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. 2022 Dec 14;69(2):2177–2206. doi: 10.1007/s12190-022-01828-6

Dynamical analysis of a stochastic non-autonomous SVIR model with multiple stages of vaccination

Mohamed Mehdaoui 1,, Abdesslem Lamrani Alaoui 1, Mouhcine Tilioua 1
PMCID: PMC9749651  PMID: 36531662

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 [212], while several other works were done in the aim of extending the deterministic results to the stochastic case [1320]. 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 [2123]. 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 V1,V2 and V3, such that V1 and V2 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 V3 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.

dS(t)=Λ(t)-βS(t)S(t)I(t)-μ(t)S(t)-κ1(t)S(t)dt-σ1(t)S(t)I(t)dB1(t),dV1(t)=-βV1(t)V1(t)I(t)+κ1(t)S(t)-μ(t)V1(t)-κ2(t)V1(t)dt-σ2(t)V1(t)I(t)dB2(t),dV2(t)=-βV2(t)V2(t)I(t)+κ2(t)V1(t)-μ(t)V2(t)-κ3(t)V2(t)dt-σ3(t)V2(t)I(t)dB3(t),dV3(t)=κ3(t)V2(t)-μ(t)V3(t)-γV3(t)V3(t)dt,dI(t)=βS(t)S(t)+βV1(t)V1(t)+βV2(t)V2(t)-γ(t)-μ(t)I(t)dt+σ1(t)S(t)I(t)dB1(t)+σ2(t)V1(t)I(t)dB2(t)+σ3(t)V2(t)I(t)dB3(t),dR(t)=γ(t)I(t)-μ(t)R(t)+γV3(t)V3(t)dt, 1

equipped with the following initial conditions

S(0):=S00,V1(0):=V100,V2(0):=V200,V3(0):=V300,I(0):=I00andR(0):=R00,

where (B1(t))t0,(B2(t))t0 and (B3(t))t0 are mutually independent Brownian motions defined on a probabilistic space (Ω,F,{Ft}t0,P) with a filtration {Ft}t0 which is increasing, right-continuous and such that F0 contains the null sets, while σ1(t),σ2(t) and σ3(t) denote the time-dependent intensities of the environmental Gaussian noise present in the disease transmission rates (Fig. 1, 1).

Fig. 1.

Fig. 1

Flow diagram of the model (1) in the deterministic case

Table 1.

Signification of the model parameters

Parameter Biological signification
Λ(t) Natural birth rate at time t
μ(t) Natural death rate at time t
βS(t) Rate in which a susceptible individual at time t becomes infected
βVi(t) Rate in which an individual at time t
and in the ith stage of vaccination (i{1,2}) becomes infected
γ(t) Natural recovery rate at time t
γV3(t) Rate in which an individual at time t and in the third stage
of vaccination possesses immunity
κi(t) Rate in which a susceptible individual at time t
reaches the ith stage of vaccination (i{1,2,3})

In order to unify the notations, we set

u(t)=Δ(S(t),V1(t),V2(t),V3(t),I(t),R(t)),u0=Δ(S0,V10,V20,V30,I0,R0),dB(t)=Δ(dB1(t),dB2(t),dB3(t),dB4(t),dB5(t),dB6(t)),θ(t)=Δ(Λ(t),βS(t),μ(t),κ1(t),κ2(t),κ3(t),βV1(t),βV2(t),γ(t),γV3(t)),f(t,u(t))=Δ(f1(t,u(t)),f2(t,u(t)),f3(t,u(t)),f4(t,u(t)),f5(t,u(t)),f6(t,u(t))),

where

f1(t,u(t)):=Λ(t)-βS(t)S(t)I(t)-μ(t)S(t)-κ1(t)S(t),f2(t,u(t)):=-βV1(t)V1(t)I(t)+κ1(t)S(t)-μ(t)V1(t)-κ2(t)V1(t),f3(t,u(t)):=-βV2(t)V2(t)I(t)+κ2(t)V1(t)-μ(t)V2(t)-κ3(t)V2(t),f4(t,u(t)):=κ3(t)V2(t)-μ(t)V3(t)-γV3(t)V3(t),f5(t,u(t)):=βS(t)S(t)I(t)+βV1(t)V1(t)I(t)+βV2(t)V2(t)I(t)-γ(t)I(t)-μ(t)I(t),f6(t,u(t)):=γ(t)I(t)-μ(t)R(t)+γV3(t)V3(t),

and

g(t,u(t)):=-σ1(t)S(t)I(t)000000-σ2(t)V1(t)I(t)000000-σ3(t)V2(t)I(t)000000000[1ex]σ1(t)S(t)I(t)σ2(t)V1(t)I(t)σ3(t)V2(t)I(t)000000000.

