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Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2021 Oct 23;31:104917. doi: 10.1016/j.rinp.2021.104917

Mathematical analysis for the effect of voluntary vaccination on the propagation of Corona virus pandemic

W Ahmad a,1, M Abbas a,1, M Rafiq b,1, D Baleanu c,d,e,⁎,1
PMCID: PMC8536489  PMID: 34722138

Abstract

In this manuscript, a new nonlinear model for the rapidly spreading Corona virus disease (COVID-19) is developed. We incorporate an additional class of vaccinated humans which ascertains the impact of vaccination strategy for susceptible humans. A complete mathematical analysis of this model is conducted to predict the dynamics of Corona virus in the population. The analysis proves the effectiveness of vaccination strategy employed and helps public health services to control or to reduce the burden of corona virus pandemic. We first prove the existence and uniqueness and then boundedness and positivity of solutions. Threshold parameter for the vaccination model is computed analytically. Stability of the proposed model at fixed points is investigated analytically with the help of threshold parameter to examine epidemiological relevance of the pandemic. We apply LaSalle’s invariance principle from the theory of Lyapunov function to prove the global stability of both the equilibria. Two well known numerical techniques namely Runge–Kutta method of order 4 (RK4), and the Non-Standard Finite Difference (NSFD) method are employed to solve the system of ODE’s and to validate our obtained theoretical results. For different coverage levels of voluntary vaccination, we explored a complete quantitative analysis of the model. To draw our conclusions, the effect of proposed vaccination on threshold parameter is studied numerically. It is claimed that Corona virus disease could be eradicated faster if a human community selfishly adopts mandatory vaccination measures at various coverage levels with proper awareness. Finally, we have executed the joint variability of all classes to understand the effect of vaccination strategy on a disease dynamics.

Keywords: COVID-19, Steady states, Voluntary vaccination, Uniqueness, Stability analysis, Covariance

Introduction

Corona virus disease (COVID-19) is a severe pandemic with an extremely high fatality rate caused by an infectious respiratory virus called SARS-CoV-2. The virus spreads uniformly among individuals and affecting people worldwide through direct and indirect physical contact. The first and overall third outbreak of novel Corona virus disease was experienced at the end of December 2019 in the Wuhan City of China. The outbreak spreads rapidly in different parts of China and then worldwide in almost 223 countries of Asia, Australia, America and Europe [1]. World Health Organization (WHO) reported that there are more than 232,636,622 confirmed cases with 4,762,089 deaths by September 29, 2021. It is remarkable that WHO reported 18,325,098 new infected cases including 90,529 serious or critical cases to date while the number of confirmed cases are continuing to increase. However, almost 210,951,891 people have been recovered. A total of 6,136,962,861 vaccine doses have been administered by 29 September, 2021. Currently, the number of highest positive cases encountered in United States of America followed by India, Brazil and Spain respectively.

The current evidence suggests that the main source of Corona virus transmission among individuals are the respiratory droplets through sneezing, coughing and spitting of an infected person [2]. During the treatment of Corona patients, health care staff can also get infected. Incubation period for the Corona virus disease normally varies from 2 to 14 and on average 5-6 days. Every individual can get Corona infection at any age and time instant and become seriously ill or die. It is observed that people 60 years and older and people who develop severe diseases like heart disease, obesity or cancer, diabetes or lung disease are at higher risk of getting seriously sick with Corona virus and can be infectious for longer. People with a variety of symptoms like fever, dry cough, sneezing, red eyes, shortness of breath, muscle pain, fatigue, severe headache, new loss of smell or taste, persistent pain in the chest, sore throat, runny nose, sleep disorders, vomiting, and diarrhea, may have Corona virus disease [3]. It may create to intense acute multi-organ failure, respiratory torture progression, blood clots, and septic shock, among other conditions [4], [5]. Without needing hospital treatment, about 80% among the people who create these indications may recover from the viral infirmity. About 15% turn critically ill and want oxygen. About 5% turn seriously sick and need medical care. They may face a rapid progression to death due to their ill condition. The virus may spread on a large scale if the pandemic is not restricted. It will threaten the entire human population. Therefore, to take care of infected patients, it is inevitable to take comprehensive preventive measures.

Public health experts worldwide are continuously learning and monitoring the dynamics of novel Corona virus these days. They always look for multiple solutions to control the pandemic. The first important step is to develop appropriate community engagement, awareness campaign and protection measures among individuals. For instance, appropriate careful steps, for example, wearing proper clothes and gloves, and washing hands subsequent to visiting the patients ought to be dealt with. To protect yourself and other people, we should wear a surgical mask that especially covers our mouth and nose. Keep a distance of at least 6 feet from other peoples who do not live with you, especially in crowded areas. Keep away from indoor spaces however much as could be expected, especially ones that are not all around ventilated. Clean up your hands with soap and water for 20 s. This trial should be repeated throughout the day. Use hand sanitizer with basically 60% liquor content. Everyone takes these actions to help slow down COVID-19. The other rigorous measures are the use of vaccination, public quarantine facilities, lock down, isolation or treatment of infected humans. This also includes raising the awareness like public health education, laboratory testing, risk communication, start of antiviral drugs, designed special hospitals and health screening at boarders. It is remarkable that antibiotics do not work against COVID-19. There is no licensed medicine which is used to cure pandemic.

The best method to control the pandemic is the prospective vaccination of human population. The vaccine is a safe and effective way to produce an immune response in the human body without causing illness. Execution of various vaccination strategies in human communities is a significant public health measure, generally been utilized to control the spread of all communicable infections. Some genuine endeavors to acquire a vaccine for COVID-19 sickness have been made after the 2019 Corona infection episode in China. No less than seven unique vaccines have been carried out in different countries by 18 February 2021. Physically weak populations from all nations are the most noteworthy need for vaccination. Throughout 2021, more potential vaccines for Corona virus disease will become available. Therefore, recommendations of vaccination strategies will expand to include more people in the whole world.

To assess the standard and safety of vaccines is the highest priority of World Health Organization (WHO). To check the efficacy, WHO works closely with researchers around the world to ensure that global standards and norms are developed and implemented during the vaccine developing process. To control the spread of epidemic diseases, numerous scientists are drawn to create different models [6], [7], [8], [9], [10] dealing with vaccination strategies while other people have analyzed stochastic delay differential models for COVID-19 pandemic [11], [12]. Recently, a group of researchers [13], [14], [15], [16] studied the stability pattern of Ebola virus epidemic models by introducing vaccination strategies in a host population. A several number of articles [17], [18], [19], [20], [21], [22] have been published recently on the efficacy of implemented vaccines. According to our little knowledge, a least number of research articles [17], [23] have been published to understand the effect of voluntary vaccination on the propagation of Corona virus epidemic. No one did a complete mathematical analysis of Corona pandemic through a vaccination model. We will move in this direction.

