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Threshold behaviour of a stochastic SIRS Lˊevy jump model with saturated incidence and vaccination


  • A stochastic SIRS system with Lˊevy process is formulated in this paper, and the model incorporates the saturated incidence and vaccination strategies. Due to the introduction of Lˊevy jump, the jump stochastic integral process is a discontinuous martingale. Then the Kunita's inequality is used to estimate the asymptotic pathwise of the solution for the proposed model, instead of Burkholder-Davis-Gundy inequality which is suitable for continuous martingales. The basic reproduction number Rs0 of the system is also derived, and the sufficient conditions are provided for the persistence and extinction of SIRS disease. In addition, the numerical simulations are carried out to illustrate the theoretical results. Theoretical and numerical results both show that Lˊevy process can suppress the outbreak of the disease.

    Citation: Yu Zhu, Liang Wang, Zhipeng Qiu. Threshold behaviour of a stochastic SIRS Lˊevy jump model with saturated incidence and vaccination[J]. Mathematical Biosciences and Engineering, 2023, 20(1): 1402-1419. doi: 10.3934/mbe.2023063

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  • A stochastic SIRS system with Lˊevy process is formulated in this paper, and the model incorporates the saturated incidence and vaccination strategies. Due to the introduction of Lˊevy jump, the jump stochastic integral process is a discontinuous martingale. Then the Kunita's inequality is used to estimate the asymptotic pathwise of the solution for the proposed model, instead of Burkholder-Davis-Gundy inequality which is suitable for continuous martingales. The basic reproduction number Rs0 of the system is also derived, and the sufficient conditions are provided for the persistence and extinction of SIRS disease. In addition, the numerical simulations are carried out to illustrate the theoretical results. Theoretical and numerical results both show that Lˊevy process can suppress the outbreak of the disease.



    The method of mathematical modelling has been an important way to study the spreading and controlling of infectious disease. Since the pioneer work of Kermack and McKendrick [1], many deterministic mathematical models have been proposed to help us understand the spreading and controlling of infectious disease [2,3,4,5]. In [6], Lahrouz et al. put forward and analyzed a deterministic SIRS model with general incidence and vaccination. The authors derived the basic reproduction number and provided sufficient conditions for the persistence and extinction of disease. However, the model does not consider the environmental fluctuations. Many researchers have demonstrated that environmental fluctuation has largely affected the spreading of infectious disease [7,8]. For human disease, due to the nondeterminacy of person-to-person contacts, the growth and spreading of infectious disease are inherently random.

    There are several ways to model the influence of environmental fluctuations by stochastic differential equations [9,10]. One of the most important way is to consider system perturbation which arises from the approach in [11]. On the basis of the work of Lahrouz et al. [6], the SIRS model incorporated by system perturbation can be described by

    {dS(t)=((1ν)ΛμSβS(t)I(t)1+aI(t)+δR(t))dt+S(t)dZ1(t),dI(t)=(βS(t)I(t)1+aI(t)(μ+c+ξ)I(t))dt+I(t)dZ2(t),dR(t)=(νΛ(μ+δ)R(t)+ξI(t))dt+R(t)dZ3(t), (1.1)

    where the numbers of the susceptible, infectious and recovered individuals at time t are represented by S(t), I(t) and R(t), respectively. S(t), I(t) and R(t) are the left limits of S(t), I(t) and R(t), respectively. Z(t)=(Z1(t), Z2(t), Z2(t)) is a 3-dimensional stochastic process which models the random perturbation of the system. The parameters are all assumed to be positive. The biological meanings of the parameters are summarised in the following Table 1.

