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Dynamical behaviors of a stochastic SIRV epidemic model with the Ornstein–Uhlenbeck process
Advances in Continuous and Discrete Models volume 2024, Article number: 9 (2024)
Abstract
Vaccination is an important tool in disease control to suppress disease, and vaccine-influenced diseases no longer conform to the general pattern of transmission. In this paper, by assuming that the infection rate is affected by the Ornstein–Uhlenbeck process, we obtained a stochastic SIRV model. First, we prove the existence and uniqueness of the global positive solution. Sufficient conditions for the extinction and persistence of the disease are then obtained. Next, by creating an appropriate Lyapunov function, the existence of the stationary distribution for the model is proved. Further, the explicit expression for the probability density function of the model around the quasi-equilibrium point is obtained. Finally, the analytical outcomes are examined by numerical simulations.
1 Introduction
Vaccination is an effective means of preventing infectious diseases. On the one hand, after vaccination, people can gain immunity to diseases, effectively reducing the risk of illness, severe illness, and death. On the other hand, through orderly vaccination, an immune barrier can be gradually established in the population, blocking the spread of diseases, and protecting people’s daily lives. Many diseases that have plagued humans for many years, such as measles, rabies, and hepatitis B, have been effectively mitigated by vaccination. In a number of articles [1–7], various dynamic behaviors of disease transmission with vaccination have been analyzed. Based on [8–10], Oke et al. [11] established a SIRV infectious disease model in 2019, which is shown below:
where \(S(t)\) denotes the susceptible individuals, \(I(t)\) denotes the infected individuals, \(R(t)\) denotes the recovered individuals and \(V(t)\) denotes the vaccinated individuals; A indicates the natural input rate, μ indicates the natural mortality of the individuals, α indicates the mortality rate of the individuals due to disease, λ indicates infection rate between susceptible individuals and infected individuals; ρ indicates the rate of vaccination of susceptible individuals, \(\delta _{1}\) and \(\delta _{2}\) indicate the rate of loss of immunity in recovered individuals and vaccinated individuals separately, γ indicates the natural recovery rate of the infected individuals, r indicates the treatment rate of the infected individuals.
The real environment is constantly changing, which leads to randomness everywhere in the natural environment, and the parameters of the model constantly fluctuate above or below the average value. Therefore, the construction of an infectious disease model considering the impact of environmental noise can better reflect the actual situation of the spread of infectious diseases in real world situations. In order to simulate the impact of environmental noise, there are generally two methods. The first method is to establish a linear function about white Gaussian noise by adding white Gaussian noise to parameters [12–20], and the second method is to introduce Ornstein–Ulenbeck process into parameters to make them driven by Ornstein–Ulenbeck process [21–31]. Kang et al. [32] noted that Gaussian colored noise, produced by the Ornstein–Ulenbeck process, is appropriate for modeling the correlation of environmental fluctuations, while Gaussian white noise, which is the formal derivative of Wiener process of stationary independent increments, is not able to represent the correlation of environmental fluctuations. Allen [33] also compared these two types of noise and reached the following conclusion:
(i) Assuming that the infection rate is affected by white Gaussian noise, its form is as follows:
where \(B(t)\) denotes the standard Brownian movement, σ denotes environmental fluctuation intensity. Dividing by t on both sides after integrating the previous equation from 0 to t, we have
It can be seen that the variance of \(\lambda (t)\) goes to infinity as t approaches 0. That is to say, successive averages of this linear function undergoes significant random fluctuations. At the same time, introducing the Ornstein–Uhlenbeck process into the infection rate gives
where \(m(t)\) obeys
where θ represents the reverse speed, ξ represents the fluctuation intensity, \(B(t)\) represents the standard Brownian motion. Integrating Eq. (3) from 0 to t, we obtain
where \({m_{0}} = m(0)\). Obviously, \(m (t)\) follows the normal distribution in the form of \(\mathbb{N}( {m_{0}}{e^{ - \theta t}}, \frac{{{\xi ^{2}}}}{{2\theta }}(1 - {e^{ - 2\theta t}}))\). As t approaches 0, the variance of the Ornstein–Uhlenbeck process also tends to 0. Obviously, using Ornstein–Ulenbeck process to simulate biological model is more appropriate.