In this manuscript, an SVEIR pandemic model is developed to predict class wise transmission dynamics of Corona infection in a population. Mathematical modeling of COVID-19 shall work confidentially to predict and comprehend how virus spread. These predictions will likewise assist with seeing how the Corona contamination might diminish or increment later on. We incorporate a class of those susceptible humans who have vaccinated through a proper vaccination programme. For this study, we assumed that any universally available vaccine is not 100% effective, means that the people will get tainted during vaccination period and can be sound toward the finish of this period. We have assessed the effect of vaccine programme on human community with the assistance of proposed model. Using some known techniques, we have presented a complete mathematical analysis of the proposed Corona model with an aim of controlling the pandemic. Additionally, we shall study the correlation between vaccinated class and the remaining classes.

In Chaos theory, an important area of research is to study various mathematical models with different descriptions and requirements for their numerical stability. Recently, the stability of various epidemic models with respect to the involved parameters was obtained [13], [24], [25]. Some appropriate reliable numerical techniques [26], [27], [28], [29], [30], [31], [32], [33], [34], [35], [36], [37], [38], [39], [40] to solve the governing equations were employed. The dynamics of epidemic diseases was examined with the help of numerical simulations. We tend to expect that our projected model also contains all vital self-propelling properties, for example, well-posedness of the problem and, boundedness and positivity of solutions. It is ascertained that most of the traditional standard methods including Euler, RK schemes sometimes become unbounded divergent when implemented to a system. Implementation of these numerical methods could cause major problems such as generating oscillations, bifurcations, chaos, negative solutions, or solutions converging to false equilibrium states as time grid size increased [13], [24], [25], [28], [29]. Subsequently, the best approach to solve our model herein is to develop NSFD scheme [30]. We have demonstrated the dynamic consistency of the developed NSFD scheme alongside a few examinations with RK4 scheme by performing detailed mathematical investigation of the given model.

The numerical examination highlights the impact of vaccination strategy on the dynamics of Corona virus disease at different levels of proposed vaccination. The effect of vaccine on susceptible and exposed class is executed reveals that number of susceptible and the exposed humans are decreased consistently with the increase in levels of vaccination. A rapid regress in the population of infected humans is observed when vaccination rates are high. It is noticed that infectivity will approach to zero as time goes to infinity. However, a quick increment in the number of recovered individuals is observed whenever the levels of vaccination are continuously increased. An addition in the number of recovered individuals and the decrease in the population of infected individuals essentially diminish the danger of Corona infection sickness. As a result, the host population will become healthy if the coverage level and effectiveness of implemented vaccination strategy is high. Furthermore, it has been observed that threshold parameter is being affected by the vaccination programme. We have discussed statistically the joint variability among all populations.

The paper is organized as follows: The derivation of the compartmental model is outlined in Section “Derivation of Corona model”. In Section “Theoretical analysis”, the existence of a unique global solution for the derived model is investigated. The positivity and boundedness of solutions is proved. Two main equilibrium points of the underlying model are obtained and the threshold parameter R0 is computed analytically. Stability of the SVEIR model is analyzed analytically. Numerical stability of the model to confirm the main theoretical results along with graphical illustrations and necessary discussions is performed in Section “Numerical simulations”. We discuss the computational advantages of NSFD scheme by comparing it with RK4 method. We conclude the present work in Section “Conclusions”.

Derivation of Corona model

There is a series of various mathematical models in the existing literature [23], [24], [41], [42], [43], [44], [45], [46], [47], [48] with different assumptions depending on the propagation mechanism of Corona virus disease. These models assist the public health planners and policy makers in lots of ways. In this section, we have developed a new real world SVEIR COVID-19 pandemic model by incorporating a class of vaccinated human. For the proposed model, all of our efforts will be to study the effect of proposed vaccination on the dynamical behavior of Corona virus disease. The variables used to model out the transmission dynamics of Corona pandemic among the individuals are given below:

We divide the total population N(t) at time t into five disjoint classes. The first class includes number of susceptible humans which is denoted by S(t). Note that there will be a limited supply of Corona virus vaccine for the host population for a while. Hence, not everyone will be able to be vaccinated right away. The second class denoted by V(t) gives the number of susceptible individuals who have been vaccinated at time instant t. The third class which represents the number of exposed humans at time instant t is denoted by E(t). The fourth epidemic class denoted by I(t) characterizes all infected people who are able to spread the infection further. Ultimately, people who have developed complete immunity from the COVID-19 are going to the fifth class of recovered humans, denoted by R(t). We assume that the recovered people will stay in the class R(t) throughout their life. Thus the variables for the Corona model (1) are S, V, E, I and R respectively. All these variables are assumed to be real valued continuously differentiable functions defined on the interval [0,1) of t values.

Fig. 1 describes a graphical representation the flow pattern of Corona virus in the host population. The physical relevance and description of the employed parameters is provided in Table 1.

Fig. 1.

Fig. 1

A schematic of the Corona virus disease in a compartmental model (1).

The following SVEIR mathematical model represents the flow pattern of Corona virus in a community:

dSdt=Ωα1SE(α3+μ)S, (1a)
dVdt=α3S(α6+μ)Vα4VEα5VI, (1b)
dEdt=α4VE+α1SEα2EI(k+μ)E, (1c)
dIdt=α5VI+α2EI(d+r+μ)I, (1d)
dRdt=α6V+rI+kEμR, (1e)

We have assumed that all the initial conditions and involved parameters of the system are non-negative.

Table 1.

Representation of involved parameters with their estimated values.

Symbol Description Value Source
Ω Recruitment rate of humans into susceptible class 0.5000 [24]
μ Natural death rate of each class 0.5000 [24]
d Death rate of infected class due to corona virus disease 0.0047876 [24]
k Rate of transfer of exposed humans into recovered class 0.00398 [24]
r Rate of transfer of infected humans into recovered class 0.09871 [24]
α1 Rate of transfer of susceptible humans into exposed class 0.005 [24]
α2 Rate of transfer of exposed humans into infected class 0.085432 Assumed
α3 Transition of susceptible humans into vaccinated class 0.6000 Assumed
α4 Rate of transfer of vaccinated humans into exposed class 0.2807 Assumed
α5 Rate of transfer of vaccinated humans into infected class 0.3813 Assumed
α6 Rate of transfer of vaccinated humans into recovered class 0.9092 Assumed

Theoretical analysis

In this section, we prove some important properties such as well-posedness of the problem (1) followed by the positivity and boundedness of all solutions for t0. Threshold parameter and the equilibrium points for the prescribed model along with their stability analysis have been presented. All these computations are done in the following steps.

