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. 2017 Jan 16;2017:7294761. doi: 10.1155/2017/7294761

Threshold Dynamics in Stochastic SIRS Epidemic Models with Nonlinear Incidence and Vaccination

Lei Wang 1, Zhidong Teng 2,*, Tingting Tang 2, Zhiming Li 2
PMCID: PMC5282465  PMID: 28194223

Abstract

In this paper, the dynamical behaviors for a stochastic SIRS epidemic model with nonlinear incidence and vaccination are investigated. In the models, the disease transmission coefficient and the removal rates are all affected by noise. Some new basic properties of the models are found. Applying these properties, we establish a series of new threshold conditions on the stochastically exponential extinction, stochastic persistence, and permanence in the mean of the disease with probability one for the models. Furthermore, we obtain a sufficient condition on the existence of unique stationary distribution for the model. Finally, a series of numerical examples are introduced to illustrate our main theoretical results and some conjectures are further proposed.

1. Introduction

As is well known, transmissions of many infectious diseases are inevitably affected by environment white noise, which is an important component in realism, because it can provide some additional degrees of realism compared to their deterministic counterparts. Therefore, in recent years, stochastic differential equation (SDE) has been used widely by many researchers to model the dynamics of spread of infectious disease (see [15] and the references cited therein). There are different possible approaches to include effects in the model. Here, we mainly introduce three approaches. The first one is through time Markov chain model to consider environment noise in SIS model (see, e.g., [6] and the references cited therein). The second is with parameters perturbation (see [2, 5, 7] and the references cited therein). The last issue to model stochastic epidemic system is to perturb around the positive equilibria of deterministic models (see, e.g., [1, 8, 9] and the references cited therein).

Now, we consider stochastic epidemic models with parameters perturbation. The incidence rate of a disease denotes the number of new cases per unit time, and this plays an important role in the study of mathematical epidemiology. In many epidemic models, the bilinear incidence rate βSI is frequently used (see [2, 5, 7, 8, 1017]), and the saturated incidence rate βSI/(1 + aI) is also frequently used (see, e.g., [1822]). Comparing with bilinear incidence rate and saturated incidence rate, Lahrouz and Omari [23] and Liu and Chen [24] introduced a nonlinear incidence rate βSI/φ(I) into stochastic SIRS epidemic models. In [25], Tang et al. investigated a class of stochastic SIRS epidemic models with nonlinear incidence rate βf(S)g(I):

dS=ΛβfSgIμS+δRdtσfSgIdBt,dI=βfSgIμ+α+γIdt+σfSgIdBt,dR=γIμ+δRdt. (1)

Lahrouz et al. [26] studied a deterministic SIRS epidemic model with nonlinear incidence rate βSI/φ(I) and vaccination. If the transmission of the disease is changed by nonlinear incidence rate βf(S)g(I), and to make the model more realistic, let us suppose that the death rates of the three classes in the population are different, then a more general deterministic SIRS model is described by the following ordinary differential equation:

S˙=1qΛβfSgIdS+pS+εR,I˙=βfSgIdI+γI,R˙=qΛ+pS+γIdR+εR, (2)

where S(t), I(t), and R(t) denote the numbers of susceptible, infectious, and recovered individuals at time t, respectively. Λ denote a constant input of new members into the susceptible per unit time. q is the rate of vaccination for the new members. p is the rate of vaccination for the susceptible individuals. dS is the natural mortality rate or the removal rate of the S. dI is the removal rate of the infectious and usually is the sum of natural mortality rate and disease-induced mortality rate. dR is the removal rate of the recovered individual. γ is the recovery rate of infective individual. ε is the rate at which the recovered individual loses immunity. β represents the transmission coefficient between compartments S and I, and βf(S)g(I) denotes the incidence rate of the disease. For biological reasons, we usually assume that functions f(S) and g(I) satisfy the following properties:

  • (H1)

    g(I) is two-order continuously differentiable function; g(I)/I is monotonically nondecreasing with respect to I; g(0) = 0 and g′(0) > 0.

  •  (H2)

    f(S) is two-order continuously differentiable function; f′(S) ≥ 0 and f′′(S) ≤ 0 for all S ≥ 0, and f(0) = 0.

It is well known that the basic reproduction number for model (2) is defined by R0 = βf(S0)g′(0)/(dI + γ), where S0 = [(1 − q)dR + ε]Λ/(dS(dR + ε) + pdR). Applying the Lyapunov function method and the theory of persistence for dynamical systems, we can prove that, when R0 < 1, model (2) has a globally asymptotically stable disease-free equilibrium E0 = (S0, 0, R0) and, when R0 > 1, model (2) has a unique endemic equilibrium E(S, I, R) and disease I is permanent.

In this paper, we extend model (1) to more general cases. As in [11], taking into account the effect of randomly fluctuating environment, we assume that fluctuations in the environment will manifest themselves mainly as fluctuations in parameters β, dS, dI, and dR in model (2) change to random variables β~, d~S, d~I, and d~R such that

β~=β+error0,d~S=dS+error1,d~I=dI+error2,d~R=dR+error3. (3)

Accordingly, model (2) becomes

dS=1qΛβfSgIdS+pS+εRdtfSgIerror0dtSerror1dt,dI=βfSgIdI+γIdt+fSgIerror0dtIerror2dt,dR=qΛ+pS+γIdR+εRdtRerror3dt. (4)

By the central limit theorem, the error term erroridt (0 ≤ i ≤ 3) may be approximated by a normal distribution with zero mean and variance σi2dt (0 ≤ i ≤ 3), respectively. That is, erroridt=N~(0,σi2dt). Since these erroridt may correlate with each other, we represent them by l-dimensional Brownian motion B(t) = (B1(t),…, Bl(t)) as follows:

erroridt=j=1lσijdBjt,0i3, (5)

where σij are all nonnegative real numbers. Therefore, model (4) is characterized by the following Itô stochastic differential equation:

dS=1qΛβfSgIdS+PS+εRdtfSgIj=1lσ0jdBjtSj=1lσ1jdBjt,dI=βfSgIdI+γIdt+fSgIj=1lσ0jdBjtIj=1lσ2jdBjt,dR=qΛ+pS+γIdR+εRdtRj=1lσ3jdBjt. (6)

Model (6) in the special case where f(S) = S, g(I) = I, and p = q = 0 has been investigated by Yang and Mao in [11] and in the special case where σ1j = σ2j = σ3j = 0  (1 ≤ jl) and p = q = 0 also has been discussed in [25]. It is well known that, in a stochastic epidemic model, the dynamical behaviors, like the extinction, persistence, stationary distribution, and stability of the model, are the most interesting topics. Therefore, in this paper, as an important extension and improvement of the results given in [11, 25], we aim to discuss the dynamical behaviors of model (6). Particularly, we will explore the stochastic extinction and persistence in the mean of disease with probability one and the existence of stationary distribution.

