Abstract
In this paper, we analyze the dynamics of a new proposed stochastic non-autonomous SVIR model, with an emphasis on multiple stages of vaccination, due to the vaccine ineffectiveness. The parameters of the model are allowed to depend on time, to incorporate the seasonal variation. Furthermore, the vaccinated population is divided into three subpopulations, each one representing a different stage. For the proposed model, we prove the mathematical and biological well-posedness. That is, the existence of a unique global almost surely positive solution. Moreover, we establish conditions under which the disease vanishes or persists. Furthermore, based on stochastic stability theory and by constructing a suitable new Lyapunov function, we provide a condition under which the model admits a non-trivial periodic solution. The established theoretical results along with the performed numerical simulations exhibit the effect of the different stages of vaccination along with the stochastic Gaussian noise on the dynamics of the studied population.
Keywords: Epidemic model, Extinction, Persistence in the mean, Stochastic differential equations, Periodic solution
Introduction
Throughout history, researchers from different disciplines have developed scientific knowledge that played a major role in the advancement of Epidemiology. In the mathematical framework, the contribution of mathematicians consists of developing adequate models, based on a good understanding of the modeled disease, which allows to describe the evolution of the latter within the studied population, predict the worst outcome by performing virtual numerical simulations and even propose control strategies that can help reduce the severity of the situation, especially when it comes to disease outbreaks. Kermack–McKendrick theory [1] has been a cornerstone to the mathematical modeling of epidemics. The basic idea is to divide the studied population into so called compartments, based on the number of clinical states induced by the modeled disease. Then, to incorporate the transition of individuals from one clinical state to another, to each compartment, a set of parameters describing all the possible transitions are considered. Once the epidemic model is derived, it takes the form of a dynamical system, which then can be interpreted from two points of view. The first one is the deterministic point of view, which assumes that the output of the system is a time-dependent function that is entirely determined by the initial conditions and the input parameters, while the second is the stochastic point of view, which assumes that the same initial conditions and input parameters can lead to different outputs due to the random effect present in the environment. Consequently, the output, in this case, takes the form of a stochastic process. In the deterministic framework, numerous pioneering results in term of the dynamical and numerical analysis of epidemic and ecological models have been established by many authors [2–12], while several other works were done in the aim of extending the deterministic results to the stochastic case [13–20]. In further work, non-autonomous stochastic models have gained the attention of several researchers, due to their ability to incorporate the seasonal variation of diseases [21–23]. We briefly outline some of the existing literature in this sense for the stochastic case. For instance, in [24], Qi et al. analyzed an SEIS model and were able to prove that it admits a non-trivial periodic solution. Additionally, conditions under which the model admits an ergodic stationary distribution were obtained. The same results were proved by Shangguan et al. [25] for an SEIR model and by Liu et al. [26] for an SIR model. In [27], Lin et al. considered an SIR model and were able to derive a threshold characterizing the persistence and extinction of the disease. Furthermore, in the case of persistence, they proved the existence of a non-trivial periodic solution. However, to the best of the authors’ knowledge, the extension of these types of results to SVIR-type models, incorporating vaccination, has not yet been done.
When it comes to stochastic epidemic models incorporating the ineffectiveness of vaccination, most of the current research works neglect the dynamics of the vaccinated population, and make use of time delays to take into consideration the duration elapsed before the effectiveness of the vaccine wears off. In this context, we mention for instance the results presented in [28, 29]. Another limitation of the aforementioned works is assuming that the immunity can be gained solely after one stage of vaccination. These assumptions can be considered in order to simplify the formulation of the model. However, for some new emerging diseases such as COVID-19 and its variants, not taking these characteristics into account in the formulation of the model can reduce the amount of information acquired from the numerical simulation. To highlight the crucial role of the multiple stages of vaccination in the acquisition of immunity, we refer the reader to the recent studies presented in [30, 31]. Hence, the main contributions of our work is to address the previous limitations by providing a different approach, allowing to incorporate the multiple stages of vaccination as well as the ineffectiveness of the first stages. More precisely, we propose a new non-autonomous stochastic model extending the standard SVIR model [2], on one hand by considering time-varying parameters, incorporating the seasonal variation, and on the other, by dividing the vaccinated population V into three sub-populations and such that and stand for the vaccinated sub-population of individuals in the first and second stages of vaccination, respectively, and are not supposed to develop immunity against the disease. Consequently, they become infected. While stands for the vaccinated sub-population of individuals who complete the third stage of vaccination and are supposed to develop immunity against the disease, for a large period of time.