Existence of a unique solution

In a compact form, the system (1) can be put into the form

dxdt=F(x),x(0)=x0, (2)

where x is a column vector of state variables in R5 and defines a mapping from [0,+) to R5. However, F(x)=(F1(x),F2(x),F3(x),F4(x),F5(x))TR5, is a vector valued function from R5 to R5 with components

F1(x)=Ωα1SE(α3+μ)S,
F2(x)=α3S(α6+μ)Vα4VEα5VI,
F3(x)=α1SE+α4VEα2EI(k+μ)E,
F4(x)=α5VI+α2EI(d+r+μ)I,
F5(x)=α6V+rI+kEμR,

The function F in (2) is Lipschitz continuous in x [49]. Hence by existence and uniqueness theorem [50], the solution of problem (2) is unique. This solution will be realistic and epidemiologically meaningful if it is nonnegative and bounded. We prove these properties in the following subsections.

Positivity of solutions

In this subsection, we have proved that all the state variables are non-negative for any t>0, that is the solution will remain positive forever corresponding to any non-negative initial data in R+5. This property is required to show our model physically realizable.

Theorem 1

The solutions of system (1) will remain positive forever with any positive initial costs.

Proof

First equation of the model (1) is rearranged to give,

dSdt=ΩH(t)S(t). (3)

where

H(t)=(α3+μ)+α1E(t).

On multiplying exp(0tH(s)ds)>0 to both sides of  Eq. (3), we get

exp(0tH(s)ds)dSdt=[ΩH(t)S(t)]exp(0tH(s)ds),

which further implies that

ddt[S(t)exp(0tH(s)ds)]=Ωexp(0tH(s)ds).

Integration of both sides with respect to s from 0 to t will leads to

S(t)exp(0tH(s)ds)S(0)=Ω0t[exp(0wH(s)ds)]dw. (4)

Multiplication of both sides of Eq. (4) with exp(0tH(s)ds) gives

S(t)=S(0)exp(0tH(s)ds)+Ωexp(0tH(s)ds)0t[exp(0wH(s)ds)]dw0.

Implies that the solution S(t) is positive for all t>0. Similarly, it can be shown that V(t)0, E(t)0, I(t)0, R(t)0 for all t>0 corresponding to any non-negative initial data. Thus the solution (S,V,E,I,R) in R+5 remain positive forever.  □

Invariant region

In this subsection, we determine the boundary of solutions of the nonlinear system (1) with an initial data S0, V0, E0, I0, R0. Our main target is to show that the obtained feasible region in R+5 is positively invariant for the proposed model (1).

Theorem 2

The solutions of system (1) given in Theorem 1 are bounded.

Proof

Addition of all the five equations in model (1) gives

dNdt=ΩμSμVμE(d+μ)Iμ6RΩμN,

provided that μ<d+μ, where N(t)=S(t)+V(t)+E(t)+I(t)+R(t), t0, is the total population under consideration. It follows that dNdt0 whenever N(t)Ωμ. By using Gronwall’s inequality [51], it can be shown that

N(t)=Ωμ[1exp(μt)]+N(0)exp(μt),

where N(0) is the initial population size. In particular, N(t)Ωμ whenever N(0)Ωμ. Thus N and all other variables of the model (1) are bounded in a region

Π={(S,V,E,I,R)R+5:0N(t)Ωμ;S,V,E,I,R0}. (5)

The solution remains x=0 for all t>0 if x0=0. Moreover, for any nonnegative set of initial conditions in Π, every solution of model (1) in R+5 approach asymptotically in finite time t, enters and remains in the region Π. Implies the set Π is closed and positively invariant for our system [1]. Whenever N(0)>Ωμ, either N(t) approaches Ωμ asymptotically or the solution enters Π. Hence the region Π attracts all solutions in R+5. Hence, the problem (2) or equivalently (1) is mathematically well-posed.

Equilibrium points

A unique non-negative Corona free equilibrium for the model (1) exists at the point

F0=(S0,V0,E0,I0,R0)=(Ωα3+μ,Ωα3(α6+μ)(α3+μ),0,0,Ωα3α6μ(α6+μ)(α3+μ)),

and a unique non-negative Corona present equilibrium exists at the point given by

F1=(S1,V1,E1,I1,R1),

in the epidemiological region Π, where

S1=Ωπ+α3+μ>0,
V1=1α4[(k+μ)+α2I1Ωα1π+α3+μ]>0,
E1=1α2(d+r+μ)α5α4[1α2(k+μ)+I1]+Ωα1α5α2α4(π+α3+μ)>0,
I1=C1(π+α3+μ)Ω2α12α5+C2(π+α3+μ)2α2(π+α3+μ)C3>0,
R1=(α2α6+rα4kα5μα4)I1+C4C5>0,

along with

π=α1E1,
C1=Ω[2α1α5(k+μ)α2α3α4α1α4(d+r+μ)],
C2=(k+μ)[α2(α6+μ)+α4(d+r+μ)α5(k+μ)]Ωα1α2(α6+μ),
C3=α2(π+α3+μ)2[α5(k+μ)α2(α6+μ)α4(d+r+μ)]Ωα1α2α5(π+α3+μ),
C4=α6(k+μ)μα4+k(d+r+μ)μα2+Ωkα1α5μα2α4(π+α3+μ),
C5=Ωα1α6μα4(π+α3+μ)+kα5(k+μ)μα2α4.

Threshold parameter R0

We can determine the dynamics of mathematical models by computing the value of threshold parameter, usually denoted by R0. The spread of any infectious disease begins when an infected person enters into a class of completely susceptible humans. Therefore, R0 gives the total number of new infections produced by an infected human at t0. It works confidentially to predict the dynamical behavior of a model. We can study the future spread of any disease in details by computing this number. Therefore, for the model (1), the value of R0 is computed by using the standard next generation matrix approach [13], [14], [25], [52].