This paper is organized as follows. In Section 2, we introduce some preliminaries to be used in later sections. In Section 3, we establish the threshold condition for stochastic extinction of disease with probability one of model (6). In Section 4, we deduce the threshold conditions for the disease being stochastically persistent and permanent in the mean with probability one. In Section 5, we discuss the existence of the stationary distribution of model (6) under some sufficient conditions. In Section 6, the numerical simulations are presented to illustrate the main results obtained in this paper and some conjectures are further proposed. Finally, in Section 7, a brief conclusion is given.

2. Preliminaries

Through this paper, we let (Ω, , {t}t≥0, P) be a complete probability space with a filtration {t}t≥0 satisfying the usual conditions (that is, it is right continuous and increasing while 0 contains all P-null sets). In this paper, we always assume that stochastic model (6) is defined on probability space (Ω, , {t}t≥0, P). Furthermore, we denote R+3 = {(x, y, z) : x > 0, y > 0, z > 0}, σi2 = ∑j=1lσij2, 0 ≤ i ≤ 3, and σ2 = ∑i=03σi2.

Firstly, on the existence and uniqueness of global positive solution for model (4) we have the following result.

Lemma 1 . —

Assume that (H1) and (H2) hold; then, for any initial value (S(0), I(0), R(0)) ∈ R+3, model (6) has a unique solution (S(t), I(t), R(t)) defined for all t ≥ 0, and the solution will remain in R+3 with probability one.

This lemma can be proved by using a similar argument as in the proof of Theorem 3.1 given in [11]. We hence omit it here.

Lemma 2 . —

Assume that (H1) and (H2) hold and let (S(t), I(t), R(t)) be the solution of model (6) with initial value (S(0), I(0), R(0)) ∈ R+3. Then lim supt(S(t) + I(t) + R(t)) <   a.s. Moreover, let h(x, y, z) be any continuous function defined on R+3; then for each 1 ≤ jl we have

limt1t0thSs,Is,RsdBjs=0. (7)

Proof —

Let N(t) = S(t) + I(t) + R(t); then we have from model (6)

dNtΛdSStdIItdRRtdtPtΛμNtdtPt, (8)

where μ = min {dS, dI, dR} and P(t) = ∑j=1l(σ1jS(t) + σ2jI(t) + σ3jR(t))dBj(t). By the comparison theorem of stochastic differential equations, we further have

NtN0eμt+Λμ1eμtQt, (9)

where

Qt=j=1l0teμtsσ1jSs+σ2jIs+σ3jRsdBjs. (10)

Define X(t) = N(0) + A(t) − U(t) − Q(t), where A(t) = (Λ/μ)(1 − eμt) and U(t) = N(0)(1 − eμt). It is clear that from Lemma 1 and (9) X(t) is nonnegative for t ≥ 0, and A(t) and U(t) are continuous adapted increasing processes for t ≥ 0 and A(0) = U(0) = 0. Therefore, by Theorem 3.9 given in [27], we obtain that limtX(t) <   a.s. exists. From (9), we further have

limsuptNt<  a.s. (11)

Denote

Mjt=0thSs,Is,RsdBjs. (12)

By (11), we have

1tMj,Mjt1t0thSs,Is,Rs2dssupt0hSt,It,Rt2<. (13)

Hence, the strong law of large number (see [27, 28]) implies limt(1/t)Mj(t) = 0  a.s. This completes the proof.

For any function h(t) defined on R+0 = [0, +), we denote the average value on [0, t] by 〈h(t)〉 = (1/t)∫0th(s)ds.

Lemma 3 . —

Assume that (H1) and (H2) hold. Let (S(t), I(t), R(t)) be any positive solution of model (6); then

St=1qdR+εΛdSdR+ε+pdRdIdR+ε+dRγdSdR+ε+pdRIt+φt, (14)

where function φ(t) is defined for all t ≥ 0 satisfying limtφ(t) = 0.

Proof —

Taking integration from 0 to t for model (6), we get

StS0t=1qΛβStgItdS+pSt+εRt1t0tj=1lSsgIsσ0j+Ssσ1jdBjs,ItI0t=βStgItdI+γIt+1t0tj=1lSsgIsσ0jIsσ2jdBjs,RtR0t=qΛ+γIt+pStdR+εRt1t0tj=1lRsσ3jdBjs. (15)

Hence, we have

dR+εStS0t+ItI0t+ε·RtR0t=1qdR+εΛdSdR+ε+pdRStdIdR+ε+dRγIt1t·0tj=1NdR+εSsσ1j+Isσ2j+εRsσ3jdBjs. (16)

With a simple calculation from (16) we can easily obtain formula (14) with which φ(t) is defined by

φt=1dSdR+ε+pdRdR+ε·StS0t+ItI0t+εRtR0t+1t·0tj=1ldR+εSsσ1j+Isσ2j+εRsσ3jdBjs. (17)

By Lemma 2, we further have limtφ(t) = 0  a.s.

Lemma 4 . —

Assume that (H1) and (H2) hold and σ1j = σ2j = σ3j = 0  (1 ≤ jl). Then, for any solution (S(t), I(t), R(t)) of system (6) with (S(0), I(0), R(0)) ∈ R+3, one has

limsuptSt+It+RtS¯,  a.s., (18)

where S¯=Λ/μ. Furthermore, the region

Γ=S,I,R:S>0,I>0,R>0,S+I+RS¯   a.s. (19)

is positive invariant with probability one for model (6), where μ = min⁡{dS, dI, dR}.