The model in question is expressed by the following system of coupled nonlinear stochastic differential equations.
| 1 |
equipped with the following initial conditions
where and are mutually independent Brownian motions defined on a probabilistic space with a filtration which is increasing, right-continuous and such that contains the null sets, while and denote the time-dependent intensities of the environmental Gaussian noise present in the disease transmission rates (Fig. 1, 1).
Fig. 1.

Flow diagram of the model (1) in the deterministic case
Table 1.
Signification of the model parameters
| Parameter | Biological signification |
|---|---|
| Natural birth rate at time t | |
| Natural death rate at time t | |
| Rate in which a susceptible individual at time t becomes infected | |
| Rate in which an individual at time t | |
| and in the stage of vaccination becomes infected | |
| Natural recovery rate at time t | |
| Rate in which an individual at time t and in the third stage | |
| of vaccination possesses immunity | |
| Rate in which a susceptible individual at time t | |
| reaches the stage of vaccination |
In order to unify the notations, we set
where
and
Then, the model (1) can be rewritten in the following abstract compact form
| 2 |
When no confusion occurs, the value of a given function h at time will occasionally be denoted h and we shall omit the explicit notation.
Given a function . The differential operator associated with (2) is defined as follows
where , tr denotes the trace operator, stands for the transpose operation, while is the Hessian matrix with respect to u.
Itô’s formula [32] states that
We now announce some definitions and notations that will be used throughout the paper.
- For denote by C([0, T]) the Banach space of real-valued continuous functions defined on [0, T]. Given we define
- For an integrable function we set
Given we set
- Consider the following open bounded set
Hereafter, T is a strictly positive real number and it is assumed that
The rest of this paper is organized as follows: In Sect. 2, we study the mathematical and biological well-posedness of the model (1). We devote Sect. 3 to establish conditions under which the infected population becomes extinct or persistent in the mean. While in Sect. 4, we provide a condition under which the model (1) admits a non-trivial periodic solution. Additionally, in order to support the theoretical results, in Sect. 5, we present the outcome of the performed numerical simulations. Finally, we leave Sect. 6 to state some conclusions and future works.
Mathematical and biological well-posedness
We begin this section by stating a remark, which will be useful overall throughout the paper.
Remark 1
It can be seen that the set is positively invariant for the stochastic system (1). Indeed, define the total population at time by Direct application of the comparison principle yields
Then if , it follows that Additionally,
Theorem 1
For every initial condition the stochastic system (2) admits a unique global, almost surely positive solution.
Proof
Since the coefficients of the stochastic system (2) satisfy the local Lipschitz condition, by the standard theory of stochastic differential equations [32], there exists a unique local solution u defined up to a maximal time of existence that we denote . In order to prove that the local solution is a global one that remains almost surely positive, let be sufficiently large such that Then, for define the following stopping time
with the usual convention , where denotes the empty set. It is clear that the sequence is increasing and . Hence, there exists such that Thus, it suffices to prove that . We argue by contradiction and suppose that there exist and such that
Now, consider the following function defined by By Itô’s formula, it holds that
Thereby, by using Remark 1, it follows that
| 3 |
where
By integrating both sides of inequality (3) from 0 to and evaluating the expectation, we obtain
On the other hand, by definition of there exists such that Consequently, Therefore, Hence, due to the positiveness of , it holds that
| 4 |
where stands for the indicator function.
Letting in inequality (4) leads to the contradiction Thus, and the solution is global and remains almost surely positive.
Analysis of the disease extinction and persistence
In this section, we are interested in establishing conditions under which the disease vanishes or persists. To this end, we define the following parameters
, and
Theorem 2
Let u be the solution of the system (2) with the initial value If one of the following conditions
where
and
is satisfied, then the infected population goes to extinction. That is,
Proof
By using Itô’s formula, it holds that
| 5 |
Dividing inequality (5) by then integrating from 0 to t yields
| 6 |
where is a local continuous martingale satisfying and is defined by
By evaluating the supremum limit on both sides of inequality (6) and by the law of large numbers for local martingales [32], we have almost surely. Consequently, we obtain
Hence, if condition (1) is satisfied. Then almost surely. Now, we suppose that By using Itô’s formula and taking Remark 1 into account, we obtain
| 7 |
By dividing inequality (7) by and integrating from 0 to t, we acquire that
| 8 |
By applying the supremum limit on both sides of inequality (8), it follows that
Hence, if it follows that almost surely.