Then, the model (1) can be rewritten in the following abstract compact form

du(t)=f(t,u(t))dt+g(t,u(t))dB(t),u(0)=u00. 2

When no confusion occurs, the value of a given function h at time t(0,T) will occasionally be denoted h and we shall omit the explicit notation.

Given a function VC1,2(R+×R6,R). The differential operator associated with (2) is defined as follows

LV(t,u)=V(t,u)t+uV(t,u).f(t,u)+12trg(t,u)Hessu(V(t,u))g(t,u),

where u:=u1,,u6, tr denotes the trace operator, stands for the transpose operation, while Hessu is the Hessian matrix with respect to u.

Itô’s formula [32] states that

dV(t,u)=LV(t,u)dt+uf(t,u(t)).g(t,u(t))dB(t).

We now announce some definitions and notations that will be used throughout the paper.

  • For T>0, denote by C([0, T]) the Banach space of real-valued continuous functions defined on [0, T]. Given fC([0,T]), we define
    f¯:=supt[0,T]|f(t)|andf_:=inft[0,T]|f(t)|.
  • For an integrable function f:(0,T)R, we set
    ft:=1t0tf(s)dst(0,T).
  • Given a,bR, we set ab=Δsup{a,b}andab=Δinf{a,b}.

  • Consider the following open bounded set
    U:=u(0,+)6,i=16ui<Λ¯μ_.

Hereafter, T is a strictly positive real number and it is assumed that

θi,σjC([0,T])andθi_,θi¯,σj_,σj¯>0,(i,j){1,,10}×{1,2,3}.

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 I:={uR+6,i=16uiΛ¯μ_}, is positively invariant for the stochastic system (1). Indeed, define the total population at time t(0,T) by N(t):=i=16ui(t). Direct application of the comparison principle yields

N(t)N(0)exp(-μ_t)+Λ¯μ_1-exp(-μ_t).

Then if u0I, it follows that u(t)It(0,T). Additionally,

limt+N(t)Λ¯μ_almost surely.

Theorem 1

For every initial condition u0I, 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 Tmax. In order to prove that the local solution is a global one that remains almost surely positive, let n~N be sufficiently large such that u01n~,Λ¯μ_)6. Then, for nn~ define the following stopping time

τn:=inft[0,Tmax)i0{1,,6}ui0(t)1n,

with the usual convention inf=+, where denotes the empty set. It is clear that the sequence (τn)nn~ is increasing and τnTmax. Hence, there exists τl such that limn+τn=τlTmax. Thus, it suffices to prove that τl=+. We argue by contradiction and suppose that there exist ϵ(0,1), T>0 and n0n~ such that

nn0,P(τnT)ϵ.

Now, consider the following function F:UR+ defined by F(u):=-i=16lnμ_uiΛ¯. By Itô’s formula, it holds that

dF=-1SΛ-βSSI-μS-κ1S-1V1-βV1V1I+κ1S-μV1-κ2V1-1V2-βV2V2I+κ2V1-μV2-κ3V2-1V3κ3V2-μV3-γV3V3-1IβSSI+βV1V1I+βV2V2I-γI-μI-1RγI-μR+γV3V3+12σ12+σ22+σ32I2+12σ12S2+σ22V12+σ32V22dt+σ1(I-S)dB1+σ2(I-V1)dB2+σ3(I-V2)dB3.

Thereby, by using Remark 1, it follows that

dFCdt+σ1(I-S)dB1+σ2(I-V1)dB2+σ3(I-V2)dB3, 3

where

C:=Λ¯μ_βS¯+βV1¯+βV2¯+6μ¯+κ1¯+κ2¯+κ3¯+γ¯+γV3¯+Λ¯2μ_2σ1¯2σ2¯2σ3¯2.

By integrating both sides of inequality (3) from 0 to Tτn and evaluating the expectation, we obtain

E(F(u(Tτn)))F(u(0))+CT.

On the other hand, by definition of τn, there exists i0{1,,6} such that ui0(τn)1n. Consequently, -lnμ_ui0(τn)Λ¯-lnμ_Λ¯n. Therefore, F(u(τn))-lnμ_Λ¯n. Hence, due to the positiveness of F, it holds that

-lnμ_Λ¯nE(F(u(τn)1τnT))E(F(u(Tτn)))F(u(0))+CT. 4

where 1 stands for the indicator function.