In fact, for N(t) = S(t) + I(t) + R(t), from model (6) we have

dNtΛdSStdIItdRRtdtΛμNtdt,  a.s. (20)

This implies that (18) holds, and set Γ is positive invariant with probability one for model (6).

Lemma 5 . —

Assume that (H1) and (H2) hold, σ1j = σ2j = σ3j = 0  (1 ≤ jl), dS = dR, and dI = dS + α with constant α ≥ 0. Then, for any solution (S(t), I(t), R(t)) of model (6) with (S(0), I(0), R(0)) ∈ R+3, one has

St=Λ1qdS+εdSdS+ε+p+Ht+Gt,  a.s.t0, (21)

where

Ht=pΛ1qdS+εdSdS+εdS+ε+pedS+ε+ptR0qΛdS+ε1p1eptedS+εt+ΛdSS0+I0+R0·1p+ε1ep+εtedSt, (22)
Gt=Itα0tedStsIsdsγ0tedS+εtsIsds+p0tedS+ε+ptsIsds+pα0tedS+ε+pts·0sedSsuIududs+pγ0tedS+ε+pts·0sedS+εsuIududs. (23)

Proof —

Since

dNt=ΛdSNtαItdt,  a.s., (24)

then

Nt=ΛdS+N0ΛdSedStα0tedStsIsds,  a.s., (25)

where N(0) = S(0) + I(0) + R(0). From the third equation of model (6) we have

Rt=qΛdS+ε+R0qΛdS+εedS+εt+p0tedS+εtsSsds+γ0tedS+εtsIsds,  a.s. (26)

Therefore,

St=Λ1qdS+εdSdS+εItR0qΛdS+εedS+εt+N0ΛdSedStp0tedS+εtsSsdsα0tedStsIsdsγ0tedS+εtsIsds. (27)

Let y(t) = ∫0te(dS + ε)sS(s)ds; then

dyt=edS+εtStdt=pyt+Λ1qdS+εdSdS+εedS+εtItedS+εtR0qΛdS+ε+N0ΛdSeεtαeεt0tedSsIsdsγ0tedS+εsIsdsdt. (28)

Solving y(t), we obtain

yt=eptΛ1qdS+εdSdS+εdS+ε+pedS+ε+pt10tedS+ε+psIsdsR0qΛdS+ε1pept1+N0ΛdS1ε+peε+pt1γ0teps0sedS+εuIududsα0tedS+ε+ps0sedSsuIudsdsdt. (29)

Substituting (29) into (27), we immediately obtain (21)–(23). This completes the proof.

Remark 6 . —

When dSdR in model (6), whether we can also establish a similar result as in Lemma 5 still is an interesting open problem.

Consider the following n-dimensional stochastic differential equation:

dxt=bxdt+r=1mσrxdBrt, (30)

where x = (x1, x2,…, xn), σr(x) = (σr1(x), σr2(x),…, σrn(x)), and Br(t)  (1 ≤ rm) are standard Brownian motions defined on the above probability space. The diffusion matrix is defined by

Ax=aijxn×n,aijx=r=1mσrixσrjx. (31)

For any second-order continuously differentiable function V(x), we define

LVx=i=1nVxxibix+12i,j=1n2Vxxixjaijx. (32)

The following lemma gives a criterion for the existence of stationary distribution in terms of Lyapunov function.

Lemma 7 (see [27]). —

Assume that there is a bounded open subset D in Rn with a regular (i.e., smooth) boundary such that

  • (i)

    there exist some i = 1,2,…, n and positive constant η > 0 such that aii(x) ≥ η for all xD;

  • (ii)

    there exists a nonnegative function V(x) : DcR such that V(x) is second-order continuously differentiable function and that, for some θ > 0, LV(x)≤−θ for all xDc, where Dc = RnD.

Then (30) has a unique stationary distribution π. That is, if function f is integrable with respect to the measure π, then for all x0Rn

Plimt1t0tfxu,x0du=Rnfx0πdx0=1. (33)

To study the permanence in mean with probability one of model (6) we need the following result on the stochastic integrable inequality.

Lemma 8 (see [13]). —

Assume that functions YC(R+ × Ω, R+) and ZC(R+ × Ω, R+) satisfy limt(Z(t)/t) = 0  a.s. If there is T > 0 such that

lnYtν0tν0tYsds+Zt  a.s., (34)

for all tT, then

liminft1t0tYsdsν0ν  a.s. (35)

3. Extinction of Disease

For the convenience of following statements, we denote

S0=1qdR+εΛdSdR+ε+pdR,S1=dIdR+ε+dRγdSdR+ε+pdR. (36)

We further define a threshold value

R~0=fS0g0β+j=1lσ0jσ2jdI+γfS0g02σ022dI+γσ222dI+γ. (37)

Theorem 9 . —

Assume that (H1) and (H2) hold. If one of the following conditions holds:

  • (a)

    R~0<1  and  σ02f(S0)g′(0) ≤ β + ∑j=1lσ0jσ2j,

  • (b)

    σ0 > 0  and  (β + ∑j=1lσ0jσ2j)2/2σ02 − (dI + γ + (1/2)σ22) < 0,

then, for any initial value (S(0), I(0), R(0)) ∈ R+3, one has

limsuptlnItt<0  a.s. (38)

That is, disease I is stochastically extinct exponentially with probability one. Moreover,

limtSt=S0,limtRt=ΛqdS+pdSdR+ε+pdR  a.s. (39)

Proof —

Applying Itô's formula to model (6) leads to

lnIt=lnI0+0tfxsds+j=1lσ0j0tfSsgIsIsdBjsσ2jBjt, (40)

where x = (S, I) and

fx=fSgIIβ+j=1lσ0jσ2jdI+γ+σ22212fSgII2σ02. (41)

