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. 2017 Jun 15;2017(1):138. doi: 10.1186/s13660-017-1418-8

Stochastic inequalities and applications to dynamics analysis of a novel SIVS epidemic model with jumps

Xiaona Leng 1, Tao Feng 1, Xinzhu Meng 1,2,
PMCID: PMC5487947  PMID: 28680241

Abstract

This paper proposes a new nonlinear stochastic SIVS epidemic model with double epidemic hypothesis and Lévy jumps. The main purpose of this paper is to investigate the threshold dynamics of the stochastic SIVS epidemic model. By using the technique of a series of stochastic inequalities, we obtain sufficient conditions for the persistence in mean and extinction of the stochastic system and the threshold which governs the extinction and the spread of the epidemic diseases. Finally, this paper describes the results of numerical simulations investigating the dynamical effects of stochastic disturbance. Our results significantly improve and generalize the corresponding results in recent literatures. The developed theoretical methods and stochastic inequalities technique can be used to investigate the high-dimensional nonlinear stochastic differential systems.

Keywords: stochastic SIVS epidemic model, Lévy jumps, persistence in mean, double epidemic diseases, Doob’s martingale inequality, Hölder’s inequality

Introduction

Mathematical inequalities are widely used in many fields of mathematical analysis, especially differential systems [15]. Recently, the inequality technique was applied to stochastic differential systems [611], impulsive differential systems [1221], and impulsive stochastic differential systems [22], thus some new results have been obtained.

As an important factor threatening the safety of human life and property, the investigation of epidemic has received extensive attention from experts in various fields [2327]. Generally speaking, medical researchers often use observation and experimental methods to study the behavior of epidemics. Recently, however, a number of experts in the field of mathematics have also been interested in the study of epidemics. They have used mathematical methods to analyze the spread and control of epidemics [2831]. Kermack and McKendrick’s pioneering work on the development of an epidemic disease is one of the typical examples. They established an SIS compartment model and proposed the famous threshold theory, which has laid a solid foundation for the study of the dynamics of infectious diseases [30].

The SIS model based on the deterministic ordinary differential equation is given by

{S˙(t)=AβS(t)I(t)uS(t)+rI(t),I˙(t)=βS(t)I(t)(u+α+r)I(t). 1

In system (1), βS(t) represents the number of people infected by a patient within a unit time at t. But in reality, the number of people who can be exposed to a patient at a time is limited. To this end, some authors have introduced a saturated infection rate to study the dynamic behavior of the disease [3234]. In addition, all creatures on the earth are infected by a variety of environmental noises, of course, the disease is no exception. Motivated by this, some scholars have studied the infection system with environmental noises (such as Brownion noise, Markov noise and Lévy noise) [3538]. Meanwhile, populations may be affected by different kinds of infectious diseases at the same time. Therefore, it is of great significance to study the epidemic model with multiple diseases [3941].

Recently, Meng et al. [39] considered a novel nonlinear stochastic SIS epidemic model with double epidemic hypothesis as follows:

{dS=(AuS(t)β1S(t)I1(t)a1+I1(t)β2S(t)I2(t)a2+I2(t)+r1I1(t)+r2I2(t))dtdS=σ1S(t)I1(t)a1+I1(t)dB1(t)σ2S(t)I2(t)a2+I2(t)dB2(t),dI1=(β1S(t)I1(t)a1+I1(t)(u+α1+r1)I1(t))dt+σ1S(t)I1(t)a1+I1(t)dB1(t),dI2=(β2S(t)I2(t)a2+I2(t)(u+α2+r2)I2(t))dt+σ2S(t)I2(t)a2+I2(t)dB2(t). 2

They obtained the threshold of system (2) for the extinction and the persistence in mean of the epidemic diseases. Based on system (2), recently, Zhang et al. [40] proposed an SIS system with double epidemic diseases driven by Lévy jumps as follows:

{dS=(AuS(t)β1S(t)I1(t)a1+I1(t)β2S(t)I2(t)a2+I2(t)+r1I1(t)+r2I2(t))dtdS=+σ1S(t)dB1(t)+Zγ1(u)S(t)N˜(dt,du),dI1=(β1S(t)I1(t)a1+I1(t)(u+α1+r1)I1(t))dtdI1=+σ2I1(t)dB2(t)+Zγ2(u)I1(t)N˜(dt,du),dI2=(β2S(t)I2(t)a2+I2(t)(u+α2+r2)I2(t))dtdI2=+σ3I2(t)dB3(t)+Zγ3(u)I2(t)N˜(dt,du). 3

In model (3), the authors discussed in detail the conditions for persistence in mean and extinction of each epidemic disease. Therefore, they discussed the persistence in mean of susceptible individuals under different conditions. The above two studies provide a theoretical basis for the study of infectious diseases. But they just discussed the persistence in mean and extinction of epidemic diseases under different conditions. In real life, however, when an epidemic outbreak occurs, we do not sit idly but take measures to control the spread of the epidemic disease. There are many ways to suppress the spread of a disease, for instance, cut off transmission routes, pay attention to food hygiene, vaccination and so on [42, 43]. Vaccination is an effective method of preventing infectious diseases and many scientists have explored the effect of vaccination on diseases [4447].