Letting n+ in inequality (4) leads to the contradiction +F(u(0))+CT<+. Thus, Tmax=+ 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

R1s(t):=Λ¯μ_βS(t)+βV1(t)+βV2(t)μ(t)+γ(t)-Λ¯2μ_2(μ(t)+γ(t))12σ12(t)+12σ22(t)+12σ32(t),

t(0,T), and

R2s:=Λ_βS_μ¯+κ2¯μ¯+κ3¯+Λ_κ1_βV1_μ¯+κ3¯+Λ_κ1_κ2_βV2_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯μ¯+γ¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

Theorem 2

Let u be the solution of the system (2) with the initial value u0I. If one of the following conditions

  1. lim supt+ϱ(t)<0, where ϱ(t):=βS2σ12t+βV12σ22t+βV22σ32t-2μt+γt,

  2. R1sT<1, and t(0,T), μ_Λ¯βS(t)>σ12(t), μ_Λ¯βV1(t)>σ22(t), μ_Λ¯βV2(t)>σ32(t),

is satisfied, then the infected population goes to extinction. That is, lim supt+I(t)=0almost surely.

Proof

By using Itô’s formula, it holds that

d(ln(I))=βSS+βV1V1+βV2V2-μ-γ-12σ12S2-12σ22V12-12σ32V22dt+σ1SdB1+σ2V1dB2+σ3V2dB3=-βS2σ1-σ1S22-βV12σ2-σ2V122-βV22σ3-σ3V222+βS22σ12+βV122σ22+βV222σ32-μ-γdt+σ1SdB1+σ2V1dB2+σ3V2dB3βS22σ12+βV122σ22+βV222σ32-μ-γdt+σ1SdB1+σ2V1dB2+σ3V2dB3. 5

Dividing inequality (5) by t>0, then integrating from 0 to t yields

ln(I(t))tln(I(0))t+12βS2σ12t+12βV12σ22t+12βV22σ32t-μt-γt+1tM1(t), 6

where M1(t) is a local continuous martingale satisfying M1(0)=0, and is defined by

M1(t):=0tσ1(s)S(s)dB1(s)+σ2(s)V1(s)dB2(s)+σ3(s)V2(s)dB3(s).

By evaluating the supremum limit on both sides of inequality (6) and by the law of large numbers for local martingales [32], we have limt+M1(t)t=0, almost surely. Consequently, we obtain

lim supt+ln(I(t))tlim supt+12βS2σ12t+βV12σ22t+βV22σ32t-μt-γt.

Hence, if condition (1) is satisfied. Then lim supt+I(t)=0 almost surely. Now, we suppose that μ_Λ¯βS(t)>σ12(t),μ_Λ¯βV1(t)>σ22(t)andμ_Λ¯βV2(t)>σ32(t),t(0,T). By using Itô’s formula and taking Remark 1 into account, we obtain

d(ln(I))=βSS-12σ12S2+βV1V1-12σ22V12+βV2V2-12σ32V22-μ-γdt+σ1SdB1+σ2V1dB2+σ3V2dB3βSΛ¯μ_-12σ12Λ¯2μ_2+βV1Λ¯μ_-12σ22Λ¯2μ_2+βV2Λ¯μ_-12σ32Λ¯2μ_2-μ-γdt+σ1SdB1+σ2V1dB2+σ3V2dB3=μ+γΛ¯μ_βS+βV1+βV2μ+γ-Λ¯2μ_2(μ+γ)12σ12+12σ22+12σ32-1dt+σ1SdB1+σ2V1dB2+σ3V2dB3. 7

By dividing inequality (7) by t>0 and integrating from 0 to t, we acquire that

ln(I(t))tln(I(0))t+μt+γtR1st-1+1tM1(t). 8

By applying the supremum limit on both sides of inequality (8), it follows that

lim supt+ln(I(t))tR1sT-1lim supt+μt+γt.

Hence, if R1sT<1, it follows that lim supt+I(t)=0 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: α>0,lim inft+Itα almost surely.