We assume ξ=(E,I,V,S,R)T and the system (1) becomes

dξdt=F(ξ)G(ξ)

where

F(ξ)=α4VE+α1SEα2EIα5VI+α2EI000=F1F2F3F4F5

and

G(ξ)=(k+μ)E(d+r+μ)Iα3S+(α6+μ)V+α4VE+α5VIΩ+(α3+μ)S+α1SEα6VrIkE+μ6R=G1G2G3G4G5

We only focus on the dynamics of classes E and I, since they are contributing to new infections. The matrix F representing the appearance rate of new cases is given by

F=α4VE+α1SEα2EIα5VI+α2EI,

whereas the matrix G representing the transition rate of existing or transported cases is computed as follows:

G=(k+μ)E(d+r+μ)I.

The jacobian of the matrices F and G evaluated at point F0 are

F¯=F1EF1IF2EF2I=Ω(α1(α6+μ)+α3α4)(α6+μ)(α3+μ)00Ωα3α5(α6+μ)(α3+μ),
G¯=G1EG1IG2EG2I=k+μ00d+r+μ.

Thus the value of threshold parameter, that is

R0=Ω[α1(α6+μ)+α3α4](α5+μ)(α3+μ)(k+μ)

is the spectral radius of the product matrix F¯G¯1.

Stability analysis

In this subsection, we analyze the stability of the model (1) at both the steady states with the help of R0 theoretically. Theorem 3, Theorem 5 are dealing with equilibrium point F0 whereas Theorem 4, Theorem 6 describe the nature of F1. Global stability of the given model is established by employing LaSalle’s invariant principle [13], [24], [25], [53], [54].

Local behavior of the vaccination model

Theorem 3

A Corona free equilibrium F0 is locally asymptotically stable (LAS) when R0<1 . If R0>1 , it is unstable.

Proof

For system (1), the Jacobian J at F0 can be written as

J(F0)=(α3+μ)0Ωα1α3+μ000(α6+μ)QΩα3α5(α6+μ)(α3+μ)000(k+μ)(R01)00000Ωα3α5(α6+μ)(α3+μ)(d+r+μ)00000μ,

where

Q=Ωα3[α4(α3+μ)+α1(α6+μ)](α6+μ)(α3+μ)2.

Jacobian matrix J(F0) has the following eigenvalues:

λ1=(α3+μ), (6)
λ2=(α6+μ), (7)
λ3=(k+μ)(R01), (8)
λ4=Ωα3α5(α6+μ)(α3+μ)(d+r+μ), (9)
λ5=μ. (10)

It is to be noted that the parameters in the proposed model are assumed to be positive. Therefore, the eigenvalues λ1, λ2 and λ5 are negative. Indeed the quantities α3+μ, α6+μ, μ are strictly positive. Now consider Eq. (8), that is λ3=(k+μ)(R01). Hence λ3<0R0<1. From Eq. (9), λ4<0 if and only if

Ωα3α5<(d+r+μ)(α6+μ)(α3+μ),

which is obviously true. Thus all the eigenvalues of J(F0) when R0 is less than unity, are negative and hence F0 is locally asymptotically stable. Once the dynamical system is stable at disease free point F0, then there will be no pandemic threat. For the later case, if R0>1,

(k+μ)(R01)>0,

which implies that λ3>0 and thus F0 is unstable.  □

Theorem 4

A Corona present equilibrium F1 is locally asymptotically stable (LAS) whenever R0>1 . Whenever R0<1 , it is unstable.

Proof

The Jacobian for the system (1) at F1 can be written as

J(F1)=J110α1S100α3J22α4V1α5V10α1E1α4E1J33α2E10α5I1α2I1J44000α6krμ,

where

J11=α1E1(α3+μ),
J22=(α6+μ)α4E1α5I1,
J33=α4V1+α1S1α2I1(k+μ),
J44=α5V1+α2E1(d+r+μ).

The eigenvalues of J(F1) are as follows:

λ1=μ, (11)
λ2=J11=α1E1(α3+μ), (12)
λ3=J22=(α6+μ)α4E1α5I1, (13)
λ4=1J11J22[J22(J11J33+α12S1E1)α4E1(α1α3S1+α4J11V1)], (14)
λ5=1Q3(Q1Q2). (15)

where

Q1=J22J44(J11J33+α12S1E1)+J11V1(J44α42E1+J33α52I1)+E1I1(α12α52S1V1+α22J11J22),
Q2=α1α3S1E1(α4J44+α2α5I1),
Q3=J11J22J33+α42J11V1E1+α1S1E1(α1J22α3α4),

Clearly from Eq. (11), Eq. (12), and Eq. (13), λ1, λ2, λ3 are negative. Since the product J11J22 is positive, so it is clear that λ4<0J22(J11J33+α12S1E1)<α4E1(α1α3S1+α4J11V1), which has been verified. As Q3 is positive, so λ5<0Q1<Q2 which is also true. Hence F1 is LAS.  □

Global behavior of the vaccination model

Theorem 5

A Corona free equilibrium F0 is globally asymptotically stable (GAS) in the domain Π when R0<1 .

Proof

Let S0=Ωα3+μ. We construct a candidate [55] Lyapunov function U0:ΠR such that,

U0=SS0S0lnSS0+VV0V0lnVV0+E+I.

Differentiating U0 with respect to time t yields

U˙0=(SS0)S˙S+(VV0)V˙V+E˙+I˙.

Substituting the values of derivatives from the system (1), we have

U˙0=(1S0S)[(S0S)μα1SE+(α6+μ)V0(1S0S)]+(1V0V)[(α6+μ)V0SS0(α6+μ+α4E+α5I)V]+(α5Vdrμ)I+(α1S+α4Vkμ)E,=μS(SS0)2+(k+μ)(R01)E+[Ωα3α5(α6+μ)(α3+μ)(d+r+μ)]I+(α6+μ)(3S0SVV0V0VSS0)

Since α3α5<(d+r+μ)(α6+μ)(α3+μ) and employing Arithmetic–Geometric inequality, it can be shown that

3S0SVV0V0VSS00.

Implies U˙00 whenever R0<1, and U˙0=0    S=S0, V=V0, E=E0=0, I=I0=0. The system (1) with these substitutions gives SS0, VV0, I0, E0 and RR0 as t. Implies {F0} is the maximal invariant set contained in

N0={(S,V,E,I,R)Π:U˙0=0}.

whenever R0<1. Hence by LaSalle’s invariance principle [53], F0 is globally asymptotically stable in Π. Subsequently, COVID-19 disappears from the human population.  □

Theorem 6

A Corona present steady state F1 is globally asymptotically stable (GAS) in the feasible region Π if R0>1 .