(ii) Compared with white Gaussian noise, the Ornstein–Uhlenbeck process is a continuous process that changes over time. For example, the correlation coefficient \({\lambda _{1}}(t)\) of the Ornstein–Uhlenbeck process admits \(\rho ({\lambda _{1}}(t),{\lambda _{1}}(t + \Delta t)) = 1 - o(t)\), while the correlation coefficient \({\lambda _{2}}(t)\) of white Gaussian noise admits \(\rho (\lambda _{2}(t), \lambda _{2}(t + \Delta t)) = 0\). This indicates that adding white Gaussian noise as a disturbance to models with short-term is more suitable. However, in reality, environmental fluctuations are influenced by multiple relationships, which are also constantly changing. Hence, introducing the Ornstein–Uhlenbeck process is more realistic for simulating this longer period interaction, suitable for the assumption that continuous fluctuations in environmental noise lead to parameter oscillations near the mean value over a period of time. This is consistent with the viewpoint of Kang et al. [32].
Considering Eq. (4) again, it can be concluded that
Then, Eq. (4) becomes
From this equation, it can be seen that no matter how \(m (t)\) changes in the previous moment, it will continue to develop towards 0 in the next moment. This is also one of the advantages of the Ornstein–Uhlenbeck process [34].
Recently, many experts and scholars have studied the property of the Ornstein–Uhlenbeck process and incorporated it into existing dynamic models with remarkable results. Zhang et al. [35] studied a stochastic SVEIR epidemic model, where the transmission rate follows the log-normal Ornstein–Uhlenbeck process. They established sufficient conditions for the persistence and extinction of the disease, and studied the local asymptotic stability of equilibrium points in the specific deterministic system with bilinear incidence and \(\sigma =1\). Zhang et al. [36] studied a stochastic constantizer model with mean-reverting Ornstein–Uhlenbeck process and Monod–Haldane response function and found that the rate of regression and volatility intensity had important effects on microbial extinction and persistence. These results can demonstrate the effectiveness of adding the Ornstein–Uhlenbeck process to the biological model. In this article, we assume that the infection rate is affected by the Ornstein–Uhlenbeck process and then establish the following stochastic SIRV model:
Suppose \((\Omega ,{\{ {F_{t}}\} _{t \ge 0}},\mathbb{P})\) is a whole space of probabilities with normal condition (Right continuous, \(F_{0}\) includes all zero measurement sets), where \({\{F_{t}\}}_{t \ge 0}\) is a σ algebra in Ω.
The main structure of this article is as follows. First, in Sect. 2, we demonstrate the existence and uniqueness of the global positive solution for model (5). In Sects. 3 and 4, we derive the conditions leading to the extinction and persistence of the disease by constructing appropriate functions. The sufficient conditions for the ergodic stationary distribution of model (5) are obtained in Sect. 5. In Sect. 6, the exact expression of the probability density function is obtained by solving the corresponding Fokker-Planck equation. Then we confirm the theoretical results by numerical simulations in Sect. 7.
2 Existence and uniqueness of global solution
Before studying this SIRV model, we first need to prove the existence and uniqueness of the global positive solutions of model (5) to demonstrate the feasibility of its dynamic behavior.
Theorem 1
Model (5) has a particular global solution \((m(t),S(t),I(t),R(t),V(t))\), specified for any \(t\geq 0\), and the solution stays in \(\mathbb{R}\times \mathbb{R}^{4}_{+}\) with probability one for any initial value \((m(0), S(0), I(0), R(0) , V(0))\in \mathbb{R}\times \mathbb{R}^{4}_{+}\).