    Table 1.  The biological meanings of each parameter in system (1).
    Notation Biological meanings
    ν The proportion of population that is vaccinated
    Λ The population influx into the susceptible component
    μ The death rates of S, I, and R
    β The transmission coefficient between S and I
    δ The rate of the recovered individuals losing immunity
    c The death rate due to the disease
    ξ The recovery rate of I
    a The parameter measuring the inhibitory or psychological effect

     | Show Table
    DownLoad: CSV

    When Zi(t)=0, system (1.1) is reduced into a deterministic model irrespective of the effects of environmental fluctuations. In fact, the spreading of disease is inevitably disturbed by environmental fluctuations. Usually, white noise [12,13] is used to model the impact of environmental noise. However, when there exist large occasionally environmental shocks, such as earthquakes and floods, a stochastic model only with white noise cannot explain these discontinuous perturbations. Since Bao et al. [14] firstly proposed that Lˊevy process should be suitable to describe large occasionally fluctuations, some researchers use non-Gaussian Lˊevy jump noise to model these discontinuous phenomena [15,16]. For the sake of modelling the influence of environmental fluctuations, the form of Zi(t) is represented by

    Zi(t)=σiBi(t)+t0Yηi(z)˜N(ds,dz),i=1,2,3, (1.2)

    and Zi(t) is a Lˊevy process and has the following Lˊevy-Khintchine representation

    E[eiu1Z1(t)+iu2Z2(t)+iu3Z3(t)]=exp(t2(u,Au)+tR0(ei(u,η(z))i(u,η(z))1)v(dz)),

    where u=(u1,u2,u3)R3 and A is a 3×3 diagonal matrix and its diagonal elements are σi.

    In (1.2), defined on a complete probability space (Ω,F,P), Bi(t) (i=1,2,3) are standard Brownian motions are independent with Bi(0)=0. The intensities of the white noise is denoted by σi (i=1,2,3). ˜N(dt,dz):=N(dt,dz)v(dz)dt represents the compensated Poisson random measure, where N(dt,dz) is the Poisson random measure and its characteristic measure is v(dz) which is finite Lˊevy measure. The Lˊevy measure satisfies Ymin(|ηi(z)|2,1)v(dz)<(i=1,2,3), see Theorem 1.2.14 in [16]. The effects of jumps is represented by ηi:YR (i=1,2,3) which is supposed to be continuously differentiable and bounded.

    On the basis of the above discussion, the model (1.1) incorporated by linear system perturbation can be described by

    {dS(t)=((1ν)ΛμSβS(t)I(t)1+aI(t)+δR(t))dt+σ1S(t)dB1(t)+Yη1(z)S(t)˜N(dt,dz),dI(t)=(βS(t)I(t)1+aI(t)(μ+c+ξ)I(t))dt+σ2I(t)dB2(t)+Yη2(z)I(t)˜N(dt,dz),dR(t)=(νΛ(μ+δ)R(t)+ξI(t))dt+σ3R(t)dB3(t)+Yη3(z)R(t)˜N(dt,dz). (1.3)

    The spreading and extinction of infectious disease are two important and interesting topics in the control of infectious disease owing to their theoretical and practical meanings. The aim of the paper is to study the extinction and persistence of stochastic model (1.3). In order to investigate the extinction and persistence of stochastic model (1.3), it is required to estimate the solution of stochastic system (1.3). Usually, for continuous martingales, Zhou and Zhang [17] have used Burkholder-Davis-Gundy (BDG) inequality to prove the asymptotic pathwise estimation (see Lemmas 2.1–2.2 in [17]) of the solution. However, in this paper, due to the introduction of Lˊevy jump, the jump stochastic integral process is a discontinuous martingale. Therefore, the Kunita's inequality which is suitable for discontinuous martingales is used to estimate the asymptotic pathwise of the solution for the proposed model, instead of BDG inequality.

    This paper is organized as follow: In Section 2, the asymptotic pathwise of the solution is estimated for stochastic model (1.3). In Section 3, sufficient conditions are provided for persistence and extinction of stochastic model (1.3). In Section 4, the paper ends with some discussions and numerical simulations.

    For the jump diffusion coefficients of stochastic model (1.3), we suppose that

    (H1) For each n>0, there exists a constant Ln>0 such that Y|Hi(x,z)Hi(y,z)|2v(dz)Ln|xy|2 (i=1,2,3), where H1(x,z)=η1(z)S(t),H2(x,z)=η2(z)I(t),H3(x,z)=η3(z)R(t) with |x||y|n;

    (H2) Y|ηi(z)ln(1+ηi(z))|v(dz)< for ηi(z)>1 (i=1,2,3).

    Theorem 2.1. Assume (H1) and (H2) hold. Then the stochastic system (1.3) has a unique global solution (S(t),I(t),R(t))R3+ for all t0 and any given initial value (S(0),I(0),R(0))R3+ a.s..

