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. 2022 Jan 15;107(3):2975–2993. doi: 10.1007/s11071-021-07095-7

Asymptotic behavior of a stochastic SIR model with general incidence rate and nonlinear Lévy jumps

Qing Yang 1, Xinhong Zhang 1,, Daqing Jiang 1,2
PMCID: PMC8760125  PMID: 35068689

Abstract

In this paper, we consider a stochastic SIR epidemic model with general disease incidence rate and perturbation caused by nonlinear white noise and Le´vy jumps. First of all, we study the existence and uniqueness of the global positive solution of the model. Then, we establish a threshold λ by investigating the one-dimensional model to determine the extinction and persistence of the disease. To verify the model has an ergodic stationary distribution, we adopt a new method which can obtain the sufficient and almost necessary conditions for the extinction and persistence of the disease. Finally, some numerical simulations are carried out to illustrate our theoretical results.

Keywords: SIR model, Lévy jumps, Incidence rate, Extinction, Ergodic stationary distribution

Introduction

The study of epidemic dynamics is to establish a mathematical model which can reflect the biological mechanisms according to the occurrence, development and environmental changes of diseases, and then to show the evolution of diseases through the study of dynamics of the model. Theories of Kermack and McKendrick laid the foundation for subsequent study of infectious disease dynamics and the generation of the most classic SIR epidemic model [1]. Since then, a large number of papers have focused on the dynamics of SIR infectious disease model [26]. And this model is usually used to denote some diseases with permanent immunity such as herpes, rabies, syphilis, whooping cough, smallpox, and measles, etc. We refer the readers to [79] for more details. In this paper, we assume that the mortality due to disease is not very high and the average daily increase in people over a period of time is constant. Then, the classic epidemic model can be given by:

dS(t)=α-βS(t)I(t)-μS(t)dt,dI(t)=βS(t)I(t)-(μ+ρ+γ)I(t)dt,dR(t)=γI(t)-μR(t)dt, 1

where S(t), I(t), R(t) represent the density of susceptible individuals, infected individuals and individuals recovered from the disease at time t, respectively. The parameter α denotes the recruitment rate of the population, β is the transmission coefficient between S(t) and I(t), μ is the natural mortality rate, ρ is the mortality due to disease, and γ is the recovery rate. All of the parameters α, β, μ, ρ, γ are assumed to be positive.

It is well known that the bilinear incidence rate βS(t)I(t) describes the number of people infected by all the patients in a unit of time t (i.e., the number of new cases). However, studies have shown there exist many biological factors that may contribute to nonlinearity of transmission rate (refer [10] and the references therein ). The nonnegligible interactions between organisms caused by the nonlinear incidence of disease have attracted many scholars to consider more complex incidence functions. For example, a study on the transmission of cholera epidemic in Bari, Italy, 1973 attracted Capasso and Serio’s attention to SIR epidemic model with saturated incidence [11], they put forward the nonlinear incidence rate βSI1+aI, which can avoid the unboundedness of the contact rate on the cholera epidemic. This incidence rate measures the behavioral change of the disease and saturation effect as the number of infected individuals increases. That is, βSI1+aI will converge to a saturation point when I is large. In addition, Chong et al. [12] considered a model of avian influenza with half-saturated incidence βSIH+I, where β>0 denotes the transmission rate and H denotes the half-saturation constant which means the density of infected individuals in the population that yields 50% possibility of contracting avian influenza. Huo and coworkers [13] proposed a rumor transmission model with Holling-type II incidence rate given by λSIm+S. Kashkynbayev and Rihan [14] studied the dynamics of a fractional-order epidemic model with general nonlinear incidence rate functionals and time-delay, they proposed that the model applied to the incidence rate βSnI1+ηSn, n2. Furthermore, they adopted the Holling-type III functional response βS2I1+ηS2 for numerical simulation to implement the theoretical results. In [15], authors assumed that the infection rate of HIV-1 was given by the Beddington–DeAngelis incidence function βSI1+aS+bI, obviously, with the different values of a and b, this nonlinear incidence rate can be transformed into Holling-type II or saturation incidence function. Similarly, when Alqahtani performed the stability and numerical analysis of a SIR epidemic system (COVID-19), they also adopted the Beddington–DeAngelis incidence function f(S,I)=β1SIa1+a2S+a3I [16]. Besides, Ruan et al. proposed an epidemic model with nonlinear incidence rate kIlS1+αIh in [17], where kIl measures the infection force of the disease and 11+αIh measures the inhibition effect from the behavioral change of the susceptible individuals when their number increases or from the crowding effect of the infective individuals. In [18], Rohith and Devika modeled the COVID-19 transmission dynamics using a susceptible-exposed-infectious-removed model with a nonlinear incidence rate β0SI1+αI2. Khan et al. [19] presented the dynamics of a fractional SIR model with a general incidence rate f(I)S which contained several most famous generalized forms. In addition, there are a lot of other studies on the subject (see [2027]). In this paper, we take a more general incidence rate F with two variables S(t) and I(t) which will contain a number of common incidence rate mentioned in studies before. To be specific, model (1) turns into the following form:

dS(t)=α-F(S(t),I(t))I(t)-μS(t)dt,dI(t)=F(S(t),I(t))I(t)-(μ+ρ+γ)I(t)dt,dR(t)=γI(t)-μR(t)dt. 2

Throughout this paper, we assume the general incidence rate F(SI) has the following properties.

Assumption 1

Suppose that F(S(t), I(t)) is locally Lipschitz continuous for both variables with F(0,I)=0 , I0. Furthermore, F is continuous at I=0 uniformly, that is

limI0supS0{F(S,I)-F(S,0)}=0.

Suppose further that F(SI) is a function non-decreasing in S, non-increasing in I and satisfies the following condition:

F(S,I)Sc,

where c is a positive constant.

Remark 1

Note that the incidence rate F(SI) contains all the disease incidence functions listed in this paper. In summary, it includes the bilinear incidence rate (F(S,I)=βS) [28], saturated incidence rate (F(S,I)=βS1+mI) [11, 29, 30], half-saturated incidence rate (F(S,I)=βSm+I) [12, 31], Holling-type II incidence rate (F(S,I)=βSm+S) [13], Holling-type III incidence rate (F(S,I)=βS2(m1+S)(m2+S)) [14], the Beddington–DeAngelis incidence rate (F(S,I)=βS1+m1S+m2I) [15, 32, 33] and some other nonlinear incidence rates that are not listed here.