Proof
Obviously, the coefficients in model (5) all satisfy the local Lipschitz condition, therefore, for any initial value \((m(0),S(0),I(0),R(0),V(0)) \in \mathbb{R} \times \mathbb{R}_{+} ^{4}\), there exists a unique local solution \((m(t),S(t),I(t),R(t),V(t)) \in \) on \(t \in [0,{\tau _{e}}]\), where \({\tau _{e}}\) an explosion time. In order to demonstrate that this particular solution is global, we need to establish that \({\tau _{e}} = \infty \). Determine a constant n that is sufficient for \(m(0)\), \(S(0)\), \(I(0)\), \(R(0)\), \(V(0)\) to fall totally within the range \([\frac{1}{n},n]\). For each instance of the integer \(k \ge n\), define the stopping time
In this article, we set \(\inf \emptyset {{ = }}\infty \). It is worth noting that \({\tau _{k}}\) increases monotonically with \(k \to \infty \). Here we make \({\tau _{\infty }}{{ = }}\lim_{k \to \infty } { \tau _{k}}\) and \({\tau _{\infty }} \le {\tau _{e}}\) a.s. If we can prove \({\tau _{\infty }}{{ = }}\infty \), then Theorem 1 can be shown to be complete.
Now we assume this situation is wrong, there is a pair of constants \(T > 0\), \(\varepsilon \in (0,1)\) obeys \(\mathbb{P} \{ {\tau _{\infty }} \le T \} > \varepsilon \). Accordingly, set an integer \({k_{1}} \ge n\) satisfies \(\mathbb{P} \{ {\tau _{k}} \le T \} > \varepsilon\) (\(\forall k \ge {k_{1}}\)). Then define a nonnegative \(C^{2}\)-function
By Itô’s formula, we obtain
From model (5), we can easily obtain that
then
Set \(K: = \max \{ \frac{A}{\mu },S(0) + I(0) + R(0) + V(0)\} \), then \(S(t) \le K\), \(I(t) \le K\), \(R(t) \le K\) and \(V(t) \le K\). Equation (6) can be reduced to that
where k̃ is a positive constant that is independent of the original value. By integrating inequality (8) from 0 to t, there is
Taking expectations on the both sides of inequality (9), one obtains
For \(k \ge {k_{1}}\), we let \({\Omega _{k}} = \{ {\tau _{k}} \le T \} \), and there exists \(\mathbb{P}({\Omega _{k}}) \ge \varepsilon \). It is noting that for all \(w \in {\Omega _{k}}\), there exists at minimum one in \({e^{m(\tau _{k}, w)}}\), \(S(\tau _{k}, w)\), \(I(\tau _{k}, w)\), \(R(\tau _{k}, w)\), \(V( \tau _{k}, w)\) reaches either k or \(\frac{1}{k}\). Therefore,
Since \(\lim_{t \to \infty } h(k) = \infty \), there is
When \(k \to \infty \), we can get \(\infty > V_{1}(m(0),S(0),I(0),R(0),V(0)) + \widetilde{k}T = \infty \) which is a contradiction. Thus, we obtain \({\tau _{\infty }}{{ = }}\infty \). The conclusion is confirmed. □
Remark 1
Through Eq. (7), we can easily obtain that
Then the feasible region of model (5) can be represented as follows:
3 Extinction
In this section, we aim to obtain the factors that lead to the demise of the disease. Before discussing this issue, we define
Theorem 2
Assume that \(R_{0}^{E} <1\). For any initial value \((m(t),S(t),I(t),R(t),V(t)) \in \mathbb{R} \times \mathbb{R}_{+}^{4}\), the following inequality holds
Proof
Define a \(C^{2}\)-Lyapunov function as follows:
Employing Itô’s formula, we have
Integrating both sides of the above inequality from 0 to t and dividing t, we have
As t tends to infinity, the Ornstein–Uhlenbeck process weakly converges to the normal distribution \(\mathbb{N}(0,\frac{{{\xi ^{2}}}}{{2\theta }})\), then its limit distribution density function is \(\pi (x) = \frac{{\sqrt {\theta}}}{{\sqrt {\pi}\xi }}{e^{ - \frac{{\theta {x^{2}}}}{\xi }}}\). And the ergodic theorem of [21, 36, 37] states that the following condition exists:
Therefore, substituting Eq. (12) into the above inequality and taking limits on both sides gives
The proof is completed. □
4 Persistence
In this section, we analyze the condition that leads to the persistence of the disease.