Proof

To show the global stability of a Corona present steady state F1, we construct a proposed [55] Lyapunov function U1:ΠR such that

U1=SS1S1lnSS1+VV1V1lnVV1+EE1E1lnEE1+II1I1lnII1.

Now, time derivative of U1 can be written as

U˙1=(SS1)S˙S+(VV1)V˙V+(EE1)E˙E+(II1)I˙I.

Using equations given in the model (1), we obtain that

U˙1=(1S1S)[μ(S1S)+α1(S1E1SE)]+V1(1S1S)[α4E1+α5I1+(α6+μ)(1SS1)(α4E1+α5I1)SS1]+(1V1V)[(α6+μ+α4E+α5I)(V1V)+(α6+μ+α4E1+α5I1)×V1VSS1(VV1)]+(EE1)[α4(VV1)+α1(SS1)α2(II1)]+(II1)[α5(VV1)+α2(EE1)].

After a simple calculation, we get

U˙1=S1(μ+α1E1)(2SS1S1S)+V1(α6+μ+α4E1+α5I1)×(3S1SVV1SS1V1V) (16)

where Arithmetic–Geometric mean inequality yields

2SS1S1S0,
3S1SVV1SS1V1V0.

Therefore the expression (16) implies that U˙10. Particularly, U˙1=0   S=S1, V=V1. Implies {F1} is the greatest invariant set contained in

N1={(S,V,E,I,R)Π:U˙1=0}.

Hence by LaSalle’s invariance principle [53], it is concluded that F1 is GAS in Π. Global stability of F1 enables that COVID-19 will persist in the community and eventually lead to pandemic.  □

Numerical simulations

The aim of this section is to analyze and predict the numerical stability of the system (1). We have developed two well-known numerical schemes namely RK4 and NSF D method to solve the system (1). Development of these schemes helps us to observe dynamical behavior of COVID-19 over time t through numerical simulations shown by graphs. We observe that solutions are in good agreement with the dynamical behavior of the continuous model. Numerical values of involved parameters are given in Table 1. The impact of proposed vaccine on human population is studied using NSFD scheme. Moreover, the correlation between model variables is computed numerically. Numerical analysis proves the reliability and dynamic consistency of NSFD scheme even for larger time step size when it compared with RK4 scheme.

RK4 scheme

To construct an explicit numerical scheme of RK4 method [13], [25], [26], [49], let us denote by Sn, Vn, En, In, and Rn the approximations of solutions S, V, E, I, and R respectively, for n=0,1,2,3,4,, and time step size h. With these substitutions, RK4 scheme may be constructed as follows:

k1=h[Ωα1SnEn(α3+μ)Sn]
w1=h[α3Sn(α6+μ)Vnα4VnEnα5VnIn]
l1=h[α1SnEn+α4VnEnα2EnIn(k+μ)En]
m1=h[α5VnIn+α2EnIn(d+r+μ)In]
n1=h[α6Vn+rIn+kEnμRn]
k2=h[Ωα1(Sn+k12)(En+l12)(α3+μ)(Sn+k12)]
w2=h[α3(Sn+k12)(α6+μ)(Vn+w12)α4(Vn+w12)(En+l12)α5(Vn+w12)(In+m12)]
l2=h[α1(Sn+k12)(En+l12)+α4(Vn+w12)(En+l12)α2(En+l12)(In+m12)(k+μ)(En+l12)]
m2=h[α5(Vn+w12)(In+m12)+α2(En+l12)(In+m12)(d+r+μ)(In+m12)]
n2=h[α6(Vn+w12)+r(In+m12)+k(En+l12)μ(Rn+n12)]
k3=h[Ωα1(Sn+k22)(En+l22)(α3+μ)(Sn+k22)]
w3=h[α3(Sn+k22)(α6+μ)(Vn+w22)α4(Vn+w22)(En+l22)α5(Vn+w22)(In+m22)]
l3=h[α1(Sn+k22)(En+l22)+α4(Vn+w22)(En+l22)α2(En+l22)(In+m22)(k+μ)(En+l22)]
m3=h[α5(Vn+w22)(In+m22)+α2(En+l22)(In+m22)(d+r+μ)(In+m22)]
n3=h[α6(Vn+w22)+r(In+m22)+k(En+l22)μ(Rn+n22)]
k4=h[Ωα1(Sn+k3)(En+l3)(α3+μ)(Sn+k3)]
w4=h[α3(Sn+k3)(α6+μ)(Vn+w3)α4(Vn+w3)(En+l3)α5(Vn+w3)(In+m3)]
l4=h[α1(Sn+k3)(En+l3)+α4(Vn+w3)(En+l3)α2(En+l3)(In+m3)(k+μ)(En+l3)]
m4=h[α5(Vn+w3)(In+m3)+α2(En+l3)(In+m3)(d+r+μ)(In+m3)]
n4=h[α6(Vn+w3)+r(In+m3)+k(En+l3)μ(Rn+n3)]

Hence

Sn+1=Sn+16(k1+2k2+2k3+k4) (17a)
Vn+1=Vn+16(w1+2w2+2w3+w4) (17b)
En+1=En+16(l1+2l2+2l3+l4) (17c)
In+1=In+16(m1+2m2+2m3+m4) (17d)
Rn+1=Rn+16(n1+2n2+2n3+n4) (17e)

where n=0,1,2,3, and the discretization time step is denoted by h.

Non-standard finite difference scheme

After RK4 technique, we now demonstrate a non-standard finite difference (NSFD) scheme for the model (1) presented herein. The scheme is based on Micken’s theory [30], [31], [32], [33] of non-standard finite difference numerical modeling. The proposed NSFD scheme has been efficiently applied to solve numerous problems [34], [35], [36], [37], [38], [39], [40], [55] in physical sciences and engineering where it is basically required that the obtained numerical solutions preserve all the properties of a dynamic model. It is shown that NSFD scheme provides more accurate solutions as compared to RK4 method for larger step sizes. For the proposed model (1), we construct NSFD numerical scheme as follows:

Sn+1=Sn+hΩ1+hα1En+h(α3+μ), (18a)
Vn+1=Vn+hα3Sn1+hα4En+hα5In+h(α6+μ), (18b)
En+1=En+hα4VnEn+hα1SnEn1+hα2In+h(k+μ), (18c)
In+1=In+hα5VnIn+hα2EnIn1+h(d+r+μ), (18d)
Rn+1=Rn+hα6Vn+hrIn+hkEn1+hμ. (18e)

where n=0,1,2,3, and the discretization time step is denoted by h.