However, from the perspective of ecology and biology, the transmission process of infectious diseases, the contact between people, the movement of people and so on are inevitably affected by various environmental disturbances [34], such as temperature, water supply or climate change, whereas the above deterministic model does not consider the effects of any random factors. May [35] has revealed that some main parameters in epidemic model, such as the birth rates, death rates and spread rates of disease, are affected by environmental noise to a certain extent. In addition, as we know, Brownian motion is the main choice for simulating random motion and noise in continuous-time system modeling. This choice is soundly based on the good statistical characteristics of Brownian motion. For example, Brownian motion has finite moments of all orders, continuous sample-path trajectories, and there are powerful analytical tools that can solve the Brownian motion problem. Thus, we aim at stochastic epidemic model which contains white noise on the basis of the deterministic model (see [36, 37]).

In order to better simulate the impact of environmental noise during disease transmission, follow the methods of Liu and Jiang [38], nonlinear perturbation is considered in this paper, because the random perturbation may be dependent on square of the state variables S, I and R. Specifically, we assume the perturbations of S, I, R have the following form, respectively.

S:-μ-μ+(σ11+σ12S)B˙1(t),I:-μ-μ+(σ21+σ22I)B˙2(t),R:-μ-μ+(σ31+σ32R)B˙3(t),

where B1(t),B2(t) and B3(t) are mutually independent standard Brownian motions. σij2>0, i=1,2,3, j=1,2 are the intensities of white noise. Thus, after taking into account the nonlinear perturbation of white noise, model (2) turns into the form of

dS(t)=α-F(S(t),I(t))I(t)-μS(t)dt+σ11S(t)+σ12S2(t)dB1(t),dI(t)=F(S(t),I(t))I(t)-(μ+ρ+γ)I(t)dt+σ21I(t)+σ22I2(t)dB2(t),dR(t)=γI(t)-μR(t)dt+σ31R(t)+σ32R2(t)dB3(t). 3

Brownian motion has many excellent properties, but in some cases advantages can also be disadvantages. In the population ecosystem, it is inevitable to suffer some abrupt massive disturbances. These disturbances could be major catastrophes, like tsunamis, hurricanes, tornadoes, earthquakes and floods, etc.; and they also could be serious, large-scale diseases, such as avian influenza, COVID-19, SARS, dengue fever and Hemorrhagic fever caused by the Ebola virus, etc. Once these disasters occur, they usually lead to drastic fluctuations in the population of the region, and even a jump in the number of people. In other words, these disturbances will lead to discontinuous sample-path trajectories in the corresponding mathematical model. Therefore, Brownian motion cannot be simply used to describe these kinds of environmental disturbances. In order to explain the above phenomenon more accurately, a stochastic differential equation with jump should be considered to continue the study of epidemic dynamics system.

According to Liu et al. [39], the jump times are always random, and the waiting time of jumps is similar to Le´vy jumps. In addition, according to the theory of Eliazar and Klafter [40], Le´vy motions—performed by stochastic processes with stationary and independent increments—constitute one of the most important and fundamental family of random motions. Consequently, some scholars incorporated jump process into the system and there have been a number of specific studies of epidemiological models with Le´vy jumps up to now. Bao et al. took the lead in considering the competitive LotKa-Volterra population dynamics with jumps in [41] and gave some results to reveal the effect of jump process on the system. In [42], authors used the stochastic differential equation with jumps to study the asymptotic behavior of stochastic SIR model. Some other studies can be found in [43, 44] and the references therein. To the best of the authors’ knowledge, there is little literature on stochastic SIR epidemic model with general disease incidence and second-order perturbation of white noise and Le´vy jumps. Inspired by the above, we develop model (3) with Le´vy jumps:

dS(t)=α-FS(t-),I(t-)I(t-)-μS(t-)dt+σ11S(t-)+σ12S2(t-)dB1(t)+Yf11(u)S(t-)+f12(u)S2(t-)N~dt,du,dI(t)=FS(t-),I(t-)I(t-)-μ+ρ+γI(t-)dt+σ21I(t-)+σ22I2(t-)dB2(t)+Yf21(u)I(t-)+f22(u)I2(t-)N~dt,du,dR(t)=γI(t-)-μR(t-)dt+σ31R(t-)+σ32R2(t-)dB3(t)+Yf31(u)R(t-)+f32(u)R2(t-)N~dt,du, 4

where S(t-), I(t-), R(t-) are the left limit of S(t), I(t) and R(t), respectively. N(·,·) is a Poisson counting measure with characteristic measure λ on a measurable subset Y of [0,) with λ(Y)<, and the compensated Poisson random measure is defined by N~(dt,du)=N(dt,du)-λ(du)dt. Throughout this paper, we assume that Bi(t), i=1,2,3 and N(·,·) are independent and all the coefficients of the system are positive. Since the dynamics of recovered population has no impact on the disease transmission dynamics of model (4), hence, we can omit the third equation in system (4) for convenience.

Assumption 2

Yfij2(u)λ(du)<.

According to this assumption, we can derive that Yln(1+fij(u))2λ(du)

<, which implies that the intensities of Le´vy jumps are not very big.

As far as we know, few papers have studied the effects of a SIR epidemic model with general incidence rate and perturbed by both nonlinear white noise and Le´vy jumps. Therefore, this paper presents a great challenge to the theoretical analysis of the model. The main innovation and contribution in this paper is that we provide a sufficient and almost necessary condition under which the disease disappears and persists. In a deterministic model, the persistence and extinction of the disease are usually reflected by the stability of the equilibrium point, while in a stochastic model, we usually discuss the existence of the stationary distribution. The common way to prove the existence of ergodic stationary distribution is the theory of Has’minskii [45], and the key to the theory is to establish befitting Lyapunov functions. However, only sufficient conditions for the existence and uniqueness of ergodic stationary distribution can be obtained by these conventional methods [4648]. To perfect the results, in this paper, we adopt a novel method which is a combination of classical Lyapunov functions and methods introduced in [49]. Finally, we obtain the desired sufficient and almost necessary condition for persistence of the disease and get a threshold λ. To be more specific, in case of λ<0, the number of the infected population will tend to zero exponentially which means the disease will become extinct. In case λ>0, system (4) exists an ergodic stationary distribution on R+2 which means the disease will persist in the population.

The structure of this paper is arranged as follows. In Sect. 2, we first give some preliminary knowledge that may be used in this paper, including the exponential martingale inequality with Le´vy jumps and the local martingale’s strong law of large numbers. Section 3 proves the existence and uniqueness of the global positive solution in system (4). In order to obtain a threshold to determine the extinction and persistence of the disease, we discuss the existence of ergodic stationary distribution of the equation on the boundary where the infected individuals are absent in Sect. 4, and then we define a λ which is a key in this paper. The extinction and the ergodic stationary distribution of the disease in model (4) are given in Sects. 5 and 6, respectively. Finally, several numerical simulation examples are conducted to illustrate our main research results.

