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Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2021 Mar 4;23:103994. doi: 10.1016/j.rinp.2021.103994

Mathematical analysis and simulation of a stochastic COVID-19 Lévy jump model with isolation strategy

Jaouad Danane a, Karam Allali b, Zakia Hammouch c,d,e, Kottakkaran Sooppy Nisar f,
PMCID: PMC7929785  PMID: 33686366

Abstract

This paper investigates the dynamics of a COVID-19 stochastic model with isolation strategy. The white noise as well as the Lévy jump perturbations are incorporated in all compartments of the suggested model. First, the existence and uniqueness of a global positive solution are proven. Next, the stochastic dynamic properties of the stochastic solution around the deterministic model equilibria are investigated. Finally, the theoretical results are reinforced by some numerical simulations.

Keywords: COVID-19, Lévy jump, White noise, Isolation strategy, Basic reproduction number

Introduction

Infectious diseases modeling has captivated the interest of many research works during the last recent years [1], [6], [2], [3], [4], [5], [7]. The basic SIR model representing the dynamics behavior of the three main populations that represent the susceptible (S), the infected (I) and the recovered (R), was firstly proposed in 1927 by Kermack and Mc Kendricks [8]; the suggested model has played an important role in starting different research works in disease dynamics field. Understanding the interaction dynamics between the different infection components becomes then an important issue to prevent many serious infectious disease outbreaks. For instance, several mathematical models have been used to better understand the behavior of various viral infections, such as the hepatitis B virus (HBV) [6], [10], [9], [11], [12] human immunodeficiency virus (HIV) [1], [14], [2], [13], [15], [3], [4] or hepatitis C virus (HCV) [16], [19], [18], [17].

COVID-19 is a recent pandemic disease that was behind a great disaster worldwide. Since there is still no efficient vaccine against COVID-19, substantial number of researches are undertaken in order to understand the disease mechanism, reduce the disease spread and find some solutions to this serious infection. As it was established, COVID-19 is the recent form of coronavirus infection induced by the already known severe acute respiratory syndrome SARS-CoV-2 [20], [21], [22], [23]. This recently discovered disease can be transmitted from an infected to any close unprotected person; likewise the susceptible can become an infected individual when touching any contaminated area [24]. Hence, isolating infected persons from the other susceptible population becomes more and more an important mean to reduce and overcome COVID-19 propagation.

Recently, different models have been investigated to study COVID-19. For instance, the risk estimation, the infection evolution and the prediction of COVD-19 infection is studied [25], [26], [27], [28]; the authors concludes that for ensuring a quick ending of the epidemic, the interventions strategy and self-protection measures should always be maintained. The meteorological role and policy measures on COVD-19 spread were studied in [29], [30]; it was concluded that the policy strategy has reduced the infection and the meteorological role can be considered as an important factor in controlling COVID-19. The effect of quarantine on coronavirus was discussed in [31]; the results confirm the importance of reducing contact between the infected and other individuals.

Since the isolation strategy is an important tool to reduce the infection, adding another component representing the isolated individuals (Q) to the classical SIR model becomes primordial; and the new epidemiological model will be under SIQR abbreviation [32].

To investigate the dynamics of COVID-19 in this paper, we subdivide the total population into four different epidemiological classes in which their descriptions are defined later. The parameters used in the co-infection model are summarized in Table 1, Table 2 , and the schematic diagram of the compartmental COVID model is shown in Fig. 1 .

Table 1.

The sensitivity indices of R0.

Parameters Sensitivity index
λ 1
β 1
ζ -2.39
υ 0.921
κ 0.514
d 0.334

Table 2.

The used parameters for the numerical simulations.

Parameters Fig. 2 Fig. 3 references
λ 1785.205 1785.205 [43]
ζ 0.35 0.49
β 0.13 0.13 [43]
υ 2.7×10-4 0.03
κ 0.15 0.35 [43]
d 0.038 0.038 [43]
σ1 10-4 10-5
σ2 2×10-4 2×10-4
σ3 2×10-4 2×10-3
σ4 2×10-4 2×10-4
q1(u) -0.04 -0.04
q2(u) -0.006 -0.006
q3(u) -0.008 -0.008
q4(u) -0.009 0.009

Fig. 1.