Theorem 3
Assume that \(R_{0}^{E} > 1\). For any initial value \((m(t),S(t),I(t),R(t),V(t)) \in \mathbb{R} \times \mathbb{R}_{+}^{4}\), the following inequality holds
Proof
Through the first line of Eq. (11), we can get
Integrating both sides of the above ineqality from 0 to t, there is
Consequently, combining Eq. (12), we have
The inequality (14) holds. This completes the proof. □
5 Stationary distribution
We first present a lemma before illustrating the ergodic stationary distribution of model (5).
Lemma 1
[38] For any initial value \(P_{0}(0)=( m(0),S(0), I(0), R(0), V(0) )\in \Gamma \), if there exists a bounded closed domain \(U_{\varepsilon }\in \Gamma \) with regular boundary, and obeys
where \(\mathbb{P}(\tau ,P_{0}(0), U_{\varepsilon})\) denotes the transition probability of \(P_{0}(t)\). In that case, the stochastic system (5) contains at least one stationary distribution.
Theorem 4
Assume that \(R_{0}^{E} > 1\). For any initial value \((m(t),S(t),I(t),R(t),V(t)) \in \mathbb{R} \times \mathbb{R}_{+}^{4}\), the system (5) has a stationary distribution \(\pi (\cdot )\).
Proof
Applying Itô’s formula, we have
Define a \(C^{2}\)-function as follows:
where M is a large enough positive constant satisfying the following inequality:
and
There exists a minimum value \(\bar{U} (S_{0},I_{0},R_{0},V_{0},m_{0})\) in the interior of Γ. Thus, we define a non-negative \(C^{2}\)-function:
where
Then, we define a closed subset of \(U_{\varepsilon}\) by
where ε is a sufficiently small constant to satisfy the following equation:
Next, the complementary set of \(U_{\varepsilon }\) can be classified into the following six subsets:
In the following, we will prove \(G(S,I,R,V,m) \le -1\) in each of the following six cases.
Case 1. For any \((S,I,R,V,m) \in U_{\varepsilon ,1}^{c}\), one obtains
Case 2. For any \((S,I,R,V,m) \in U_{\varepsilon ,2}^{c}\), one obtains
Case 3. For any \((S,I,R,V,m) \in U_{\varepsilon ,3}^{c}\), one obtains
Case 4. For any \((S,I,R,V,m) \in U_{\varepsilon ,4}^{c}\), one obtains
Case 5. For any \((S,I,R,V,m) \in U_{\varepsilon ,5}^{c}\), one obtains
Case 6. For any \((S,I,R,V,m) \in U_{\varepsilon ,6}^{c}\), one obtains
As a result, we are able to easily obtain
for sufficiently small ε. Moreover, there exists a positive constant Y that satisfies \(G(S,I, R,V,m) \le Y\). Here, denote \(K_{0}(t)=(S(t),I(t),R(t),V(t),m(t))\). Thus, we can get
Taking the infimum bound for both sides of the above inequality and combining it with Eq. (12), we have
where \({{\mathbf{1}}_{\{ {K_{0}}(\tau ) \in {U_{\varepsilon }}\} }}\) and \({{\mathbf{1}}_{\{ {K_{0}}(\tau ) \in \Gamma \backslash {U_{ \varepsilon }}\} }}\) are the indicator functions of the set \(\{ K_{0}(\tau ) \in {U_{\varepsilon }}\} \) and \(\{ K_{0}(\tau ) \in \Gamma \backslash {U_{\varepsilon }}\} \). This indicates that
then
The Inequality (21) and the invariance of Γ indicate the existence of an invariance probability measure for model (5) on Γ. Moreover, the positive recurrence of model (5) is easily derived from the existence of the invariant probability measure. Hence, the system (5) has a stationary distribution \(\pi (\cdot )\). □
6 Density function
In this section, we concentrate on the analysis of the probability density function. First, if \(R_{0}^{E} > 1\), there is a quasi-equilibrium \(E^{*} = ({S^{*}},{I^{*}},{R^{*}},{V^{*}},{m^{*}}) = ({S^{*}},{I^{*}},{R^{*}},{V^{*}},0)\) that satisfies the following equations:
Notice that when the random factors in the model are not taken into account, the quasi-equilibrium \(E^{*}\) is same as the equilibrium in the deterministic model. Taking \({L_{1}} = S - {S^{*}}\), \({L_{2}} = I - {I^{*}}\), \({L_{3}} = R - {R^{*}}\), \({L_{4}} = V - {V^{*}}\), \({L_{5}} = m - {m^{*}}\), we are able to obtain the corresponding linearized system
where
Theorem 5
If \(R_{0}^{E} > 1\), the solution of system (23) is given by the specific normal probability density function \(\Phi ({L_{1}},{L_{2}},{L_{3}},{L_{4}},{L_{5}})\), which has the following form.