Preliminaries

Unless otherwise stated, throughout this paper, let (Ω, F, {Ft}t0, P) be a complete probability space with a filtration {Ft}t0 satisfying the usual conditions. We denote R+=[0,), R+n={xiRn:xi>0,i=1,2,,n}.

Now we shall give some primary basic knowledge in stochastic population systems with Le´vy jumps, more details on Le´vy process can be found in [50].

Definition 1

X is a Le´vy process if:

  1. X(0) = 0 a.s.;

  2. X has independent and stationary increments;

  3. X is stochastically continuous, i.e., for all a>0 and s>0,
    limtsP(X(t)-X(s)>a)=0.

In general, let x(t) be a d-dimensional Le´vy process on t0 presented as the following stochastic differential equation with Le´vy jumps

dx(t)=f(t-)dt+g(t-)dB(t)+Yγ(t-,u)N~(dt,du), 5

where fL1(R+,Rd), gL2(R+,Rd×m) and γL1(R+×Y,Rd).

B(t)={Bt1,Bt2,,BtmT}t0 is an m-dimensional Brownian motion defined on the complete probability space (Ω,F,P). Integrating both sides of (5) from 0 to t, we can get

x(t)=x(0)+0tf(s-)ds+0tg(s-)dB(s)+0tYγ(s-,u)N~(ds,du).

Let C2,1(Rd×R+;R) denote the family of all real-valued functions V(xt) defined on Rd×R+ such that they are continuously twice differentiable in x and once in t. For any function UC2,1(Rd×R+;R), define the differential operator LU(x(t),t) as follows:

LU(x(t),t)=Ut(x(t),t)+Ux(x(t),t)f(t)+12trace(gT(t)Uxx(x(t),t)g(t))+YU(x(t)+γ(t,u),t)-U(x(t),t)-Ux(x(t),t)γ(t,u)λ(du),

where

Ut=Ut,Ux=Ux1,,Uxd,Uxx=2Ux1x12Ux1xd2Uxdx12Uxdxd.

According to the Ito^’s formula,

dU(x(t),t)=LU(x(t),t)dt+Uxg(t)dB(t)+YU(x(t)+γ(t,u),t)-U(x(t),t)N~(dt,du).

Next, we shall introduce the exponential martingale inequality with jumps as follows [41].

Definition 2

Assume that gL2(R+,Rd×m),γL1(R+×Y,Rd). For any constants T,α,β>0,

P{sup0tT0tg(s)dB(s)-α20tg(s)2ds+0tYγ(s,u)N~(ds,du)-1α0tYeαγ(s,u)-1-αγ(s,u)λ(du)ds>β}e-αβ.

To make the theory more complete, the following lemma cited by [50] is concerning the local martingale’s strong law of large numbers.

Lemma 1

Assume that M(t) is a local martingale vanishing at t=0, define

ρM(t):=0tdM(s)(1+s)2,t0,

where M(t):=M,M(t) is Meyer’s angle bracket process.

If limtρM(t)<a.s. holds, then

limtM(t)t=0a.s..

From the relevant introduction in [51], we cite the proposition as follows.

Remark 2

Assume that

Γloc2:=γ(t,u)predictable|0tYγ(t,u)2λ(du)dt<.

For any γΓloc2,

M(t):=0tYγ(s,u)N~(ds,du),

then one can see that

M(t)=0tYγ(s,u)2λ(du)ds,M(t)=0tYγ(s,u)2N~(ds,du),

where M(t)=M,M(t) denotes the quadratic variation process of M(t).

Existence and uniqueness of the global positive solution

In order to study the dynamics of an epidemic system, the first thing we concerned is whether the solution of model (4) is global and positive. Here, we give the following conclusion which is a fundamental condition for the long time behavior of model (4).

Theorem 1

For any initial value (S(0),I(0))R+2, stochastic system (4) has a unique positive solution (S(t),I(t))R+2 on t0, and the solution will remain in R+2 with probability one.

Proof

Our proof is motivated by the methods of [34]. Since the drift and diffusion (i.e., the coefficients of model (4)) are locally Lipschitz continuous, hence there is a unique local solution S(t),I(t) on t[0,ρe) for any given initial value S(0),I(0)R+2, where ρe is an explosion time. To testify this solution is global, we only need to show that ρe= a.s.. Let k0>0 be sufficiently large such that both S(0) and I(0) can lie within the interval [1k0,k0]. For each integer kk0, define the following stopping time

τk=inf{t(0,ρe):S(t)1k,korI(t)1k,k}.

Apparently, τk is increasing as k. Set τ=limkτk, hence τρe a.s.. Once we prove that τ= a.s., then we can get ρe= and S(t),I(t)R+2 a.s..

If τ< a.s., then there exists a pair of constants T>0 and 0<ε<1 such that P(τT)>ε. Hence, there is an integer k1k0 such that P(τkT)ε for all kk1.

Define a C2-function V: R+2R+ as follows:

V(S,I)=(1+S)p-1-plogS+Ip-1-plogI,

where 0<p<1. The nonnegativity of V(SI) is due to k-1-logk0 for k0. It is easy to see V(SI) is continuously twice differentiable with respect to S and I.

Applying Ito^’s formula to function V(SI), we have

dV(S,I)=LV(S,I)dt+p(1+S)p-1-pSσ11S+σ12S2dB1(t)+pIp-1-pIσ21I+σ22I2dB2(t)+Y(1+S+f11(u)S+f12(u)S2)p-(1+S)pN~(dt,du)-pYlog(S+f11(u)S+f12(u)S2)-logSN~(dt,du)+Y(I+f21(u)I+f22(u)I2)p-IpN~(dt,du)-pYlogI+f21(u)I+f22(u)I2-logIN~(dt,du), 6

where

LV(S,I)=p(1+S)p-1α-F(S,I)I-μS+p(p-1)2(1+S)p-2(σ11S+σ12S2)2+Y1+S+f11(u)S+f12(u)S2p-(1+S)p-p(1+S)p-1(f11(u)S+f12(u)S2)λ(du)-pαS+pF(S,I)IS+pμ+pσ1122+pσ1222S2+pσ11σ12S-pYlogS+f11(u)S+f12(u)S2-logS-1Sf11(u)S+f12(u)S2λ(du)+pF(S,I)Ip-pμ+ρ+γIp+p(p-1)2Ip-2σ21I+σ22I22+YI+f21(u)I+f22(u)I2p-Ip-pIp-1f21(u)I+f22(u)I2λ(du)-pF(S,I)+p(μ+ρ+γ)+pσ2122+pσ2222I2+pσ21σ22I-pYlogI+f21(u)I+f22(u)I2-logI-1If21(u)I+f22(u)I2λ(du).