We now proceed to derive the condition under which the infected population becomes persistent in the mean. Namely, under a suitable condition, we prove that: almost surely.
Theorem 3
Let u be the solution of the system (2) with the initial value Under the following condition
| 9 |
the infected population is persistent in the mean. More precisely, almost surely, where
Proof
By using Itô’s formula, it holds that
| 10 |
An integration of inequality (10) from 0 to t and a divison by lead to
| 11 |
where is the local continuous martingale defined in the proof of Theorem 2.
Now, by taking Remark 1 into account, an integration of the first three equations of the stochastic system (1) from 0 to t and a division by yield
| 12 |
where and are continuous local martingales, satisfying and are defined by , , and By injecting the inequalities of (12) into the inequality (11) and rearranging the terms, we obtain
Consequently
| 13 |
where and are as defined in Theorem 3, and
By the law of large numbers for local martingales and by taking Remark 1 into account, it follows that almost surely. The result follows by letting in (13).
Remark 2
We emphasize that in the case of non-autonomous epidemic models with Gaussian noise in the disease transmission, the characterization of the disease extinction and persistence in terms of one stochastic threshold has not been done, due to major difficulties caused by the considered type of noise as well as the time varying parameters, prohibiting to define a unified stochastic threshold. Such a characterization can be obtained for the autonomous case (see e.g. [19]).
On the other hand, for the model (1), considered in this paper, the characterization of the disease extinction and persistence is given independently, in terms of the two stochastic parameters and . However, for the autonomous counterpart of the model, that is, when the model parameters don’t depend on time, following the approach used in Theorem 3, it can be proved that when , the infected population goes to extinction. Consequently, can be seen as a stochastic threshold characterizing the disease persistence and extinction, in the stochastic case. Furthermore, in the absence of Gaussain noise, coincides with the basic reproduction number corresponding to the deterministic counterpart of the model.
Existence of a non-trivial periodic solution
In this section, we investigate the condition under which the system (2) admits a non-trivial periodic solution. From the biological point of view, the existence of such a solution means that the susceptible, vaccinated, infected and recovered populations are persistent. Meaning that their corresponding densities remain strictly positive throughout time. Hence, for diseases with seasonal characteristics, by analyzing the existence of such solutions, one can obtain additional conditions under which, the disease persists within the studied population. In order to achieve the main result of this section, we recall the definition of a periodic stochastic process.
Definition 1
(See [33]) A stochastic process is said to be periodic with period if for every finite sequence of numbers the joint distribution of random variables is independent of h, where
Lemma 1
(See [33]) Let be an l-dimensional stochastic process, consider the following system such that the corresponding coefficients are -periodic in t and satisfy the local Lipschitz condition with respect to X. If there exists a function such that
V is -periodic with respect to .
outside some compact set.
Then, there exists a solution of the above system, which is a -periodic Markov process.
Theorem 4
Suppose that and are periodic functions and denote by their corresponding period. Moreover, let u be the solution of the system (2) with the initial value Define the following parameters
and
Set If the following condition
| 14 |
is satisfied, then the stochastic system (2) admits a -periodic solution.
Proof
We consider the following function defined by
such that
and
while which will both be chosen thereafter accordingly. For simplicity, set
By applying Itô’s formula and rearranging the terms, we obtain
Owing to the inequality of arithmetic and geometric means, we acquire that
For , set
and
so that
Let satisfy
Then, clearly the -periodicity of implies that of . Indeed, taking into account that
we obtain
Thus
Since
and
it follows that
On the other hand, by Itô’s formula, one can obtain
and Thereby,
Now, consider the following compact set
such that will be chosen later.
