Skip to main content
Computational and Mathematical Methods in Medicine logoLink to Computational and Mathematical Methods in Medicine
. 2022 May 29;2022:4617685. doi: 10.1155/2022/4617685

Stationary Distribution and Extinction of a Stochastic Brucellosis Model with Standard Incidence

Dilnaray Iskandar 1, Xamxinur Abdurahman 1,, Ahmadjan Muhammadhaji 1
PMCID: PMC9201711  PMID: 35720044

Abstract

In this paper, we proposed a stochastic SVEI brucellosis model with stage structure by introducing the effect of environmental white noise on transmission dynamics of brucellosis. By Has'minskii theory and constructing suitable Lyapunov functions, we established sufficient conditions on the existence of ergodic stationary distribution for the considered model. Moreover, we also established sufficient condition for extinction of the disease. Finally, two examples with numerical simulations are given to illustrate the main results of this paper.

1. Introduction

Brucellosis, which is recognized as a major public health problem, is a serious and economically devastating zoonosis which can infect animals, such as sheep, cattle, pig, and dogs. The disease is caused by bacteria of the genus Brucella, of which there are six species: B. abortus, B. melitensis, B. suis, B. ovis, B. canis, and B. neotomae [1]. Brucella can survive for long periods in dust, dung, water, slurry, aborted fetuses, soil, meat, and dairy products. In animals, brucellosis can be infected by contact with the infected animals (direct way of infection) and by contact of polluted environment (indirect way of transmission), and the disease mainly affects reproduction and fertility and reduces survival of newborns [2]. Brucellosis also can infect human being; the main transmission sources of human brucellosis include exposure to a contaminated environment by infected animals, direct contact with infected animals, and the ingestion of fresh milk or dairy products prepared from unpasteurized milk and unheated meat and animal liver [3]; there is no recorded cases of the infection between humans. Most of the human brucellosis cases are infected by Brucella melitensis (which is infected in sheep and goats), accounting for 84.5% of the total cases [4]. In humans, disease-related mortality is negligible, but the illness can last for several years [5]. Therefore, the key to solve the problem of this public health problem is the elimination of animal brucellosis.

It is worth noting that, mathematical models are widely used not only to study the transmission dynamics of brucellosis, but also to study the epidemiological characteristics of brucellosis [18]. Recently, the authors in [6] presented a sheep brucellosis model with immigration and proportional birth, considering both direct and indirect transmission. In [7], the authors proposed a multigroup SEIRV dynamical model with bidirectional mixed cross infection between cattle and sheep and investigated the influence of cross infection of mixed feeding on the brucellosis transmission. In [8], the authors proposed the following deterministic brucellosis transmission model:

dS2dt=η1S1βS2IθS2μ2S2+δV,dVdt=θS2εβVIμ2+δV,dEdt=βεVI+βS2Iμ2+η2E,dIdt=η2Eμ2+cI, ((1))

and studied the dynamical behavior of the model, where sheep population is classified into five compartments: the susceptible young sheep S1(t), the susceptible adult (or sexually mature) sheep S2(t), the vaccinated sheep V(t), the exposed sheep E(t), and the infectious sheep I(t). A and b are the input number of young sheep and the natural birth rate of sheep, and τ is the extent of the birth being delayed. μ1 and μ2 are the young sheep natural mortality rate and the elimination rate of adult sheep. η1 and η2 are the transfer rate from young sheep to adult sheep and exposed sheep to infected sheep. d is the output number of young sheep, δ is the vaccination rate, β is sheep-to-sheep transmission rate, ε is the ineffective vaccination rate, and c is the elimination rate caused by brucellosis. All the parameters are assumed to be positive.

However, the epidemics in the real world are often disturbed by some uncertain factors, such as environmental white noises. Therefore, it is difficult to describe these epidemic dynamics by using determined differential equation [9]. Thus, the deterministic models has some limitations in mathematical modeling of epidemics, and it is quite difficult to fitting data perfectly and to predicting the future dynamics of the epidemic system. In the past years, there has been a lot of researchers who are interested in the stochastic dynamical models [3, 928]. In particular, the stochastic epidemic models have been extensively studied [3, 1025]. For example, in [3], the authors proposed and studied a periodic stochastic brucellosis model and obtained some conditions on the existence of nontrivial positive periodic solution of the model. In [11], the authors studied a stochastic SIRS epidemic model with standard incidence rate and partial immunity and obtained sufficient conditions on the extinction and existence of a stationary probability measure for the disease of the system. In [12], the authors studied a kind of stochastic SEIR epidemic model with standard incidence and obtained sufficient conditions for the existence of stationary distribution and the extinction of the disease in the system. In [24], the authors discussed a stochastic SIRS epidemic model with logistic growth and nonlinear incidence and obtained sufficient conditions on the ergodic stationary distribution and extinction of the considered model.