Theorem 3

Let u be the solution of the system (2) with the initial value u0I. Under the following condition

R2s>1, 9

the infected population is persistent in the mean. More precisely, lim inft+Itλλ0 almost surely, where

λ:=μ¯+γ¯+12σ1¯2Λ¯2μ2_+12σ2¯2Λ¯2μ2_+12σ3¯2Λ¯2μ2_R2s-1,
λ0:=α3βS_βS¯Λ¯α2+βV1_βV1¯Λ¯α1+Λ¯βS¯κ1_βV1_μ_α1α2α3+α1βV2¯βV2_Λ¯α2+Λ¯κ2_βV1¯βV2_+Λ¯βS¯κ1_κ2_βV2_μ_α1α2α3,
α1:=μ¯+κ1¯,α2:=μ¯+κ2¯andα3:=μ¯+κ3¯.

Proof

By using Itô’s formula, it holds that

d(ln(I))=βSS+βV1V1+βV2V2-μ-γ-12σ12S2-12σ22V12-12σ32V22dt+σ1SdB1+σ2V1dB2+σ3V2dB3βS_S+βV1_V1+βV2_V2-μ¯-γ¯-12σ1¯2Λ¯2μ2¯-12σ2¯2Λ¯2μ2_-12σ3¯2Λ¯2μ2_dt+σ1SdB1+σ2V1dB2+σ3V2dB3. 10

An integration of inequality (10) from 0 to t and a divison by t>0 lead to

ln(I(t))-ln(I(0))tβS_St+βV1_V1t+βV2_V2t-μ¯-γ¯-12σ1¯2Λ¯2μ2_-12σ2¯2Λ¯2μ2_-12σ3¯2Λ¯2μ2_+M1(t)t, 11

where M1(t) 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 t>0 yield

St1μ¯+κ1¯-βS¯Λ¯μ_It+Λ_-S(t)-S(0)t+M2(t)t,V1t1μ¯+κ2¯-βV1¯Λ¯μ_It+κ1_μ¯+κ1¯Λ_-βS¯Λ¯μ_It-S(t)-S(0)t+M2(t)t-V1(t)-V1(0)t+M3(t)t,V2t1μ¯+κ3¯-βV2¯Λ¯μ_It+κ2_μ¯+κ2¯-βV1¯Λ¯μ_It+κ1_μ¯+κ1¯×Λ_-βS¯Λ¯μ_It-S(t)-S(0)t+M2(t)t-V1(t)-V1(0)t+M3(t)t-V2(t)-V2(0)t+M4(t)t, 12

where M2(t),M3(t) and M4(t) are continuous local martingales, satisfying M2(0)=M3(0)=M4(0)=0, and are defined by M2(t):=0t-σ1(s)S(s)I(s)dB1(s), M3(t):=0t-σ2(s)V1(s)I(s)dB2(s), and M4(t):=0t-σ3(s)V2(s)I(s)dB3(s). By injecting the inequalities of (12) into the inequality (11) and rearranging the terms, we obtain

ln(I(t))-ln(I(0))tμ¯+γ¯+12σ1¯2Λ¯2μ2_+12σ2¯2Λ¯2μ2_+12σ3¯2Λ¯2μ2_R2s-1+M1(t)t+βS_μ¯+κ1¯+κ1_βV1_μ¯+κ1¯μ¯+κ2¯+κ1_κ2_βV2_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯×M2(t)t+βV1_μ¯+κ2¯+κ2_βV2_μ¯+κ2¯μ¯+κ3¯M3(t)t+βV2_μ¯+κ3¯M4(t)t-Λ¯βS¯βS_μ_μ¯+κ1¯+Λ¯βV1¯βV1_μ_μ¯+κ2¯+κ1_βV1_βS¯Λ¯μ_μ¯+κ1¯μ¯+κ2¯+κ2_βV2_βV1¯Λ¯μ_μ¯+κ2¯μ¯+κ3¯+Λ¯βV2¯βV2_μ_μ¯+κ3¯+κ1_κ2_βV2_βS¯Λ¯μ_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯It-βS_μ¯+κ1¯+κ1_βV1_μ¯+κ1¯μ¯+κ2¯+κ1_κ2_βV2_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯S(t)-S(0)t-βV1_μ¯+κ2¯+κ2_βV2_μ¯+κ2¯μ¯+κ3¯V1(t)-V1(0)t-βV2_μ¯+κ3¯×V2(t)-V2(0)t.