Fig. 1

The transfer diagram for the SIQR model.

The SIQR deterministic system of equations may take the following form:

dSdt(t)=λ-ζS(t)-βS(t)I(t),dIdt(t)=βS(t)I(t)-(ζ+υ)I(t),dQdt(t)=υI(t)-(ζ+κ+d)Q(t),dRdt(t)=κQ(t)-ζR(t), (1)

where λ is the birth average of the susceptibles, their mortality rate is denoted by ζS. The susceptible become infected at a rate βSI, the death rate of infected population is denoted by ζI; the infected become isolated at rate υI. The death rate of the isolated individuals due to the infection is represented dQ and due to others means is ζQ. Finally, the isolated become recovered at rate κQ; the death rate of the recovered is denoted by ζR.

On the hand, stochastic quantification of several real life phenomena have been much helpful in understanding the random nature of their incidence or occurrence. This also helped in finding solutions to such problems arising from them either in form of minimization of their undesirability or maximizing their rewards. Besides, the infectious diseases are exposed to randomness and uncertainty in terms of normal infection progress. Therefore, the stochastic modeling are more appropriate comparing to the deterministic models; considering the fact that the stochastic systems do not take into account only the variable mean but also the standard deviation behavior surround it. Moreover, the deterministic systems generate similar results for initial fixed values, but the stochastic ones can give different predicted results. Several stochastic infectious models describe the effect of white noise on viral dynamics have been deployed [33], [7], [34]. Recently and in the same context, a stochastic SIQR model is studied in [35], the authors introduce the Brownian perturbation to the four components of the model and study the different conditions of extinction and persistence of the infection. Both of white and telegraph noises were taken into consideration to study SIQR model [36], sufficient different conditions to establish persistence in mean were studied.

In addition to the cited random noises, Lévy jumps present an important tool to model many real dynamical phenomena [37], [38]. Indeed, because of the unpredictable stochastic properties of the disease progression, infection dynamical model may know sudden significant perturbations in the disease process [39]. Then, it will be more reasonable to illustrate those sudden fluctuations through an introduction of the Lévy jump behavior into the infection model. For instance, Berrhazi et al. [40] studied, recently, a stochastic SIRS model under Lévy jumps fluctuations and considering bilinear function describing the infection. The uniqueness of global solution was established, also through suitable Lyapunov functions, it was demonstrated that the stochastic stability of steady states depends on some sufficient conditions for persistence or extinction of the studied infection. Motivated by the previous works, we will consider in this paper the following stochastic SIQR model driven by Lévy noise:

dS(t)=λ-ζS(t)-βS(t)I(t)dt+σ1S(t)dW1(t)+Uq1(u)S(t-)N~(dt,du),dI(t)=βS(t)I(t)-(ζ+υ)I(t)dt+σ2I(t)dW2(t)+Uq2(u)I(t-)N~(dt,du),dQ(t)=υI(t)-(ζ+κ+d)Q(t)dt+σ3Q(t)dW3(t)+Uq3(u)Q(t-)N~(dt,du),dR(t)=κQ(t)-ζR(t)dt+σ4R(t)dW4(t)+Uq4(u)R(t-)N~(dt,du), (2)

where Wi(t) is a standard Brownian motion defined on a complete probability space Ω,F,(Ft)t0,P with the filtration (Ft)t0 satisfying the usual conditions. We denote by S(t-),I(t-) , Q(t-) and R(t-) the left limits of S(t),I(t),Q(t) and R(t) respectively. N(dt,du) is a Poisson counting measure with the stationary compensator ν(du)dt,N~(dt,du)=N(dt,du)-ν(du)dt with ν(U)< and σi is the intensity of Wi(t). The jumps intensities are represented by qi(u) with i=1,,4.

The present work will be organized as follows. The next section is devoted to establish the existence and uniqueness of the global positive solution to the studied model (2). We calculate the basic reproduction number and the different problem equilibria in Section “The basic reproduction number and equilibria”. The stochastic behavior of the solution of the disease-free equilibrium is studied in Section “The stochastic property around the free-infection equilibrium”. The dynamics of the solution of the endemic equilibrium is studied in Section “The stochastic property around the endemic equilibrium”. The sensitivity analysis is presented in Section “Sensitivity analysis”. The final part of this paper is dedicated to some numerical results in order to support the theoretical findings.