Assume that condition (b) holds. Since

fxtβ+j=1lσ0jσ2j22σ02dI+γ+12σ22, (42)

then from (40)

lnIttlnI0t+β+j=1lσ0jσ2j22σ02dI+γ+12σ22+j=1lσ0j1t0tfSsgIsIsdBjsσ2j1t0tdBjs. (43)

By Lemma 2, we have

limt1t0tSsgIsIsdBjs=0,limt1t0tdBjs=0  a.s.,1jl. (44)

Therefore,

limsuptlnIttβ+j=1lσ0jσ2j22σ02dI+γ+12σ22<0. (45)

Assume that condition (a) holds. Choose constant ϵ > 0 such that β + ∑j=1lσ0jσ2jg′(0)f(ϵ)σ02. We compute that

fx=fSgIIβ+j=1lσ0jσ2jdI+γ+σ22212fSgII2σ02=fSgIIβ+j=1lσ0jσ2jdI+γ+σ222+12f2ϵg2II2σ0212fSfϵ2g2II2σ02fSfϵg2II2σ02β+j=1lσ0jσ2jgIIfϵσ02g2II2fSdI+γ+σ222+12fϵg02σ02. (46)

When σ02 = 0, which implies σ0j = 0  (1 ≤ jl), we have from (46)

fxβfSgIIdI+γ+σ222βg0fSdI+γ+σ222. (47)

Since

fSfS0+fSfS0=fS0+fξSS0, (48)

where ξ ∈ (S, S0), from (H2), we can obtain f′(ξ)(SS0) ≤ f′(S0)(SS0). Hence, we have

fSfS0+fS0SS0. (49)

According to (14), (40), and (49), we have

lnIttlnI0t+βg01t0tfSsdsdI+γ+σ222+j=1lσ0j1t0tfSsgIsIsdBjsσ2jBjtt=lnI0t+βg0fS0βg0·fS0S1It+βfS0g0φtdI+γ+σ222+j=1lσ0j1t0tfSsgIsIsdBjsσ2j1t0tdBjs. (50)

Hence, from (44) and Lemma 3, we finally have

limsuptlnIttβfS0g0dI+γ+σ222  a.s. (51)

When σ02 ≠ 0, from (40) and (46) we have

lnIttlnI0t+1t0tβ+j=1Nσ0jσ2jgIsIsfϵσ02g2IsIs2fSsds+j=1Nσ0j1t0tfSsgIsIsdBjsσ2jBjttdI+γ+σ222+12fϵg02·σ02. (52)

Define a function

Fu=β+j=1lσ0jσ2jufϵσ02u2. (53)

Clearly, F(u) is a monotone increasing for u ∈ [0, (β + ∑j=1lσ0jσ2j)/2f(ϵ)σ02] and monotone decreasing for u ∈ [(β + ∑j=1lσ0jσ2j)/2f(ϵ)σ02, ). With condition β + ∑j=1lσ0jσ2jg′(0)f(ϵ)σ02, that is, g(I)/Ig′(0) ≤ (β + ∑j=1lσ0jσ2j)/2f(ϵ)σ02, we have

FgIIFg0=β+j=1lσ0jσ2jg0fϵσ02g02. (54)

Hence, by (14) and (49), we have

lnIttlnI0t+g0β+j=1lσ0jσ2jfϵ·σ02g01t0tfSsds+j=1lσ0j1t0tfSsgIsIsdBjsσ2j1t0tdBjsdI+γ+σ222+12g0·fϵ2σ02lnI0t+g0β+j=1lσ0jσ2jfϵσ02g0fS0+fS0φtdI+γ+σ222+12g0fϵ2σ02+j=1lσ0j1t0tSsgIsIsdBjsσ2j1t0tdBjs. (55)

Choose ϵ = S0; from (44) and Lemma 3, we finally have

limsuptlnIttfS0g0β+j=1lσ0jσ2jdI+γ+σ22212fS0g02σ02  a.s. (56)

From (45), (51), and (56), it follows that (38) holds.

Since limtI(t) = 0  a.s., by (14) of Lemma 3 and the last equation of (15), we further obtain

limtSt=S0,limtRt=ΛqdS+pdSdR+ε+pdR  a.s. (57)

This completes the proof.

Remark 10 . —

Condition (b) in Theorem 9 can be rewritten in the following form:

σ02>β+j=1lσ0jσ2j22dI+γ+1/2σ22. (58)

It is clear that

fS0g0β+j=1lσ0jσ2jdI+γ+1/2σ22fS0g02β+j=1lσ0jσ2j24dI+γ+1/2σ2221. (59)

Therefore, when condition (b) holds, from (58) we also have

R~0=fS0g0β+j=1lσ0jσ2jdI+γfS0g02σ022dI+γσ222dI+γ<fS0g0β+j=1lσ0jσ2jdI+γfS0g02β+j=1lσ0jσ2j24dI+γdI+γ+1/2σ22σ222dI+γ=fS0g0β+j=1lσ0jσ2jdI+γ+1/2σ22fS0g02β+j=1lσ0jσ2j24dI+γ+1/2σ222×dI+γ+1/2σ22dI+γσ222dI+γ1. (60)

Remark 11 . —

From Remark 10 above, we see that in Theorem 9 if condition (a) holds, then we directly have R~0<1, and if condition (b) holds, then we also have R~0<1. Therefore, an interesting open problem is whether we can establish the extinction of disease I with probability one for model (6) only when R~0<1.

4. Stochastic Persistence in the Mean

In this section, we discuss the stochastic persistence and permanence in the mean with probability one for model (6) only for the following two special cases: (1) σ0j = 0  (1 ≤ jl) and (2) σ1j = σ2j = σ3j = 0  (1 ≤ jl). Furthermore, we also assume that in model (6) function f(S) ≡ S.