Let To verify that in it suffices to investigate the following distinguished seven cases
- Case 1
:
- Case 2
:
- Case 3
:
- Case 4
:
- Case 5
:
- Case 6
:
- Case 7
:
For case 1, we obtain
For case 2, we obtain
For case 3, we obtain
For case 4, we obtain
For case 5, we obtain
For case 6, we obtain
For case 7, we obtain
Now, set
Then, for case 1 and in case 7, choose
For case 2, case 3, case 4, case 5, case 6 and in case 7, choose
Consequently, On the other hand, since and taking into consideration the -periodicity of with respect to t, the assumptions of Lemma 1 are verified. Conclusively, the stochastic system (2) admits a -periodic solution.
Remark 3
For the deterministic autonomous counterpart of the model (1), that is One can use the Next Generation Method [34] to compute the basic reproduction number which yields that Hence, the value of coincides with that of and stated in Sects. 3 and 4, respectively.
Numerical simulations
We consider the time horizon (0, 200) and we choose the following initial condition We simulate the model (1) numerically by relying on Matlab software [35] to develop a script implementing the Milstein method presented in [36], which was chosen due to its accuracy. The resulting numerical scheme of the model (1) is the same one presented in [37, 38] and hence is omitted here for brevity. To support all the established theoretical results, five cases are numerically simulated. In the first and second cases, the parameters are chosen such that the conditions (1) and (2) stated in Theorem 2 are verified, respectively. In the third case, the parameters are chosen such that the condition (9) of Theorem 3 is verified. While the fourth and fifth cases correspond to choices of parameters in which the condition (14) of Theorem 4 is verified in both deterministic and stochastic non autonomous cases. For the first case, Fig. 2 shows that the condition (1) of Theorem 2 is satisfied. For the second case, by using Simpson’s method, we have (Fig. 3). Moreover, from Fig. 4, it can be deduced that the condition (2) of Theorem 2 is satisfied. The numerical outcomes are shown in Figs. 3 and 5 and exhibit in both cases that the disease goes to extinction. For the third case, by calculation, we have , thereby, the condition (4) of Theorem 3 holds (Fig. 6). Consequently, which is illustrated by Fig. 7. Figures 6 and 8 show the obtained solution. For the fourth case, by using Simpson’s method, we have Similarly, for the fifth case, we have Consequently, the condition (14) of Theorem 4 is verified. Figures 9 and 10 illustrate the deterministic and stochastic periodicity of the obtained solution (Fig. 11).
Fig. 2.

Verification of the first disease extinction condition
Fig. 3.
Paths of S, , , , I and R when the first condition of the disease extinction holds
Fig. 4.

Verification of the second disease extinction condition
Fig. 5.
Paths of S, , , , I and R when the second condition of the disease extinction holds
Fig. 6.
Paths of S, , , , I and R when the condition of the disease persistence in the mean holds
Fig. 7.

Persistence in the mean of the infected population
Fig. 8.
Probability density functions of S, , , , I and R at time when the condition of the disease persistence in the mean holds
Fig. 9.
Paths of S, , , , I and R in the deterministic non-autonomous case and under the condition
Fig. 10.
Paths of S, , , , I and R in the stochastic non-autonomous case and under the condition
Fig. 11.
Probability density functions of and R at time in the stochastic non-autonomous case and under the condition
The assigned values to the parameters in each case are as follows
- Case 1
- :
- Case 2
- :
- Case 3
- :
- Case 4
- :
- Case 5
- :
Conclusions and future work
The appearance of new emerging diseases requires the enhancement of existing epidemic models, in order to have a more pertinent interpretation of reality [39–43]. In this context, inspired by the characteristics of new emerging diseases such as COVID-19, in this paper, we have conducted a dynamical study of a new-proposed stochastic SVIR model, in the aim of studying the effect of the multiple stages of vaccination, required to gain immunity, along with the environmental noise on the dynamics of the studied population. Our results are briefly outlined as follows.
For a large values of the Gaussian noise intensities, the infected population goes to extinction if . For sufficiently small values of the Gaussian noise intensities, a sufficient condition guaranteeing that the infected population goes to extinction is and and .
Under the condition , the infected population becomes persistent in the mean.
For diseases with seasonal patterns, under the condition the susceptible, infected, vaccinated and recovered subpopulations become persistent.