    Proof. According to the assumption (H1), the coefficients of the model (1.3) satisfy local Lipschitz conditions. By Theorem 2.1 of [14], for any t[0,τe), there is a unique local solution (S(t),I(t),R(t))R3+ and τe is the explosion time. To illustrate the solution is global, it is necessary to show that τe=+ a.s.. Define the stopping time as

    τm=inf{t[0,τe):min{S(t),I(t),R(t)}1mormax{S(t),I(t),R(t)}m}.

    Set τ=limmτmτe a.s.. It is sufficient to prove τ=+ a.s.. If it does not hold, then there exist constants T>0 and ϵ(0,1) such that

    P(τT)ϵ.

    Consequently, for all mm1, there is an integer m1 such that P(τmT)ϵ. Define

    V(S(t),I(t),R(t))=(SbblnSb)+(I1lnI)+(R1lnR),

    where 0<b<μ+cβ. By Itô's formula with Lˊevy jump process, we have

    dV(S(t),I(t),R(t))=LVdt+σ1(S(t)b)dB1(t)+σ2(I(t)1)dB2(t)+σ3(R(t)1)dB3(t)+Y[η1(z)S(t)bln(1+η1(z))+η2(z)I(t)ln(1+η2(z))+η3(z)R(t)ln(1+η3(z))]˜N(dt,dz),

    where LV is the generating operator of stochastic system (1.3):

    LV=(1bS)[(1ν)ΛμSβSI1+aI+δR]+(11I)[(μ+c+ξ)I+βSI1+aI]+(11R)[νΛ(μ+δ)R+ξI]+b2σ21+12σ22+12σ23+Y[η1(z)bln(1+η1(z))+η2(z)ln(1+η2(z))+η3(z)ln(1+η3(z))]v(dz)=Λ+μb+2μ+c+ξ+δμSb(1ν)ΛSbδRSβS1+aIνΛRξIR(μ+cbβ1+aI)I+b2σ21+12σ22+12σ23+Y[η1(z)bln(1+η1(z))+η2(z)ln(1+η2(z))+η3(z)ln(1+η3(z))]v(dz).

    Applying the inequality ηi(z)ln(1+ηi(z))0 for ηi(z)>1 and assumption (H2), we obtain

    LVΛ+μb+2μ+c+ξ+δ+b2σ21+12σ22+12σ23+Y[η1(z)bln(1+η1(z))+η2(z)ln(1+η2(z))+η3(z)ln(1+η3(z))]v(dz):=K,

    where K is a positive constant.

    The remaining steps are similar to [8], so they are omitted.

    Firstly, we provide some preliminary results for the asymptotic pathwise estimation of the solution of stochastic system (1.3).

    For continuous martingales, Zhou and Zhang [17] used BDG inequality to prove asymptotic pathwise estimation of the solution. However, in this paper, for discontinuous martingales, Kunita's inequality is needed to prove asymptotic pathwise estimation of the solution and it is different from the BDG inequality for continuous martingales used by Zhou and Zhang [17].

    Let us first state the Kunita inequality (Theorem 4.4.23 of [16]). Consider the stochastic integral for jump process

    Y(t)=t0YH(s,z)(N(ds,dz)v(dz)ds),tR+ (3.1)

    of the predictable integrand (H(s,z))(s,z)R+×Y.

    Lemma 3.1. Assume that Y(t) is a semi-martingale represented by (3.1) [16]. Then there exists a constant Cp>0 such that for any p2,

    E[sup0<st|Y(s)|p]Cp{E[(t0Y|H(s,z)|2dsv(dz))p/2]+E[t0Y|H(s,z)|pdsv(dz)]}

    For convenience, denote

    ab=max{a,b};ab=min{a,b};σ2=σ21σ22σ23;λ=Y[(1+η1(z)η2(z)η3(z))p1]v(dz).

    Now, let us state the results on the asymptotic pathwise estimation.

    Theorem 3.1. Suppose (H1)(H2) hold. If μp12σ21pλ>0 for some p>1, then

    limtS(t)+I(t)+R(t)t=0a.s..

