ1, b2 = −λ1, and the diagonal entries are b3 = 1 + 2λ2. The entries of C in the off-diagonal are c1 = −2λ3, c2 = −λ3, and the diagonal entries are c3 = 1 + 2λ3. The off-diagonal entries of D are d1 = −2λ4, d2 = −λ4, and the diagonal entries are d3 = 1 + 2λ4. The off-diagonal entries of G are g1 = −2λ5, g2 = −λ5, and the diagonal entries are g3 = 1 + 2λ5. Thus, A, B, C, D, and G are M-matrices, and Equations (81), (82), (83), (84), and (85) are:

Sm+1=A-1Sm    (91)
Em+1=B-1Em    (92)
Im+1=C-1Im    (93)
Qm+1=D-1Im    (94)
Vm+1=G-1Im    (95)

If we consider that Sm > 0, Em > 0, Im > 0, Qm > 0, and Vm > 0, then the M-matrix along with (60) implies that the values of all of the state variables, i.e., Sm+1, Em+1, Im+1, Qm+10, and Vm+1 are positive. Hence, the theorem is done by using the principle of mathematical induction.

This theorem is applied for drawing the conclusion that the proposed scheme, which is implicit in nature, guarantees the positive solution unconditionally.

7. Numerical Experiment and Simulations

A numerical test is performed on both the points of equilibrium for all the schemes under consideration. The set of parametric values considered for the test problem at disease-free equilibrium point [7] is given as:

b = 0.7, μ = 0.06, σ = 0.7, β = 0.35, γ = 0.15, ω = 0.3, q1 = 0.2, q2 = 0.2, q3 = 0.1, ϕ = 0.4, ϵ = 0.05, α = 2, d1 = 0.05, d2 = 0.01, d3 = 0.001, d4 = 0.01, d5 = 0.01.

For the endemic equilibrium point, the following parametric values are used:

b = 0.7, μ = 0.06, σ = 0.7, β = 0.35, γ = 0.15, ω = 0.06, q1 = 0.2, q2 = 0.2,

q3 = 0.1, ϕ = 0.4, ϵ = 0.05, α = 2, d1 = 0.05, d2 = 0.01, d3 = 0.001, d4 = 0.01, d5 = 0.01.

The initial condition for the model (6)–(10) is:

S(x,0)={0.7xif x[0,0.5)0.7(10-x)if x[0.5,1]    (96)
E(x,0)={0.5xif x[0,0.5)0.5(10-x)if x[0.5,1]    (97)
I(x,0)={0.3xif x[0,0.5)0.3(10-x)if x[0.5,1]    (98)
Q(x,0)={0.1xif x[0,0.5)0.1(10-x)if x[0.5,1]    (99)
V(x,0)={0.1xif x[0,0.5)0.1(10-x)if x[0.5,1]    (100)

7.1. Disease-Free Equilibrium Point

In this section, graphs of all the state variables against time are presented (for DFE) to illustrate the behavior of the schemes. In Figures 1, 2, we consider h = 0.5, λ1 = 0.3, λ2 = 0.06, λ3 = 0.006, λ4 = 0.06, and λ5 = 0.06.

FIGURE 1
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Figure 1. The explicit operator splitting NSFD scheme is used to simulate the graphs (A–E). (A) Mesh graph of S; (B) Mesh graph of E; (C) Mesh graph of I; (D) Mesh graph of Q; (E) Mesh graph of V.

FIGURE 2
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Figure 2. The implicit operator splitting NSFD scheme is used to simulate graphs (A–E). (A) Mesh graph of S; (B) Mesh graph of E; (C) Mesh graph of I; (D) Mesh graph of Q; (E) Mesh graph of V.

Figures 1, 2 validate the preservation of the positivity property in both of the proposed operator splitting NSFD schemes. Also, all the graphs in Figures 1, 2 show that both proposed NSFD schemes achieve convergence to the DFE point. Next, we examine the behavior of forward Euler and backward Euler splitting schemes at different values of h and τ.

In parts (a) and (b) of Figure 3, we take the same values of h and τ as in Figures 1, 2 for the graphs of forward Euler operator splitting scheme and backward Euler operator splitting scheme. The graphs clearly show the failure of the positivity property of both classic schemes. In parts (c) and (d) of Figure 3, both existing splitting schemes converge to the false DFE equilibrium point for susceptible individuals.

FIGURE 3
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Figure 3. (A) The forward Euler FD operator splitting method is used to simulate the graph of exposed persons for the DFE point at h = 0.5, λ1 = 0.3. (B) The backward Euler FD operator splitting method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.3. (C) The forward Euler FD operator splitting method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4. (D) The backward Euler FD operator splitting method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4.

In parts (a) and (b) of Figure 4, we take the same values of h and τ as given in parts (c) and (d) of Figure 3 for the explicit and implicit NSFD operator splitting schemes, respectively. The graphs clearly show that both of the proposed NSFD schemes not only preserve the positivity property but also achieve convergence to the true equilibrium point.