On the other hand, there are different approaches used in the literature to introduce random perturbations into population models, both from a mathematical and biological perspective [3, 928]. In this paper, in light of the above analysis and reasons, we consider the stochastic perturbations for deterministic system (1) and we employ the approach used in Mao et al. [26] and assume that the parameters involved in the model always fluctuate around some average value due to continuous fluctuations in the environment. This approach is reasonable and well justified biologically [27, 28]. By this approach, we study a stochastic S1S2VEI brucellosis model with standard incidence, and we assume that the environmental white noise affects the natural mortality rate, the elimination rate, transfer rate, and transmission rate. In order to obtain the stochastic S1S2VEI brucellosis model, we let X(t) = (S1(t), S2(t), V(t), E(t), I(t))T, and then it is appropriate to model X = (S1, S2, V, E, I)T as a Markov process; thus, from [15] and model (1), we can get the following properties when 0 ≤ Δt ≪ 1, the conditional mean

ES1t+ΔtS1tX=xA+bS2+V1+τS2+Vμ1+d+η1S1Δt,ES2t+ΔtS2tX=xη1S1βS2IθS2μ2S2+δVΔt,EVt+ΔtVtX=xθS2εβVIμ2+δVΔt,EEt+ΔtEtX=xβεVI+βS2Iμ2+η2EΔt,EIt+ΔtItX=xη2Eμ2+cIΔt, (2)

and the conditional covariance

VarS1t+ΔtS1tX=xσ12S12Δt,VarS2t+ΔtS2tX=xσ22S22Δt,VarVt+ΔtVtX=xσ32V2Δt,VarEt+ΔtEtX=xσ42E2Δt,VarIt+ΔtItX=xσ52I2Δt. (3)

Then, we derive the following stochastic form of system (1)

dS1t=A+bS2+V1+τS2+Vμ1+d+η1S1dt+σ1S1dB1t,dS2t=η1S1βS2IθS2μ2S2+δVdt+σ2S2dB2t,dVt=θS2εβVIμ2+δVdt+σ3VdB3t,dEt=βεVI+βS2Iμ2+η2Edt+σ4EdB4t,dIt=η2Eμ2+cI+σ5IdB5t, (4)

where B1(t), B2(t), B3(t), B4(t), and B5(t) are the standard one-dimensional independent Brownian motions and σi2 > 0(i = 1, 2, 3, 4, 5) are the intensity of the white noises.

The main purpose of the paper is to obtain the conditions for the existence of ergodic stationary distribution and extinction of the disease for model (4).

This paper is organized as follows. In Section 2, we present some preliminaries which will be used in the following analysis. In Section 3, we show that there is a unique global positive solution of system (4). In Section 4, we prove the existence of ergodic stationary distribution for system (4) under certain conditions. In Section 5, we establish sufficient conditions for the disease extinction.

2. Preliminaries

Throughout this paper, let (Ω, F, ) be a complete probability space with a filtration {Ft}t≥0 satisfying the usual conditions (i.e., it is increasing and right continuous, while F0 contains all -null sets); Bi(t)(i = 1, 2, 3, 4) are defined on this complete probability space, and also let ℝ+d = {x ∈ ℝd : xi > 0, 1 ≤ id}.

In general, consider the d-dimensional stochastic differential equation

dxt=fxt,tdt+gxt,tdBtfor t0,, (5)

with initial value x(0) = x0 ∈ ℝd. B(t) denotes an n-dimensional standard Brownian motion defined on the complete probability space (Ω, F, {Ft}t≥0, ). C2,1(ℝd × [t0, ∞]; ℝ+) denotes the family of all nonnegative functions V(x, t) defined on ℝd × [t0, ∞] such that they are continuously twice differentiable in x and once in t. The differential operator L of equation (5) is defined by [16].

Ł=t+i=1dfix,txi+12i,j=1dgTx,tgx,tij2xixj. (6)

If L acts on a function VC2,1(ℝd × [t0, ∞]; ℝ+), then

LVx,t=Vtx,t+Vxx,tfx,t+12tracegTx,tVxxx,tgx,t, (7)

where Vt = ∂V/∂t, Vx = ((∂V/∂x1), ⋯, (∂V/∂xd)), Vxx = (2V/∂xi∂xj)d×d. By Itô's formula, if x(t) ∈ ℝd, then

dVxt,t=LVxt,tdt+Vxxt,tgxt,tdBt. (8)

Next, we present a result about the existence of stationary distribution (see Has'minskii [17]).

Let X(t) be a homogeneous Markov process in Ed (Ed denotes d-dimensional Euclidean space) and be described by the following stochastic differential equation:

dXt=bXdt+r=1kgrXdBrt. (9)

The diffusion matrix is defined as follows:

Ax=aijx,aijx=r=1kgrixgrjx. (10)

Lemma 1 . —

The Markov process X(t) has a unique ergodic stationary distribution Π(·) if there exists a bounded domain DEd with regular boundary Γ and

A 1: there is a positive number M such that ∑i,j=1daij(x)ξiξjM|ξ|2, xD, ξ ∈ ℝd.

A 2: there exists a nonnegative C2-function V such that LV is negative for any Ed\D. Then

xlimT1T0Tfxtdt=EdfxΠdx=1, (11)

for all xEd, where f(·) is a function integrable with respect to the measure π.

3. Main Results

3.1. Existence and Uniqueness of the Positive Solution

In studying the dynamical behavior of an epidemic model, the first importance is whether the solution is global and positive. Hence, in the following theorem, we will study the existence and uniqueness of the global positive solution, which is a prerequisite for researching the long-term behavior of model (4).

Theorem 1 . —

For any initial value X0 = (S1(0), S2(0), V(0), E(0), I(0)) ∈ ℝ+5, there is a unique solution X(t) = (S1(t), S2(t), V(t), E(t), I(t)) of system (4) on t ≥ 0, and the solution will remain in ℝ+5 with probability one.