    Moreover,

    limtS(t)t=0,limtI(t)t=0,limtR(t)t=0,a.s..

    Proof. The proof is enlightened by [18]. Let X(t)=S(t)+I(t)+R(t). Define

    V(X)=(1+X)p,

    where p>0 is a constant to be determined later. It follows that

    dV(X(t))=LVdt+p(1+X(t))p1[σ1S(t)dB1(t)+σ2I(t)dB2(t)+σ3R(t)dB3(t)]+Y(1+X(t)+η1(z)S(t)+η2(z)I(t)+η3(z)R(t))p(1+X(t))p˜N(dt,dz), (3.2)

    where

    LV(X)p(1+X)p1[ΛμS(μ+c)IμR]+p(p1)2(1+X)p2(σ21S2+σ22I2+σ23R2)+Y(1+X(t))p[(1+η1(z)η2(z)η3(z))p1]v(dz)p(1+X)p2{[μp12σ21pλ]X2+(Λμ+2pλ)X+Λ+λp}.

    Set ρ=μp12σ21pλ. It follows from ρ=μp12σ21pλ>0 that

    LV(X)p(1+X)p2{ρX2+(Λ+2pλμ)X+Λ+λp}. (3.3)

    For any κR, direct calculation yields that

    deκtV(X(t))=L[eκtV(X(t))]dt+eκtp(1+X(t))p1[σ1S(t)dB1(t)+σ2I(t)dB2(t)+σ3R(t)dB3(t)]+eκtY{(1+X(t)+η1(z)S(t)+η2(z)I(t)+η3(z)R(t))p(1+X(t))p}˜N(dt,dz). (3.4)

    Integrating from 0 to t, we have

    eκt(1+X(t))p=(1+X(0))p+t0[κeκs(1+X(s))p+eκsLV(X(s))]ds+t0eκsp(1+X(s))p1[σ1S(s)dB1(s)+σ2I(s)dB2(s)+σ3R(s)dB3(s)]+t0eκsY{(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p}˜N(ds,dz). (3.5)

    Taking expectations of (3.5) leads to

    eκtE[(1+X(t))p]=(1+X(0))p+E{t0[κeκs(1+X(s))p+eκsLV(X(s))]ds}. (3.6)

    According to the inequality (3.3), for any κ<ρp, we have

    κeκt(1+X(t))p+eκtLV(X(t))κeκt(1+X(t))p+peκt(1+X(t))p2[ρX2(t)+(Λ+2pλμ)X(t)+Λ+λp]=peκt(1+X(t))p2[(ρκp)X2(t)+(Λ+2pλμ+2κp)X(t)+Λ+λ+κp]peκtH, (3.7)

    where

    0<H:=1+supXR+(1+X)p2[(ρκp)X2+(Λ+2pλμ+2κp)X+Λ+λ+κp]<.

    Therefore, for any κ(0,ρp), according to (3.6) and (3.7), we obtain

    E[eκt(1+X(t))p](1+X(0))p+pHt0eκsds=(1+X(0))p+pHκeκt.

    Consequently,

    lim suptE[(1+X(t))p]pHκ,

    which indicates that we have M>0 such that

    E[(1+X(t))p]M,t0. (3.8)

    For k=1,2, and sufficiently small θ>0, by (3.2) and (3.3) that

    (1+X(t))p(1+X(kθ))pptkθ(1+X(s))p2[ρX2(s)+(Λ+2pλμ)X(s)+Λ+λp]ds+ptkθ(1+X(s))p1(σ1S(s)dB1(s)+σ2I(s)dB2(s)+σ3R(s)dB3(s))+tkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]˜N(ds,dz),tkθ.

    Direct calculation yields that

    supkθt(k+1)θ(1+X(t))p(1+X(kθ))p+psupkθt(k+1)θ|tkθ(1+X(s))p2[ρX2(s)+(Λ+2pλμ)X(s)+Λ+λp]ds|+psupkθt(k+1)θtkθ(1+X(s))p1(σ1S(s)dB1(s)+σ2I(s)dB2(s)+σ3R(s)dB3(s))+supkθt(k+1)θtkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]˜N(ds,dz).