Consequently

ln(I(t))tλ-λ0It+H(t)talmostsurely,t0, 13

where λ and λ0 are as defined in Theorem 3, and

H(t):=M1(t)+βS_μ¯+κ1¯+κ1_βV1_μ¯+κ1¯μ¯+κ2¯+κ1_κ2_βV2_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯M2(t)+βV1_μ¯+κ2¯+κ2_βV2_μ¯+κ2¯μ¯+κ3¯M3(t)+βV2_μ¯+κ3¯M4(t)-βS_μ¯+κ1¯+κ1_βV1_μ¯+κ1¯μ¯+κ2¯+κ1_κ2_βV2_μ¯+κ1¯μ¯+κ2¯μ¯+κ3¯S(t)-S(0)-βV1_μ¯+κ2¯+κ2_βV2_μ¯+κ2¯μ¯+κ3¯V1(t)-V1(0)-βV2_μ¯+κ3¯V2(t)-V2(0)+ln(I(0)).

By the law of large numbers for local martingales and by taking Remark 1 into account, it follows that limt+H(t)t=0, almost surely. The result follows by letting t+ 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 R1s and R2s. 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 R2s<1, the infected population goes to extinction. Consequently, R2s can be seen as a stochastic threshold characterizing the disease persistence and extinction, in the stochastic case. Furthermore, in the absence of Gaussain noise, R2s 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 (η(t))tR is said to be periodic with period ν if for every finite sequence of numbers t1,t2,,tn, the joint distribution of random variables ηt1+h,ηt2+h,,ηtn+h, is independent of h, where h:=kν(k=±1,±2,).

Lemma 1

(See [33]) Let (X(t))tt0 be an l-dimensional stochastic process, consider the following system dX(t)=b(t,X(t))dt+σ(t,X(t))dB(t), such that the corresponding coefficients are ν-periodic in t and satisfy the local Lipschitz condition with respect to X. If there exists a function VC1,2((0,+)×Rl,R) such that

  1. V is ν-periodic with respect to t(0,+).

  2. inf|x|>RV(t,x)+asR+t(0,+).

  3. LV(t,x)-1 outside some compact set.

Then, there exists a solution of the above system, which is a ν-periodic Markov process.

Theorem 4

Suppose that (θi)i=110 and (σ)i=13 are periodic functions and denote by ν>0 their corresponding period. Moreover, let u be the solution of the system (2) with the initial value u0I. Define the following parameters

R1:=ΛβS12ν2μ+γν+12σ12+σ22+σ32νΛ¯2μ2_μ+κ1ν+12σ12νΛ¯2μ2_,
R2:=Λκ1βV113ν3μ+γν+12σ12+σ22+σ32νΛ¯2μ2_μ+κ2ν+12σ22νΛ¯2μ2_×1μ+κ1ν+12σ12νΛ¯2μ2_,

and

R3:=Λκ1κ2βV214ν4μ+γν+12σ12+σ22+σ32νΛ¯2μ2_μ+κ3ν+12σ32νΛ¯2μ2_×1μ+κ2ν+12σ22νΛ¯2μ2_.

Set R:=R1+R2+R3. If the following condition

R>1, 14

is satisfied, then the stochastic system (2) admits a ν-periodic solution.

Proof

We consider the following function V:(0,+)×UR defined by

V(t,u):=M(-b1+b2+b3lnμ_Λ¯S-b4+b5lnμ_Λ¯V1-b6lnμ_Λ¯V2-lnμ_Λ¯I+ω(t))+S+V1+V2+V3+I+R-lnμ_Λ¯S-lnμ_Λ¯V1-lnμ_Λ¯V2-lnμ_Λ¯V3-lnμ_Λ¯R,

such that

b1:=ΛβS12ν2μ+κ1ν+12σ12νΛ¯2μ2_2,b2:=Λκ1βV113ν3μ+κ2ν+12σ22νΛ¯2μ2_μ+κ1ν+12σ12νΛ¯2μ2_2,b3:=Λκ1κ2βV214ν4μ+κ3ν+12σ32νΛ¯2μ2_μ+κ2ν+12σ22νΛ¯2μ2_μ+κ1ν+12σ12νΛ¯2μ2_2,b4:=Λκ1βV113ν3μ+κ2ν+12σ22νΛ¯2μ2_2μ+κ1ν+12σ12νΛ¯2μ2_,b5:=Λκ1κ2βV214ν4μ+κ3ν+12σ32νΛ¯2μ2_μ+κ2ν+12σ22νΛ¯2μ2_2μ+κ1ν+12σ12νΛ¯2μ2_,

and

b6:=Λκ1κ2βV214ν4μ+κ3ν+12σ32νΛ¯2μ2_2μ+κ2ν+12σ22νΛ¯2μ2_μ+κ1ν+12σ12νΛ¯2μ2_,

while MR+andω:(0,T)Ris a periodic function, which will both be chosen thereafter accordingly. For simplicity, set

V1(u):=-b1+b2+b3lnμ_Λ¯S-b4+b5lnμ_Λ¯V1-b6lnμ_Λ¯V2-lnμ_Λ¯I.