where
Proof
Taking \({\mathrm{{d}}}L = AL{\,\mathrm{d} }t + G{\,\mathrm{d} }B(t)\), the matrix form of system (23) can be expressed as
Then the characteristic polynomial of A can be represented as
where
By the Routh–Hurwitz criterion and \({b_{1}}{b_{2}} - {b_{3}} > 0\), \({b_{1}}{b_{2}}{b_{3}} - b_{3}^{2} - b_{1}^{2}{b_{4}} > 0\), the real parts of the eigenvalues of matrix A are all negative. By [39], the probability density function \(\Phi (m,{L_{1}},{L_{2}},{L_{3}},{L_{4}})\) of the system (23) can thus be written as the following Fokker–Planck equation:
which can be denoted as the formula of Gaussian distribution
where Q satisfies \(Q{G^{2}}Q + {A^{T}}Q + QA = 0\). Suppose that Q is is invertible and let \({Q^{ - 1}} = \Sigma \), one obtains
Two transformation matrices \(J_{1}\) and \(J_{2}\), which we import here, can be written as
Then we can conclude that
where
Define
then we can get
where
Next, consider the transform matrix
where
Then
where \({d_{1}} = \theta + {b_{1}}\), \({d_{2}} = \theta {b_{1}} + {b_{2}}\), \({d_{3}} = \theta {b_{2}} + {b_{3}}\), \({d_{4}} = \theta {b_{3}} + {b_{4}}\), \({d_{5}} = \theta {b_{4}}\). Then we can transform Eq. (24) into the following form for the corresponding equation:
Set \(\Sigma _{1} = \frac{1}{{q_{1}^{2}{\xi ^{2}}}}{M_{1}}{J_{3}}{J_{2}}{J_{1}} \Sigma {({M_{1}}{J_{3}}{J_{2}}{J_{1}})^{T}}\), then we can get
where \(G_{0}=\operatorname{diag}(1,0,0,0,0)\) and
where
Note that \(\Sigma _{1}\) is a positive definite matrix, hence, \(\Sigma = {q_{1}^{2}{\xi ^{2}}}(M_{1} J_{3} J_{2} J_{1})^{ - 1}{ \Sigma _{1}}{[(M_{1} J_{3} J_{2} J_{1})^{ - 1}]^{T}}\) is also positive definite. Consequently, the density function around the quasi-equilibrium point \(E^{*}\) can be written as
The proof is completed. □
Remark 2
Derived from Theorem 5, the solution \((S(t),I(t),R(t),V(t),m(t))\) to model (5) around \(((S^{*},I^{*},R^{*},V^{*},m^{*})^{T})\) fulfils the normal density function \(\mathbb{N}((S^{*},I^{*},R^{*},V^{*},m^{*})^{T}, \Sigma ) \). Then, if \(R_{0}^{E} >1\), the solution \((S(t), I(t), R(t), V(t))\) has a unique normal density function
Therefore, \(S(t)\), \(I(t)\), \(R(t)\) and \(V(t)\) will converge to the marginal density functions \(\Phi _{S}\), \(\Phi _{I}\), \(\Phi _{R}\), \(\Phi _{V}\), respectively, where
\(\varphi _{i}^{2}\) is the ith element on the main diagonal of Σ, respectively. Similarly, \(S (t)\), \(I (t)\), \(R(t)\), and \(V (t)\) also converge to the marginal distribution functions \(\mathbb{N}(S^{*},\varphi _{1}^{2})\), \(\mathbb{N}(I^{*},\varphi _{2}^{2})\), \(\mathbb{N}(R^{*},\varphi _{3}^{2})\) and \(\mathbb{N}(V^{*},\varphi _{4}^{2})\).