Motivated by the above works, in this paper, we propose a stochastic SIVS model with double epidemic diseases and Lévy jumps under vaccination as follows:

{dS=((1q)Λ(u+p)S(t)β1S(t)I1(t)α1+I1(t)β2S(t)I2(t)α2+I2(t)dS=+r1I1(t)+r2I2(t)+δV(t))dtdS=+σ3SdB3(t)+Zγ3(u)S(t)N˜(dt,du),dI1=(β1S(t)I1(t)α1+I1(t)(u+d1+r1)I1(t))dtdI1=+σ1I1dB1(t)+Zγ1(u)I1(t)N˜(dt,du),dI2=(β2S(t)I2(t)α2+I2(t)(u+d2+r2)I2(t))dtdI2=+σ2I2dB2(t)+Zγ2(u)I2(t)N˜(dt,du),dV=[qΛ+pS(t)(u+δ)V(t)]dt+σ4VdB4(t)dV=+Zγ4(u)V(t)N˜(dt,du), 4

where S(t), I1(t), I2(t), V(t), respectively, stand for the density of susceptible, infective A, infective B and vaccinated individuals at time t, Λ is a constant input of new numbers into the population, q means a fraction of vaccinated for the newborn, βi is the infection rate coefficient from Ii(t) (i=1,2) to S(t), respectively. u represents the natural death rate of S(t), I1(t), I2(t), V(t), p is the proportional coefficient of vaccinated for the susceptible, ri, di is the recovery rate and disease-caused death rate of Ii(t), i=1,2, respectively. δ stands for the rate of losing their immunity for vaccinated individuals, α1 and α2 are the so-called half-saturation constants, respectively. B(t)=(B1(t),B2(t),B3(t),B4(t)) is a standard Brownian motion with intensity σi>0 (i=1,2,3,4).

Throughout this paper, let (Ω,F,{F}t0,P) be a complete probability space with a filtration {Ft}t0 satisfying the usual conditions (i.e. it is increasing and right continuous while F0 contains all P-null sets). Function Bi(t) (i=1,2,3,4) is a Brownian motion defined on the complete probability space Ω, the intensity of Bi(t) is σi (i=1,2,3,4). N˜(dt,du)=N(dt,du)λ(du)dt, N is a Poisson counting measure on (0,+)×Z, λ is the characteristic measure of N on a measurable subset Z, λ(Z)<+, γi (i=1,2,3,4) is bounded and continuous with respect to λ and is B(Z)×Ft-measurable. For an integrable function X(t) on [0,+), we define X(t)=1t0tX(s)ds.

The main purpose of this paper is to investigate the threshold dynamics of the stochastic SIVS epidemic model. In this paper, by using the Lyapunov method and the technique of a series of stochastic inequalities, we obtain sufficient conditions for the persistence in mean and extinction of the stochastic system and the threshold which governs the extinction and the spread of the epidemic diseases. Our results significantly improve and generalize the corresponding results in recent literatures. The developed theoretical methods and stochastic inequalities technique can be used to investigate the high-dimensional nonlinear stochastic differential systems. In Section 2, we firstly give some lemmas and recall some necessary notations and definitions. Furthermore, we obtain the main results for stochastic disease-free dynamics and stochastic endemic dynamics which imply the extinction and the spread of the epidemic diseases. Finally, this paper gives the conclusions and numerical simulations investigating the dynamical effects of stochastic disturbance.

Main results

The main purpose of this paper is to investigate the threshold dynamics of the stochastic SIVS epidemic model. In this section, by using the technique of a series of stochastic inequalities, we obtain sufficient conditions for the persistence in mean and extinction of the stochastic system and the threshold which governs the extinction and the spread of epidemic diseases.

Preliminary knowledge

For the sake of notational simplicity, we define

bi=12σi2+Z[γi(u)ln(1+γi(u))]λ(du),i=1,2,3,4;Ri=βi(u+δuq)Λu2+uδ+upαi(u+di+ri+bi),i=1,2;γˇ(u)=max{γ1(u),γ2(u),γ3(u),γ4(u)};γˆ(u)=min{γ1(u),γ2(u),γ3(u),γ4(u)};ϕ=Z[(1+γˇ(u))ϱ1γˆ(u)]v(du);σ=max{σ1,σ2,σ3,σ4}.

Throughout this paper, suppose that the following two assumptions hold.

Assumption 2.1

The following hold:

  • (i)

    1+γi(u)>0;

  • (ii)

    Z[γi(u)ln(1+γi(u))]λ(du)<, i=1,2,3,4, uZ.

Remark 2.1

This assumption means that the intensities of Lévy noises are not infinite.

Assumption 2.2

Suppose that there exists some ϱ>1 such that the following inequality holds:

b=uϱ12σ2ϕϱ>0.

Definition 2.1

[39]

  • (i)

    The species X(t) is said to be extinctive if limt+X(t)=0;

  • (ii)

    The species X(t) is said to be persistent in mean if limt+X(t)>0.

The following elementary inequality will be used frequently in the sequel.

Lemma 2.1

Burkholder-Davis-Gundy inequality [48]

Let gL2(R+;Rd×m). For any t0, define

x(t)=0tg(s)dB(s),A(t)=t0|g(s)|2ds.

Then, for every p>0, there exist two positive constants cp, Cp such that

cpE|A(t)|p/2E(sup0st|x(s)|p)CpE|A(t)|p/2,t0,

where cp, Cp only depend on p.

Lemma 2.2

Chebyshev inequality [48]

For any c>0, p>0, XLp, the following inequality holds:

P{w:|X(w)|c}cpE|X|p.

Lemma 2.3

Hölder inequality [48]

For any ai,biR and k2, if p,q>1 and 1p+1q=1, the following inequality holds:

|i=1kaibi|(i=1k|ai|p)1/p(i=1k|bi|q)1/q.

Lemma 2.4

Doob’s martingale inequality [48]

Let X be a submartingale taking nonnegative real values, either in discrete or continuous time. That is, for all times s and t with s<t,

XsE[Xt|Fs].

Then, for any constant C>0,

P[sup0tTXtC]E[|XT|]C,

where P denotes the probability measure on the sample space Ω of the stochastic process X:[0,T]×Ω[0,+) and E denotes the expected value with respect to the probability measure P.