    Taking expectations of the above inequality, it follows that

    E[supkθt(k+1)θ(1+X(t))p]E[(1+X(kθ))p]+I1+I2+I3M+I1+I2+I3,

    where

    I1=pE{supkθt(k+1)θ|tkθ(1+X)p2[ρX2+(Λ+2pλμ)X+Λ+λp]ds|};I2=pE{supkθt(k+1)θtkθ(1+X(s))p1(σ1S(s)dB1(s)+σ2I(s)dB2(s)+σ3R(s)dB3(s))};I3=E{supkθt(k+1)θtkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]˜N(ds,dz)}.

    Now let us estimate I1, I2 and I3. It is easy to see that there exists c11>0 and c12>0 such that

    ρ(1+X)p2X20;(Λ+2pλμ)(1+X)p2Xc11(1+X)p;(Λ+λp)(1+X)p2c12(1+X)p,

    then we have

    I1c1E{supkθt(k+1)θ|tkθ(1+X)pds|}c1E{(k+1)θkθ(1+X)pds}c1θE{supkθt(k+1)θ(1+X)p},

    where c1=p(c11+c12) is a positive constant. By using BDG inequality, it follows that

    I232pE{((k+1)θkθ(1+X)2(p1)(σ21S2+σ22I2+σ23R2)ds)12}c2θ12pσE{(supkθt(k+1)θ(1+X)2p)12}=c2θ12pσE{supkθt(k+1)θ(1+X)p},

    where c2 is positive constant. Since ˜N(dt,dz):=N(dt,dz)v(dz)dt, then,

    I3E{(k+1)θkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]N(ds,dz)}+E{(k+1)θkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]dsv(dz)}=2E{(k+1)θkθY[(1+X(s)+η1(z)S(s)+η2(z)I(s)+η3(z)R(s))p(1+X(s))p]dsv(dz)}2θE[supkθt(k+1)θ(1+X)p]Y(1+η1(z)η2(z)η3(z))p1v(dz).

    Therefore, it follows that

    E[supkθt(k+1)θ(1+X(t))p]E[(1+X(kθ))p]+{c1θ+c2θ12pσ+2θY(1+η1(z)η2(z)η3(z))p1v(dz)}E[supkθt(k+1)δ(1+X(t))p]. (3.9)

    Moreover, it is easy to see that we can choose θ>0 small enough such that

    c1θ+c2θ12pσ+2θY(1+η1(z)η2(z)η3(z))p1v(dz)<12.

    It follows from (3.8) and (3.9) that

    E[supkθt(k+1)θ(1+X(t))p]2E[(1+X(kθ))p]2M. (3.10)

    Set arbitrary ϵ>0. For all k1, applying Chebyshev's inequality yields

    P{supkθt(k+1)θ(1+X(t))p>(kθ)1+ϵ}E[supkθt(k+1)θ(1+X(t))p](kθ)1+ϵ2M(kθ)1+ϵ

    By Borel-Cantelli Lemma ([19]),

    supkθt(k+1)θ(1+X(t))p(kθ)1+ϵ (3.11)

    holds for all but finitely many k. Then, there exists k0(ω) such that whenever kk0, then

    ln(1+X(t))plnt(1+ϵX)lnkθln(kθ)=1+ϵ,ϵ>0,kθt(k+1)θ.

    Therefore, we have

    lim suptln(1+X(t))plnt1+ϵ,a.s..

    Letting ϵ0 yields

    lim suptln(1+X(t))plnt1,a.s..

    For p>1,

    lim suptlnX(t)lntlim suptln(1+X(t))lnt1p,a.s.,

    i.e., for any b(0,11p), we can find a finite random time T(ω) such that

    lnX(t)(1p+b)lnt,tT(ω).

    It implies

    lim suptX(t)tlim suptt1p+bt=0.

    Thus, we get

    limtX(t)t=limtS(t)+I(t)+R(t)t=0. (3.12)

    The positivity of the solution and the equality (3.12) imply

    limtS(t)t=0,limtI(t)t=0,limtR(t)t=0,a.s..

    In the following, Kunita's inequality is used to estimate the asymptotic pathwise of the jump stochastic integral process instead of BDG inequality.