For any 0<p<1, by the inequation xr1+r(x-1) for x0,0r1, we have

Y1+S+f11(u)S+f12(u)S2p-(1+S)p-p(1+S)p-1f11(u)S+f12(u)S2λ(du)<0,YI+f21(u)I+f22(u)I2p-Ip-pIp-1f21(u)I+f22(u)I2λ(du)<0.

On the basis of Assumption 1 and the above results, then

LV(S,I)pα-pF(S,I)I(1+S)p-1-pμS(1+S)p-1+p(p-1)2(1+S)pσ11S+σ12S21+S2-pαS+pcI+pμ+pσ1122+pσ1222S2+pσ11σ12S+pYf11(u)+f12(u)Sλ(du)+pF(S,I)Ip-p(μ+ρ+γ)Ip+p(p-1)2Ip+2σ21+σ22II2-pF(S,I)+p(μ+ρ+γ)+pσ2122+pσ2222I2+pσ21σ22I+pYf21(u)+f22(u)Iλ(du)pα+pμ+pσ1122+p(μ+ρ+γ)+pσ2122+pYf11(u)+f21(u)λ(du)-p(1-p)2(1+S)pσ11S+σ12S21+S2-p(1-p)2Ip+2σ22+σ21I2+pF(S,I)Ip+pσ1222S2+pσ2222I2+pcI+pσ11σ12S+pσ21σ22I+pYf12(u)λ(du)S+pYf22(u)λ(du)Ipα+2μ+ρ+γ+σ112+σ2122+Yf11(u)+f21(u)λ(du)-p(1-p)2min{σ11,σ12}2(1+S)pS2-p(1-p)2σ222Ip+2+pcSIp+p2σ122S2+σ222I2+pc+pσ21σ22+pYf22(u)λ(du)I+pσ11σ12+pYf12(u)λ(du)Sk2+pα+2μ+ρ+γ+σ112+σ2122+pYf11(u)+f21(u)λ(du)=:k3,

where

k2=supS0,I0{-p(1-p)2min{σ11,σ12}2(1+S)pS2-p(1-p)2σ22Ip+2+pcSIp+p2σ122S2+σ222I2+pc+pσ21σ22+pYf22(u)λ(du)I+pσ11σ12+pYf12(u)λ(du)S}.

Integrating both sides of (6) from 0 to τkT and then taking expectations

EVS(τkT),I(τkT)VS(0),I(0)+k3EτkTVS(0),I(0)+k3T.

Let Ωk={τkT} for kk1, then we have p(Ωk)ε. Note that for every ωΩk, S(τk,ω) or I(τk,ω) equals either k or 1k. Consequently,

VS(0),I(0)+k3TE[IΩkV(S(τk,ω),I(τk,ω))]ε[(1+k)p-1-plogk(1+1k)p-1-plog1kkp-1-plogk1kp-1-plog1k],

where IΩk is the indicator function of Ωk. Taking k, we obtain that >VS(0),I(0)+k3T= which is a contradiction, therefor we have τ= a.s. (i.e., S(t) and I(t) will not explode in a finite time with probability one). The conclusion is confirmed.

Exponential ergodicity for the system without disease

In this section, a threshold λ will be defined by exploring the exponential ergodicity of a one-dimensional disease-free system. To proceed, we first consider the following equation if there is no infective at time t=0:

dS^(t)=α-μS^(t)dt+σ11S^(t)+σ12S^2(t)dB1(t)+Yf11(u)S^(t)+f12(u)S^2(t)N~dt,du. 7

In terms of the comparison theorem, it is easy to check out that S(t)S^(t), t0 a.s. provided S(0)=S^(0)>0. In order to obtain the exponential ergodicity of model (7), we first give the following lemma which has been discussed in [38].

Lemma 2

The following equation

dS¯(t)=α-μS¯(t)dt+σ11S¯(t)+σ12S¯2(t)dB1(t),S¯(0)>0 8

admits an ergodic stationary distribution with the density:

π(x)=Qx-2-2(2ασ12+μσ11)σ113σ11+σ12x-2+2(2ασ12+μσ11)σ113e-2σ11σ11+σ12xαx+2ασ12+μσ11σ11, 9

where Q is a constant such that 0π(x)dx=1,x(0,) and it follows limt1t0tS¯(τ)dτ=0xπ(dx)a.s..

Theorem 2

Markov process S^(t) is exponentially ergodic and it has a unique stationary distribution denoted by π¯ on R+.

Proof

In order to prove the existence of the ergodic stationarity of S^(t), according to [49], it is equivalent to proving the following two conditions: (a) The auxiliary process S¯(t) determined by (8) has a positive transition probability density with respect to Lebesgue measure. (b) There exists a nonnegative C2-function V(S^(t)) such that LV(S^(t))-H2V(S^(t))+H1, in which H1,H2 are positive constants. In view of Lemma 2, condition (a) has been given; therefore, we just need to verify condition (b) in the following.

Consider the Lyapunov function

V(S^(t))=1+S^(t)pp-lnS^(t),

where 0<p<1.

Applying Ito^’s formula , one sees that

L1+S^(t)pp-lnS^(t)=1+S^p-1α-μS^+p-121+S^p-2σ11S^+σ12S^22+Y1+S^+f11(u)S^+f12(u)S^2pp-1+S^pp-1+S^p-1f11(u)S^+f12(u)S^2λ(du)-αS^+μ+σ11S^+σ12S^222S^2-YlnS^+f11(u)S^+f12(u)S^2-lnS^-f11(u)+f12(u)S^λ(du)-μ1+S^p-αS^+μ(1+S^)p-1+α(1+S^)p-1+p-121+S^pσ11S^+σ12S^21+S^2+μ+σ11+σ12S^22+1+S^ppY1+S^1+S^f11(u)+S^21+S^f12(u)p-1-pS^1+S^f11(u)+S^21+S^f12(u)λ(du)+Yf11(u)+f12(u)S^-ln(1+f11(u)+f12(u)S^)λ(du).