Lemma 2.5

[49, 50]

Assume that X(t)R+ is an Itô’s-Lévy process of the form

dX(t)=F(X(t),t)dt+G(X(t),t)dB(t)+ZH(X(t),t,u)N˜(dt,du),

where F:Rn×R+×SRn, G:Rn×R+×SRn and H:Rn×R+×S×ZRn are measurable functions.

Given VC2,1(Rn×R+×S;R+), we define the operator LV by

LV(X,t)=Vt(X,t)+VX(X,t)F(X,t)+12trace[GT(X,t)VXX(X,t)G(X,t)]+Z{V(X+H(X,t))V(X,t)VX(X,t)H(X,t,u)}λ(du),

where

Vt(X,t)=VX(X,t)t,VX(X,t)=(VX(X,t)X1,,VX(X,t)Xn),VXX(X,t)=(2VX(X,t)XiXj)n×n.

Then the generalized Itô’s formula with Lévy jumps is given by

dV(X,t)=LV(X,t)dt+VX(X,t)G(X,t)dB(t)+Z{V(X+H(X,t))V(X,t)}N˜(dt,du).

Lemma 2.6

[51]

Let X(t)C(Ω×[0,+),R+). We have the following conclusions.

  • (i)
    If there exist T>0, λ0>0, λ, m, ni such that when tT,
    lnX(t)λtλ00tX(s)ds+mB(t)+i=1jni0tZln(1+γi(u))Γ˜(ds,du)a.s.,
    then
    {Xλλ0a.s., if λ0;limt+X(t)=0a.s., if λ<0.
  • (ii)
    If there exist T>0, λ0>0, λ>0, m, ni such that when tT,
    lnX(t)λtλ00tX(s)ds+mB(t)+i=1jni0tZln(1+γi(u))Γ˜(ds,du)a.s.,
    then Xλλ0 a.s.

Lemma 2.7

For any initial value (S(0),I1(0),I2(0),V(0))R+4, the solution (S(t),I1(t),I2(t),V(t)) of model (4) has the following property:

limtS(t)+I1(t)+I2(t)+V(t)t=0a.s.

Moreover,

limtS(t)t=0,limtI1(t)t=0,limtI2(t)t=0,limtV(t)t=0a.s.limtlnS(t)t0,limtlnI1(t)t0,limtlnI2(t)t0,limtlnV(t)t0a.s.

Proof

Define

X=S+I1+I2+V,Q(X)=Xϱ.

Applying the generalized Itô’s formula to Q(X), we have

dQ(X)LQdt+ϱXϱ1(σ1I1dB1(t)+σ2I2dB2(t)+σ3SdB3(t)+σ4VdB4(t))+XϱZ[(1+γˇ(u))ϱγˆ]N˜(dt,du), 5

where

LQϱXϱ1(ΛuXd1I1d2I2)+ϱ(ϱ1)2Xϱ2σ2X2+ϕXϱϱXϱ2[ΛX(uϱ12σ2ϕϱ)X2].

Choose a positive constant ϱ>1 that satisfies

b=uϱ12σ2ϕϱ>0.

For any constant k satisfying k(0,bϱ), one has

dektQ(X(t))L[ektQ(X(t))]dt+ektϱXϱ1[σ1I1(s)dB1(s)+σ2I2(s)dB2(s)+σ3S(s)dB3(s)+σ4V(s)dB4(s)]+ektϱXϱZ[(1+γˇ(u))ϱγˆ]N˜(dt,du).

Integrating from 0 to t and taking expectation on both sides of (5), we have

EektQ(X(t))Q(X(0))+E[0t[keksQ(X(s))+eksLQ(X(s))]ds].

Easily, one has

kektQ(X(t))+ektLQ(X(t))kektXϱ(t)+ϱektXϱ2(t)[bX2(t)+ΛX(t)]ϱektsupXR+{Xϱ2[(bkϱ)X2+ΛX]+1}:=ϱektH.

Therefore

E(Xϱ)Xϱ(0)ekt+ϱHkXϱ(0)+ϱH:=M. 6

By Lemma 2.1, applying the Burkholder-Davis-Gundy inequality, integrating equation (5) from 0 to t, and for an arbitrarily small positive constant δ, one has

E[supkδt(k+1)δ(Xϱ(t))]E(X(kδ))ϱ+Y1+Y2M+Y1+Y2,

where

Y1=E{supkδt(k+1)δ|kδtϱXϱ2(s)[bX2(s)+ΛX(s)]ds|}cϱE[supkδt(k+1)δ|kδtXϱ(s)ds|]cϱE[kδ(k+1)δXϱ(s)ds]cϱδE[supkδt(k+1)δXϱ(s)ds],k=1,2,

and

Y2=E{supkδt(k+1)δ|kδtϱXϱ1(s)[σ1I1(s)dB1(s)+σ2I2(s)dB2(s)+σ3S(s)dB3(s)+σ4V(s)dB4(s)]+kδtXϱ(s)Z[(1+γˇ(u))ϱγˆ]N˜(dt,du)|}CϱE[kδ(k+1)δϱ2X2(ϱ1)(σ12I12+σ22I22+σ32S2+σ42V2)ds]12+CϱE{kδ(k+1)δX2ϱZ[(1+γˇ(u))ϱγˆ(u)]2v(du)ds}12Cϱδ12[ϱσ+Z[(1+γˇ(u))ϱγˆ(u)]2v(du)]E[supkδt(k+1)δXϱ],k=1,2,,

where cϱ,Cϱ>0.

So we have

E[supkδt(k+1)δ(Xϱ(t))]E(X(kδ))ϱ+cϱδE[supkδt(k+1)δXϱ(s)ds]+Cϱδ12[ϱσ+Z[(1+γˇ(u))ϱγˆ(u)]2v(du)]×E[supkδt(k+1)δXϱ].