Theorem 7

The only fixed points of the scheme (18) are either the F0 or F1 of the dynamic model (1) . Moreover, fixed points of proposed scheme (18) has the same stability properties as that of F0 and F1 of the given model.

Theorem 8

WheneverR0<1, the NSFD scheme (18) has a globally asymptotically stable equilibrium point F0 and a globally asymptotically stable endemic point F1 whenever R0>1 . For the later case, F0 will become unstable.

Analysis through comparisons

In the current section, the comparison of the nonstandard computational method with well known standard computational method is presented. In Fig. 2, Fig. 3, Fig. 4, Fig. 5, Fig. 6, Fig. 7, we can observe that RK4 method converge for small time step sizes. Although for larger time step sizes, RK4 scheme fails to restore the desired properties like positivity and boundedness of solutions. As time increases, RK4 method also loses dynamical consistency of the continuous model (1). By this property, all the fixed points of an implemented numerical scheme should be the same as the continuous model for the any set of parameter values. For details, we will refer the Fig. 9, Fig. 10, Fig. 11. To check the validity of analytical results, We first solve the system (1) using both RK4 and NSFD method with time step sizes h=1.0 and h=1.2 respectively. In Fig. 2, Fig. 3, Fig. 4, Fig. 5, Fig. 6, Fig. 7, both the numerical schemes are seen to be convergent to the same equilibrium states F0 (whenever R0<1) and F1 (whenever R0>1) of the model. Furthermore, both the numerical schemes exhibit positive and bounded solutions in the region Π for these step sizes. Additionally, if we increase the value of h, for example h=1.5 and h=2.0, it is observed that RK4 method do not converge to both F0 and F1. Moreover, for these values of h, RK4 scheme exhibit unexpected negative solutions as observed in Fig. 9, Fig. 10, Fig. 11. However, the NSFD scheme converges to true states with the same set of condition applied on R0, and preserves all the essential properties of the model (1). For comparisons, see Fig. 2, Fig. 3, Fig. 4, Fig. 5, Fig. 6, Fig. 7, Fig. 8, Fig. 9, Fig. 10, Fig. 11. We have presented four numerical experiments for NSFD and RK4 scheme respectively using different values of h, and the obtained results are given in Table 2.

Fig. 2.

Fig. 2

Graphical behavior of NSFD scheme at F0=(0.4545,0.1935,0,0,0.3519) of the model (1) with h=1.0.

Fig. 3.

Fig. 3

Graphical behavior of NSFD scheme at F1=(0.2066,0.07896,0.5283,0.03185,0.1541) of the model (1) with h=1.0.

Fig. 4.

Fig. 4

Graphical behavior of RK4 scheme at F0=(0.4545,0.1935,0,0,0.3519) of the model (1) with h=1.0.

Fig. 5.

Fig. 5

Graphical behavior of RK4 scheme at F1=(0.2066,0.07896,0.5283,0.03185,0.1541) of the model (1) with h=1.0.

Fig. 6.

Fig. 6

The solutions are obtained by NSFD and RK4 techniques with step size h=1.2. It is seen that both techniques converge numerically to the point F0=(0.4545,0.1935,0,0,0.3519).

Fig. 7.

Fig. 7

The solutions are obtained by NSFD and RK4 techniques with step size h=1.2. It is seen that both techniques converge numerically to the point F1=(0.2066,0.07896,0.5283,0.03185,0.1541).

Fig. 9.

Fig. 9

The solutions are obtained by NSFD and RK4 techniques with step size h=1.5. It is observed that RK4 scheme diverges and gives unexpected negative solutions whereas NSFD converges to the true equilibrium point F1=(0.2066,0.07896,0.5283,0.03185,0.1541).

Fig. 10.

Fig. 10

The solutions are obtained by NSFD and RK4 techniques with step size h=2.0. It is observed that RK4 scheme diverges and gives unexpected negative solutions whereas NSFD converges to the true equilibrium point F0=(0.4545,0.1935,0,0,0.3519).

Fig. 11.

Fig. 11

The solutions are obtained by NSFD and RK4 techniques with step size h=2.0. It is observed that RK4 scheme diverges and gives unexpected negative solutions whereas NSFD converges to the true equilibrium point F1=(0.2066,0.07896,0.5283,0.03185,0.1541).

Fig. 8.

Fig. 8

The solutions are obtained by NSFD and RK4 techniques with step size h=1.5. It is seen that both techniques converge numerically to the point F0=(0.4545,0.1935,0,0,0.3519).

Table 2.

Convergence of numerical schemes vs. time step size h.

Step size h=1.0 h=1.2 h=1.5 h=2.0
RK4 Convergent Convergent Divergent Divergent
NSFD Convergent Convergent Convergent Convergent

Projected scheme and its computational advantages

This section is dedicated to showing the numerical advantages and dynamic consistency of the proposed NSFD technique. The numerical comparisons discussed in Section “Analysis through comparisons” demonstrates that the RK4 scheme is not always convergent, rather conditionally convergent and stable. It is very sensitive to the time step size h and fails to converge especially for larger step sizes. In contrast with other widely utilized standard numerical strategies including RK4, our proposed NSFD scheme is seen to be convergent for any step size used. It is clear from Table 2 that the adopted NSFD scheme is more competitive in terms of numerical stability of the model (1) at fixed points. The Fig. 2, Fig. 3, and Fig. 6, Fig. 7, Fig. 8, Fig. 9, Fig. 10, Fig. 11, Fig. 12, Fig. 13, Fig. 14, Fig. 15 illustrate the potential of NSFD scheme. Furthermore, it is concluded that the developed NSFD scheme is unconditionally convergent and stable, gives positive and bounded solutions, convergence to the equilibrium points and maintains its dynamical consistency with the vaccination model.

Fig. 12.

Fig. 12

Behavior of the population proportion of susceptible humans at corona present point F1 for different coverage levels (%) of voluntary vaccination. Numerical results are obtained by NSFD scheme using h=0.1.

Fig. 13.

Fig. 13

Behavior of the population proportion of exposed humans at corona present point F1 for different coverage levels (%) of voluntary vaccination. Numerical results are obtained by NSFD scheme using h=0.1.

Fig. 14.

Fig. 14

Behavior of the population proportion of infected humans at corona present point F1 for different coverage levels (%) of voluntary vaccination. Numerical results are obtained by NSFD scheme using h=0.1.