The existence and uniqueness of global positive solution

The existence and uniqueness of the problem (2) global positive solution is guaranteed by the next following theorem.

Theorem 1

For any initial condition inR+4, the model(2)has a unique global solutionS(t),I(t),Q(t),R(t)R+4almost surely.

Proof

First, we know that the diffusion and the drift are locally Lipschitz functions, therefore for any initial condition S(0),I(0),Q(0),R(0)R+4, we have the existence of a unique local solution S(t),I(t),Q(t),R(t) for t[0,te), where te is the time of explosion.

In order to demonstrate that this solution is globally defined, we need to check that te= a.s. Firstly, we will demonstrate that S(t),I(t),Q(t),R(t) do not tend to infinity for a bounded time. Let m0>0, be sufficiently a large number, in such manner that S(0),I(0),Q(0),R(0) be within the interval [1m0,m0]. We define, for each integer mm0, the stopping time

tm=inf{t[0,te)/S(t)(1m,m)orI(t)(1m,m)orQ(t)(1m,m)orR(t)(1m,m)},

where tm is an increasing number when m. Let t=limmtm, where tte a.s. We need to show that t= which means that te= and S(t),I(t),Q(t),R(t)R+4 a.s. Assume the opposite case is verified, i.e. t< a.s. Therefore, there exist two constants 0<<1 and T>0 such that P(tT).

Therefore, there exists an integer m1m0 such that P(tmT)forallmm1.

Let’s now consider the following functional

VS(t),I(t),Q(t),R(t)=S-a-alogSa+,I-1-log,I+Q-1-logQ+R-1-logR,

with a is a positive constant.

Let mm0 and T>0 be arbitrary. For any 0ttmT=min(tm,T). From Itô’s formula, we will have

dVS,I,Q,R=LVdt+σ1(S-a)dW1+σ2(I-1)dW2+σ3(Q-1)dW3+σ4(R-1)dW4+Uq1(u)S-alog1+q1(u)N~(dt,du)+Uq2(u)I-log1+q2(u)N~(dt,du)+Uq3(u)Q-log1+q3(u)N~(dt,du)+Uq4(u)R-log1+q4(u)N~(dt,du), (3)

where

LV=1-aSλ-ζS(t)-βS(t)I(t)+aσ122+1-1IβS(t)I(t)-(ζ+υ)I(t)+σ222+1-1QυI(t)-(ζ+κ)Q(t)+σ322+1-1RκQ(t)-ζR+σ422+Uq1(u)-log1+q1(u)ν(du)+Uq2(u)-log1+q2(u)ν(du)+Uq3(u)-log1+q3(u)ν(du)+Uq4(u)-log1+q4(u)ν(du),

therefore, we will have

LVλ+ζ+aζ+aβ-ζI+ζ+υ+(ζ+κ)+aσ122+σ222+σ322+σ422+Uaq1(u)-alog1+q1(u)ν(du)+Uq2(u)-log1+q2(u)ν(du)+Uq3(u)-log1+q3(u)ν(du)+Uq4(u)-log1+q4(u)ν(du),

by choosing a=ζβ, we will get

LVλ+ζ+ζ2β+ζ+υ+(ζ+κ)+ζσ122β+σ222+σ322+4M=M,

where

M=maxUζβq1(u)-log1+q1(u)ν(du),Uq2(u)-log1+q2(u)ν(du),Uq3(u)-log1+q3(u)ν(du),Uq4(u)-log1+q4(u)ν(du).

Integrating both sides of the Eq. (3) between 0 and tmT, we get

0tmTdVS(t),I(t),Q(t),R(t)dt0tmTMdt+σ10tmT(S-ζβ)dW1(t)+σ20tmT(I-1)dW2(t)+σ30tmT(Q-1)dW3(t)+σ40tmT(R-1)dW4(t)+0tmTUq1(u)S-ζβlog1+q1(u)N~(dt,du)dt+0tmTUq2(u)I-log1+q2(u)N~(dt,du)dt+0tmTUq3(u)Q-log1+q3(u)N~(dt,du)dt+0tmTUq4(u)R-log1+q4(u)N~(dt,du)dt.