Choose a positive constant δ that satisfies

cϱδ+Cϱδ12[ϱσ+Z[(1+γˇ(u))ϱγˆ(u)]2v(du)]12.

Combining it with equation (6), one has

E[supkδt(k+1)δ(Xϱ(t))]2E(X(kδ))ϱ2M.

Applying the arbitrariness of κX>0 and Lemma 2.2 for Chebyshev’s inequality, one obtains

P{supkδt(k+1)δXϱ(t)>(kδ)1+κX}E[supkδt(k+1)δXϱ(t)](kδ)1+κX2M(kδ)1+κX,k=1,2,.

Applying the Borel-Cantelli lemma [48], for almost all ωΩ, one has

supkδt(k+1)δXϱ(t)(kδ)1+κX 7

holds for all but finitely many k. Therefore, for any positive constant kk0 and almost all ωΩ, there is k0(ω) such that equation (7) holds.

Thus, for almost all ωΩ, once conditions kk0 and kδt(k+1)δ hold, then we have

lnXϱ(t)lnt(1+κX)ln(kδ)ln(kδ)=1+κX. 8

Taking the limit superior on both sides of equation (8) and applying the arbitrariness of κX>0, one has

lim suptlnXϱ(t)lnt1a.s.

Easily, for any ϱ satisfying 1<ϱ<1+2(uϕ)σ2, one has u>ϱ12σ2+ϕ. Therefore

lim suptlnXϱ(t)lnt1ϱa.s.

That is to say, for any constant τ satisfying 0<τ<11ϱ, there is a constant N=N(ω), and once condition tN holds, then we have

lnX(t)(1ϱ+τ)lnt.

Therefore

limtX(t)t=limtS(t)+I1(t)+I2(t)+V(t)t=0lim suptt1ϱ+τt=0a.s.

So

limtS(t)t=0,limtI1(t)t=0,limtI2(t)t=0,limtV(t)t=0a.s.

and

limtlnS(t)t0,limtlnI1(t)t0,limtlnI2(t)t0,limtlnV(t)t0a.s.

This completes the proof. □

Lemma 2.8

For any initial value (S(0),I1(0),I2(0),V(0))R+4, the solution (S(t),I1(t),I2(t),V(t)) of model (4) has the following property:

limt0tI1(s)dB1(s)t=0,limt0tZγ1(u)I1(s)N˜(ds,du)t=0a.s.,limt0tI2(s)dB2(s)t=0,limt0tZγ2(u)I2(s)N˜(ds,du)t=0a.s.,limt0tS(s)dB3(s)t=0,limt0tZγ3(u)S(s)N˜(ds,du)t=0a.s.,limt0tV(s)dB4(s)t=0,limt0tZγ4(u)V(s)N˜(ds,du)t=0a.s.

Proof

Define

X1(t)=0tI1(s)dB1(s),Y1(t)=0tZγ1(u)I1(s)N˜(ds,du),X2(t)=0tI2(s)dB2(s),Y2(t)=0tZγ2(u)I2(s)N˜(ds,du),X3(t)=0tS(s)dB3(s),Y3(t)=0tZγ3(u)S(s)N˜(ds,du),X4(t)=0tV(s)dB4(s),Y4(t)=0tZγ4(u)V(s)N˜(ds,du).

Applying Lemma 2.1 for the Burkholder-Davis-Gundy inequality and Lemma 2.3 for Hölder’s inequality, one has

E[sup0st|X1(s)|ϱ]CϱE[0tI12(θ)dθ]ϱ2CϱE[0t|I12(θ)|dθ]ϱ2,E[sup0st|Y1(s)|ϱ]CϱE[0tZI12(θ)γ12(u)dθ]ϱ2E[sup0st|Y1(s)|ϱ]Cϱ(Zγ12(u)v(du))ϱ2E[0t|I1(θ)|dθ]ϱ2

for 2<ϱ<1+2(uϕ)σ2. Here Cϱ=[ϱϱ+12(ϱ1)ϱ1]ϱ2>0 is a constant.

Applying equation (6), we have

E[supkt(k+1)|X1(s)|ϱ]2MCϱ(k+1)ϱ221+ϱ2MCϱkϱ2.

For any constant κX1>0, applying Lemma 2.4 for Doob’s martingale inequality, one obtains

P{ω:supkt(k+1)|X1(t)|ϱ>k1+κX1+ϱ2}E[supkt(k+1)|X1(k+1)|ϱ]k1+κX1+ϱ221+ϱ2MCϱkϱ2k1+κX1+ϱ221+ϱ2MCϱk1+κX1,k=1,2,.

Applying the Borel-Cantelli lemma, one has

ln|X1(t)|ϱlnt(1+κX1+ϱ2)lnklnk=1+κX1+ϱ2. 9

Taking the limit superior on both sides of equation (9) and applying the arbitrariness of κX>0, one has

lim suptln|X1(t)|lnt12+1ϱa.s.

That is to say, for any constant τ satisfying 0<τ<121ϱ, there is a constant N=N(ω), and once tN, wΩτ holds, then we have

ln|X1(t)|(12+1ϱ+τ)lnt. 10

Dividing both sides of equation (10) by t and taking the limit superior, we have

lim supt|X1(t)|tlim suptt12+1ϱ+τt=0.

Combining it with lim inft|X1(t)|t0, one has

limt|X1(t)|t=limtX1(t)t=0a.s.

Similarly, one obtains

limtlnX2(t)t=0,limtlnX3(t)t=0,limtlnX4(t)t=0,limtlnY1(t)t=0,limtlnY2(t)t=0,limtlnY3(t)t=0,limtlnY4(t)t=0.

This completes the proof. □

Lemma 2.9

For any initial value (S(0),I1(0),I2(t),V(0))R+4, model (4) has a unique positive solution (S(t),I1(t),I2(t),V(t))R+4 on t0 with probability 1.