4.1. Case σ0j = 0  (1 ≤ jl)

When f(S) = S and σ0j = 0  (1 ≤ jl) in model (6), we have

R~0=S0g0βdI+γσ222dI+γ. (61)

Theorem 12 . —

Assume that (H1) holds, f(S) = S, and σ0j = 0  (1 ≤ jl). If R~0>1; then disease I in model (6) is stochastically persistent in the mean; that is,

liminft1t0tIrdr>0  a.s. (62)

Proof —

Let (S(t), I(t), R(t)) be any positive solution of model (6). Lemma 2 implies that there is a constant M0 > 0 such that S(t) + I(t) + R(t) ≤ M0  a.s. for all ≥0. Define a Lyapunov function

UI=I0It1gIdI. (63)

Using Itô's formula to model (6) leads to

dUI=βSdI+γIgIσ222I2g2IgIdtj=1lσ2jIgIdBjt=βSdI+γIgI1g0σ222I2g2IgI1g0dI+γg0+σ222g0dtj=1lσ2jIgIdBjt. (64)

From (H1), which implies that g′(I) ≤ g(I)/Ig′(0), we have

I2g2IgI1g0=I2g2IgIg0+g0I2g2I1g02g0IgI+1g0IgI1g0Mg0+1IgI1g0, (65)

where M = sup0≤IM0{I/g(I)}. Since limI→0+(I/g(I)) = 1/g′(0), then 0 < M < . Substituting (65) into (64) and then integrating from 0 to t ≥ 0, we get

UIt1t0tβSrdI+γ+σ222Mg0+1·IrgIr1g0dI+γg0+σ222g0drj=1l1tMjt, (66)

where Mj(t) = ∫0tσ2j(I(r)/g(I(r)))dBj(r). From Lemma 2, we have

limt1tMjt=0  a.s.,1jl. (67)

Define a function G(I) as follows. When I > 0, G(I) = I/g(I), and when I = 0, G(0) = limI→0(I/g(I)) = 1/g′(0). Then G(I) is continuous for I ≥ 0 and differentiable for I > 0. Applying Lagrange's mean value theorem to G(I) − G(0), we have from (66)

UIt1t0tβSrdI+γ+σ222Mg0+1·sup0IM0GIIrdI+γg0+σ222g0drj=1l1tMjt, (68)

Substituting (14) into (68), it follows that

UItβS0βS1+dI+γ+σ222Mg0+1sup0IM0GI·ItdI+γg0+σ222g0j=1l1tMjt+βφt. (69)

Since

UIt1tI0ItIgI1IdI1tI0ItM1IdI=MlnItlnI0t, (70)

we have

lnItt1MβS0dI+γg0σ222g01MβS1+dI+γ+σ222Mg0+1sup0IM0GI·It+Φt, (71)

where

Φt=1Mj=1l1tMjt+βφtM+1tlnI0. (72)

From (67) and Lemma 3 we have limtΦ(t) = 0. Finally, by Lemma 8, we obtain

liminft1t0tIrdrI, (73)

where

I=dI+γR~01βS1+dI+γ+1/2σ22Mg0+1sup0IM0GIg0. (74)

This completes the proof.

Remark 13 . —

In the proof of Theorem 12, we easily see that three constants M0, M = sup0≤IM0{I/g(I)}, and I given in (74) are dependent on every solution (S(t), I(t), R(t)) of model (6). This shows that in Theorem 12 we only obtain the stochastic persistence in the mean of the disease.

4.2. Case σ1j = σ2j = σ3j = 0  (1 ≤ jl)

When f(S) = S and σ1j = σ2j = σ3j = 0  (1 ≤ jl) in model (6), we have

R~0=βS0g0dI+γS02g02σ022dI+γ. (75)

In order to obtain the stochastic permanence in the mean with probability one for model (6), we need to introduce a new threshold value

R¯0=βS0g0dI+γS¯2g02σ022dI+γ. (76)

Obviously, we have R¯0R~0.

Theorem 14 . —

Assume that (H1) holds, f(S) = S, and σ1j = σ2j = σ3j = 0  (1 ≤ jl). If R¯0>1, then disease I in model (6) is stochastically permanent in the mean, that is,

liminft1t0tIrdrdI+γR¯01βS1+dI+γmax0IS¯GIg0  a.s., (77)

where function G(I) is defined in Theorem 12 above.

Proof —

Let U(I) = ∫I(0)I(t)(1/g(I))dI; using Itô's formula to model (6) and (18) leads to

dUI=βSdI+γIgIσ022S2gIdtj=1lSσ0jdBjtβSdI+γIgI1g0σ02S¯2g02+dI+γg0dtj=1lSσ0jdBjt. (78)

Similarly to above proof of Theorem 12, we have

UIt1t0tβSrdI+γmax0IS¯GIIrσ02S¯2g02+dI+γg0drj=1l0tSrσ0jdBjr. (79)

Substituting (14) into (79) yields

UItβS0βS1+dI+γmax0IS¯GI1t0tIrdrσ02S¯2g02+dI+γg0j=1l1t0tSrσ0jdBjr+βφt. (80)

Since by (18)

UIt1tI0ItS¯gS¯1IdIS¯lnS¯lnI0gS¯t, (81)

(80) can be rewritten as

1t0tIrdrdI+γR¯01+g0ΦtβS1+dI+γmax0IS¯GIg0, (82)

where

Φt=j=1l1t0tSrσ0jdBjr+βφtS¯lnS¯lnI0gS¯t. (83)

By Lemmas 2 and 3, it follows that limtΦ(t) = 0. Therefore, taking t in (82) it follows that (77) holds. This completes the proof.

Using Lemma 5, we can establish the following result which shows that R~0 can be a threshold value for the stochastic permanence of disease I in the mean for a more special case of model (6): dS = dR and dI = dS + α with constant α ≥ 0.

Theorem 15 . —

Assume that (H1) holds, f(S) = S, σ1j = σ2j = σ3j = 0  (1 ≤ jl), dS = dR, and dI = dS + α with constant α ≥ 0. If R~0>1; then disease I in model (6) is stochastically permanent in the mean; that is,

liminft1t0tIrdrdS+α+γR~01βS1+dI+γmax0IS¯GI+M0g0  a.s., (84)

where function G(I) is defined in above Theorem 12 and

M0=61+α2dS2+γ2dS+ε2+p2dS+ε+p2+pα2dS2dS+ε+p2+pγ2dS+ε2dS+ε+p2ΛdS. (85)

Proof —

Firstly, when dS = dR and dI = dS + α, then threshold value R~0 becomes

R~0=βS0g0dS+α+γS02g02σ022dS+α+γ, (86)

where S0 = Λ[(1 − q)dS + ε]/dS(dS + ε + p).