Proof —

Since the coefficients of system (4) satisfy the local Lipschitz condition, then for any initial value (S1(0), S2(0), V(0), E(0), I(0)) ∈ ℝ+5, there is a unique local solution (S1(t), S2(t), V(t), E(t), I(t)) on [0, τe), where τe is the explosion time [16]. To show this solution is global, we only need to prove that τe = ∞ a.s. To this end, let n0 > 0 be sufficiently large such that every component of X0 lying within the interval [(1/n0), n0]. For each integer n > n0, define the stopping time as follows:

τn=inft0,τe: minS1t,S2t,Vt,Et,It1nor maxS1t,S2t,Vt,Et,Itn. (12)

Throughout this paper, we set inf∅ = ∞ (as usual ∅ denotes the empty set). It is easy to see that τn is increasing as n⟶∞. Let τ = limn⟶∞τn, then ττe a.s. In what follows, we need to verify τ = ∞ a.s. If this assertion is violated, there is a constant T > 0 and an ε ∈ (0, 1) such that {τT} > ε. As a result, there exists an integer n1n0 such that

τnTε,nn1. (13)

Define a C2-function V: ℝ+5⟶ℝ+ by

VS1,S2,V,E,I=S11lnS1+S21lnS2+V1lnV+E1lnE+I1lnI. (14)

Using Ito^'s formula, we have

dVS1S2,V,E,I=LVS1S2,V,E,Idt+σ1S11dB1t+σ2S21dB2t+σ3V1dB3t+σ4E1dB4t+σ5I1dB5t, (15)

where

LV=11S1A+bS2+V1+τS2+Vμ1+d+η1S1+11S2η1S1βS2IθS2μ2S2+δV+11VθS2εβVIμ2+δV+11EβεVI+βS2Iμ2+η2E+11Iη2Eμ2+cI+σ12+σ22+σ32+σ42+σ522. (16)

By applying the following invariant set of model (1) which is obtained in [8]

Ω=S1,S2,V,E,IR+5:S1+S2+V+E+IAτ+bμτ, (17)

and from the following inequalities

bS2+V1+τS2+Vbτ,Iβε+1βε+1Aτ+bμτ, (18)

and also cancel the items less than zero, so we have

LV=A+bS2+V1+τS2+V+μ1+d+η1+βI+θ+4μ2+εβI+δ+η2+cμ1+dS1AS1bS2+VS11+τS2+Vμ2S2+V+E+Iη1S1S2δVS2θS2VβεVIEβS2IEcIη2EI+σ12+σ22+σ32+σ42+σ522A+bτ+βε+1Aτ+bμτ+μ1+d+η1+θ+4μ2+δ+η2+c+σ12+σ22+σ32+σ42+σ522=ζ. (19)

Since ζ is positive constant which is independent of S1, S2, V, E, I, and t, we can get

dVS1S2,V,E,Iζdt+σ1S11dB1t+σ2S21dB2t+σ3V1dB3t+σ4E1dB4t+σ5I1dB5t. (20)

Integrating both sides (20) from 0 to Tτε and taking expectations, then we can obtain

EVS1τεT,S2τεT,VτεT,EτεT,IτεTVS10,S20,V0,E0,I0+ζT<. (21)

Set Ωε = {τεt} for nn1 by (13), P(Ωn) ≥ ε. Notice that for every ωΩε, there is at least one of S1(τε, ω), S2(τε, ω), V(τε, ω), E(τε, ω), and I(τε, ω) that equal either n or 1/n. Hence, S1(τε, ω), S2(τε, ω), V(τε, ω), E(τε, ω), and I(τε, ω) are no less than

n1logn or 1n1logn. (22)

Consequently,

VS1τε,ω,S2τε,ω,Vτε,ω,Eτε,ω,Iτε,ωn1logn1n1logn, (23)

where ab donates the minimum of a and b. In view of (21) and (23) we have

VS10,S20,V0,E0,I0+ζTE1ΩωVS1τεT,S2τεT,VτεT,EτεT,IτεTδ~n1logn1n1+logn, (24)

where 1Ω(ω) is the indicator function of Ωn. Let n⟶∞ leads to the contradiction

>VS10,S20,V0,E0,I0+ζT=. (25)

Therefore, we must have τ = ∞ a.s.

3.2. Stationary Distribution and Ergodicity

The difference between model (1) and the stochastic model is that the stochastic model does not have the endemic equilibrium. Hence, we cannot study the persistence of the disease by studying the stability of the endemic equilibrium and turn to check out the existence and uniqueness of the stationary distribution for the system (4) which implies the persistence of the disease in some sense. In this section, based on the theory of Has'minskii [17], we verify that there is an ergodic stationary distribution, which reveals the persistence of the disease.

Define a parameter

R0s=η1η2βεθμ1+d+η1+σ12/2θ+μ2+σ22/2μ2+η2+σ42/2μ2+c+σ52/2. (26)

Theorem 2 . —

Assume that R0s > 1, then system (4) has a unique stationary distribution Π(·) and it has the ergodic property.

Proof —

In view of Theorem 2, we have obtained that for any initial value (S1(0), S2(0), V(0), E(0), I(0)) ∈ ℝ+5), there is a unique global solution (S1, S2, V, E, I) ∈ ℝ+5..

The diffusion matrix of system (4) is given by

A=σ12S1200000σ22S2200000σ32V200000σ42E200000σ52I2. (27)

Choose M=minS1,S2,V,E,ID¯σR+5σ12S12,σ12S22,σ32V2,σ42E2,σ52I2; one can get that

i,j=15aijS1,S2,V,E,Iξiξj=σ12S12ξ12+σ12S22ξ22+σ32V2ξ32+σ42E2ξ42+σ52I2ξ52Mξ2,S1,S2,V,E,ID¯σ,ξ=ξ1,ξ2,ξ3,ξ4,ξ5+5. (28)

Then the condition A1 in Lemma 1 is satisfied.