By reason of the inequations 1x-1+lnx0 for x0 and xr1+r(x-1) for x0, 0r1, we derive that

LV(S^(t))-μp1+S^pp+αlnS^+μ(1+S^)p-1+α(1+S^)p-1-1-p2min{σ11,σ12}21+S^pS^2+μ+σ11+σ12S^22+Yf11(u)+f12(u)S^-ln(1+f11(u)+f12(u)S^)λ(du)-μp1+S^pp-α(-lnS^)+max{h,1}-min{μp,α}1+S^(t)pp-lnS^(t)+max{h,1}=-H2V(S^(t))+H1,

where

H1=max{h,1},H2=min{μp,α},h=supS^[0,){μ(1+S^)p-1+α(1+S^)p-1-1-p2min{σ11,σ12}21+S^pS^2+μ+σ11+σ12S^22+Yf11(u)+f12(u)S^-ln(1+f11(u)+f12(u)S^)λ(du)}.

This completes the proof of the theorem.

Remark 3

For any π¯-integrable f(x): R+2R, according to the ergodicity of S^(t),

limt1t0tfS^(τ)dτ=0fxπ¯(dx).

Furthermore, integrating both sides of (7) from 0 to t and then taking expectation, then it yields

limtES^(t)t=α-μlimt1t0tES^(τ)dτ=α-μE0xπ¯(dx),

combining the above result and limtES^(t)t=0, we can obtain

limt1t0tS^(τ)dτ=0xπ¯(dx)=αμ.

Remark 4

Now, we define a critical value which will play an important role in determining the extinction and persistence of the disease.

λ=0Fx,0π¯(dx)-μ+ρ+γ+σ2122+Yf21u-ln1+f21uλdu. 10

According to Assumption (1), one can see that F(S,I)cS, hence,

0Fx,0π¯(dx)c0xπ¯(dx)=limtct0tS^(τ)dτ=cαμ<.

Therefore, λ is well defined.

Extinction of the disease

In this section, we will present sufficient conditions for the demise of the disease, which will provide theoretical guidance for the prevention and control of the spread of disease. The following theorem is vital in this paper.

Theorem 3

Let S(t),I(t) be the solution of system (4) with any given positive initial value S(0),I(0)R+2, then it has the property

limtlnI(t)tλa.s..

If λ<0 holds, I(t) will go to zero exponentially with probability one.

Proof

Applying Ito^’s formula to lnI(t), we have

dlnI(t)=F(S,I)-μ+ρ+γ-σ21I+σ22I222I2+YlnI+f21(u)I+f22(u)I2-lnI-f21(u)+f22(u)Iλdudt+σ21+σ22IdB2(t)+YlnI+f21(u)I+f22(u)I2-lnIN~(dt,du)F(S^,0)-μ+ρ+γ+σ2122+Yf21(u)-ln1+f21(u)λ(du)-σ21σ22I-σ2222I2+Yln1+f22(u)I1+f21(u)-f22(u)Iλ(du)dt+σ21dB2(t)+σ22IdB2(t)+Yln1+f21(u)N~(dt,du)+Yln1+f22(u)I1+f21(u)N~(dt,du). 11

Integrating both sides of (11), we obtain

lnI(t)lnI(0)-σ22220tI2(τ)dτ-0tσ21σ22I(τ)dτ+0tF(S^(τ),0)-μ+ρ+γ+σ2122dτ+0tYf21(u)-ln1+f21(u)λ(du)dτ-0tYln1+f22(u)I(τ)1+f21(u)-f22(u)I(τ)λ(du)dτ+0tσ21dB2(τ)+0tσ22I(τ)dB2(τ)+0tYln1+f21(u)N~(dτ,du)+0tYln1+f22(u)I(τ)1+f21(u)N~(dτ,du)=lnI(0)-0tσ21σ22I(τ)dτ-σ22220tI2(τ)dτ+0tF(S^(τ),0)-μ+ρ+γ+σ2122dτ-0tYf21(u)-ln1+f21(u)λ(du)dτ+0tYln1+f22(u)I(τ)1+f21(u)-f22(u)I(τ)λ(du)dτ+0tσ22I(τ)dB2(τ)+w1(t)+w2(t)+0tYln1+f22(u)I(τ)1+f21(u)N~(dτ,du), 12

where

w1(t)=0tσ21dB2(τ),w2(t)=0tYln1+f21(u)N~(dτ,du).

It is obvious that w1,w1(t)=σ212t. In view of Remark 2, one can obtain that w2,w2(t)=tYln1+f21(u)2λ(du). Consequently, according to the strong law of large numbers presented in Lemma 1 we have

limtw1(t)t=0,limtw2(t)t=0a.s..

Furthermore, on the basis of exponential martingale inequality introduced in Definition 2, we choose α=1, β=2lnn, then it follows

P{sup0tn0tσ22I(τ)dB2(τ)-120tσ222I2(τ)dτ+0tYln1+f22(u)I(τ)1+f21(u)N~(dτ,du)-0tY1+f22(u)I(τ)1+f21(u)-1-ln1+f22(u)I(τ)1+f21(u)λ(du)dτ2lnn}1n2,

since 1n2<, the Borel–Cantelli lemma implies that there exist a set Ω0F with P(Ω0)=1 and an integer-valued random variable n0 such that for every ωΩ0,

sup0tn0tσ22I(τ)dB2(τ)-120tσ222I2(τ)dτ+0tYln1+f22(u)I(τ)1+f21(u)N~(dτ,du)-0tY1+f22(u)I(τ)1+f21(u)-1-ln1+f22(u)I(τ)1+f21(u)λ(du)dτ2lnn,ifnn0.

That is, for all 0tn and nn0 a.s., it follows

0tσ22I(τ)dB2(τ)+0tYln1+f22(u)I(τ)1+f21(u)N~(dτ,du)2lnn+σ22220tI2(τ)dτ+0tYf22(u)I(τ)1+f21(u)-ln1+f22(u)I(τ)1+f21(u)λ(du)dτ.

Then, substituting the above results into (12) deduces that

lnI(t)-lnI(0)t1t0tF(S^(τ),0)-μ+ρ+γ+σ2122dτ-1t0tYf21(u)-ln1+f21(u)λ(du)dτ+2lnnt-1t0tYf22(u)I(τ)-f22(u)I(τ)1+f21(u)λ(du)dτ-1t0tσ21σ22I(τ)dτ+w1(t)t+w2(t)t1t0tF(S^(τ),0)-μ+ρ+γ+σ2122dτ-1t0tYf21(u)-ln1+f21(u)λ(du)dτ+2lnnt+w1(t)t+w2(t)t,

for all 0tn and nn0 a.s..

Therefore, for almost all ωΩ0, if nn0, 0<n-1tn, by taking the limit of both sides we obtain

lim suptlnI(t)tlimt1t0tF(S^(τ),0)dτ-μ+ρ+γ+σ2122dτ-limt1t0tYf21(u)-ln1+f21(u)λ(du)dτ+limn2lnnn-10Fx,0π¯(dx)-μ+ρ+γ+σ2122+Yf21(u)-ln1+f21(u)λ(du)=λa.s..