This leads to

0EVS(tmT),I(tmT),Q(tmT),R(tmT)VS(0),I(0),Q(0),R(0)+ME[tmT]VS(0),I(0),Q(0),R(0)+MT. (4)

Set Ωm=tmT for mm1. From (3), we obtain P(Ωm). Noting that for every ωΩm, there exists S(tm,ω) or I(tm,ω) or Q(tm,ω) or R(tm,ω) equals to either m or 1/m,

VS(tm,ω),I(tm,ω),Q(tm,ω),R(tm,ω) is not less than either

m-1-log(m)or1m-1+log(m).

This fact implies that,

VS(tm,ω),I(tm,ω),Q(tm,ω),R(tm,ω)m-1-log(m)1m-1+log(m).

It follows from (4) that

VS(0),I(0),Q(0),R(0)+MTEIΩm(ω)VS(tm,ω),I(tm,ω),Q(tm,ω),R(tm,ω)P(tmT)m-1-log(m)1m-1+log(m),

where IΩm denotes the indicator function of Ωm, letting m, we will have

limmP(tmT)=0.

Since T>0 is arbitrary, then

P(t<)=0.

So,

P(t=)=1.

Therefore, the model has a unique global solution S(t),I(t),Q(t),R(t) a.s. □

The basic reproduction number and equilibria

The model basic reproduction number (1) is given by R0=λβυζ(ζ+υ)(ζ+d+κ). Its biological meaning stands for the average number of secondary infected individuals generated by only one infected person at the start of the infection process. The problem (1) has a unique free-infection equilibrium Ef=λζ,0,0,0 and an endemic equilibrium E=S,I,Q,R given as follows

S=υ+ζβ,I=λβ-ζ(υ+ζ)β(υ+ζ),Q=ζR0β2λβλ-ζ(υ+ζ),R=ζκR0υβ2λβλ-ζ(υ+ζ).

Following the same reasoning as in [41], [32] concerning the equilibria stability of the deterministic SIQR model, we can establish that Ef is globally asymptotically stable when R01. Besides, when R0>1,Ef losses it stability and the other equilibrium E becomes stable.

The stochastic property around the free-infection equilibrium

Around the free-infection equilibrium Ef, we have the following stochastic property.

Theorem 2

IfR01and

l1=2ζ-2σ12-6Uq12(u)ν(du)0,
l2=2ζ-2σ22-3Uq12(u)ν(du)0,
l3=2ζ-2σ32-3Uq12(u)ν(du)0,
l4=λζ(16υ-(ζ+κ+d)4υκ0,

then,

limt+sup1tE0tS(η)-λζ2+I2(η)+Q2(η)+R(η)dηM1ρ1,

where

M1=σ12+6Uq12(u)ν(du)λζ2

and

ρ1=min{l1,l2,l3,l4}.

Proof

We set X(t)=S(t)-λζ,Y(t)=I(t),V(t)=Q(t) and R(t)=Z(t), then the model (2) becomes

dX(t)=-ζX(t)-βX(t)Y(t)-βλζY(t)dt+σ1X(t)+λζdW1(t)+Uq1(u)X(t-)+λζN~(dt,du),dY(t)=βX(t)Y(t)+βλζY(t)-(ζ+υ)Y(t)dt+σ2Y(t)dW2(t)+Uq2(u)Y(t-)N~(dt,du),dV(t)=υY(t)-(ζ+κ+d)V(t)dt+σ3V(t)dW3(t)+Uq3(u)V(t-)N~(dt,du),dZ(t)=κV(t)-ζZ(t)dt+σ4Z(t)dW4(t)+Uq4(u)Z(t-)N~(dt,du).

We consider the following functional

F(X,Y,V,Z)=X+Y+V2+c1Y+c2V+c3Z,

where c1,c2 and c3 are three constants that will be determined later.