    Theorem 3.2. Assume (H1)(H2) hold. If there exists some p>2 such that μp12σ21pλ>0, then

    limtt0Yη1(z)S(s)˜N(ds,dz)t=0,limtt0Yη2(z)I(s)˜N(ds,dz)t=0,limtt0Yη3(z)R(s)˜N(ds,dz)t=0,a.s..

    Proof. Denote

    X1(t)=t0Yη1(z)S(s)˜N(ds,dz),X2(t)=t0Yη2(z)I(s)˜N(ds,dz),X3(t)=t0Yη3(z)R(s)˜N(ds,dz).

    By Kunita's inequality, there exists Cp>0 for any p2 such that

    E[sup0st|X1(s)|p]CpE[(t0Y|η1(z)S(s)|2v(dz)ds)p2]+CpE[t0Y|η1(z)S(s)|pv(dz)ds]=Cp(Yη21(z)v(dz))p2E[(t0|S(s)|2ds)p2]+Cp(Yηp1(z)v(dz))E[t0|S(s)|pds]Cptp2(Yη21(z)v(dz))p2E[sup0st|S(s)|p]+CptMYηp1(z)v(dz),

    where the inequality (3.8) has been used in the last inequality. By the above inequality and (3.10), then

    E[supkθt(k+1)θ|X1(t)|p]Cp2M((k+1)θ)p2(Yη21(z)v(dz))p2+CpM(k+1)θYηp1(z)v(dz).

    Let ϵ>0 be arbitrary. Then, by Doob's martingale inequality,

    P{ω:supkθt(k+1)θ|X1(t)|p>(kθ)1+ϵ+p2}E[supkθt(k+1)θ|X1(t)|p](kθ)1+ϵ+p22MCp((k+1)θ)p2(kθ)1+ϵ+p2(Yη21(z)v(dz))p2+MCp(k+1)θ(kθ)1+ϵ+p2Yηp1(u)v(dz).

    By Borel-Cantelli Lemma ([19]),

    supkθt(k+1)θ|X1(t)|p(kθ)1+ϵ+p2a.s.

    holds for all but finitely many k. Therefore, there exists a positive k0(ω) such that for all k>k0, we have

    ln|X1(t)|plnt(1+ϵ+p2)lnkθln(kθ)=1+ϵ+p2,ϵ>0,kθt(k+1)θ.

    Therefore, we obtain

    lim suptln|X1|lnt12+1+ϵp.

    Letting ϵ0, we have

    lim suptln|X1(t)|lnt12+1p,p>2.

    Similar to the proof of Theorem 3.1, it follows that

    lim suptX1(t)tlim suptt12+1pt=0.

    Together with lim inft|X1(t)|t0, this yields

    limt|X1(t)|t=0,a.s..

    We also obtain

    limtX2(t)t=0,limtX3(t)t=0,a.s..

    Theorem 3.3. Assume (H1)(H2) hold. If there exists some p>1 such that μp12σ21pλ>0, then

    limtt0S(s)dB1(s)t=0,limtt0I(s)dB2(s)t=0,limtt0R(s)dB3(s)t=0,a.s..

    The proof is omitted here because it is similar to that of Lemma 2.2 in [18].

    When Zi(t)=0 (i=1,2,3), the stochastic system (1.3) is reduced into a deterministic system investigated by Lahrouz et al. [6]. In [6], the basic reproduction number R0 is derived represented by

    R0=βΛ((1ν)μ+δ)μ(μ+δ)(μ+c+ξ).

    The purpose of this paper is to provide sufficient conditions for the persistence and extinction of disease for stochastic model (1.3). Define

    Rs0=R01μ+c+ξ(σ222+Y[η2(z)ln(1+η2(z))]v(dz)).

    In the following, we will show that Rs0 completely determines the persistence and extinction of the disease. Throughout this section, always assume

    (H3) Y[ln(1+ηi(z))]2v(dz)<.

    For convenience, denote x(t)=1tt0x(s)ds.

    Theorem 4.1. Suppose (H1)(H3) hold. If Rs0<1 and there exists some p>2 such that μp12σ21pλ>0, then

    limtS(t)=Λ(μ+δ+μν)μ(μ+δ),limtI(t)=0,limtR(t)=νΛμ+δ,a.s.,

    i.e., the disease will die out a.s..