If λ<0, then lim suptlnI(t)t<0, i.e., limtI(t)=0 a.s., which means the disease will die out in a long term.

Ergodic stationary distribution

In biology, the persistence of disease is closely related to the balance and stability of the entire ecosystem. In theoretical research, different from the deterministic model, the stochastic model has no endemic equilibrium point, so there is no way to get the desired result by analyzing the stability of the equilibrium point. In this part, we will investigate the existence of the ergodic stationary distribution of model (4) in a new way on the basis of the method mentioned in [5355].

Theorem 4

Assume that λ>0, for any initial value S(0),I(0)R+2, system (4) has a unique stationary distribution π and it has ergodic property.

Furthermore, the following assertions are valid.

  1. For any π-integrable f(x,y) : R+2R, it follows that
    limt1t0tf(S(τ),I(τ))dτ=R+2f(x,y)π(dx,dy)a.s..
  2. limt||P(t,(S(0),I(0)),·)-π||=0(S(0),I(0))R+2, where

    P(t,(S(0),I(0)),·) is the transition probability of (S(t),I(t)).

Proof

At first, we define a C2-function

V^(S(t),I(t))=M-lnI(t)+cμS^(t)-S(t)-lnS(t)+1+S(t)pp+Ip(t)p,

where p (0,1), M is a positive constant which satisfies -Mλ+L-2 and constant L will be determined later. In view of S(t)^-S(t)>0,t0 and the partial derivative equations, it is easy to know that the following function has a minimum point, i.e.,

V^(S(t),I(t))-MlnI(t)-lnS(t)+1+S(t)pp+Ip(t)pl1.

Then, we consider the following nonnegative function

V(S(t),I(t))=V^(S(t),I(t))-l1.

Denote

V1=-lnI(t),V2=S^(t)-S(t),V3=-lnI(t)+cμS^(t)-S(t),V4=-lnS(t),V5=1+S(t)pp,V6=Ip(t)p.

An application of Ito^’s formula , one can see that

L(V1)=-F(S,I)+μ+ρ+γ+σ21+σ22I22+Yf21(u)+f22(u)I-ln1+f21(u)+f22(u)Iλdu=-F(S,I)+μ+ρ+γ+σ2122+Yf21(u)-ln1+f21(u)λ(du)+σ21σ22I+σ2222I2+Yf22(u)I-ln1+f22(u)I1+f21(u)λ(du)-F(S^,0)+μ+ρ+γ+σ2122+Yf21(u)-ln1+f21(u)λ(du)+F(S^,0)-F(S,0)+F(S,0)-F(S,I)+σ21σ22+Yf22(u)λ(du)I+σ2222I2-F(S^,0)+μ+ρ+γ+σ2122+c(S^-S)+Yf21(u)-ln1+f21(u)λ(du)+F(S,0)-F(S,I)+σ21σ22+Yf22(u)λ(du)I+σ2222I2. 13
L(V2)=-μ(S^-S)+F(S,I)I-μ(S^-S)+cSI, 14

where Assumption 1 has been used.

Combining Eqs. (13) and (14), we obtain

L(V3)-0F(x,0)π¯(dx)+μ+ρ+γ+σ2122+Yf21(u)-ln1+f21(u)λ(du)+0F(x,0)π¯(dx)-F(S^,0)+F(S,0)-F(S,I)+σ21σ22+Yf22(u)λ(du)I+σ2222I2+c2μSI.

Moreover,

L(V4)=-αS+μ+F(S,I)IS+12σ11+σ12S2+Yf11(u)+f12(u)S-ln1+f11(u)+f12(u)Sλ(du)-αS+μ+σ1122+cI+σ11σ12S+σ1222S2+Yf11(u)+f12(u)Sλ(du)=-αS+μ+σ1122+Yf11(u)λ(du)+cI+σ11σ12+Yf12(u)λ(du)S+σ1222S2.L(V5)1+Sp-1α-F(S,I)I-μS-1-p21+Sp-2σ11S+σ12S22+1+SppY1+S1+Sf11(u)+S21+Sf12(u)p-1-pS1+Sf11(u)+S21+Sf12(u)λ(du)α-1-p2min{σ11,σ12}2(1+S)pS2.L(V6)=F(S,I)I-(μ+ρ+γ)IIp-1-1-p2Ip-2σ21I+σ22I22+IppY1+f21+f22Ip-1-pf21+f22Iλ(du)cSIp-1-p2σ222Ip+2.

Now, combining the inequalities what we have got above, it follows

LV(S,I)-Mλ+MF(S,0)-F(S,I)+Mσ21σ22+Yf22(u)λ(du)I+σ2222MI2+c2μMSI-αS+μ+σ1122+Yf11(u)λ(du)+cI+σ11σ12+Yf12(u)λ(du)S+σ1222S2+α-1-p2min{σ11,σ12}2(1+S)pS2+cSIp-1-p2σ222Ip+2+M0F(x,0)π¯(dx)-F(S^,0)-Mλ+L-αS-1-p4min{σ11,σ12}2(1+S)pS2-1-p4σ222Ip+2+σ2222MI2+c2μMSI+MF(S,0)-F(S,I)+Mσ21σ22+Yf22(u)λ(du)I+M0F(x,0)π¯(dx)-F(S^,0)=G(S,I)+M0F(x,0)π¯(dx)-F(S^,0),

where

L=supt{μ+σ1122+Yf11(u)λ(du)+cI+σ11σ12+Yf12(u)λ(du)S+σ1222S2+α-1-p4min{σ11,σ12}2(1+S)pS2+cSIp-1-p4σ222Ip+2},G(S,I)=-Mλ+L-αS-1-p4min{σ11,σ12}2(1+S)pS2-1-p4σ222Ip+2+σ2222MI2+c2μMSI+MF(S,0)-F(S,I)+Mσ21σ22+Yf22(u)λ(du)I.

From the expression of G(SI), we can deduce that

Case 1. If S0+, then it is obvious that G(S,I)-;

Case 2. If S+, obviously we have G(S,I)-;

Case 3. If I+, then G(S,I)-;

Case 4. If I0+, it is easy to see that

G(S,I)-Mλ+L+σ2222MI2+c2μMSI+MF(S,0)-F(S,I)+Mσ21σ22+Yf22(u)λ(du)I,

according to Assumption 1, F(SI) is continuous at I=0 uniformly, hence it is obvious that F(S,0)-F(S,I) tends to 0 as I tends to 0+. Consequently, we obtain that

G(S,I)-Mλ+L-2.