It is worth mentioning that while our primal focus in this work resided in the dynamical analysis, this paper brings about other interesting questions that need to be investigated. Case in point, we can think of dealing with the identification problem for COVID-19 in Morocco, due to the availability of the data [44], which will permit us to identify the stochastic thresholds characterizing the disease extinction and persistence and then test the effectiveness of the vaccination strategy adopted by the authorities. On the other hand, the model (1) can be further generalized. For instance, taking into account that a certain amount of time is necessary between each stage of vaccination as well as the mean time in which the effectiveness of each stage wears off, we can add delay variables to the model and analyze the changes induced in the dynamics. Finally, by taking into account that the population may suffer from sudden environmental shocks. Precisely, ones exhibited by socio-cultural changes such as anti-vaccination movements, adding Lévy jumps to the model can increase its pertinence. All these questions will be the subjects of future work.
Acknowledgements
The authors would like to express their gratitude to the editor and anonymous reviewers for their careful reading and valuable suggestions.
Code availability
The Matlab code used for the numerical simulations is available from the corresponding author upon request.
Declarations
Conflicts of interest
The authors declare that they have no conflicts of interest.
Footnotes
Publisher's Note
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Contributor Information
Mohamed Mehdaoui, Email: m.mehdaoui@edu.umi.ac.ma.
Abdesslem Lamrani Alaoui, Email: abdesslemalaoui@gmail.com.
Mouhcine Tilioua, Email: m.tilioua@umi.ac.ma.
References
- 1.Kermack WO, McKendrick AG. A contribution to the mathematical theory of epidemics. Proc. R. Soc. Lond. Ser. A Contain Papers Math. Phys. Charact. 1927;115:700–721. doi: 10.1098/rspa.1927.0118. [DOI] [Google Scholar]
- 2.Liu X, Takeuchi Y, Iwami S. SVIR epidemic models with vaccination strategies. J. Theor. Biol. 2008;253(1):1–11. doi: 10.1016/j.jtbi.2007.10.014. [DOI] [PubMed] [Google Scholar]
- 3.Kumar S, Ahmadian A, Kumar R, Kumar D, Singh J, Baleanu D, Salimi M. An efficient numerical method for fractional sir epidemic model of infectious disease by using Bernstein wavelets. Mathematics. 2020;8(4):558. doi: 10.3390/math8040558. [DOI] [Google Scholar]
- 4.Khan ZA, Lamrani Alaoui A, Zeb A, Tilioua M, Djilali S. Global dynamics of a SEI epidemic model with immigration and generalized nonlinear incidence functional. Results Phys. 2021;27:104477. doi: 10.1016/j.rinp.2021.104477. [DOI] [Google Scholar]
- 5.Kumar S, Kumar A, Samet B, Gómez-Aguilar J, Osman M. A chaos study of tumor and effector cells in fractional tumor-immune model for cancer treatment. Chaos Solitons Fractals. 2020;141:110321. doi: 10.1016/j.chaos.2020.110321. [DOI] [Google Scholar]
- 6.Kumar S, Kumar R, Osman M, Samet B. A wavelet based numerical scheme for fractional order SEIR epidemic of measles by using Genocchi polynomials. Numer. Methods Partial Differ. Equ. 2021;37(2):1250–1268. doi: 10.1002/num.22577. [DOI] [Google Scholar]
- 7.Mohammadi H, Kumar S, Rezapour S, Etemad S. A theoretical study of the Caputo-Fabrizio fractional modeling for hearing loss due to mumps virus with optimal control. Chaos Solitons Fractals. 2021;144:110668. doi: 10.1016/j.chaos.2021.110668. [DOI] [Google Scholar]
- 8.Ghanbari B, Kumar S, Kumar R. A study of behaviour for immune and tumor cells in immunogenetic tumour model with non-singular fractional derivative. Chaos Solitons Fractals. 2020;133:109619. doi: 10.1016/j.chaos.2020.109619. [DOI] [Google Scholar]
- 9.Mehdaoui M, Alaoui AL, Tilioua M. Optimal control for a multi-group reaction-diffusion SIR model with heterogeneous incidence rates. Int. J. Dyn. Control. 2022 doi: 10.1007/s40435-022-01030-3. [DOI] [Google Scholar]