Proof

The proof is similar to Refs. [9, 44] by defining Q(S,I1,I2,V)=S1lnS+I11lnI1+I21lnI2+V1lnV, and hence is omitted. □

Stochastic disease-free dynamics

Theorem 2.1

Suppose that conditions R1<0 and R2<0 hold. Then, for any initial value (S(0),I1(0),I2(0),V(0))R+4, the solution (S(t),I1(t),I2(t),V(t)) of model (4) has the following property:

limtIi(t)=0,i=1,2,limtS(t)=(u+δuq)Λu2+uδ+up,limtV(t)=(p+uq)Λu2+uδ+up.

That is to say, the two epidemic diseases go to extinct almost surely.

Proof

By equation (4), one has

d(S+I1+I2+δu+δV)=(u+δuq)Λu+δu2+uδ+upu+δSi=12(u+di)Ii+σ3SdB3(t)+Zγ3(u)S(t)N˜(dt,du)+i=12[σiIidBi(t)+Zγi(u)Ii(t)N˜(dt,du)]+δu+δ(σ4VdB4(t)+Zγ4(u)V(t)N˜(dt,du)). 11

Dividing both sides of equation (11) by t and integrating over the time interval 0 to t yield

S(t)=u+δu2+uδ+up[(u+δuq)Λu+δi=12(u+di)Ii(t)Φ(t)], 12

where

Φ(t)=1t{S(t)S(0)+i=12(Ii(t)Ii(0))+δu+δ(V(t)V(0))i=120t[σiIidBi(s)+Zγi(u)Ii(s)N˜(dt,du)]0t[σ3SdB3(s)+Zγ3(u)S(s)N˜(dt,du)]δu+δ0t[σ4VdB4(s)+Zγ4(u)V(s)N˜(dt,du)]}.

Applying Lemmas 2.7 and 2.8, we obtain that

limt+Φ(t)=0a.s. 13

Applying the generalized Itô’s formula in Lemma 2.5 to α1lnI1(t)+I1(t) yields

d[α1lnI1(t)+I1(t)]=[β1S(u+d1+r1)I1α1(u+d1+r1)α1b1]dt+(α1+I1)σ1dB1(t)+Z[α1ln(1+γ1(u))+I1γ1(u)]N˜(dt,du). 14

Dividing both sides of equation (14) by t, integrating over the time interval 0 to t and taking the limit, one obtains that

α1lnI1(t)+I1(t)t=α1lnI1(0)+I1(0)t+β1S(t)(u+d1+r1)I1(t)α1(u+d1+r1)α1b1+1t0t(α1+I1(s))σ1dB1(s)+1t0tZ[α1ln(1+γ1(u))+I1(s)γ1(u)]N˜(dt,du). 15

Combining equations (12) and (15), one obtains

α1lnI1(t)t=β1(u+δuq)Λu2+uδ+upα1(u+d1+r1+b1)β1(u+δ)(u+d2)u2+uδ+upI2(t)(β1(u+δ)(u+d1)u2+uδ+up+(u+d1+r1))I1(t)+αlnI1(0)+I1(0)tI1(t)tβ1(u+δ)u2+uδ+upΦ(t)+1t0t(α1+I1(s))σ1dB1(s)+1t0tZ[α1ln(1+γ1(u))+I1(s)γ1(u)]N˜(dt,du)=β1(u+δuq)Λu2+uδ+upα1(u+d1+r1+b1)β1(u+δ)(u+d2)u2+uδ+upI2(t)(β1(u+δ)(u+d1)u2+uδ+up+(u+d1+r1))I1(t)+Ψ1(t), 16

where

Ψ1(t)=α1lnI1(0)+I1(0)tI1(t)tβ1(u+δ)u2+uδ+upΦ(t)+1t0t(α1+I1(s))σ1dB1(s)+1t0tZ[α1ln(1+γ1(u))+I1(s)γ1(u)]N˜(dt,du).

Similarly, applying the generalized Itô’s formula in Lemma 2.5 to α2lnI2(t)+I2(t) yields

α2lnI2(t)t=β2(u+δuq)Λu2+uδ+upα2(u+d2+r2+b2)β2(u+δ)(u+d1)u2+uδ+upI1(t)(β2(u+δ)(u+d2)u2+uδ+up+(u+d2+r2))I2(t)+Ψ2(t), 17

where

Ψ2(t)=α2lnI2(0)+I2(0)tI2(t)tβ2(u+δ)u2+uδ+upΦ(t)+1t0t(α2+I2(s))σ2dB2(s)+1t0tZ[α2ln(1+γ2(u))+I2(s)γ2(u)]N˜(dt,du).

Applying Lemmas 2.7 and 2.8, we obtain that

limt+Ψi(t)=0,i=1,2 a.s. 18

By taking the limit superior of both sides of equation (16) and equation (17), respectively, one has

lim suptα1lnI1(t)tβ1(u+δuq)Λu2+uδ+upα1(u+d1+r1+b1)=R1<0,lim suptα2lnI2(t)tβ2(u+δuq)Λu2+uδ+upα2(u+d2+r2+b2)=R2<0.