Now we proceed to define the bounded closed set

Uε=(S,I)R+2,εS1ε,εI1ε, taking ε>0 sufficiently small. From what we have discussed it follows that

G(S,I)-1,(S,I)R+2\Uε.

On the other hand, for any (S,I)R+2, there exists a positive constant H such that G(S,I)H. Consequently, we have

-EV(S(0),I(0))EV(S(t),I(t))-EV(S(0),I(0))=0tELV(S(τ),I(τ))dτ0tEGS(τ),I(τ)dτ+ME0t0F(x,0)π¯(dx)dτ-0tF(S^(τ),0)dτ.

According to the ergodicity of S^(t), we get

0lim inft1t0tEG(S(τ),I(τ))dτ=lim inft1t0tE(G(S(τ),I(τ)))I{(S(τ),I(τ))Uεc}+E(G(x(s),y(s)))I{(S(τ),I(τ))Uε}dτlim inft1t0t-P((S(τ),I(τ))Uεc)+HP((S(τ),I(τ))Uε)dτ-1+(1+H)lim inft1tP((S(τ),I(τ))Uε)dτ,

which follows that

lim inft1t0tP(τ,(S(0),I(0)),Uε)dτ11+H,(S(0),I(0))R+2, 15

where P(t,(S(0),I(0)),·) is the transition probability of (S(t), I(t)). Inequality (15) and the invariance of R+2 imply that there exist an invariant probability measure of system (x(t), y(t)) on R+2. Furthermore, the independence between standard Brownian motions Bi(t),  i=1,2,3 indicates that the diffusion matrix is non-degenerate. In addition, it is easy to see the existence of an invariant probability measure is equivalent to a positive recurrence. Therefore, system (4) has a unique stationary distribution π and it has the ergodic property. On the other hand, assertions (a) and (b) can refer to [13, 56]. The proof is complete.

Lemma 3

Assume that S(t),I(t) is the positive solution of system (4) with initial value S(0),I(0)R+2, then for any 0θ1, there exists a positive constant K(θ) such that

limtsupESθK(θ),limtsupEIθK(θ).

Proof

Consider the Lyapunov function

V(S(t),I(t))=(1+S+I)θ.

By simple calculation on the basis of Ito^’s formula, we obtain

dV(S(t),I(t))=θ(1+S+I)θ-1α-μS-μ+ρ+γI+θ(θ-1)2(1+S+I)θ-2σ11S+σ12S22+σ21I+σ22I22+Y1+S+I+f11S+f12S2+f21I+f22I2θ-1+S+Iθ-θ1+S+Iθ-1f11S+f12S2+f21I+f22I2λ(du)dt+θ1+S+Iθ-1σ11S+σ12S2dB1(t)+σ21I+σ22I2dB2(t)+Y1+S+I+f11S+f12S2+f21I+f22I2θ-1+S+IθN~(dt,du).

Applying Ito^’s formula to eηtV(S(t),I(t)), we have

d(eηtV(S(t),I(t)))=ηeηtV(S(t),I(t))+eηtdV(S(t),I(t))=eηtη(1+S+I)θ+eηtθ(α+μ)(1+S+I)θ-1-θμ(1+S+I)θ-θ(ρ+γ)I(1+S+I)θ-1dt+θ(θ-1)2eηt(1+S+I)θ-2σ11S+σ12S22+σ21I+σ22I22dt+eηtY1+S+I+f11S+f12S2+f21I+f22I2θ-1+S+Iθ-θ1+S+Iθ-1f11S+f12S2+f21I+f22I2λ(du)dt+eηtθ(1+S+I)θ-1σ11S+σ12S2dB1(t)+σ21I+σ22I2dB2(t)+eηtY1+S+I+f11S+f12S2+f21I+f22I2θ-1+S+IθN~(dt,du), 16

where η is a positive constant which satisfies η>μθ.

Denote

G=θ(α+μ)(1+S+I)θ-1-(η-μθ)(1+S+I)θ-θ(ρ+γ)I(1+S+I)θ-1+θ(θ-1)2(1+S+I)θ-2σ11S+σ12S22+σ21I+σ22I22+Y1+S+I+f11S+f12S2+f21I+f22I2θ-1+S+Iθ-θ1+S+Iθ-1f11S+f12S2+f21I+f22I2λ(du).

According to the inequation

xr1+r(x-1),x0,0r1,i=1kaipkp-1i=1kaip,p1,

it follows

Gθ(α+μ)(1+S+I)θ-1-(η-μθ)(1+S+I)θ-θ(1-θ)54min{σ122,σ222,1}(1+S+I)θ+2K(θ),θ[0,1].

Integrating both sides of (16) from 0 to t and then taking expectations

EeηtV(S(t),I(t))V(S(0),I(0))+K(θ)(eηt-1)η

This completes the proof.

Remark 5

If θ=1, by virtue of Lemma 3 and Theorem 4, one can see that

limt1t0tS(τ)dτ=R+2xπ(dx,dy),limt1t0tI(τ)dτ=R+2yπ(dx,dy)a.s..

Although information about the stationary distribution π is not known yet, the above result implies that S(t) and I(t) are persistent in the mean.

Examples and numerical simulations

Numerical simulation only with white noise

In this section, we give some numerical simulation examples to illustrate the effect of disturbances on the SIR epidemic model. Since it is difficult to get the explicit value of λ, we first consider the following equation with saturated incidence rate but without the perturbation of Le´vy jumps, i.e., fij=0, i=1,2,3, j=1,2.

dS(t)=α-μS(t)-βS(t)I(t)1+mI(t)dt+σ11S(t)+σ12S2(t)dB1(t),dI(t)=βS(t)I(t)1+mI(t)-(μ+ρ+γ)I(t)dt+σ21I(t)+σ22I2(t)dB2(t),dR(t)=γI(t)-μR(t)dt+σ31R(t)+σ32R2(t)dB3(t), 17

The values of parameters in model (17) and initial values of SIR are shown in the following table.

Example 1

Consider model (17) with parameters in Table 1, we take the white noise intensities as σij=0.01, i=1,2,3, j=1,2. By using MATLAB software, we compute that

λ=0F(x,0)π(dx)-(μ+ρ+γ+σ2122)=β0xπ(dx)-(μ+ρ+γ+σ2122)0.046>0,

According to Theorem 4, this means that the disease will persist and system (17) has an unique ergodic stationary distribution. Through the trajectory images of S(t), I(t) and R(t) shown in Fig. 1, one can easily find that the number of all the three sub-populations fluctuated around a nonzero number, which means that the disease persists in a long term.