Construct a C2-function Q : ℝ+5⟶ℝ in the following from

QS1,S2,V,E,I=MS1+S2+V+E+Ic1lnS1c2lnS2c3lnEc4lnIlnV+1χ+1S1+S2+V+E+Iχ+1lnS1lnS2lnElnV+S1+S2+V+E+I=MV1+V2+V3+V4+V5+V6, (29)

where χ is a constant satisfying 0 < χ < 2μ/σ12σ22σ32σ42σ52,

c1=Aμ1+d+η1+σ12/2,c2=Aθ+μ2+σ22/2,c3=Aμ2+η2+σ42/2,c4=Aμ2+c+σ52/2, (30)

and M > 0 satisfies the following condition

Mλ+C2, (31)

where

λ=5Aη1η2βεθμ1+d+η1+σ12/2θ+μ2+σ22/2μ2+η2+σ42/2μ2+c+σ52/21/51=5AR0s1/51>0, (32)
C=supS1,S2,V,E,Iε+512μ12σσ12σ22σ32σ42σ52·S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422. (33)

It is easy to check that

liminfk,S1,S2,V,E,I+5\UkQS1,S2,V,E,I=, (34)

where Uk = ((1/k), k) × ((1/k), k) × ((1/k), k) × ((1/k), k) × ((1/k), k). Furthermore, Q(S1, S2, V, E, I) is a continuous function. Hence, Q(S1, S2, V, E, I) must have a minimum point S¯10,S¯20,V¯0,E¯0,I¯0 in the interior of ℝ+5. Then we define a nonnegative C2-function V : ℝ+5⟶ℝ+ as follows:

VS1,S2,V,E,I=QS1,S2,V,E,IQS¯10,S¯20,V¯0,E¯0,I¯0. (35)

Making use of Ito^'s formula, we have

LV1=μ2S2+V+E+I+μ1+dS1+c1AS1+c1bS2+VS11+τS2+V+c2η1S1S2+c2δVS2+c3βεVIE+c3βS2IE+c4η2EI+θS2VcI+A+bS2+V1+τS2+V+εβI+c2βI+μ2+δ+σ322+c1μ1+d+η1+σ122+c2θ+μ2+σ222+c3μ2+η2+σ422+c4μ2+c+σ522. (36)

Using the inequality a+b+c+d+e5abcde5,a,b,c,d,e>0 leads to

LV1c1AS1+c2η1S1S2+c3βεVIE+c4η2EI+θS2V+A+bτ+εβI+c2βI+μ2+δ+σ322+c1μ1+d+η1+σ122+c2θ+μ2+σ222+c3μ2+η2+σ422+c4μ2+c+σ5225c1c2c3c4Aη1βεη2θ1/5+A+bτ+εβI+c2βI+μ2+δ+σ322+c1μ1+d+η1+σ122+c2θ+μ2+σ222+c3μ2+η2+σ422+c4μ2+c+σ522=5A5η1βεη2θμ1+d+η1+σ12/2θ+μ2+σ22/2μ2+η2+σ42/2μ2+c+σ52/21/5+5A+μ2+δ+bτ+βIc2+ε+σ322=5Aη1βεη2θμ1+d+η1+σ12/2θ+μ2+σ22/2μ2+η2+σ42/2μ2+c+σ52/21/51+μ2+δ+bτ+βIc2+ε+σ322=λ+μ2+δ+bτ+βIc2+ε+σ322, (37)

where λ is defined in (32).

Similarly

LV2=S1+S2+V+E+IχA+bS2+V1+τS2+Vμ1+dS1μ2S2+V+E+IcI+12χS1+S2+V+E+Iχ1×σ12S12+σ22S22+σ32V2+σ42E+σ52I2S1+S2+V+E+IχA+bτμS1+S2+V+E+I+12χS1+S2+V+E+Iχ+1σ12σ22σ32σ42σ52=A+bτS1+S2+V+E+Iχμ12χσ12σ22σ32σ42σ52S1+S2+V+E+Iχ+1. (38)

Then

LV2B12μ12χσ12σ22σ32σ42σ52S1+S2+V+E+Iχ+1B12μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1, (39)

where

B=supS1,S2,V,E,I+5A+bτS1+S2+V+E+Iχ12μ12χσ12σ22σ32σ42σ52S1+S2+V+E+Iχ+1<. (40)

We can also get

LV3=AS1bS2+VS11+τS2+V+μ1+d+η1+σ122, (41)
LV4=η1S1S2+βI+θ+μ2δVS2+σ222, (42)
LV5=βεVIEβS2IE+μ2+η2+σ422, (43)
LV6=θS2V+εβI+μ2+δ+σ322, (44)
LV7=A+S2+V1+τS2+Vμ1+dS1μ2S2+V+E+IcIA+bτμ1+dS1μ2S2+V+E+I. (45)

Hence, by (37)-(45), we obtain

LVMλ+MβIc2+ε+1+εM+B12μ12χσ12σ22σ32σ42σ52×S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1AS1bS2+VS11+τS2+Vη1S1S2δVS2βεVIEβS2IEθS2Vμ1+dS1μ2S2+V+E+I+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422. (46)

Thus, we can construct a compact subset D such that the condition A2 in Lemma 1 holds. Define the bounded closed set

D=ε1S11ε1,ε2S21ε2,ε3I1ε3,ε4E1ε4,ε5V1ε5, (47)

where εi > 0(i = 1, 2, 3, 4, 5) are sufficiently small constants satisfying the following conditions:

1ε1+F1, (48)
Mλε5ε2+C1, (49)
Mλ+Mβε31+εM+c2+ε+C1, (50)
βε2ε3ε4+F1, (51)
θS2ε5+F1, (52)
14μ12χσ12σ22σ32σ42σ521ε1χ+1+G1, (53)
14μ12χσ12σ22σ32σ42σ521ε2χ+1+H1, (54)
14μ12χσ12σ22σ32σ42σ521ε4χ+1+J1, (55)
14μ12χσ12σ22σ32σ42σ521ε3χ+1+K1, (56)
14μ12χσ12σ22σ32σ42σ521ε5χ+1+L1, (57)

where F, G, H, J, K, and L are positive constants which can be seen from (60), (68), (70), (72), (74), and (76), respectively. Note that for sufficiently small εi, i = 1, 2, 3, 4, 5. For convenience, we divide ℝ+5\D into ten domains

D1=S1,S2,V,E,I+5:0<S1<ε1,D2=S1,S2,V,E,I+5:0<S2<ε2,Vε5,D3=S1,S2,V,E,I+5:0<I<ε3,D4=S1,S2,V,E,I+5:S2ε2,Iε3,0<E<ε4,D5=S1,S2,V,E,I+5:0<V<ε5S2ε2,D6=S1,S2,V,E,I+5:S1>1ε1,D7=S1,S2,V,E,I+5:S2>1ε2,D8=S1,S2,V,E,I+5:I>1ε3,D9=S1,S2,V,E,I+5:E>1ε4,D10=S1,S2,V,E,I+5:V>1ε5. (58)

Next, we will show that LV(S1, S2, V, E, I) ≤ −1 on ℝ+5\D, which is equivalent to proving it on the above ten domains.

Case 1 . —

If (S1, S2, V, E, I) ∈ D1, one can get that

LVAS1+MβIc2+ε+1+εM12μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422AS1+FAε1+F1, (59)

where

F=supS1,S2,V,E,I+5MβIc2+ε+1+εM12μ12χσ12σ22σ32σ42σ52×S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422. (60)

According to (48), we have

LV1,for any S1,S2,V,E,ID1. (61)

Case 2 . —

If (S1, S2, V, E, I) ∈ D2, we have

LVMλδVS212μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422MλδVS2+CMλε5ε2+C, (62)

where C is defined in (33).

In view of (49), we can obtain that for sufficiently small εi(i = 2, 5), LV ≤ −1 for any (S1, S2, V, E, I) ∈ D2.

Case 3 . —

If (S1, S2, V, E, I) ∈ D3, one can see that

LVMλ+MβIc2+ε+1+εM12μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422. (63)

We obtain that

LV1 for any S1,S2,V,E,ID3. (64)

Case 4 . —

If (S1, S2, V, E, I) ∈ D4, one can see that

LVβS2IE+MβIc2+ε+1+εM12μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422βS2IE+Fβε2ε3ε4+F. (65)

In view of (51), we can obtain that for sufficiently small εi(i = 3, 4), LV ≤ −1 for any (S1, S2, V, E, I) ∈ D4.

Case 5 . —

If (S1, S2, V, E, I) ∈ D5, one can see that

LVθS2V+MβIc2+ε+1+εM12μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+σ12+σ22+σ32+σ422θS2V+Fθε2ε5+F. (66)

We can obtain that for sufficiently small εi(i = 2, 5), LV ≤ −1 for any (S1, S2, V, E, I) ∈ D5.

Case 6 . —

If (S1, S2, V, E, I) ∈ D6, one can see that

LV14μ12χσ12σ22σ32σ42σ52S1χ+114μ12χσ12σ22σ32σ42σ52×S1χ+112μ12χσ12σ22σ32σ42σ52S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ42214μ12χσ12σ22σ32σ42σ52S1χ+1+G14μ12χσ12σ22σ32σ42σ521ε1χ+1+G, (67)

where

G=supS1,S2,V,E,I+514μ12χσ12σ22σ32σ42σ52S1χ+112μ12χσ12σ22σ32σ42σ52×S2χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ422. (68)

By (53), we conclude that LV ≤ −1 onD6.

Case 7 . —

If (S1, S2, V, E, I) ∈ D7, one can see that

LV14μ12χσ12σ22σ32σ42σ52S2χ+114μ12χσ12σ22σ32σ42σ52×S2χ+112μ12χσ12σ22σ32σ42σ52S1χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ42214μ12χσ12σ22σ32σ42σ52S2χ+1+H14μ12χσ12σ22σ32σ42σ521ε2χ+1+H, (69)

where

H=supS1,S2,V,E,I+514μ12χσ12σ22σ32σ42σ52S2χ+112μ12χσ12σ22σ32σ42σ52×S1χ+1+Vχ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ422. (70)

Together with (54), we can deduce that LV ≤ −1 onD7.

Case 8 . —

If (S1, S2, V, E, I) ∈ D8, one can see that

LV14μ12χσ12σ22σ32σ42σ52Eχ+114μ12χσ12σ22σ32σ42σ52×Eχ+112μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ42214μ12χσ12σ22σ32σ42σ52Eχ+1+J14μ12θσ12σ22σ32σ42σ521ε4χ+1+J, (71)

where

J=supS1,S2,V,E,I+514μ12χσ12σ22σ32σ42σ52Eχ+112μ12χσ12σ22σ32σ42σ52×S1χ+1+S2χ+1+Vχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ422. (72)

which together with (55) implies that LV ≤ −1 onD8.