FIGURE 4
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Figure 4. (A) The explicit operator splitting NSFD method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.3. (B) The implicit operator splitting NSFD method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4.

7.2. Endemic Equilibrium Point

In this section, we present simulations of the SEIQV epidemic model at the EE point using all of the operator splitting FD schemes. In Figures 5, 6, we consider h = 0.5, λ1 = 0.3, λ2 = 0.06, λ3 = 0.006, λ4 = 0.06, and λ5 = 0.06.

FIGURE 5
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Figure 5. (A) The explicit operator splitting NSFD scheme is used to simulate graphs (A–E). (A) Mesh graph of S; (B) Mesh graph of E; (C) Mesh graph of I; (D) Mesh graph of Q; (E) Mesh graph of V.

FIGURE 6
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Figure 6. The implicit operator splitting NSFD scheme is used to simulate graphs (A–E). (A) Mesh graph of S; (B) Mesh graph of E; (C) Mesh graph of I; (D) Mesh graph of Q; (E) Mesh graph of V.

Figures 5, 6 depict the graphs of susceptible, exposed, infected, quarantined, and vaccinated individuals for the EE point using the explicit operator splitting NSFD scheme and implicit operator splitting NSFD scheme, respectively. All the graphs in Figures 5, 6 demonstrate that both of the proposed operator splitting NSFD schemes preserve the property of positivity. These graphs also show that both proposed schemes converge to the EE point.

Again, both the forward and backward Euler FD schemes fail to preserve the positivity property and converge to the false EE point, as shown in Figure 7.

FIGURE 7
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Figure 7. (A) The forward Euler FD operator splitting method is used to simulate the graph of exposed persons for the DFE point at h = 0.5, λ1 = 0.3. (B) The backward Euler FD operator splitting method is used to simulate the graph of exposed persons for the DFE point at h = 0.5, λ1 = 0.3. (C) The forward Euler FD operator splitting method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4. (D) The backward Euler FD operator splitting method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4.

Figure 8 shows that the proposed NSFD operator splitting methods are consistent with the continuous reaction-diffusion system as they not only preserve the positivity property but converge to the EE point.

FIGURE 8
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Figure 8. (A) The explicit operator splitting NSFD method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4. (B) The implicit operator splitting NSFD method is used to simulate the graph of susceptible persons for the DFE point at h = 0.5, λ1 = 0.4.

8. Conclusion

In this work, we consider the SEIQV reaction-diffusion epidemic model. The stability of the SEIQV model is guaranteed numerically by using criteria defined by Routh-Hurwitz. We also find the bifurcation value of the important vaccination parameter ω of SEIQV epidemic systems with diffusion and without diffusion. We design two novel and efficient operator splitting NSFD schemes for the SEIQV reaction-diffusion system. The NSFD schemes put forth, which are technically operator splitting schemes, possess the same behavior as is possessed by the SEIQV epidemic system. To conclude regarding the designed methods, we present two novel numerical schemes, one of which is explicit and the other of which is implicit in nature. The explicit scheme is more computationally efficient than the implicit scheme, but it has conditional stability while the implicit scheme is stable unconditionally. Both schemes employ structural splitting, due to which they deal adroitly with the nonlinearity of the reaction-diffusion system. These schemes avoid the false chaos that is a part of many existing methods. The positive solution of the SEIQV model is sustained by both schemes. Also, the nature of the stability of equilibria is preserved effectively by the proposed NSFD schemes. It is also shown that classical schemes, in parallel to our proposed schemes, produce chaos, leading to inconsistencies and instabilities numerically. The currently designed schemes are a valuable contribution for finding the solutions of nonlinear dynamical systems comprising differential equations. These NSFD schemes will become very efficient for the solution of one- and multi-dimensional reaction-diffusion population models, auto-catalytic chemical reaction models, and many more.

Author Contributions

NA, MR, and MAR designed the study. NA, MF, and MR developed the methodology. NA and MF collected the data. NA, DB, KN, and IK performed the analysis. NA, MF, DB, MA, and IK wrote the manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors are grateful to the referees for their suggestions and useful comments on this paper.

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Keywords: splitting methods, NSFD schemes, positivity, epidemic model, stability, bifurcation value

Citation: Ahmed N, Fatima M, Baleanu D, Nisar KS, Khan I, Rafiq M, Rehman MA and Ahmad MO (2020) Numerical Analysis of the Susceptible Exposed Infected Quarantined and Vaccinated (SEIQV) Reaction-Diffusion Epidemic Model. Front. Phys. 7:220. doi: 10.3389/fphy.2019.00220

Received: 06 October 2019; Accepted: 28 November 2019;
Published: 17 January 2020.

Edited by:

Devendra Kumar, University of Rajasthan, India

Reviewed by:

Yudhveer Singh, Amity University Jaipur, India
Vinod Gill, Government Post Graduate College, Hisar, India

Copyright © 2020 Ahmed, Fatima, Baleanu, Nisar, Khan, Rafiq, Rehman and Ahmad. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ilyas Khan, aWx5YXNraGFuJiN4MDAwNDA7dGR0dS5lZHUudm4=

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