That is to say,

limtIi(t)=0,i=1,2 a.s. 19

Applying (13) and (19) into equation (12), we obtain that

limtS(t)=u+δu2+uδ+up[(u+δuq)Λu+δi=12(u+di)limtIi(t)limtΦ(t)]=(u+δuq)Λu2+uδ+up. 20

By equation (4), one has

d(S+I1+I2+V)=[ΛuSuV(u+d1)I1(u+d2)I2]dt+i=12[σiIidBi(t)+Zγi(u)Ii(t)N˜(dt,du)]+σ3SdB3(t)+Zγ3(u)S(t)N˜(dt,du)+σ4VdB4(t)+Zγ4(u)V(t)N˜(dt,du). 21

Dividing both sides of equation (21) by t, integrating over the time interval t=0 to t and taking the limit, one obtains that

limtV(t)=ΛulimtS(t)i=12u+diulimtIi(t)limtS(t)S(0)+i=12(Ii(t)Ii(0))+V(t)V(0)ut+1ulimt1t0t{i=12[σiIi(s)dBi(s)+Zγ1(u)I1(s)N˜(ds,du)]+σ3S(s)dB3(s)+Zγ3(u)S(s)N˜(ds,du)+σ4V(s)dB4(s)+Zγ4(u)V(s)N˜(ds,du)}ds. 22

Applying (19), (20), Lemmas 2.7 and 2.8, we have

limtV(t)=Λu(u+δuq)Λu2+uδ+up=(p+uq)Λu2+uδ+up.

This completes the proof. □

Stochastic endemic dynamics

Theorem 2.2

For any initial value (S(0),I1(0),I2(0),V(0))R+4, the solution (S(t),I1(t),I2(t),V(t)) of model (4) has the following property:

  • (i)
    If R1>0 and R2<0, then the epidemic disease I1(t) is persistent in mean and I2(t) goes extinct, i.e. limtI1(t)=R1ϒ11>0, limtI2(t)=0 a.s. Moreover,
    limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upR1ϒ11a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)R1ϒ11a.s.
  • (ii)
    If R1<0 and R2>0, then the epidemic disease I1(t) goes extinct and I2(t) is persistent in mean, i.e. limtI1(t)=0, limtI2(t)=R2ϒ21>0 a.s. Moreover,
    limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d2)u2+uδ+upR2ϒ21a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d2)pu(u+δ+p)R2ϒ21a.s.

Proof

Case (i): From equation (16) we have

α1lnI1(t)t=β1(u+δuq)Λu2+uδ+upα1(u+d1+r1+b1)[β1(u+δ)(u+d1)u2+uδ+up+(u+d1+r1)]I1(t)β1(u+δ)(u+d2)u2+uδ+upI2(t)+Ψ1(t)=R1ϒ11I1(t)ϒ12I2(t)+Ψ1(t), 23

where

ϒ11=β1(u+δ)(u+d1)u2+uδ+up+(u+d1+r1),ϒ12=β1(u+δ)(u+d2)u2+uδ+up.

From Theorem 2.1, when R2<0 one has

limtI2(t)=0a.s. 24

Therefore, there exists an arbitrarily small constant ε>0 such that when t is large enough, we have I2(t)<ε. Applying this into equation (23) leads to

R1ϒ11I1(t)+Ψ1(t)α1lnI1(t)tR1ϒ11I1(t)ϒ12ε+Ψ1(t).

Applying Lemma 2.6 and the arbitrariness of ε, we obtain

limtI1(t)=R1ϒ11a.s. 25

Applying (13), (24) and (25) into equation (12), we obtain that

limtS(t)=u+δu2+uδ+up[(u+δuq)Λu+δi=12(u+di)limtIi(t)limtΦ(t)]=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upR1ϒ11. 26

Applying (24), (25), (26), Lemmas 2.7 and 2.8 into equation (22), we have

limtV(t)=Λu(u+δuq)Λu2+uδ+up+(u+δ)(u+d1)u2+uδ+upR1ϒ11u+d1uR1ϒ11=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)R1ϒ11.

Case (ii): From equation (17) we have

α2lnI2(t)t=β2(u+δuq)Λu2+uδ+upα2(u+d2+r2+b2)β2(u+δ)(u+d1)u2+uδ+upI1(t)[β2(u+δ)(u+d2)u2+uδ+up+(u+d2+r2)]I2(t)+Ψ2(t)=R2ϒ21I1(t)ϒ22I2(t)+Ψ2(t), 27

where

ϒ21=β2(u+δ)(u+d1)u2+uδ+up,ϒ22=β2(u+δ)(u+d2)u2+uδ+up+(u+d2+r2).

From Theorem 2.1, when R1<0 one has

limtI1(t)=0a.s. 28

Therefore, there exists an arbitrarily small constant ε>0 such that when t is large enough, we have I1(t)<ε. Applying this into equation (23) leads to

R2ϒ21I2(t)+Ψ2(t)α2lnI2(t)tR2ϒ21I2(t)ϒ22ε+Ψ2(t).

Applying Lemma 2.6 and the arbitrariness of ε, we obtain

limtI2(t)=R2ϒ21a.s. 29

Applying equations (13), (28), (29) into equation (12), we obtain that

limtS(t)=u+δu2+uδ+up[(u+δuq)Λu+δi=12(u+di)limtIi(t)limtΦ(t)]=(u+δuq)Λu2+uδ+up(u+δ)(u+d2)u2+uδ+upR2ϒ21. 30

Applying (28), (29), (30), Lemmas 2.7 and 2.8 into equation (22), we have

limtV(t)=Λu(u+δuq)Λu2+uδ+up+(u+δ)(u+d2)u2+uδ+upR2ϒ21u+d1uR2ϒ21=(p+uq)Λu2+uδ+up(u+d2)pu(u+δ+p)R2ϒ21.

This completes the proof. □

Theorem 2.3

Suppose that conditions R1>0 and R2>0 hold. Let (S(t),I1(t),I2(t),V(t)) be the solution of model (4) with the initial value (S(0),I1(0),I2(0),V(0))R+4.