Case 9 . —

If (S1, S2, V, E, I) ∈ D9, we obtain

LV14μ12χσ12σ22σ32σ42σ52Iχ+114μ12χσ12σ22σ32σ42σ52×Iχ+112μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Vχ+1+Eχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ42214μ12χσ12σ22σ32σ42σ52Iχ+1+K14μ12χσ12σ22σ32σ42σ521ε3χ+1+K, (73)

where

K=supS1,S2,V,E,I+514μ12χσ12σ22σ32σ42σ52Iχ+112μ12χσ12σ22σ32σ42σ52×S1χ+1+S2χ+1+Vχ+1+Eχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ422. (74)

By (56), we can conclude that LV ≤ −1 on D9.

Case 10 . —

If (S1, S2, V, E, I) ∈ D10, it follows that

LV14μ12χσ12σ22σ32σ42σ52Vχ+114μ12χσ12σ22σ32σ42σ52×Vχ+112μ12χσ12σ22σ32σ42σ52S1χ+1+S2χ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ42214μ12χσ12σ22σ32σ42σ52Vχ+1+L14μ12χσ12σ22σ32σ42σ521ε5χ+1+L, (75)

where

L=supS1,S2,V,E,I+514μ12χσ12σ22σ32σ42σ52Vχ+112μ12χσ12σ22σ32σ42σ52×S1χ+1+S2χ+1+Eχ+1+Iχ+1+μ1+d+η1+θ+3μ2+η2+δ+A+bτ+Mσ322+μ2+δ+bτ+MβIc2+ε+1+εM+σ12+σ22+σ32+σ422. (76)

Combining with (57) yields LV ≤ −1 on D10.

Obviously, A2 in Lemma 2.1 is satisfied. According to Lemma 2.1, we can obtain that system (4) is ergodic and has a unique stationary distribution.

Remark 1 . —

Theorem 3 reveals that system (4) has a unique ergodic stationary distribution π(·) if R0s = η1η2βεθ/((μ1 + d + η1 + (σ12/2))(θ + μ2 + (σ22/2))(μ2 + η2 + (σ42/2))(μ2 + c + (σ52/2))) > 1. Note that the expression of R0s coincide with the threshold R0 of the deterministic system (1) if there is no stochastic perturbation. This shows that we generalize the result of the deterministic system.

3.3. Extinction of the Disease

As it is well known, one of the main concern of epidemiology is how we regulate the disease dynamics in order to eradicate the disease in the long term. Moreover, in [10], Allen et al. proposed and studied several types of stochastic epidemic models and pointed out that the stochastic models should suit the question of disease extinction better. Hence, in this section, we shall establish some sufficient conditions for extinction of the disease in stochastic model (4).

Theorem 3 . —

Let S1(t), S2(t), V(t), E(t), I(t) be the solution of system (4) with any initial value (S1(0), S2(0), V(0), E(0), I(0)) ∈ ℝ+5. If (β(ε + 1)( + b)(μ2 + η2))/μτη2 < ((σ52/2) + μ2 + c)∧(σ42/2), then the disease I(t) will extinct exponentially with probability one, i.e., moreover

limtsup1tlogE+μ2+η2η2Iβη2ε+1Aτ+bμ2+η2μτη2μ2+η22σ522+μ2+cσ422. (77)

Proof —

Applying Ito^'s formula to log[E + (μ2 + η2/η2)I], we have

dlogE+μ2+η2η2I=βεV+S2IE+μ2+η2/η2Iμ2+η2μ2+cIE+μ2+η2/η2Iη2σ42E2+σ52μ2+η2/η2I22E+μ2+η2/η2I2dt+σ4EE+μ2+η2/η2IdB4t+σ5μ2+η2Iη2E+μ2+η2/η2IdB5t=βεV+S2IE+μ2+η2/η2Idt1E+μ2+η2/η2I2μ2+η2η2μ2+cIE+σ522+μ2+cμ2+η2η22I2+σ42E22dt+σ4EE+μ2+η2/η2IdB4t+σ5μ2+η2Iη2E+μ2+η2/η2IdB5tβεV+S2η2μ2+η2dt1E+μ2+η2/η2I2σ522+μ2+cμ2+η2η22I2+σ42E22dt+σ4EE+μ2+η2/η2IdB4t+σ5μ2+η2Iη2E+μ2+η2/η2IdB5tβη2ε+1Aτ+bμ2+η2Aτdtη2μ2+η22σ522+μ2+cσ422dt+σ4EE+μ2+η2/η2IdB4t+σ5μ2+η2Iη2E+μ2+η2/η2IdB5t. (78)

Integrating the above inequality from 0 to t, and the fact that limt⟶∞Bi(t)/t = 0, i = 4, 5 [16], yields

limtsup1tlogE+μ2+η2η2Iβη2ε+1Aτ+bμ2+η2μτη2μ2+η22σ522+μ2+cσ422=x0. (79)

For any ε¯>0, and almost ωΩ, ∃T = T(ω) such that

Itη2μ2+η2expx0+ε¯t,tT. (80)

Remark 2 . —

Theorem 5 suggests that the disease will become extinct if (β(ε + 1)( + b)(μ2 + η2))/μτη2 < ((σ52/2) + μ2 + c)∧(σ42/2).