Table 1.

Parameters of the epidemic system (4)

Description and Parameters Value References
Recruitment rate (α) 2 person day-1 [57, 58]
Natural death rate of each sub-population (μ) 0.05 day-1 [57, 58]
Mortality rate induced by the disease (ρ) 0.001 day-1 [57, 58]
Recovery rate of infected individuals (γ) 0.002 day-1 [57, 58]
Transmission rate (β) 0.004 person-1 day-1 [57, 58]
Saturation factor that measures the inhibitory effect (m) 0.002 person-1 day-1 [57, 58]
Initially susceptibles (S0) 20 [57, 58]
Initially infected (I0) 15 [57, 58]
Initial recovered (R0) 10 [57, 58]
Fig. 1.

Fig. 1

Simulations of the solution in stochastic system (17) with white noise σ11=σ12=σ21=σ22=σ31=σ32=0.01. The graph shows that the three sub-populations are persistent, which means that the disease will spread among people

Next, we choose other parameter values such that λ<0, which can indicate the disease will be extinct in a long time. The only difference between the two examples is the intensities of white noise. Consider model (17) with σ11=0.01,σ12=0.01,σ21=0.8,σ22=0.01,σ31=0.01,σ32=0.01, then by software we obtain λ-0.274<0. According to Theorem 3, we can know that I(t) will go to zero exponentially with probability one while S(t) converges to the ergodic process S¯(t). Through the curve trajectories in Fig. 2, one can see that the number of infected and recovered populations tends to zero eventually, and this implies that the disease can be brought under control and stopped spreading among people.

Fig. 2.

Fig. 2

Simulations of the solution in stochastic system (17) with white noise σ11=0.01,σ12=0.01,σ21=0.8,σ22=0.01,σ31=0.01,σ32=0.01. The curves in the graph show that both the infected and the recovered population will eventually decrease to zero, which means that the disease will eventually disappear

Numerical simulation with white noise and Le´vy jumps

Although we cannot get the exact mathematical expression of λ at present, some corresponding visualized results can be obtained by numerical simulation. Now, we take into account the interference of Le´vy jumps to study the effects of this noise. At first, we present the equation.

dS(t)=α-μS(t-)-βS(t-)I(t-)1+mI(t-)dt+σ11S(t-)+σ12S2(t-)dB1(t)+Yf11(u)S(t-)+f12(u)S2(t-)×N~dt,du,dI(t)=βS(t-)I(t-)1+mI(t-)-(μ+ρ+γ)I(t-)dt+σ21I(t-)+σ22I2(t-)dB2(t)+Yf21(u)I(t-)+f22(u)I2(t-)×N~dt,du,dR(t)=γI(t-)-μR(t-)dt+σ31R(t-)+σ32R2(t-)dB3(t)+Yf31(u)R(t-)+f32(u)R2(t-)×N~dt,du, 18

Example 2

Based on the parameter values in Table 1, we set the intensities of white noise and Le´vy noise as σij=fij=0.01, i=1,2,3, j=1,2. When the noise intensities are relatively small, the effect of external disturbance on epidemic system (18) is weak, in addition, the dynamic properties of the stochastic model are similar to those of the deterministic model. From Fig. 3, it is easy to see that the numbers of S(t), I(t), R(t) are stable in the mean which also indicates that the disease will be persistent in a long term under the relatively weak noise.

Fig. 3.

Fig. 3

Simulations of the solution in stochastic system (18) with white noise σij=0.01, i=1,2,3, j=1,2 and jump noise fij=0.01, i=1,2,3, j=1,2. The curves in the figure indicate a persistent presence of susceptible, infected and recovered individuals

On the other hand, we increase the intensity of Le´vy noise and set it to f21=f22=0.8. It is obvious that the only difference between the two examples is the value of f21 and f22. Now, the external noise plays an important role in the dynamics of disease transmission, and its influence on the stochastic system cannot be ignored. Through the curve trajectories in Fig. 4, it is obvious that the susceptible still remain stable on average, while both the infected and the recovered disappeared eventually. This also reflects that when there is a strong external disturbance, the disease can be controlled and does not spread in the population.

Fig. 4.

Fig. 4

Simulations of the solution in stochastic system (18) with white noise σij=0.01, i=1,2,3, j=1,2 and jump noise f11=f12=f31=f32=0.01 while 21=f22=0.8. As time goes on, the number of infected and recovered people tends to zero, which means that the disease will stop spreading and eventually disappear

Based on the numerical simulations above, it is easy to find that both white noise and Le´vy jumps can suppress the spread of the disease. As the intensities of the white noise and Le´vy jumps increase, the disease disappeared eventually.

Conclusion

Based on the pervasiveness of randomness in nature, which includes mild noises and some massive, abrupt fluctuations, a stochastic SIR epidemic model with general disease incidence rate and Le´vy jumps is studied in this paper. Through rigorous theoretical analysis, we first present that the solution of model (4) is global and unique. Then, we investigate the existence of exponential ergodicity for the corresponding one-dimensional disease-free system (7) and a threshold λ is established, which is represented by the stationary distribution π¯ of (7) and the parameters in model (4). Through the symbol of the threshold, we can classify the extinction and persistence of the disease. To be specific, when λ<0, the number of the infected population will tend to zero exponentially which means the disease will extinct finally. Meanwhile, in case of λ>0, system (4) exists an ergodic stationary distribution on R+2 which also means the disease is permanent.

However, since the explicit analytic formula of invariant measure π¯ cannot be obtained so far, the exact expression of λ cannot be known accordingly, whereas from the threshold we can still get a series of dynamic behaviors and characteristics of model (4). According to the mathematical expression of the threshold λ, a surprising finding is that neither f11(u) nor f12(u) has an effect on the value of λ. In addition, both the linear perturbation parameters σ21 of white noise and f21(u) of Le´vy jumps have a negative effect on the value of λ, while the second-order perturbation parameters have little effect.

In our numerical simulation, one can easily find that when the intensities of noises are relatively small, the disease will persist. However, with the increase in noise intensity, the curves of the solution (SIR) to model (4) fluctuate more obvious. Finally, when noise intensity is relatively high, the number of infected and recovered people tends to zero, which indicates that the disease tends to disappear. In other words, it implies that both the white noise and Le´vy jumps can suppress the outbreak of the disease.

Funding

The authors thank the support of the National Natural Science Foundation of China (Grant nos. 11801566, 11871473) and the Fundamental Research Funds for the Central Universities of China (No. 19CX02059A).

Data availability

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Data Availability Statement

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.


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