By applying Itô’s formula and rearranging the terms, we obtain

L(V1(u))=-b1ΛS-βSS+b1μ+κ1+12σ12I2-b2ΛS-βV1V1-b4κ1SV1+b2μ+κ1+12σ12I2+b4μ+κ2+12σ22I2-b3ΛS-b5κ1SV1-b6κ2V1V2-βV2V2+b3μ+κ1+12σ1I2+b5μ+κ2+12σ22I2+b6μ+κ3+12σ32I2+b1+b2+b3βS+b4+b5βV1+b6βV2I+μ+γ+12σ12S2+σ22V12+σ32V22.

Owing to the inequality of arithmetic and geometric means, we acquire that

L(V1(u))-2ΛβSb112+b1μ+κ1+12σ12Λ¯2μ_2-3Λκ1βV1b2b413+b2μ+κ1+12σ12Λ¯2μ_2+b4μ+κ2+12σ22Λ¯2μ_2-4Λκ1κ2βV2b3b5b614+b3μ+κ1+12σ12Λ¯2μ_2+b6μ+κ3+12σ32Λ¯2μ_2+b5μ+κ2+12σ22I2+b1+b2+b3βS+b4+b5βV1+b6βV2I+μ+γ+12Λ¯2μ_2σ12+σ22+σ32.

For t(0,T), set

ζ(t):=-2Λ(t)βS(t)b112+b1μ(t)+κ1(t)+12σ12(t)Λ¯2μ_2-3Λ(t)κ1(t)βV1(t)b2b413+b2μ(t)+κ1(t)+12σ12(t)Λ¯2μ_2+b4μ(t)+κ2(t)+12σ22(t)Λ¯2μ_2+b5μ(t)+κ2(t)+12σ22(t)Λ¯2μ_2-4Λ(t)κ1(t)κ2(t)βV2(t)b3b5b614+b3μ(t)+κ1(t)+12σ12(t)Λ¯2μ_2+b6μ(t)+κ3(t)+12σ32(t)Λ¯2μ_2+μ(t)+γ(t)+12Λ¯2μ_2σ12(t)+σ22(t)+σ32(t),

and

ξ:=b1+b2+b3βS¯+b4+b5βV1¯+b6βV2¯,

so that

L(V1(u(t)))ζ(t)+ξI.

Let ω satisfy

ω(t)=ζν-ζ(t),ω(0)=0.

Then, clearly the ν-periodicity of ζ implies that of ω. Indeed, taking into account that

ω(ν)=νζν-0νζ(s)ds=νζν-1ν0νζ(s)ds=ν(ζν-ζν)=0,

we obtain

ω(t+ν)=ω(ν)+νt+νζν-ζ(s)ds=0tζν-ζ(u+ν)du=0tζν-ζ(u)du=ω(t).

Thus

L(V1(u)+ω(t))ζν+ξI.

Since

-2ΛβSb112ν=-2ΛβS12ν2μ+κ1ν+12σ12νΛ¯2μ2_,-3Λκ1βV1b2b413ν=-3Λκ1βV113ν3μν+12σ22νΛ¯2μ2_μ+κ1ν+12σ12νΛ¯2μ2_,

and

-4Λκ1κ2βV2b3b5b614ν=-4Λκ1κ2βV214ν4μ+κ3ν+12σ32νΛ¯2μ2_μ+κ2ν+12σ22νΛ¯2μ2_×1μ+κ1ν+12σ12νΛ¯2μ2_,

it follows that

L(V1(u)+ω(t))-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξI.

On the other hand, by Itô’s formula, one can obtain

L-lnμ_Λ¯S-Λ_S+βS¯I+μ¯+κ1¯+12σ1¯2Λ¯2μ_2,L-lnμ_Λ¯V1βV1¯I-κ1_SV1+μ¯+κ2¯+12σ2¯2Λ¯2μ_2,L-lnμ_Λ¯V2βV2¯I-κ2_V1V2+μ¯+κ3¯+12σ3¯2Λ¯2μ_2,L-lnμ_Λ¯V3-κ3_V2V3+μ¯+γV3¯,L-lnμ_Λ¯Rμ¯-γV3_V3R,

and LS+V1+V2+V3+I+RΛ¯-μ_S+V1+V2+V3+I+R. Thereby,

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32R-1+ξI+Λ¯-μ_S+V1+V2+V3+I+R-Λ_S+βS¯+βV1¯+βV2¯I+κ1¯+κ2¯+κ3¯-κ1_SV1-κ2_V1V2-κ3_V2V3+5μ¯+γV3¯-γV3_V3R+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

Now, consider the following compact set

K:=uU,ϵiui1ϵii{1,,6},

such that ϵ1,,ϵ6>0 will be chosen later.