    Proof. From stochastic model (1.3),

    d(S(t)+I(t))+δμ+δdR(t)=(1ν)Λ+νΛδμ+δμS(t)(ξμμ+δ+μ+c)I(t)+σ1S(t)dB1(t)+σ2I(t)dB2(t)+σ3δμ+δR(t)dB3(t)+Yη1(z)S(t)˜N(dt,dz)+Yη2(z)I(t)˜N(dt,dz)+δμ+δYη3(z)R(t)˜N(dt,dz).

    Integrating the above equality from 0 to t and dividing both sides by t,

    (1ν)Λ+νΛδμ+δμS(t)(ξμμ+δ+μ+c)I(t)=Ψ1(t), (4.1)

    where

    Ψ1(t)=S(t)S(0)t+I(t)I(0)t+δμ+δR(t)R(0)tσ1tt0S(s)dB1(s)σ2tt0I(s)dB2(s)σ3tδμ+δt0R(s)dB3(s)1tt0Yη1(z)S(s)˜N(ds,dz)1tt0Yη2(z)I(s)˜N(ds,dz)1tδμ+δt0Yη3(z)R(s)˜N(ds,dz).

    Similarly, for the first equation of system (1.3),

    =(1ν)ΛμS(t)βS(t)(1+aI(t))S(t)a(1+aI(t))+δR(t)=(1ν)Λ(μ+βa)S(t)+1aβS1+aI+δR(t)=Ψ2(t), (4.2)

    where

    Ψ2(t)=S(t)S(0)tσ1tt0S(s)dB1(s)1tt0Yη1(z)S(s)˜N(ds,dz).

    For the third equation in system (1.3), we obtain

    νΛ(μ+δ)R(t)+ξI(t)=Ψ3(t), (4.3)

    where

    Ψ3(t)=R(t)R(0)tσ3tt0R(s)dB3(s)1tt0Yη3(z)R(s)˜N(ds,dz).

    According to Theorem 3.1–3.3, then

    limtΨ1(t)=0,limtΨ2(t)=0,limtΨ3(t)=0. (4.4)

    By Itô's formula with jump process,

    dlnI(t)={βS1+aI(μ+c+ξ)σ222Y[η2(z)ln(1+η2(z))]v(dz)}dt+σ2dB2(t)+Yln(1+η2(z))˜N(dt,dz).

    It follows that

    lnI(t)lnI(0)t=βS1+aI(μ+c+ξ)σ222Y[η2(z)ln(1+η2(z))]v(dz)+σ2B2(t)t+1tt0Yln(1+η2(z))˜N(ds,dz). (4.5)

    Substituting (4.1)–(4.3) into (4.5) leads to

    lnI(t)t=lnI(0)t+βΛ((1ν)μ+δ)μ(μ+δ)(μ+c+ξ)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ]I(t)+aΨ2(t)aμ+βμΨ1(t)+aδμ+δΨ3(t)σ222Y[η2(z)ln(1+η2(z))]v(dz)+σ2B2(t)t+1tt0Yln(1+η2(z))˜N(ds,dz)(μ+c+ξ)(Rs01)+aΨ2(t)aμ+βμΨ1(t)+aδμ+δΨ3(t)+σ2B2(t)t+1tt0Yln(1+η2(z))˜N(ds,dz)+lnI(0)t. (4.6)

    Besides, define

    M1(t):=t0Yln(1+η2(z))˜N(ds,dz).

    By assumption (H3), we obtain

    t0dM1,M1(s)(1+s)2ds=t1+tY(ln(1+η2(z)))2v(dz)<+.

    Law of large numbers (Theorem 1 of [20]) yields that

    limtM1(t)t=0,a.s.. (4.7)

    Employing the law of large number yields limtB2(t)t=0, a.s.. This with (4.4) and (4.7) yields

    lim suptlnI(t)t(μ+c+ξ)(Rs01),a.s..

    Then

    limtI(t)=0,a.s.. (4.8)

    Moreover, from (4.1), (4.3) and (4.4) we obtain

    limtS(t)=Λ(μ+δ+μν)μ(μ+δ),limtR(t)=νΛμ+δ,a.s..