7 Numerical simulation
In this section, various situations are simulated by giving special values of parameters. First, we discretize model (5) through the Milstein method. The discretized form is as follows:
where Δt is time variation, \(\eta _{k}\) is a random variable conforming to the standard normal distribution.
Next, we verify our scientific results in the following four aspects.
-
(i)
When \(R_{0}^{E}<1\), whether the disease will become extinct with probability 1.
-
(ii)
When \(R_{0}^{E}>1\), whether the disease will become persistent with probability 1.
-
(iii)
Average evolution and variance of infected individuals.
-
(iv)
The existence of the stationary distribution.
Example 1
Choose \(A=0.014\), \(\mu =0.014\), \(\lambda =0.25\), \(\rho =0.03\), \(\delta _{1}=0.37\), \(\delta _{2}=0.0014\), \(\alpha =0.03\), \(\gamma =0.05\), \(r=0.001\), \(\theta =0.1\), \(\xi =0.05\), and the initial value \((m(0), S(0), I(0), R(0), V(0))=(-0.002, 0.03, 0.95, 0.01, 0.01)\). In this case, \(R_{0}^{E} \approx 0.979<1\) meets Theorem 2. Figure 1 simulates the number of four types of population, and it can be seen that \(I(t)\) and \(R(t)\) extinct after a period of time, while \(S(t)\) and \(V(t)\) stabilize with probability 1.
Example 2
Choose \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\theta =0.1\), \(\xi =0.05\), and the initial value \((m(0), S(0), I(0), R(0), V(0))= (-0.002, 0.03, 0.95 , 0.01, 0.01 )\). In this case, \(R_{0}^{E} \approx 23.3>1\) meets Theorem 3. Figure 2 simulates the number of four types of population, and it indicates that \(I(t)\) and \(R(t)\) do not extinct, but become endemic diseases.
Example 3
Choose (a) \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\theta =0.1\), \(\xi =0.05\), (b) \(A=0.014\), \(\mu =0.014\), \(\lambda =0.25\), \(\rho =0.03\), \(\delta _{1}=0.37\), \(\delta _{2}=0.0014\), \(\alpha =0.03\), \(\gamma =0.05\), \(r=0.001\), \(\theta =0.1\), \(\xi =0.05\), and the initial value \((m(0), S(0), I(0), R(0), V(0)) =(-0.002, 0.03, 0.95, 0.01, 0.01)\). Figure 3 simulates the expectation and standard deviation of the number of infected individuals, which demonstrates that in case (a), the disease spreads and becomes endemic, but in case (b), it quickly disappears.
Example 4
Choose \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\theta =0.1\), \(\xi =0.05\), and the initial value \((m(0), S(0), I(0), R(0), V(0))=(-0.002, 0.03, 0.95, 0.01, 0.01)\). In this case, \(R_{0}^{E} \approx 23.3>1\) and the positive equilibrium \(E_{2}^{*} = ({S^{*}},{I^{*}},{R^{*}},{V^{*}}) = (0.6,0.653,0.759,0.477 )\). In addition, we get that the solution \((S(t), I(t), R(t), V(t), m(t))\) follows the normal density function \(\Phi (S,I,R,V,m) \sim \mathbb{N}_{4}((0.6,0.653, 0.759,0.477,0 )^{T}, \Sigma )\), where
and
Figure 4 simulates the density histogram and marginal density curve of model (5), which can verify the existence of the stationary distribution. It can be seen that the curve is basically consistent with the histogram.
Example 5
Choose \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\theta =0.1\), \(\xi =0.05\), and the initial value \((m(0), S(0), I(0), R(0), V(0))=(-0.002, 0.03, 0.95, 0.01, 0.01)\). Figure 5 simulates the comparison chart of the stochastic model and the deterministic model. It can be seen that when the random disturbance is not too large, the trend of the stochastic model is the same as that of the deterministic model.