  • (i)
    If ϒ11R2<ϒ21R1, then the epidemic disease I1(t) is persistent in mean and I2(t) goes extinct, i.e. limtI1(t)=R1ϒ11>0, limtI2(t)=0 a.s. Moreover,
    limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upR1ϒ11a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)R1ϒ11a.s.
  • (ii)
    If ϒ22R1<ϒ12R2, then the epidemic disease I1(t) goes extinct and I2(t) is persistent in mean, i.e. limtI1(t)=0, limtI2(t)=R2ϒ21>0 a.s. Moreover,
    limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d2)u2+uδ+upR2ϒ21a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d2)pu(u+δ+p)R2ϒ21a.s.
  • (iii)
    If ϒ11R2>ϒ21R1, ϒ22R1>ϒ12R2, then the epidemic diseases I1 and I2 are persistent in mean. Moreover,
    limtI1(t)=ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21,limtI2(t)=ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.,limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21limtS(t)=(u+δ)(u+d2)u2+uδ+upϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21limtV(t)=(u+d2)u(u+δ+p)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.

Proof

Case (i): Note that

lim supt+lnI1(t)t0,

there exists an arbitrarily small constant ε>0 such that when t is large enough, we have

lnI1(t)t<ε.

From equation (23) and equation (27), when t is large enough, one has

ϒ11α2lnI2(t)t=ϒ11R2ϒ21R1(ϒ11ϒ22ϒ12ϒ21)I2(t)+ϒ21α1lnI1(t)t+ϒ11Ψ2(t)ϒ21Ψ1(t)ϒ11R2ϒ21R1(ϒ11ϒ22ϒ12ϒ21)I2(t)+ϒ21α1ε+ϒ11Ψ2(t)ϒ21Ψ1(t). 31

Since ϒ11R2<ϒ21R1 and ϒ11ϒ22>ϒ12ϒ21, taking the limit superior of both sides of equation (31), applying equation (18) and the arbitrariness of ε, we have

lim supt+lnI2(t)tϒ11R2ϒ21R1ϒ11α2<0.

That is to say,

limtI2(t)=0a.s.

By using the method of Case (ii) in Theorem 2.2, one obtains the persistence in mean of I1(t), S(t) and V(t), and hence is omitted.

Case (ii): The proof of Case (ii) is similar to the proof of Case (i) in this subsection and hence is omitted.

Case (iii): Since ϒ11R2>ϒ21R1 and ϒ11ϒ22>ϒ12ϒ21, using Lemma 2.6 and the arbitrariness of ε for equation (31), one obtains that

lim supt+I2(t)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s. 32

Similarly, when ϒ22R1>ϒ12R2, we have

lim supt+I1(t)ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21a.s. 33

From equation (32), there exists an arbitrarily small constant ε>0 such that when t is large enough, we have

I2(t)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21+ε. 34

Applying equation (23) into equation (34), one obtains that

α1lnI1(t)t=R1ϒ11I1(t)ϒ12I2(t)+Ψ1(t)R1ϒ11I1(t)ϒ12εϒ12ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21+Ψ1(t).

By using Lemma 2.6 and the arbitrariness of ε, we obtain that

lim inft+I1(t)ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21a.s. 35

Similarly, one obtains

lim inft+I2(t)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s. 36

Applying equations (32), (33), (35) and (36) leads to

limt+I1(t)=ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21,limt+I2(t)=ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s. 37

Applying (13) and (37) into equation (12), we obtain that

limtS(t)=u+δu2+uδ+up[(u+δuq)Λu+δi=12(u+di)limtIi(t)limtΦ(t)]=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21(u+δ)(u+d2)u2+uδ+upϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21. 38

Applying (37), (38), Lemmas 2.7 and 2.8 into equation (22), we have

limtV(t)=Λu(u+δuq)Λu2+uδ+up+(u+δ)(u+d1)u2+uδ+upϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21u+d1uϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21+(u+δ)(u+d2)u2+uδ+upϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21u+d2uϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21(u+d2)pu(u+δ+p)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21.

This completes the proof. □

Conclusions and numerical simulations

In this paper, we propose a novel stochastic epidemic system with double epidemic diseases under vaccination. By using stochastic differential equation theory, we study the persistence in mean and extinction of the two diseases. Compared with the existing work in Refs. [39] and [40], the model constructed in this paper also considers the efficiency of vaccination. When all the coefficients related to the vaccination are 0, system (4) is similar to systems (2) and (3) in Refs. [39] and [40], in addition, our conclusion is consistent with them. That is to say, systems (2) and (3) in Refs. [39] and [40] are a special case of our system (4). The theoretical results of this article can be used as a reference for the control of infectious diseases.

To sum up, we have the following conclusions:

I.

Stochastic disease-free dynamics

When R1<0 and R2<0 hold, we have
limtIi(t)=0,i=1,2,limtS(t)=(u+δuq)Λu2+uδ+up,limtV(t)=(p+uq)Λu2+uδ+up.
That is to say, the two epidemic diseases go to extinct almost surely.
II.
Stochastic endemic dynamics
  • (i)
    If one of the following conditions holds:
    • R1>0, R2<0,
    • R1,R2>0, ϒ11R2<ϒ21R1,
    then we have
    limtI1(t)=R1ϒ11>0,limtI2(t)=0a.s.,limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upR1ϒ11a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)R1ϒ11a.s.
    That is to say, the epidemic disease I1(t) is persistent in mean and I2(t) is extinct.
  • (ii)
    If one of the following conditions hold:
    • R1<0, R2>0,
    • R1,R2>0, ϒ22R1<ϒ12R2,
    then we have
    limtI1(t)=0,limtI2(t)=R2ϒ21>0a.s.,limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d2)u2+uδ+upR2ϒ21a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d2)pu(u+δ+p)R2ϒ21a.s.
    That is to say, the epidemic disease I1(t) is extinct and I2(t) is persistent in mean.
  • (iii)
    If ϒ11R2>ϒ21R1, ϒ22R1>ϒ12R2 hold, then we have
    limtI1(t)=ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21,limtI2(t)=ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.,limtS(t)=(u+δuq)Λu2+uδ+up(u+δ)(u+d1)u2+uδ+upϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21limtS(t)=(u+δ)(u+d2)u2+uδ+upϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.,limtV(t)=(p+uq)Λu2+uδ+up(u+d1)pu(u+δ+p)ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21limtV(t)=(u+d2)u(u+δ+p)ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21a.s.
    That is to say, the epidemic diseases I1 and I2 are persistent in mean.