4. Numerical Examples

In this section, we will give two numerical examples to illustrate the main theoretical results obtained in this paper. The numerical simulation method can be found in [9, 22, 23]. The following is a corresponding discrete equations of system (4):

S1k+1=S1k+A+bS2k+Vk1+τS2k+Vkμ1+d+η1S1kΔt+S1kσ1ξkΔt+12σ12ξk21Δt,S2k+1=S2k+η1S1kβS2kIkθS2kμ2S2k+δVkΔt+S2kσ2ξkΔt+12σ22ξk21Δt,Vk+1=Vk+θS2kεβVkIkμ2+δVkΔt+Vkσ3ξkΔt+12σ32ξk21Δt,Ek+1=Ek+βεVkIk+βS2kIkμ2+η2EkΔt+Ekσ4ξkΔt+12σ42ξk21Δt,Ik+1=Ik+η2Ekμ2+cIkΔt+Ikσ5ξkΔt+12σ52ξk21Δt, (81)

where ξk (k = 1, 2, ⋯) are the Gaussian random variables which follow standard normal distribution N(0, 1), and σi, 1 ≤ i ≤ 5, are intensities of white noises.

Example 1 . —

We take parameters as A = 45, β = 0.05, μ1 = 0.05, μ2 = 0.06, ε = 3.2, τ = 0.01, b = 0.3, η1 = 0.25, η2 = 0.5, and θ = 1.1, δ = 0.01, c = 0.02, σ1 = 0.2, σ2 = 0.05, σ3 = 0.31, σ4 = 0.03, and σ5 = 0.02. It is clear that conditions of Theorem 3 are satisfied; by calculating, we have the basic reproduction number R0s = η1η2βεθ/((μ1 + d + η1 + (σ12/2))(θ + μ2 + (σ22/2))(μ2 + η2 + (σ42/2))(μ2 + c + (σ52/2))) = 1.17080128

The histogram and the smoothing curves of the probability density functions of S1(t), S2(t), V(t), E(t), I(t) are given in Figure 1.

Figure 1.

Figure 1

Dynamic behaviors of the system.

Example 2 . —

We take parameters as A = 1000, β = 0.0001, μ1 = 0.1, μ2 = 0.25ε = 0.18, τ = 0.002, b = 1.5, η1 = 1.06, η2 = 3.4, and θ = 0.1, δ = 0.4, c = 0.05, σ1 = 0.2, σ2 = 0.5, σ3 = 0.31, σ4 = 1.65, and σ5 = 1.5. It is clear that conditions of Theorem 5 are satisfied.

The curves on the persistence of S1(t), S2(t), V(t), E(t) and extinction of I(t) for stochastic model (4) are given in Figure 2, where the initial value is (S1(0), S2(0), V(0), E(0), I(0)) = (1,1.5,1, 1, 1).

Figure 2.

Figure 2

Dynamic behaviors of the system.

Remark 3 . —

In this paper, we consider the stochastic perturbations for deterministic model (1) and derived model (4). Thus, model (4) can be specialized as models (1). Hence, model (4) can be seen as a general model compared to model (1), and the theoretical results obtained in this article can be seen as the extensions and supplements of the model and the theoretical results obtained in [8].

5. Conclusion

In this paper, firstly, we have considered the stochastic perturbations for deterministic system (1) and established corresponding stochastic system (4). Secondly, under the condition R0s > 1 and applying the theory of stochastic differential equations, Has'minskii theory, Ito's formula, and Lyapunov function method, we obtained some sufficient conditions on the existence of ergodic stationary distribution of model (4). We also established sufficient conditions on the extinction of the disease. Finally, two examples are presented to validate the main results of this paper. The results obtained in this paper suggest that stochastic perturbations have remarkable effects on the disease in model (4). Especially, from the numerical simulations, we can see that, under the stochastic perturbations, the disease in the stochastic system will become extinct more quickly than the corresponding deterministic one.

Acknowledgments

This project is supported by the National Natural Science Foundation of China (Grant No. 11861063) and the National Natural Science Foundation of Xinjiang (Grant No. 2021D01C067) .

Data Availability

No data were used to support this study.

Conflicts of Interest

The authors declare that they have no competing interests.