- 10.Mezouaghi A, Djilali S, Bentout S, Biroud K. Bifurcation analysis of a diffusive predator-prey model with prey social behavior and predator harvesting. Math. Methods Appl. Sci. 2022;45(2):718–731. doi: 10.1002/mma.7807. [DOI] [Google Scholar]
- 11.Djilali S, Bentout S. Pattern formations of a delayed diffusive predator-prey model with predator harvesting and prey social behavior. Math. Methods Appl. Sci. 2021;44(11):9128–9142. doi: 10.1002/mma.7340. [DOI] [Google Scholar]
- 12.Djilali S, Bentout S. Spatiotemporal patterns in a diffusive predator-prey model with prey social behavior. Acta Appl. Math. 2020;169(1):125–143. doi: 10.1007/s10440-019-00291-z. [DOI] [Google Scholar]
- 13.Kiouach, D., Sabbar, Y.: Ergodic stationary distribution of a stochastic hepatitis B epidemic model with interval-valued parameters and compensated poisson process. Comput. Math. Methods Med. 2020 (2020) [DOI] [PMC free article] [PubMed]
- 14.Kiouach D, Sabbar Y. Global dynamics analysis of a stochastic SIRS epidemic model with vertical transmission and different periods of immunity. Int. J. Dyn. Syst. Differ. Equ. 2020;10(5):468–491. [Google Scholar]
- 15.Kiouach D, Sabbar Y. Dynamic characterization of a stochastic SIR infectious disease model with dual perturbation. Int. J. Biomath. 2021;14(04):2150016. doi: 10.1142/S1793524521500169. [DOI] [Google Scholar]
- 16.Liu Q, Jiang D, Hayat T, Alsaedi A, Ahmad B. Dynamical behavior of a higher order stochastically perturbed SIRI epidemic model with relapse and media coverage. Chaos Solit. Fractals. 2020;139:110013. doi: 10.1016/j.chaos.2020.110013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Kiouach D, Sabbar Y, El Azami El-idrissi S. New results on the asymptotic behavior of an SIS epidemiological model with quarantine strategy, stochastic transmission, and Lévy disturbance. Math. Methods Appl. Sci. 2021;44(17):13468–13492. doi: 10.1002/mma.7638. [DOI] [Google Scholar]
- 18.Shangguan D, Liu Z, Wang L, Tan R. A stochastic epidemic model with infectivity in incubation period and homestead-isolation on the susceptible. J. Appl. Math. Comput. 2021;67(1):785–805. doi: 10.1007/s12190-021-01504-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Jiang D, Yu J, Ji C, Shi N. Asymptotic behavior of global positive solution to a stochastic SIR model. Math. Comput. Model. 2011;54(1–2):221–232. doi: 10.1016/j.mcm.2011.02.004. [DOI] [Google Scholar]
- 20.Sabbar Y, Khan A, Din A, Kiouach D, Rajasekar S. Determining the global threshold of an epidemic model with general interference function and high-order perturbation. AIMS Math. 2022;7(11):19865–19890. doi: 10.3934/math.20221088. [DOI] [Google Scholar]
- 21.Keeling MJ, Rohani P, Grenfell BT. Seasonally forced disease dynamics explored as switching between attractors. Phys. D Nonlinear Phenom. 2001;148(3–4):317–335. doi: 10.1016/S0167-2789(00)00187-1. [DOI] [Google Scholar]
- 22.Weber A, Weber M, Milligan P. Modeling epidemics caused by respiratory syncytial virus (RSV) Math. Biosci. 2001;172(2):95–113. doi: 10.1016/S0025-5564(01)00066-9. [DOI] [PubMed] [Google Scholar]
- 23.Greenhalgh D, Moneim IA. SIRS epidemic model and simulations using different types of seasonal contact rate. Syst. Anal. Model. Simul. 2003;43(5):573–600. doi: 10.1080/023929021000008813. [DOI] [Google Scholar]
- 24.Qi H, Leng X, Meng X, Zhang T. Periodic solution and ergodic stationary distribution of SEIS dynamical systems with active and latent patients. Qual. Theory Dyn. Syst. 2019;18(2):347–369. doi: 10.1007/s12346-018-0289-9. [DOI] [Google Scholar]
- 25.Shangguan, D., Liu, Z., Wang, L., Tan, R.: Periodicity and stationary distribution of two novel stochastic epidemic models with infectivity in the latent period and household quarantine. J. Appl. Math. Comput. 1–20 (2021) [DOI] [PMC free article] [PubMed]