    Now, sufficient condition for the persistence of the disease is provided.

    Theorem 4.2. Suppose (H1)(H3) hold. If Rs0>1 and there exists some p>2 such that μp12σ21pλ>0, then

    limtS(t)=1μ((1ν)Λ+νΛδμ+δ)1μ(ξμμ+δ+μ+c)(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ];limtI(t)=(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ];limtR(t)=νΛμ+δ+ξμ+δ(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ],a.s.,

    i.e., the disease will persist a.s..

    Proof. According to (4.6), we have

    lnI(t)t=(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ]I(t)+Ψ(t),

    where

    Ψ(t):=aΨ2(t)aμ+βμΨ1(t)+aδμ+δΨ3(t)+σ2B2(t)t+1tt0Yln(1+η2(z))˜N(ds,dz)+lnI(0)t.

    Theorem 3.1–3.3, the law of large number, (4.4) and (4.7) yield that limtΨ(t)=0. It follows from Lemma 2 of Liu and Wang [21] that

    limtI(t)=(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ].

    Meanwhile, from (4.1) and (4.4) we obtain

    limtS(t)=1μ((1ν)Λ+νΛδμ+δ)1μ(ξμμ+δ+μ+c)limtI(t).

    Consequently, it follows that

    limtS(t)=1μ((1ν)Λ+νΛδμ+δ)1μ(ξμμ+δ+μ+c)(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ].

    By virtue of (4.3), we have

    limtR(t)=νΛμ+δ+ξμ+δ(μ+c+ξ)(Rs01)a[(μ+βa)(ξμ+δ+μ+cμ)+ξδμ+δ].

    In the paper, we analyze the asymptotic behaviour of a stochastic SIRS system with Lˊevy process. Due to the introduction of Lˊevy jump, the jump stochastic integral process is a discontinuous martingale. Thus the Kunita's inequality is used to estimate the asymptotic pathwise of solution for stochastic system (1.3). On this basis, the basic reproduction number for stochastic system (1.3) is defined:

    Rs0=βΛ((1ν)μ+δ)μ(μ+δ)(μ+c+ξ)1μ+c+ξ(σ222+Y[η2(z)ln(1+η2(z))]v(dz)).

    If Rs0<1 and some other conditions hold, the disease will die out. If Rs0>1 and some other conditions hold, the disease will persist. By comparing R0=βΛ((1ν)μ+δ)μ(μ+δ)(μ+c+ξ), it is easy to see that Rs0<R0. This indicates that Lˊevy noise can suppress the outbreak of infectious disease.

    Next, let us make numerical simulations to verify the theoretical results. The initial value is given by (S(0),I(0),R(0))=(80,8,5). The parameters ν, Λ, μ, β, a, δ, c and ξ are chosen as 0.7346, 6, 0.04, 0.02, 1, 0.005, 0.01 and 0.8, respectively. By calculation, we can obtain R0=1.1023. This implies that the disease will persist when the system does not have environmental perturbation.

    To consider the effect of Lˊevy process in the spreading of disease, the values of σ2 are both taken as 0.4. We first choose η2 as 0.08. By calculating the value of Rs0, we get the value is 1.0046. It follows from Theorem 4.2 that the disease will persist. The simulated result is shown in Figure 1(a). Then we choose η2 as 0.2. The value of Rs0 is 0.9874 in this case. By Theorem 4.1, the disease will die out. The simulation result is presented in Figure 1(b). From Figure 1, it can be seen that the larger jump noise induces the extinction of disease, i.e., the Lˊevy noise suppress the outbreak of infectious disease while the corresponding deterministic model is persist.

    Figure 1.  The paths of the infected for two different values of η2.

    Y. Zhu is supported by the Postgraduate Research & Practice Innovation Program of Jiangsu Province (No. KYCX22_0391) and the Fundamental Research Funds for the Central Universities (No. 30922010813). L. Wang is supported by the National Natural Science Foundation of China (No. 12001271), the Natural Science Foundation of Jiangsu Province (No. BK20200484) and the Fundamental Research Funds for the Central Universities (No. 30922010813). Z. Qiu is supported by the National Natural Science Foundation of China (No. 12071217).

    The authors declare that there is no conflict of interest.



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