Let U(I) = ∫I(0)I(t)(1/g(I))dI; similarly to above proof of Theorem 12, we have

dUIβSdS+α+γmax0IS¯GII12σ02S2g0dS+α+γg0dtj=1lSσ0jdBjt. (87)

Since S2 = S02 + 2S0(SS0)+(SS0)2, we further have

UItβStdS+α+γmax0IS¯GIIt12σ02S02g0σ02S0g0StS0dS+α+γg012σ02g0StS02j=1l1t0tSσ0jdBjs. (88)

Substituting (14) and (21) of Lemma 5 into (88), using inequality (a + b)2 ≤ 2(a2 + b2), it follows that

UItdS+α+γg0R~01βS1+dS+α+γmax0IS¯GIIt+βσ02S0g0φtσ02g0H2t+G2tj=1l1t0tSσ0jdBjs. (89)

From expression (22) of H(t), we easily have limtH2(t)〉 = 0. By (18), without loss of generality, we can assume that S(t) + I(t) + R(t) ≤ Λ/dS  a.s. for all t ≥ 0. Hence,

G2t6I2t+α20tedStsIsds2+γ20tedS+εtsIsds2+p20tedS+ε+ptsIsds2+pα2·0tedS+ε+pts0sedSsuIududs2+pγ20tedS+ε+pts·0sedS+εsuIududs26ΛdSIt+α2ΛdS20tedStsIsds+γ2ΛdSdS+ε·0tedS+εtsIsds+p2ΛdSdS+ε+p·0tedS+ε+ptsIsds+pα2λdS2dS+ε+p·0tedS+ε+pts0sedSsuIududs+pγ2ΛdSdS+εdS+ε+p0tedS+ε+pts·0sedS+εsuIududs. (90)

By computing, we obtain

1t0t0sedSsuIududs1dSIt,1t0t0sedS+εsuIududs1dS+εIt,1t0t0sedS+ε+psuIududs1dS+ε+pIt,1t0t0sedS+ε+psu0uedSuvIvdvduds1dSdS+ε+pIt,1t0t0sedS+ε+psu0uedS+εuvIvdvduds1dS+εdS+ε+pIt. (91)

Therefore, we finally have

G2tM0It. (92)

From (81), (89), and (92) we further obtain

1t0tIrdrdS+α+γR~01+g0ΦtβS1+dI+γmax0IS¯GI+M0g0, (93)

where

Φt=j=1l1t0tSrσ0jdBjr+βσ02S0g0φtσ02g0H2tS¯lnS¯lnI0gS¯t. (94)

By Lemmas 2 and 3, it follows that limtΦ(t) = 0. Therefore, taking t in (93) it follows that (84) holds. This completes the proof.

5. Stationary Distribution

In this section, we discuss the stationary distribution of model (6) by using Lyapunov function method. We firstly define the diffusion matrix A(x) = h(x)hT(x), where x = (S, I, R),

hx=h11xh12xh1lxh21xh22xh2lxh31xh32xh3lx,h1jx=fSgIσ0jfSσ1j,h2jx=fSgIσ0jIσ2j,h3jx=Rσ3j. (95)

Furthermore, we denote by aii(x)  (i = 1,2, 3) the diagonal elements of matrix A(x). We have aii(x) = ∑j=1lhij2(x).

Theorem 16 . —

Assume that (H1) holds, f(S) = S, and there is a constant ρ > 0 such that aii(x) > ρ, for any xR+3 and i = 1,2, 3, γ > p, dI > dS, and γ(dS + dR) > p(dI + dR). If R0 > 1 and

dS+pγdS+dRpdI+dRγpε+dSC1S2dI+γγdS+dRpdI+dRγpε+dIC2I2dIdSdR+εγp+dRC3R2>dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIσ22εβgIγp+C1S2+C2I2+C3R2, (96)

where

C1=2dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIg02σ02εβgIγp+2γdS+dRpdI+dRσ12γpε+σ2,C2=2γdS+dRpdI+dRσ22γpε+σ2,C3=dIdSσ32γp+σ2 (97)

and (S, I, R) is the unique endemic equilibrium of model (2), then model (6) has a unique stationary distribution.

Proof —

We here use the Lyapunov function method to prove this theorem. The proof given here is similar to Theorem 5.1 in [11]. But, due to nonlinear function g(I), the Lyapunov function structured in the following is different from that given in [11].

By Lemma 7, it suffices to find a nonnegative Lyapunov function V(x) and compact set KR+3 such that LV(x)≤−C for some C > 0 and xR+3/K.

Denote x = (S, I, R) ∈ R+3. Define the function

V1x=12RR2. (98)

Calculating LV1(x), we have

LV1x=RR·pSS+γIIdR+εRR+12σ32R2dR+εσ32RR2+pSSRR+γIIRR+σ32R2. (99)

Define the function

V2x=IIIlnII. (100)

Calculating LV2(x), we have

LV2x=1IIβSgIdI+γI+I2·j=1lSgIIσ0jσ2j2=II·βSgIIgII+βgIISS+12Iσ22+12Iσ02S2g2II2j=1lISgIIσ0jσ2jβgIISSII+12Iσ22+12·Iσ02g02S2j=1lISgIIσ0jσ2jβ·gIISSII+2Iσ02g02·SS2+2Iσ02g02S2+Iσ22. (101)

Define the function

V3x=12S+ISI2. (102)

Calculating LV3(x), we get

LV3x=S+ISIdS+pSS+εRRdI+γII+12σ12S2+12·σ22I2+j=1lSIσ1jσ2jdS+p2σ12SS2dI+γ2σ22II2+εSSRRdS+p+dI+γSSII+εIIRR+2σ12S2+2σ22I2. (103)

Define the function

V4x=12S+I+RSIR2. (104)

