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 [1–8]. 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:
| ((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, 9–28]. In particular, the stochastic epidemic models have been extensively studied [3, 10–25]. 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, 9–28]. 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
| (2) |
and the conditional covariance
| (3) |
Then, we derive the following stochastic form of system (1)
| (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, ℙ) 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 ℙ -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 ≤ i ≤ d}.
In general, consider the d-dimensional stochastic differential equation
| (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, ℙ). 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].
| (6) |
If L acts on a function V ∈ C2,1(ℝd × [t0, ∞]; ℝ+), then
| (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
| (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:
| (9) |
The diffusion matrix is defined as follows:
| (10) |
Lemma 1 . —
The Markov process X(t) has a unique ergodic stationary distribution Π(·) if there exists a bounded domain D ⊂ Ed with regular boundary Γ and
A 1: there is a positive number M such that ∑i,j=1daij(x)ξiξj ≥ M|ξ|2, x ∈ D, ξ ∈ ℝd.
A 2: there exists a nonnegative C2-function V such that LV is negative for any Ed\D. Then
(11) for all x ∈ Ed, 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:
(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 τ∞ ≤ τe 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 ℙ{τ∞ ≤ T} > ε. As a result, there exists an integer n1 ≥ n0 such that
| (13) |
Define a C2-function V: ℝ+5⟶ℝ+ by
| (14) |
Using It's formula, we have
| (15) |
where
| (16) |
By applying the following invariant set of model (1) which is obtained in [8]
| (17) |
and from the following inequalities
| (18) |
and also cancel the items less than zero, so we have
| (19) |
Since ζ is positive constant which is independent of S1, S2, V, E, I, and t, we can get
| (20) |
Integrating both sides (20) from 0 to T∧τε and taking expectations, then we can obtain
| (21) |
Set Ωε = {τε ≤ t} for n ≥ n1 by (13), P(Ωn) ≥ ε. Notice that for every ω ∈ Ωε, 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
| (22) |
Consequently,
| (23) |
where a∧b donates the minimum of a and b. In view of (21) and (23) we have
| (24) |
where 1Ω(ω) is the indicator function of Ωn. Let n⟶∞ leads to the contradiction
| (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
| (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
(27)
Choose ; one can get that
| (28) |
Then the condition A1 in Lemma 1 is satisfied.
Construct a C2-function Q : ℝ+5⟶ℝ in the following from
| (29) |
where χ is a constant satisfying 0 < χ < 2μ/σ12∨σ22∨σ32∨σ42∨σ52,
| (30) |
and M > 0 satisfies the following condition
| (31) |
where
| (32) |
| (33) |
It is easy to check that
| (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 in the interior of ℝ+5. Then we define a nonnegative C2-function V : ℝ+5⟶ℝ+ as follows:
| (35) |
Making use of It's formula, we have
| (36) |
Using the inequality leads to
| (37) |
where λ is defined in (32).
Similarly
| (38) |
Then
| (39) |
where
| (40) |
We can also get
| (41) |
| (42) |
| (43) |
| (44) |
| (45) |
Hence, by (37)-(45), we obtain
| (46) |
Thus, we can construct a compact subset D such that the condition A2 in Lemma 1 holds. Define the bounded closed set
| (47) |
where εi > 0(i = 1, 2, 3, 4, 5) are sufficiently small constants satisfying the following conditions:
| (48) |
| (49) |
| (50) |
| (51) |
| (52) |
| (53) |
| (54) |
| (55) |
| (56) |
| (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
| (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
(59) where
(60)
According to (48), we have
| (61) |
Case 2 . —
If (S1, S2, V, E, I) ∈ D2, we have
(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
(63)
We obtain that
| (64) |
Case 4 . —
If (S1, S2, V, E, I) ∈ D4, one can see that
(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
(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
(67) where
(68)
By (53), we conclude that LV ≤ −1 on D6.
Case 7 . —
If (S1, S2, V, E, I) ∈ D7, one can see that
(69) where
(70)
Together with (54), we can deduce that LV ≤ −1 on D7.
Case 8 . —
If (S1, S2, V, E, I) ∈ D8, one can see that
(71) where
(72) which together with (55) implies that LV ≤ −1 on D8.
Case 9 . —
If (S1, S2, V, E, I) ∈ D9, we obtain
(73) where
(74)
By (56), we can conclude that LV ≤ −1 on D9.
Case 10 . —
If (S1, S2, V, E, I) ∈ D10, it follows that
(75) where
(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)(Aτ + b)(μ2 + η2))/μτη2 < ((σ52/2) + μ2 + c)∧(σ42/2), then the disease I(t) will extinct exponentially with probability one, i.e., moreover
(77)
Proof —
Applying It's formula to log[E + (μ2 + η2/η2)I], we have
(78)
Integrating the above inequality from 0 to t, and the fact that limt⟶∞Bi(t)/t = 0, i = 4, 5 [16], yields
| (79) |
For any , and almost ω ∈ Ω, ∃T = T(ω) such that
| (80) |
Remark 2 . —
Theorem 5 suggests that the disease will become extinct if (β(ε + 1)(Aτ + 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):
| (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.

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.

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.
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Data Availability Statement
No data were used to support this study.