By using Itô’s formula, we have

dF=LFdt+2X+Y+Vσ1X+λζdW1+σ2YdW2+σ3VdW3+c1σ2YdW2+c2σ3VdW3+c3σ4ZdW4+Uq1(u)X+λζ+q2(u)Y+q3(u)V2N~(dt,du)+2X+Y+VUq1(u)X+λζN~(dt,du)+c1Uq2(u)N~(dt,du)+c2Uq3(u)N~(dt,du)+c3Uq4(u)N~(dt,du), (5)

where

LF=2X+Y+V-ζX-ζY-(ζ+κ+d)V+σ12X+λζ2+c1βX+βλζ-(ζ+υ)Y+σ22Y2+c2υY-(ζ+κ+d)V+σ32V2+c3κV-ζZ+Uq1(u)X+λζ+q2(u)Y+q3(u)V2ν(du)=-2ζX2-2ζY2-2(ζ+κ+d)V2+(c1β-4ζ)XY-(4ζ+κ+d)(XV+YV)+c2υ-c1(ζ+υ-βλζ)+c3κ-c2(ζ+κ+d)V-c3ζZ+σ12X+λζ2+σ22Y2+σ32V2+Uq1(u)X+λζ+q2(u)Y+q3(u)V2ν(du).

Now, we choose c1=4ζβ and c2=λ(16υ-(ζ+κ+d)4υ(ζ+κ+d) and c3=λ(16υ-(ζ+κ+d)4υκ, we get c1β-4ζ=0, c2υ-c1(ζ+υ-βλζ)=4ζ(ζ+υ)β(R0-1) and c3κ-c2(ζ+κ+d)=0, since R01 , 2aba2+b2 and (a+b+c)23a2+3b2+3c2. We will obtain

LF-2ζ-2σ12-6Uq12(u)ν(du)X2-2ζ-2σ22-3Uq22(u)ν(du)Y2-2ζ-2σ32-3Uq32(u)ν(du)V2-λζ(16υ-(ζ+κ+d)4υκZ+σ12+6Uq12(u)ν(du)λζ2.

Therefore

LF-l1X2-l2Y2-l3V2-l4Z+M1,

where

M1=σ12+6Uq12(u)ν(du)λζ2.

Integrating both sides of the Eq. (5) between 0 and t and taking into account expectation, we have

0EFX(t),Y(t),V(t),Z(t)E0t-l1S(τ)-λζ2-l2I(τ)2-l3Q(τ)2-l4R(τ)dτ+FX(0),Y(0),V(0),Z(0)+M1t,

let now ρ1=min{l1,l2,l3,l4}, then

E0tS(τ)-λζ2+I(τ)2+Q(τ)2+R(τ)dτFX(0),Y(0),V(0),Z(0)ρ1+M1ρ1t,

we conclude that

limt+sup1tE0tS(τ)-λζ2+I(τ)2+Q(τ)2+R(τ)dτM1ρ1.

 □

Remark 1

From our last result, one can conclude that when R01, the solution fluctuates around the free steady state Ef.

The stochastic property around the endemic equilibrium

The infection steady state E has the following stochastic property.

Theorem 3

IfR0>1,

l5=(8ζ-d)(8ζ+2d)16ζ+2d-σ12-4Uq12(u)ν(du)0,
l6=(8ζ-d)(8ζ+2d)16ζ+2d-σ22-4Uq22(u)ν(du)0,
l7=d2-σ12-4Uq12(u)ν(du)0,
l8=(8ζ-d)(8ζ+2d)16ζ+2d-σ42-4Uq42(u)ν(du)0

and

8ζ-d0,

then,

limt+sup1tE0tS(τ)-S2+(I(τ)-I2+(Q(τ)-Q2+(R(τ)-R2dτM2ρ2,

where

M2=σ12S2+σ22I2+σ32Q2+σ42R2+3Uq12(u)S2+q22(u)I2+q32(u)Q2+q42(u)R2ν(du)

and

ρ2=min{l5,l6,l7,l8}.

Proof

First, let the following function:

GS,I,Q,R=12S-S+I-I+Q-Q+R-R2,

By using Itô’s formula, we will have

dG=LGdt+S-S+I-I+Q-Q+R-Rσ1SdW1+σ2IdW2+σ3QdW3+σ4RdW4+U12q1(u)SS+q2(u)I+q3(u)Q+q4(u)R2+S-S+I-I+Q-Q+R-Rq1(u)S+q2(u)I+q3(u)Q+q4(u)RN~(dt,du), (6)

with

LG=S-S+I-I+Q-Q+R-Rλ-ζS+I+Q+R-dQ+12σ12S2+12σ22I2+12σ32Q2+12σ42R2+U12q1(u)S+q2(u)I+q3(u)Q+q4(u)R2ν(du).