Calculating LV4(x), we get

LV4x=S+I+RSIR·ΛdSSdIIdRR+12·j=1lSσ1j+Iσ2j+Rσ3j2dSSS2dIII2dRRR2dS+dI·SSIIdS+dRSSRRdI+dRIIRR+12σ12+σ22+σ32·S2+I2+R2dSσ2SS2dIσ2II2dRσ2RR2dS+dISSIIdS+dRSS·RRdI+dRIIRR+σ2S2+I2+R2. (105)

Define the Lyapunov function for model (6) as follows:

Vx=dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIεβgIγpV2x+dIdSγpV1x+γdS+dRpdI+dRγpεV3x+V4x. (106)

Then from (99), (101), (103), and (105) we have

LVxdS+pγdS+dRpdI+dRγpε+dSC1SS2dI+γγdS+dRpdI+dRγpε+dIC2II2dIdSdR+εγp+dRC3RR2+C1S2+C2I2+C3R2+dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIσ22εβgIγp. (107)

If condition (96) holds, then the surface

dS+pγdS+dRpdI+dRγpε+dSC1SS2+dI+γγdS+dRpdI+dRγpε+dIC2II2+dIdSdR+εγp+dRC3RR2=dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIσ22εβgIγp+C1S2+C2I2+C3R2 (108)

lies in the interior of R+3. Hence, we can easily obtain that there exists a constant C > 0 and a compact set K of R+3 such that, for any xR+3/K,

LVxC. (109)

Therefore, model (6) has a unique stationary distribution. This completes the proof.

Remark 17 . —

In fact, the variances of errors usually should be small enough to justify their validity of real data; otherwise, the data may not be considered as a good one. It is clear that when σij are very small, condition (96) is always satisfied.

6. Numerical Examples

To verify the theoretical results in this paper, we next give numerical simulations of model (6).

Throughout the following numerical simulations, we choose l = 2 and g(I) = I/(1 + ωI2), where ω is a positive constant. It is easy to verify that assumption (H1) holds. By Milstein's higher-order method [29, 30], we drive the corresponding discretization equations of model (6):

Si+1=Si+1qΛβfSiIi1+ωIi2dSi+PSi+εRiΔtfSiIi1+ωIi2j=1lσ0jξjiΔt+12σ0j2ξji21ΔtSij=1lσ1jξjiΔt+12σ1j2ξji21Δt,Ii+1=Ii+βfSiIi1+ωIi2dI+γIiΔt+fSiIi1+ωIi2·j=1lσ0jξjiΔt+12σ0j2ξji21ΔtIij=1lσ2jξjiΔt+12σ2j2ξji21Δt,Ri+1=Ri+qΛ+pSi+γIidR+εRiΔtRij=1lσ3jξjiΔt+12σ3j2ξji21Δt. (110)

Here, ξji  (i = 1,2,…, j = 1,…, l) are N(0,1)-distributed independent Gaussian random variables and Δt > 0 is time increment.

Example 1 . —

In model (6), we take f(S) = S/(1 + 0.2S), Λ = 1.85, q = 0.52, β = 0.52, p = 0.24, ε = 0.2, γ = 0.3, ω = 2, dS = 0.4, dI = 0.21, dR = 0.3, σ01 = 0.15, σ02 = 0.99, σ11 = 0.23, σ12 = 0.17, σ21 = 0.14, σ22 = 0.72, σ31 = 0.47, and σ32 = 0.93. By computing, we obtain R~0=0.8939<1, σ02f(S0)g′(0)−(β + ∑j=12σ0jσ2j) = 0.3442 > 0, and (β + ∑j=12σ0jσ2j)2/2σ02 − (dI + γ + (1/2)σ22) = 0.005 > 0. This shows that conditions (a) and (b) of Theorem 9 do not hold. The numerical simulations (see Figure 1) suggest that disease I(t) of model (6) is still stochastically extinct with probability one. Therefore, as an improvement of Theorem 9, we have the following interesting conjecture.

Figure 1.

Figure 1

The path of I(t) for the stochastic model (6) with parameters in Example 1, compared to the corresponding deterministic model. (a) is trajectories of the solution I(t) with the initial value I(0) = 0.05 and (b) with the initial value I(0) = 0.5. The disease of model (6) is extinct with probability one.

Conjecture 2 . —

Assume (H1) holds. The disease I(t) in model (6) is stochastically extinct with probability one only when R~0<1 holds.

Example 3 . —

In model (6), we take f(S) = S/(1 + 1.5S), Λ = 3, q = 0.2, β = 2.1, p = 0.3, ε = 0.8, γ = 0.1, ω = 2, dS = 0.5, dI = 0.8, dR = 0.4, σ01 = 0.8, σ02 = 1.2, σ11 = 0.3, σ12 = 0.75, σ21 = 0.45, σ22 = 0.8, σ31 = 0.8, and σ32 = 0.3. By computing, we obtain R~0=1.3554>1. From the numerical simulations given in Figure 2, it is shown that disease I(t) of model (6) is not only stochastically persistent in the mean but also stochastically persistent with probability one. Therefore, as an improvement of Theorem 12, we have the following interesting conjecture.

Figure 2.

Figure 2

The paths of I(t) and (1/t)∫0tI(s)ds for the stochastic model (6) with parameters in Example 3, (a) with the initial value I(0) = 0.05 and (b) with the initial value I(0) = 0.5.

Conjecture 4 . —

Assume (H1) holds. The disease I(t) in model (6) is stochastically persistent in the mean only when R~0>1.

Example 5 . —

In model (6), we take f(S) = S/(1 + 0.1S), Λ = 1.2, q = 0.5, β = 1.5, p = 0.9, ε = 1.1, γ = 0.9, ω = 2, dS = 0.6, dI = 0.35, dR = 0.4, σ01 = 0.4, σ02 = 0.2, σ11 = 0.1, σ12 = 0.45, σ21 = 0.2, σ22 = 0.1, σ31 = 0.2, and σ32 = 0.3. By computing, we obtain R¯0=0.8687<1 and R~0=1.2931>1. The numerical simulations given in Figure 3 show that disease I(t) of model (6) is still stochastically permanent in the mean. Therefore, combining Theorem 12 and Theorem 14, we can obtain the following interesting conjecture about the stochastic permanence in the mean of disease I(t).