- 26.Liu Q, Jiang D, Hayat T, Ahmad B. Periodic solution and stationary distribution of stochastic SIR epidemic models with higher order perturbation. Phys. A Stat. Mech. Appl. 2017;482:209–217. doi: 10.1016/j.physa.2017.04.056. [DOI] [Google Scholar]
- 27.Lin Y, Jiang D, Liu T. Nontrivial periodic solution of a stochastic epidemic model with seasonal variation. Appl. Math. Lett. 2015;45:103–107. doi: 10.1016/j.aml.2015.01.021. [DOI] [Google Scholar]
- 28.El Fatini M, Pettersson R, Sekkak I, Taki R. A stochastic analysis for a triple delayed SIQR epidemic model with vaccination and elimination strategies. J. Appl. Math. Comput. 2020;64(1):781–805. doi: 10.1007/s12190-020-01380-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Zhang X, Liu M. Dynamical analysis of a stochastic delayed sir epidemic model with vertical transmission and vaccination. Adv. Contin. Discrete Models. 2022;2022(1):1–18. doi: 10.1186/s13662-022-03707-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Burki TK. Omicron variant and booster COVID-19 vaccines. Lancet Respir. Med. 2022;10(2):17. doi: 10.1016/S2213-2600(21)00559-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Mattiuzzi, C., Lippi, G.: Primary COVID-19 vaccine cycle and booster doses efficacy: analysis of Italian nationwide vaccination campaign. Eur. J. Public Health (2022) [DOI] [PMC free article] [PubMed]
- 32.Mao X. Stochastic Differential Equations and Applications. New York: Elsevier; 2007. [Google Scholar]
- 33.Khasminskii R. Stochastic Stability of Differential Equations. Berlin: Springer; 2011. [Google Scholar]
- 34.Van den Driessche P, Watmough J. Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission. Math. Biosci. 2002;180(1–2):29–48. doi: 10.1016/S0025-5564(02)00108-6. [DOI] [PubMed] [Google Scholar]
- 35.MATLAB: Version 9.4.0 (R2018a). The MathWorks Inc., Natick, Massachusetts (2010)
- 36.Higham DJ. An algorithmic introduction to numerical simulation of stochastic differential equations. SIAM Rev. 2001;43(3):525–546. doi: 10.1137/S0036144500378302. [DOI] [Google Scholar]
- 37.Bao K, Zhang Q. Stationary distribution and extinction of a stochastic sirs epidemic model with information intervention. Adv. Differ. Equ. 2017;2017(1):1–19. doi: 10.1186/s13662-017-1406-9. [DOI] [Google Scholar]
- 38.Rao, F.: Dynamics analysis of a stochastic sir epidemic model. In: Abstract and Applied Analysis, vol. 2014 (2014). Hindawi
- 39.Soufiane B, Touaoula TM. Global analysis of an infection age model with a class of nonlinear incidence rates. J. Math. Anal. Appl. 2016;434(2):1211–1239. doi: 10.1016/j.jmaa.2015.09.066. [DOI] [Google Scholar]
- 40.Bentout S, Tridane A, Djilali S, Touaoula TM. Age-structured modeling of Covid-19 epidemic in the USA, UAE and Algeria. Alex. Eng. J. 2021;60(1):401–411. doi: 10.1016/j.aej.2020.08.053. [DOI] [Google Scholar]
- 41.Bentout S, Chekroun A, Kuniya T. Parameter estimation and prediction for coronavirus disease outbreak 2019 (Covid-19) in Algeria. AIMS Public Health. 2020;7(2):306. doi: 10.3934/publichealth.2020026. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Soufiane B, Touaoula TM. Global analysis of an infection age model with a class of nonlinear incidence rates. J. Math. Anal. Appl. 2016;434(2):1211–1239. doi: 10.1016/j.jmaa.2015.09.066. [DOI] [Google Scholar]
- 43.Bentout S, Chen Y, Djilali S. Global dynamics of an SEIR model with two age structures and a nonlinear incidence. Acta Appl. Math. 2021;171(1):1–27. doi: 10.1007/s10440-020-00369-z. [DOI] [Google Scholar]
- 44.The Moroccan Ministry of Public Health: COVID-19 Platform. http://www.covidmaroc.ma/pages/Accueilfr.aspx (2022)
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The Matlab code used for the numerical simulations is available from the corresponding author upon request.