In [39, 41], Meng and Chang et al. obtained the lower boundedness of the persistence in mean for I1 and I2 as follows:

lim inft+I1(t)+I2(t)m,

where m is a positive constant. However, this paper proves that I1 and I2 have their own limit, that is,

limt+I1(t)=m1,limt+I2(t)=m2,

where m1=ϒ22R1ϒ12R2ϒ11ϒ22ϒ12ϒ21 and m2=ϒ11R2ϒ21R1ϒ11ϒ22ϒ12ϒ21. Thus this paper contains and significantly improves the results for persistence in mean in [39, 41]. The developed theoretical methods can be used to investigate the high-dimensional nonlinear stochastic differential systems.

To numerically illustrate our results, we employ a numerical method from [52] with ©Matlab2013b to the following discrete equations:

{Sn+1=Sn+[(1q)Λ(u+p)Snβ1SnI1,nα1+I1,nβ2SnI2,nα2+I2,n+r1I1,n+r2I2,n+δVn]ΔtSn+1=+σ3SnΔW1k+Snγ3ΔΓ3k,I1,n+1=I1,n+[β1SnI1,nα1+I1,n(u+d1+r1)I1,n]Δt+σ1I1,nΔW1k+I1,nγ1ΔΓ1k,I2,n+1=I2,n+[β2SnI2,nα2+I2,n(u+d2+r2)I2,n]Δt+σ2I2,nΔW2k+I2,nγ2ΔΓ2k,Vn+1=Vn+[qΛ+pSn(u+δ)Vn]Δt+σ4VnΔW4k+Vnγ4ΔΓ4k,

where Δt=0.01, ΔWikW(tk+1)W(tk) (i=1,2,3,4) obeys the Gaussian distribution N(0,Δt), ΔΓikΓ(tk+1)Γ(tk) obeys the Poisson distribution with intensity λ.

To this end, we set Λ=1, q=0.1, u=0.2, p=0.2, β1=0.24, β2=0.27, α1=1, α2=1, r1=0.2, r2=0.1, δ=0.2, d1=0.2, d2=0.4.

Figure 1(a) is the time sequence diagram of system (4) with σi=γi=0, i=1,2,3,4; Figure 1(b) is the corresponding phase diagram of I1(t) and I2(t). In this case, the two epidemic diseases are persistent.

Figure 1.

Figure 1

Time sequence diagram and phase diagram of model (4) without stochastic effects.

In Figure 2, we choose σ1=0.6, σ2=0.8, σ3=0.1, σ4=0.1, γ1=0.2, γ2=0.3, γ3=0.1, γ4=0.2. In this case, R1=0.0377<0, R2=0.2026<0. We see that in the time sequence diagram Figure 2(a) and the corresponding phase diagram Figure 2(b), the two epidemic diseases are extinct.

Figure 2.

Figure 2

Time sequence diagram and phase diagram of model (4) for extinction of two epidemic diseases.

In Figure 3, we choose σ1=0.2, σ2=0.6, σ3=0.1, σ4=0.1, γ1=0.3, γ2=0.3, γ3=0.1, γ4=0.2. In this case, R1=0.1024>0, R2=0.0626<0. We see that in the time sequence diagram Figure 3(a) and the corresponding phase diagram Figure 3(b), the epidemic disease I1(t) is persistent in mean and I2(t) is extinct.

Figure 3.

Figure 3

Time sequence diagram and phase diagram of model (4) for extinctions of disease 2 and persistence of disease 1.

In Figure 4, we choose σ1=0.6, σ2=0.2, σ3=0.1, σ4=0.1, γ1=0.3, γ2=0.3, γ3=0.1, γ4=0.2. In this case, R1=0.0576<0, R2=0.0974>0. We see that in the time sequence diagram Figure 4(a) and the corresponding phase diagram Figure 4(b), the epidemic disease I2(t) is persistent in mean and I1(t) is extinct.

Figure 4.

Figure 4

Time sequence diagram and phase diagram of model (4) for extinctions of disease 1 and persistence of disease 2.

In Figure 5, we choose σ1=0.3, σ2=0.14, σ3=0.1, σ4=0.1, γ1=0.1, γ2=0.1, γ3=0.1, γ4=0.1. In this case, R1=0.0123>0, R2=0.0079>0. We see that in the time sequence diagram Figure 2(a) and the corresponding phase diagram Figure 2(b), the two epidemic diseases are persistent in mean.

Figure 5.

Figure 5

Time sequence diagram and phase diagram of model (4) for persistence of two diseases.

Obviously, the numerical simulation results are consistent with the conclusion of our theorems.

Acknowledgements

This research was partially supported by the National Natural Science Foundation of China (11371230, 11501331, 11561004), by the SDUST Research Fund (2014TDJH102), Shandong Provincial Natural Science Foundation, China (ZR2015AQ001, BS2015SF002), by Joint Innovative Center for Safe And Effective Mining Technology and Equipment of Coal Resources, the Open Foundation of the Key Laboratory of Jiangxi Province for Numerical Simulation and Emulation Techniques, Gannan Normal University, China, by SDUST Innovation Fund for Graduate Students (SDKDYC170225).

Footnotes

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

The work presented in this paper has been accomplished through contributions of all authors. All authors read and approved the final manuscript.

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