Since

λ=ζS+I+Q+R+dQ,

therefore,

LG=S-S+I-I+Q-Q+R-R-ζS-S+I-I+Q-Q+R-R-dQ-Q+12σ12S2+12σ22I2+12σ32Q2+12σ42R2+U12q1(u)S+q2(u)I+q3(u)Q+q4(u)R2ν(du),

then,

LG=-ζS-S+I-I+Q-Q+R-R2-dQ-Q2+dQ-QS-S+dQ-QI-I+dQ-QR-R+12σ12S2+12σ22I2+12σ32Q2+12σ42R2+U12q1(u)S+q2(u)I+q3(u)Q+q4(u)R2ν(du).

Using the inequalities 2aba2+b2,(a+b+c+d)24a2+4b2+4c2+4d2 and 2aba2+b2 with =8ζ+dd, we will obtain

LG-(8ζ-d)(8ζ+2d)16ζ+2d-σ12-4Uq12(u)ν(du)S-S2-(8ζ-d)(8ζ+2d)16ζ+2d-σ22-4Uq22(u)ν(du)I-I*2-d2-σ42-4Uq32(u)ν(du)Q-Q2-(8ζ-d)(8ζ+2d)16ζ+2d-σ42-4Uq42(u)ν(du)R-R2+σ12S2+σ22I2+σ32Q2+σ42R2+3Uq12(u)S2+q22(u)I2+q32(u)Q2+q42(u)R2ν(du).

Since 8ζ-d>0, therefore (8ζ-d)(8ζ+2d)>0, which implies

LG-l5S-S2-l6I-I*2-l7Q-Q2-l8R-R2+M2,

where

M2=σ12S2+σ22I2+σ32Q2+σ42R2+3Uq12(u)S2+q22(u)I2+q32(u)Q2+q42(u)R2ν(du).

Integrating both sides of the Eq. (6) between 0 and t and taking expectation, we will get

0EGS(t),I(t),Q(t),R(t)E0t-l5S(τ)-S2-l6I(τ)-I2-l7Q(τ)-Q2-l8R(τ)-R2dτ+GS(0),I(0),Q(0),R(0)+M2t,

let ρ2=min{l5,l6,l7,l8}, then

E0tS(τ)-S2+I(τ)-I2+Q(τ)-Q2+R(τ)-R2dτM2ρ2t+GS(0),I(0),Q(0),R(0)ρ2,

therefore,

limt+sup1tE0tS(τ)-S2+I(τ)-I2+Q(τ)-Q2+R(τ)-R2dτM2ρ2.

 □

Remark 2

From our last finding, one can conclude that when R0>1 the solution will fluctuate around the steady state E.

Sensitivity analysis

The sensitivity analysis is used principally to determine which model parameter can change significantly infection dynamics. This allows to detect the parameters that have a high impact on the basic reproduction number R0. To perform such analysis we will need the following normalized sensitivity index of R0 with respect to any given parameter θ:

φθ=R0θθR0,

therefore, we obtain

φλ=1,
φβ=1,
φυ=ζζ+υ,
φd=-dζ+d+κ,
φκ=-κζ+d+κ,

and

φζ=-(ζ+υ)(ζ+d+κ)+ζ(ζ+d+κ)+ζ(ζ+υ)(ζ+υ)(ζ+d+κ).

From Table 1, we observe that the parameters λ,β and υ are positive sensitivity indices and the other remaining parameters ζ,κ and d are negative sensitivity indices. We remark that the parameters λ,β and υ have large magnitude, in their absolute values, which means that they are the most sensitive parameters of our model equations. This indicates that any increase of the parameters λ,β and υ will cause an increase of the basic reproduction number, which have as consequence of an increase of the infection. Oppositely, an increase of the parameters ζ,d and κ will decrease R0 which leads to a reduce of the infection.

Fig. 2 illustrates the contour plot of R0, we observe that for β=1 and υ=0 the value of R0 reaches the maximum value 5.11×103. By decreasing β and υ from 1 to 0, we remark that the value of R0 decreases also and tends toward 8.75×10-3 (corresponding to β=0;υ=0). This result reflects the impact of these two key parameters in controlling the infection.