Let uU\K. To verify that L(V(t,.))-1 in U\K, it suffices to investigate the following distinguished seven cases

Case 1

: uuU,I<ϵ5.

Case 2

: uuU,Iϵ5,S<ϵ1.

Case 3

: uuU,Iϵ5,Sϵ1,V1<ϵ2.

Case 4

: uuU,Iϵ5,Sϵ1,V1ϵ2,V2<ϵ3.

Case 5

: uuU,Iϵ5,Sϵ1,V1ϵ2,V2ϵ3,V3<ϵ4.

Case 6

: uuU,Iϵ5,Sϵ1,V1ϵ2,V2ϵ3,V3ϵ4R<ϵ6.

Case 7

: uuU,j{1,,6},uj>1ϵj.

For case 1, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξϵ5+Λ¯+βS¯+βV1¯+βV2¯ϵ5+κ1¯+κ2¯+κ3¯+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 2, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯-Λ_ϵ1+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 3, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯-κ1_ϵ1ϵ2+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 4, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯-κ2_ϵ2ϵ3+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 5, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯-κ3_ϵ3ϵ4+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 6, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯-γV3_ϵ4ϵ6+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

For case 7, we obtain

L(V(t,u))M-μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1+ξΛ¯μ_+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯-μ_1ϵj+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2.

Now, set

M2+Λ¯+βS¯+βV1¯+βV2¯Λ¯μ_+κ1¯+κ2¯+κ3¯+5μ¯+γV3¯+12Λ¯2μ_2σ1¯2+σ2¯2+σ3¯2μν+γν+12Λ¯μ_σ12+σ22+σ32νR-1.

Then, for case 1 and j=5 in case 7, choose

ϵ5:=min1,1Mξ+βS¯+βV1¯+βV2¯,μ_2Λ¯Mξ.

For case 2, case 3, case 4, case 5, case 6 and j5 in case 7, choose

ϵ1=min1,μ_Λ_MξΛ¯,μ_κ1_MξΛ¯,κ2_μ_MΛ¯ξ,κ3_μ_MΛ¯ξ,γV3_μ_MΛ¯ξ,μ_2λ¯Mξ,μ_2λ¯Mξ12,μ_2λ¯Mξ13,μ_2λ¯Mξ14,μ_2λ¯Mξ15,
ϵ2=ϵ12,ϵ3=ϵ13,ϵ4=ϵ14andϵ6=ϵ15.

Consequently, L(V(t,.))-1inU\K. On the other hand, since inf|u|>RV(t,u)+asR+t(0,+), and taking into consideration the ν-periodicity of V with respect to t,  the assumptions of Lemma 1 are verified. Conclusively, the stochastic system (2) admits a ν-periodic solution.

Remark 3

For the deterministic autonomous counterpart of the model (1), that is σ1(t)=σ2(t)=σ3(t)=0andθ(t)=θ(0,+)10t(0,T). One can use the Next Generation Method [34] to compute the basic reproduction number R0, which yields that R0=ΛβSμ+κ2μ+κ3+Λκ1βV1μ+κ3+Λκ1κ2βV2μ+κ1μ+κ2μ+κ3μ+γ. Hence, the value of R0 coincides with that of R2s and R stated in Sects. 3 and 4, respectively.

Numerical simulations

We consider the time horizon (0, 200) and we choose the following initial condition u0=0.8,0.1,0.01,0.04,0.03,0.02. 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 R1s2000.7812<1 (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 R2s=1.2192>1, thereby, the condition (4) of Theorem 3 holds (Fig. 6). Consequently, lim inft+It0.0029, 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 R1.4697>1. Similarly, for the fifth case, we have R1.3340>1. 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.

Fig. 2

Verification of the first disease extinction condition

Fig. 3.

Fig. 3

Paths of S, V1, V2, V3, I and R when the first condition of the disease extinction holds

Fig. 4.

Fig. 4

Verification of the second disease extinction condition

Fig. 5.