Example 6
Choose \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\theta =0.1\), and the initial value \((m(0), S(0), I(0), R(0), V(0))=(-0.002, 0.03, 0.95, 0.01, 0.01)\). Then, the impact of fluctuation intensity on the disease is identified by selecting three different ξ. Here we select three scenarios: \(\xi =0.005\), \(\xi =0.01\), and \(\xi =0.03\). From Fig. 6, it can be seen that as ξ increases, the disease becomes increasingly unstable.
Example 7
Choose \(A=0.16\), \(\mu =0.016\), \(\lambda =0.5\), \(\rho =0.014\), \(\delta _{1}=0.07\), \(\delta _{2}=0.0016\), \(\alpha =0.084\), \(\gamma =0.1\), \(r=0.1\), \(\xi =0.02\), and the initial value \((m(0), S(0), I(0), R(0), V(0))=(-0.002, 0.03, 0.95, 0.01, 0.01)\). Then, the impact of the reverse speed on the disease is identified by selecting three different θ. Here we select three scenarios: \(\theta =0.00001\), \(\theta =0.01\), and \(\theta =0.95\). From Fig. 7, it can be seen that as θ decreases, the disease becomes increasingly unstable.
8 Conclusion
This article studies a stochastic SIRV model with vaccination to illustrate the random transmission of diseases in ecosystems. By comparing with classical white Gaussian noise, the reason why the Ornstein–Uhlenbeck process is more in line with reality is explained. Firstly, we prove the existence and uniqueness of global positive solutions for model (5) with constructing appropriate functions. Secondly, the conditions leading to the extinction and persistence of diseases are studied, and it is found that when \(R_{0}^{E}<1\), the disease will become extinct with probability 1, while when \(R_{0}^{E}>1\), the disease will continue to exist as an endemic disease. These results are beneficial for people to eliminate the disease or control its spread. Once again, it is studied that model (5) has a stationary distribution when \(R_{0}^{E}>1\), and an explicit expression for the corresponding probability density function of the model is obtained. Finally, by providing specific parameter values, model (5) is simulated using Python to obtain sample trajectories and density histograms under different conditions. These results have certain reference value for reality.
Although the research conducted in this paper on the dynamic properties of the stochastic SIRV model, there are still numerous issues worthy of further exploration:
-
1.
Given that the stochastic system is perturbed by the Ornstein–Uhlenbeck process, its diffusion matrix exhibits singular characteristics and does not satisfy the uniform ellipticity condition. This indicates that the model admits at least one stationary distribution, but to ensure its uniqueness, we still need to explore more appropriate methods and theories.
-
2.
In the model presented in this paper, we only considered the impact of environmental fluctuations on the infection rate. However, in reality, every parameter in the biological model is potentially subject to environmental interference. Therefore, our next research focus will be on studying the influence of environmental fluctuations on more parameters in the biological model, in order to more comprehensively reveal the complexity and dynamic characteristics of the model.
Data availability
Not applicable.
Code availability
The code used in this article is original.
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Acknowledgements
We thank to the reviewers for their helpful comments and suggestions. This work is supported by the National Natural Science Foundation of China Tianyuan Mathematical Foundation (No. 12126312, No. 12126328). The authors gratefully acknowledge the Natural Science Foundation of Heilongjiang Province (No. LH2022E023), Heilongjiang Provincial Postdoctoral Science Foundation (LBH-Z23259), and the Northeast Petroleum University Special Research Team Project (No. 2022TSTD-05) for the support in publishing this paper.
Funding
The National Natural Science Foundation of China Tianyuan Mathematical Foundation (No. 12126312, No. 12126328), the Natural Science Foundation of Heilongjiang Province (No. LH2022E023) and the Northeast Petroleum University Special Research Team Project (No. 2022TSTD-05).
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Shang, J., Li, W. Dynamical behaviors of a stochastic SIRV epidemic model with the Ornstein–Uhlenbeck process. Adv Cont Discr Mod 2024, 9 (2024). https://doi.org/10.1186/s13662-024-03807-6
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DOI: https://doi.org/10.1186/s13662-024-03807-6