Fig. 15.

Fig. 15

Behavior of the population proportion of recovered humans at corona present point F1 for different coverage levels (%) of voluntary vaccination. Numerical results are obtained by NSFD scheme using h=0.1.

Vaccination effect on human populations

In this subsection, the effect of voluntary vaccination on the human population is studied, just to handle the spread of Corona virus pandemic in a community. The study indicates that susceptibility of humans decreases with the increase in proportion of vaccinated humans. It is observed that the number of exposed and infected humans are significantly reduced with the increase in the rate of vaccination. However, the number of recovered individuals is increased by increasing the number of vaccinated humans. As time t, an increment in vaccination levels (%), will help automatically all populations approach F0, see Fig. 12, Fig. 13, Fig. 14, Fig. 15. The analysis proves that the spread of Corona virus disease could be controlled if people adopt proper vaccination strategies at least up to the level of 60%. The dynamical behavior of Corona virus disease in all populations through a vaccination programme is observed in Fig. 12, Fig. 13, Fig. 14, Fig. 15. These profiles are illustrated in Table 3, Table 4, Table 5, Table 6 respectively.

Table 3.

Rate of vaccination versus proportion of susceptible humans at F1.

Vaccination rate (%) Proportion of susceptible humans
0 0.4985
20 0.4896
40 0.4720
60 0.4546

Table 4.

Rate of vaccination versus proportion of exposed humans at F1.

Vaccination rate (%) Proportion of exposed humans
0 0.4365
20 0.2561
40 0.0785
60 0.0000

Table 5.

Rate of vaccination versus proportion of infected humans at F1 .

Vaccination rate (%) Proportion of infected humans
0 0.1072
20 0.0603
40 0.0209
60 0.0000

Table 6.

Effect of vaccination on the proportion of recovered humans at F1 .

Vaccination rate (%) Proportion of recovered humans
0 0.0034
20 0.1340
40 0.2624
60 0.3519

Effect of vaccination on R0

Our goal is to lift up the proportion of recovered humans and to decrease the number of humans in susceptible, exposed and the infected compartments by adopting proper vaccination measures. It is important to compute the value of R0 at different levels of voluntary vaccination to get the better understanding of the problem. Therefore, the effectiveness of voluntary vaccination on threshold parameter R0 has been examined in Fig. 16. We saw that increment in the level of vaccination diminishes the value of R0. It is likewise seen that the Corona virus disease will remain continue in the community at all vaccination levels goes from 0% to 60%. Indeed, for this range, the value of R0 is greater than one. However, from 60% onward, the value of threshold parameter R0 will become less than one as given in Table 7 and the infectivity goes to zero as illustrated in Fig. 13, Fig. 14 already. This shows that Corona virus disease will be eliminated from the host population if we vaccinate around 60% of the human population, which legitimizes the title of our manuscript.

Fig. 16.

Fig. 16

Portrait of threshold parameter R0 plotted against vaccination coverage levels. It is observed that R0 gives a small decease in its value by increasing the levels of voluntary vaccination.

Table 7.

Threshold parameter R0 under the effect of persistent vaccination.

Vaccination levels (%) Threshold parameter R0
0 1.9860>1
20 1.4750>1
40 1.1910>1
60 1.0110>1
61 0.9991<1

Covariance

In the current subsection, the joint variability [40] of all classes is studied numerically. For each pair of populations, we have elaborated the consequences of relationship quantity ρ as illustrated in Table 8. A numerical study performed in Fig. 12, Fig. 13, Fig. 14 authentically justified the inverse relationship among susceptible, exposed, infected and the vaccinated humans. However, it is noticed that there is a direct correlation between the recovered and vaccinated class as demonstrated in Fig. 15. Subsequently, a continuous rapid increment in the recovered class will lead the total population to F0.

Table 8.

Joint variability of populations.

Populations ρ Relationship
(V,S) −0.8842 Inverse
(V,E) −0.6574 Inverse
(V,I) −0.6971 Inverse
(V,R) 0.6765 Direct

Conclusions

In this research article, we proposed a mathematical model for COVID-19 that provides a good description about the spread of a Corona virus within the community. Dynamical behavior of Corona virus disease is investigated through this dynamic model using some comprehensive mathematical techniques. First, we proved existence and uniqueness and then positivity and the boundedness of solutions. Subsequently, our problem is well-posed and solutions are physically realizable.

We evaluated two main equilibrium states of the proposed model respectively. The value of threshold parameter R0 was computed using the method of next generation to study the dynamics of the vaccination model. Existence of a Corona free point F0 is proved for the condition R0<1 in the local and global sense. When R0>1, it is also proved that F1 exists and is locally and globally stable, where F0 got unstable. LaSalle’s invariance principle from the theory of Lyapunov functions was established to carry out the proofs of global stability.

Furthermore, we have investigated stability analysis of COVID-19 within the community numerically by employing NSFD and RK4 methods. We have made this effort to solve the system and to validate our obtained analytical results. Numerical simulations show that RK4 is not suitable especially when the time step size is large. It produces non-physical oscillations, fails to preserve positivity of solutions and converges to false steady states and diverges. On the other hand, the projected NSFD scheme is reliable and consistent with the SVEIR model and preserves all the essential properties of solutions. Moreover, the developed NSFD scheme is unconditionally convergent and stable.

We also discussed graphically the dynamical behavior of the Corona model under the effect of four vaccination levels. It is proved that the disease can be controlled efficiently if the level of voluntary vaccination is increased in susceptible, exposed, and infected population. We also studied the effect of vaccination on the value of R0. As time goes to infinity, the value of R0 regresses with the increase in levels of voluntary vaccination. It is found that Corona virus disease will persist in the community if the susceptible humans are vaccinated up to the level of 60%. An increase in this percentage significantly reduces the risk of Corona virus disease.

Covariances among susceptible, exposed, infected, recovered and the vaccinated humans is computed to check the statistical relationship between all the classes. We have discussed the corresponding joint variability.

CRediT authorship contribution statement

W. Ahmad: Conceptualization, Methodology, Computations, Writing – original draft. M. Abbas: Supervision, Visualization, Investigation, Validation. M. Rafiq: Project administration, Resources, Data curation, Revision of original draft, Formal analysis. D. Baleanu: Writing – review & editing, Software.

Uncited references

[56], [57], [58], [59], [60], [61], [62], [63], [64], [65], [66], [67], [68], [69]

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

The authors are grateful to the anonymous reviewers and the handling editor for their constructive comments and suggestions, which lead to improvements of the original manuscript.