Fig. 2.

Fig. 2

Contour plot of R0 depending on β and υ.

From the contour plot of R0 given in Fig. 3 , we observe that for β=1 and κ=0 the value of R0 reaches the maximum value 1.03×103. When the parameter κ is increased from 0 to 1 and the parameter β is decreased also from 1 to 0, we observe that f R0 gradually decreases and tends to the limit value 1.93×10-1 (corresponding to β=0;κ=1). Hence, the parameters x and y play an essential role in controlling the infection spread.

Fig. 3.

Fig. 3

Contour plot of R0 depending on β and κ.

The last contour plot of R0 in illustrated in Fig. 4 . We observe that when β=1 and d=0 the value of R0 reaches its maximal value of 5.74×102. By decreasing β from 1 to 0 and increasing d from 0 to 1, we observe that the value of R0 gradually decreases and tends towards 1.57×10-1 (corresponding to β=0;d=1). This confirm the impact of the β and d in controlling the progression of the infection.

Fig. 4.

Fig. 4

Contour plot of R0 depending on β and d.

Numerical simulations and discussion

This section will illustrate our mathematical results by different numerical simulations. To this end, we will apply the algorithm given in [42] to solve the system (2). The parameters of our model representing the infection and the recovery rates are estimated from COVID-19 Morocco case [43]. The different used values of our parameters in our numerical simulations are given in Table 1.

Figure 5 shows the dynamics of COVID-19 infection during the period of observation for the case of the disease extinction. From this figure, we clearly observe that the curves representing to the deterministic model converge towards the endemic-free equilibrium Ef=5.1×102,0,0,0. The curves that represent the stochastic model fluctuate around the curves representing the deterministic ones. Moreover, it will be worthy to notice that in this case, the susceptible increase to reach their maximum and the other SIQR components that are the infected, the quarantined (the isolated) and the recovered vanish which means that the disease dies out. Within the used parameters in this figure (see Table 1), we have R0=0.95<1 which indicates the die out of the infection. This is consistent with our theoretical findings concerning the extinction of SIQR infection.

Fig. 5.

Fig. 5

The evolution of the infection when R0=0.95.

The evolution of the infection for both the deterministic model and the stochastic with Lévy jumps model is illustrated in Fig. 6 in the case of the disease persistence. Regarding the depicts of this figure, we can see that the plots corresponding to the deterministic model converge towards the endemic equilibrium E=4,3.42×103,117.17,83.69. The fluctuation around the endemic equilibrium E is clearly remarked for the stochastic numerical results. We note that in this epidemic situation, all the four SIQR compartments, i.e. the susceptible, the infected, the quarantined (the isolated) and the recovered remain at constant level which means that the disease persists. Within the used parameters in this figure (see Table 1), we have R0=31.12>1 which indicates the persistence of the infection. This is consistent with our theoretical findings concerning the infection persistence.

Fig. 6.

Fig. 6

The evolution of the infection when R0=31.12.

Conclusion

In this present work, a stochastic coronavirus model with Lévy noise is presented and analyzed. We have given a four compartments SIQR model representing the interaction between the susceptible, the infected, the quarantined (the isolated) and the recovered. A white noise as well as a Lévy jump perturbations are incorporated in all model compartments. We have proved the existence and the uniqueness of the global positive solution for the stochastic COVID-19 epidemic model which ensures the well-posedness of our mathematical model. By using some appropriate functionals, we have shown that the solution fluctuates around the steady states under sufficient conditions. Different numerical results support our theoretical findings. Indeed, the extinction of the disease is observed for the basic reproduction number less than unity. However, the persistence of the disease is observed for the basic reproduction number greater than one. Moreover, the fluctuation of the stochastic solution around the disease-free equilibrium is observed for the extinction case and the fluctuation of the stochastic solution around the endemic equilibrium is observed for the persistence case.

Funding

None.

CRediT authorship contribution statement

Jaouad Danane: Conceptualization, Writing - original draft, Software. Karam Allali: Conceptualization, Writing - original draft, Software. Zakia Hammouch: Writing - original draft, Software, Formal analysis, Visualization, Methodology. Kottakkaran Sooppy Nisar: Writing - original draft, Formal analysis, Software, Writing - review & editing.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgement

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