Fig. 5

Paths of S, V1, V2, V3, I and R when the second condition of the disease extinction holds

Fig. 6.

Fig. 6

Paths of S, V1, V2, V3, I and R when the condition of the disease persistence in the mean holds

Fig. 7.

Fig. 7

Persistence in the mean of the infected population

Fig. 8.

Fig. 8

Probability density functions of S, V1, V2, V3, I and R at time t=200 when the condition of the disease persistence in the mean holds

Fig. 9.

Fig. 9

Paths of S, V1, V2, V3, I and R in the deterministic non-autonomous case and under the condition R>1

Fig. 10.

Fig. 10

Paths of S, V1, V2, V3, I and R in the stochastic non-autonomous case and under the condition R>1

Fig. 11.

Fig. 11

Probability density functions of S,V1,V2,V3,I and R at time t=200 in the stochastic non-autonomous case and under the condition R>1

The assigned values to the parameters in each case are as follows

Case 1
: t[0,200],
Λ(t)=0.3+0.02sin(t),βS(t)=0.2+0.06sin(t),βV1(t)=0.1+0.02sin(t),βV2(t)=0.1+0.05sin(t),γ(t)=0.3+0.001sin(t),γV3(t)=0.2+0.001sin(t),κ1(t)=0.1+0.02sin(t),κ2(t)=0.1+0.02sin(t),κ3(t)=0.2+0.02sin(t),μ(t)=0.3+0.02sin(t).
Case 2
: t[0,200]
σ1(t)=0.3+0.1sin(t),σ2(t)=0.2+0.1sin(t),σ3(t)=0.1+0.05sin(t),Λ(t)=0.3+0.02sin(t),βS(t)=0.2+0.1sin(t),βV1(t)=0.2+0.05sin(t),βV2(t)=0.3+0.02sin(t),γ(t)=0.3+0.001sin(t),γV3(t)=0.2+0.001sin(t),κ1(t)=0.3+0.02sin(t),κ2(t)=0.2+0.02sin(t),κ3(t)=0.3+0.02sin(t),μ(t)=0.3+0.02sin(t).
Case 3
: t[0,200]
σ1(t)=0.1+0.01sin(t),σ2(t)=0.05+0.01sin(t),σ3(t)=0.04+0.01sin(t),Λ(t)=0.1+0.02sin(t),βS(t)=0.6+0.3sin(t),βV1(t)=0.7+0.2sin(t),βV2(t)=0.8+0.4sin(t),γ(t)=0.01+0.001sin(t),γV3(t)=0.2+0.001sin(t),κ1(t)=0.03+0.01sin(t),κ2(t)=0.02+0.01sin(t),κ3(t)=0.05+0.02sin(t),μ(t)=0.1+0.02sin(t).
Case 4
: t[0,200]
σ1(t)=0,σ2(t)=0,σ3(t)=0,Λ(t)=0.1+0.02sin(t),βS(t)=0.3+0.2sin(t),βV1(t)=0.4+0.2sin(t),βV2(t)=0.3+0.2sin(t),γ(t)=0.01+0.001sin(t),γV3(t)=0.01+0.001sin(t),κ1(t)=0.3+0.02sin(t),κ2(t)=0.2+0.02sin(t),κ3(t)=0.3+0.02sin(t),μ(t)=0.1+0.02sin(t).
Case 5
: t[0,200]
σ1(t)=0.06+0.02sin(t),σ2(t)=0.03+0.02sin(t),σ3(t)=0.05+0.02sin(t),Λ(t)=0.1+0.02sin(t),βS(t)=0.3+0.2sin(t),βV1(t)=0.4+0.2sin(t),βV2(t)=0.3+0.2sin(t),γ(t)=0.01+0.001sin(t),γV3(t)=0.01+0.001sin(t),κ1(t)=0.3+0.02sin(t),κ2(t)=0.2+0.02sin(t),κ3(t)=0.3+0.02sin(t),μ(t)=0.1+0.02sin(t).

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 [3943]. 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 lim supt+ϱ(t)<0. For sufficiently small values of the Gaussian noise intensities, a sufficient condition guaranteeing that the infected population goes to extinction is R1sT<1, and t(0,T), μ_Λ¯βS(t)>σ12(t), μ_Λ¯βV1(t)>σ22(t), and μ_Λ¯βV2(t)>σ32(t).

  • Under the condition R2s>1, the infected population becomes persistent in the mean.

  • For diseases with seasonal patterns, under the condition R>1, 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

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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.

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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.


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