Figure 3.

Figure 3

The paths of I(t) and (1/t)∫0tI(s)ds for the stochastic model (6) with parameters in Example 5, (a) with the initial value I(0) = 0.05 and (b) with the initial value I(0) = 0.5.

Conjecture 6 . —

Assume (H1) holds. The disease I(t) in model (6) is stochastically permanent in the mean only when R~0>1.

Example 7 . —

In model (6), we take f(S) = S, Λ = 0.67, q = 0.02, β = 1.7, p = 0.05, ε = 3, γ = 0.99, ω = 4, dS = 0.29, dI = 0.53, dR = 0.39, σ01 = 0.025, σ02 = 0.02, σ11 = 0.0121, σ12 = 0.01, σ21 = 0, σ22 = 0, σ31 = 0.02, and σ32 = 0.01. By computing, we obtain that the basic reproduction number for deterministic model (2) is R0 = 2.5279 > 1 and the unique endemic equilibrium of model (2) is (S, I, R) = (1.4230,0.3845,0.1372). Furthermore, we can verify that there is a constant ρ > 0 such that aii(x) > ρ for any xR+3  (i = 1,2, 3), dI  −  dS = 0.24 > 0, γ  −  p = 0.94 > 0, γ(dS + dR) − p(dI + dR) = 0.6272 > 0, and

dS+pγdS+dRpdI+dRγpε+dSC1S2dI+γγdS+dRpdI+dRγpε+dIC2I2dIdSdR+εγp+dRC3R2dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIσ22εβgIγp+C1S2+C2I2+C3R2=0.0147>0. (111)

That is, all conditions in Theorem 16 are satisfied. The stationary distributions about the susceptible, infected, and removed individuals obtained through the numerical simulations are reported in Figure 4, which shows that after some initial transients the population densities fluctuate around the deterministic steady-state values S = 1.4230, I = 0.3845, and R = 0.1372.

Figure 4.

Figure 4

The solution of stochastic model (6) and its histogram with parameters in Example 7.

Example 8 . —

In model (6), we take f(S) = S/(1 + 0.4S), Λ = 2.5, q = 0.5, β = 1.4, p = 0.7, ε = 0.9, γ = 0.51, ω = 1.89, dS = 0.7, dI = 0.45, dR = 0.58, σ01 = 0.4, σ02 = 0.2, σ11 = 0.21, σ12 = 0.1, σ21 = 0.1, σ22 = 0.24, σ31 = 0.2, and σ32 = 0.1. By computing, we obtain that the basic reproduction number for deterministic model (2) is R0 = 1.6484 > 1 and the unique endemic equilibrium of model (2) is (S, I, R) = (1.7242,0.5082,1.8352). Furthermore, we can verify that there is not a constant ρ > 0 such that aii(x) > ρ for any xR+3 and i = 1,2, 3, dIdS = −0.25 < 0, γp = −0.19 < 0, γ(dS + dR) − p(dI + dR) = −0.0682 < 0 and

dS+pγdS+dRpdI+dRγpε+dSC1S2dI+γγdS+dRpdI+dRγpε+dIC2I2dIdSdR+εγp+dRC3R2dS+dIγpε+dS+p+dI+γγdS+dRpdI+dRIσ22εβgIγp+C1S2+C2I2+C3R2=5.5051<0. (112)

That is, the conditions in Theorem 16 are not satisfied. However, we obtain that threshold value R~0=2.7192>1. The numerical simulations given in Figure 5 show the stationary distributions about the susceptible, infected, and removed individuals. Therefore, we can obtain the following interesting conjecture about the stationary distribution for model (6), as described in the conclusion part.

Figure 5.

Figure 5

The solution of stochastic model (6) and its histogram with parameters in Example 8.

Conjecture 9 . —

Assume (H1) holds. Model (6) has a unique stationary distribution only when R~0>1.

7. Conclusion

In this paper, as an extension of the results given in [11, 25], we investigated the dynamical behaviors for a stochastic SIRS epidemic model (6) with nonlinear incidence and vaccination. In model (6), the disease transmission coefficient β and the removal rates dS, dI, and dR are affected by noise. Some new basic properties of model (6) are found in Lemmas 2, 3, and 5. Applying these lemmas, we established a series of new threshold value criteria on the stochastic extinction, persistence in the mean, and permanence in the mean of the disease with probability one. Furthermore, by using the Lyapunov function method, a sufficient condition on the existence of unique stationary distribution for model (6) is also obtained.

The stochastic persistence and permanence in the mean of the disease for model (6) are established in this paper only for the special cases: f(S) ≡ S and (1) σ0j = 0  (1 ≤ jl) or (2) σ1j = σ2j = σ3j = 0  (1 ≤ jl). However, for the general model (6), particularly, f(S) ≠ S and (σ1j, σ2j, σ3j)≠(0,0, 0)  (1 ≤ jl), whether we also can establish similar results still is an interesting open problem.

In fact, under the above case, from the proofs of Theorems 12 and 14, we can see that an important question is to deal with terms βf(S(t)) and f2(S(t))g′(I(t)). If we may get

βfStβfS0+v1StS0  a.s.,f2StgItf2S0g0+v2StS0  a.s., (113)

where v1 and v2 are two positive constants; then the following perfect result may be established.

Assume that (H1) holds. If R~0>1, then disease I in model (6) is stochastically persistent in the mean; that is,

liminft1t0tIrdr>0  a.s. (114)

Another important open problem is about the existence of stationary distribution of model (6), that is, whether we can establish a similar result as in Theorem 16 when f(S) is a nonlinear function. The best perfect result on the stationary distribution is to prove that model (6) possesses a unique stationary distribution only when threshold value R~0>1. But this is a very difficult open problem.

However, the numerical examples given in Section 6 propose some affirmative answer for above open problems.

Acknowledgments

This research is supported by the Natural Science Foundation of Xinjiang (Grant no. 2016D03022) and the National Natural Science Foundation of China (Grant nos. 11401512, 11271312, and 11660176).

Competing Interests

The authors declare that they have no competing interests.

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