References

  • 1.MacMillan A. Brucellosis: freedom but the risk remains. Cattle Practice . 1994;2:469–474. [Google Scholar]
  • 2.Sewell M. M. H., Brocklesby D. W. Handbook on Animal Diseases in the Tropics . London: Bailliere Tindall; 1990. [Google Scholar]
  • 3.Wang L., Wang K., Jiang D. Q., Hayat T. Nontrivial periodic solution for a stochastic brucellosis model with application to Xinjiang, China. Physica A: Statistical Mechanics and its Applications . 2018;510:522–537. doi: 10.1016/j.physa.2018.06.061. [DOI] [Google Scholar]
  • 4.Shang D. Q., Xiao D. L., Yin J. M. Epidemiology and control of brucellosis in China. Veterinary Microbiology . 2002;90:165–182. doi: 10.1016/s0378-1135(02)00252-3. [DOI] [PubMed] [Google Scholar]
  • 5.Madkour M. M. Madkour’s Brucellosis . Berlin: Springer; 2001. [DOI] [Google Scholar]
  • 6.Sun G. Q., Zhang Z. K. Global stability for a sheep brucellosis model with immigration. Applied Mathematics and Computation . 2014;246:336–345. doi: 10.1016/j.amc.2014.08.028. [DOI] [Google Scholar]
  • 7.Li M. T., Sun G. Q., Wu Y. F., Zhang J., Jin Z. Transmission dynamics of a multi-group brucellosis model with mixed cross infection in public farm. Applied Mathematics and Computation . 2014;237:582–594. doi: 10.1016/j.amc.2014.03.094. [DOI] [Google Scholar]
  • 8.Hou Q., Sun X. D. Modeling sheep brucellosis transmission with a multi-stage model in Changling County of Jilin Province, China. Journal of Applied Mathematics and Computing . 2016;51(1-2):227–244. doi: 10.1007/s12190-015-0901-y. [DOI] [Google Scholar]
  • 9.Muhammadhajia A., Teng Z., Rehim M. On a two species stochastic Lotka-Volterra competition system. Journal of Dynamical and Control Systems . 2015;21(3):495–511. doi: 10.1007/s10883-015-9276-5. [DOI] [Google Scholar]
  • 10.Allen L. J. S. Mathematical Epidemiology . Springer; 2008. An introduction to stochastic epidemic models; pp. 81–130. (Lecture Notes in Mathematics). [DOI] [Google Scholar]
  • 11.Zhang X. B., Wang X. D., Huo H. F. Extinction and stationary distribution of a stochastic SIRS epidemic model with standard incidence rate and partial immunity. Physica A: Statistical Mechanics and its Applications . 2019;531, article 121548 doi: 10.1016/j.physa.2019.121548. [DOI] [Google Scholar]
  • 12.Liu Q., Jiang D. Q., Shi N. Z., Hayat T., Ahmad B. Stationary distribution and extinction of a stochastic SEIR epidemic model with standard incidence. Physica A: Statistical Mechanics and its Applications . 2017;476:58–69. doi: 10.1016/j.physa.2017.02.028. [DOI] [Google Scholar]
  • 13.Liu Z. Dynamics of positive solutions to SIR and SEIR epidemic models with saturated incidence rates. Nonlinear Analysis: Real World Applications . 2013;14(3):1286–1299. doi: 10.1016/j.nonrwa.2012.09.016. [DOI] [Google Scholar]
  • 14.Imhof L., Walcher S. Exclusion and persistence in deterministic and stochastic chemostat models. Journal of Differential Equations . 2005;217(1):26–53. doi: 10.1016/j.jde.2005.06.017. [DOI] [Google Scholar]
  • 15.Evans S. N., Ralph P., Schreiber S. J., Sen A. Stochastic population growth in spatially heterogeneous environments. Journal of Mathematical Biology . 2013;66(3):423–476. doi: 10.1007/s00285-012-0514-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Mao X. Stochastic Differential Equations and their Applications . Chichester: Horwood; 1997. [Google Scholar]
  • 17.Khasminskii R. Stochastic Stability of Differential Equations . Berlin: Springer; 2012. [Google Scholar]
  • 18.Yang Q. S., Jiang D. Q., Shi N. Z., Ji C. Y. The ergodicity and extinction of stochastically perturbed SIR and SEIR epidemic models with saturated incidence. Journal of Mathematical Analysis and Applications . 2012;388(1):248–271. doi: 10.1016/j.jmaa.2011.11.072. [DOI] [Google Scholar]
  • 19.Zhao D. L., Zhang T. S., Yuan S. L. The threshold of a stochastic SIVS epidemic model with nonlinear saturated incidence. Physica A: Statistical Mechanics and its Applications . 2016;443:372–379. doi: 10.1016/j.physa.2015.09.092. [DOI] [Google Scholar]
  • 20.Lahrouz A., Settati A., Akharif A. Effects of stochastic perturbation on the SIS epidemic system. Journal of Mathematical Biology . 2017;74(1-2):469–498. doi: 10.1007/s00285-016-1033-1. [DOI] [PubMed] [Google Scholar]
  • 21.Rifhat R., Muhammadhaji A., Teng Z. Asymptotic properties of a stochastic SIRS epidemic model with nonlinear incidence and varying population sizes. Dynamical Systems . 2020;35(1):56–80. doi: 10.1080/14689367.2019.1620689. [DOI] [Google Scholar]
  • 22.Carletti M., Burrage K., Burrage P. Numerical simulation of stochastic ordinary differential equations in biomathematical modelling. Mathematics and Computers in Simulation . 2004;64(2):271–277. doi: 10.1016/j.matcom.2003.09.022. [DOI] [Google Scholar]
  • 23.Higham D. J. An algorithmic introduction to numerical simulation of stochastic differential equations. SIAM Review . 2001;43(3):525–546. doi: 10.1137/S0036144500378302. [DOI] [Google Scholar]
  • 24.Rajasekar S. P., Pitchaimani M. Ergodic stationary distribution and extinction of a stochastic SIRS epidemic model with logistic growth and nonlinear incidence. Applied Mathematics and Computation . 2020;377, article 125143 doi: 10.1016/j.amc.2020.125143. [DOI] [Google Scholar]
  • 25.Rajasekar S. P., Pitchaimani M., Zhu Q. Progressive dynamics of a stochastic epidemic model with logistic growth and saturated treatment. Physica A: Statistical Mechanics and its Applications . 2020;538, article 122649 doi: 10.1016/j.physa.2019.122649. [DOI] [Google Scholar]
  • 26.Mao X., Marion G., Renshaw E. Environmental brownian noise suppresses explosions in population dynamics. Stochastic Processes and their Applications . 2002;97(1):95–110. doi: 10.1016/S0304-4149(01)00126-0. [DOI] [Google Scholar]
  • 27.Liu M., Bai C. Analysis of a stochastic tri-trophic food-chain model with harvesting. Journal of Mathematical Biology . 2016;73(3):597–625. doi: 10.1007/s00285-016-0970-z. [DOI] [PubMed] [Google Scholar]
  • 28.Liu M., Fan M. Permanence of stochastic Lotka-Volterra systems. Journal of Nonlinear Science . 2017;27(2):425–452. doi: 10.1007/s00332-016-9337-2. [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

No data were used to support this study.


Articles from Computational and Mathematical Methods in Medicine are provided here courtesy of Wiley

RESOURCES