Funding

Funding is not applicable for this research paper.

References

  • 1.HuiDS I.A.E., Madani T., Ntoumi F., Koch R., Dar O., et al. The continuing 2019- nCoV epidemic threat of novel coronaviruses to global health: the latest 2019 novel coronavirus outbreak in Wuhan, China. Int J Infect Dis. 2020;91:264–266. doi: 10.1016/j.ijid.2020.01.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.He S., Tang S., Rong L. A discrete stochastic model of the COVID-19 outbreak: forecast and control. Math Biosci Eng. 2020;17(4):2792–2804. doi: 10.3934/mbe.2020153. [DOI] [PubMed] [Google Scholar]
  • 3.Liang T., et al. The First Affiliated Hospital, Zhejiang University School of Medicine. Compiled According to Clinical Experience; 2020. Handbook of COVID-19 prevention and treatment. [Google Scholar]
  • 4.Murthy S., Gomersall C.D., Fowler R.A. Care for critically ill patients with COVID-19. JAMA. 2020;323(15) doi: 10.1001/jama.2020.3633. [DOI] [PubMed] [Google Scholar]
  • 5.Bikdeli B., Madhavan M.V., Jimenez D., Chuich T., Dreyfus I., Driggin E., Der Nigoghos-sian C., Ageno W., Madjid M., Guo Y., et al. COVID-19 and thrombotic or thromboembolic disease: implications for prevention, antithrombotic therapy, and follow-up. J Am Coll Cardiol. 2020 doi: 10.1016/j.jacc.2020.04.031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Li T., Xue Y. Global stability analysis of a delayed SEIQR epidemic model with quarantine and latent. Appl Math. 2013;4:109–117. [Google Scholar]
  • 7.Chen S., Small M., Fu X. Global stability of epidemic models with imperfect vaccination and quarantine on scale-free networks. IEEE Trans Netw Sci Eng. 2020;7:1583–1596. [Google Scholar]
  • 8.Li F., Meng X., Wang X. Analysis and numerical simulations of a stochastic SEIQR epidemic system with quarantine-adjusted incidence and imperfect vaccination. Comput Math Methods Med. 2018;2018 doi: 10.1155/2018/7873902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Yongzhena P., Shaoying L., Shujing G., Shuping L., Changguoc L. A delayed SEIQR epidemic model with pulse vaccination and the quarantine measure. Comput Math Appl. 2009;58:135–145. [Google Scholar]
  • 10.Volpert V., Banerjee M., Petrovskii S. On a quarantine model of coronavirus infection and data analysis. Math Model Nat Phenom. 2020;15(24):1–6. [Google Scholar]
  • 11.Rihan F.A., Alsakaji H.J. Dynamics of a stochastic delay differential model for COVID-19 infection with asymptomatic infected and interacting people: Case study in the UAE. Results Phys. 2021;28 doi: 10.1016/j.rinp.2021.104658. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Rihan F.A., Alsakaji H.J., Rajivganthi C. Stochastic SIRC epidemic model with time-delay for COVID-19. Adv Difference Equ. 2020;2020(1):1–20. doi: 10.1186/s13662-020-02964-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Ahmad W., Rafiq M., Abbas M. Mathematical analysis to control the spread of Ebola virus epidemic through voluntary vaccination. Eur Phys J Plus. 2020;135(10) 1-34. [Google Scholar]
  • 14.Brettin A., Goldthorpe R.R.R., Weishaar K., Erovenko I.V. Ebola could be eradicated through voluntary vaccination. R Soc Open Sci. 2018;5 doi: 10.1098/rsos.171591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Tulu T.W., Tian B., Wu Z. Modeling the effect of quarantine and vaccination on Ebola disease. Adv Difference Equ. 2017;2017:178. doi: 10.1186/s13662-017-1225-z. [DOI] [Google Scholar]
  • 16.Ahmad M.D., Usman M., Khan A., Imran M. Optimal control analysis of Ebola disease with control strategies of quarantine and vaccination. Infect Dis Poverty. 2016;5(72):12. doi: 10.1186/s40249-016-0161-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Acuna-Zegarra M.A., Diaz-Infanteb S., Baca-Carrasco D., Liceaga D.O. COVID-19 optimal vaccination policies: a modeling study on efficacy, natural and vaccine-induced immunity responses. MedRxiv. 2020 doi: 10.1016/j.mbs.2021.108614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Belete T.M. A review on Promising vaccine development progress for COVID-19 disease. Vacunas. 2020;21:121–128. doi: 10.1016/j.vacun.2020.05.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Kaur S.P., Gupta V. COVID-19 Vaccine: A comprehensive status report. Virus Res. 2020;288 doi: 10.1016/j.virusres.2020.198114. (1-12) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Shah A., Marks P.W. Unwavering regulatory safeguards for COVID-19 vaccines. J Am Med Assoc. 2020;324:931–932. doi: 10.1001/jama.2020.15725. [DOI] [PubMed] [Google Scholar]
  • 21.Ivanova P. 2020. Russia says its sputnik v covid-19 vaccine is 92% effective. press release, November 11, 2020. [Google Scholar]
  • 22.Cohen E. 2020. Moderna’s coronavirus vaccine is 94.5% effective, according to company data. URL: https://edition.cnn.com/2020/11/16/health/moderna-vaccine-results-coronavirus/index.html, prees release updated November 16, 2020. [Google Scholar]
  • 23.Ahmed A., Salam B., Mohammad M., Akgul A., Khoshnaw S.H.A. Analysis coronavirus disease (COVID-19) model using numerical approaches and logistic model. AIMS Bioeng. 2020;7(3):130–146. [Google Scholar]
  • 24.Rafiq M., Macias-Diaz J.E., Raza A., Ahmed N. Design of a nonlinear model for the prop- agation of COVID-19 and its efficient nonstandard computational implementation. Appl Math Model. 2021;89:1835–1846. doi: 10.1016/j.apm.2020.08.082. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Rafiq M, Ahmad W, Abbas M, Baleanu D. A reliable and competitive mathematical analysis of Ebola epidemic model. Adv Difference Equ 2020(1):540, p. 1–24.
  • 26.Villanueva RJ, Arenas AJ, Gonzalez-Parra G. A nonstandard dynamically consistent numerical scheme applied to obesity dynamics. J Appl Math 2008:640154, p. 14.
  • 27.Iqbal Z., Ahmed N., Baleanu D., Adel W., Rafiq M., A.-u. Rehman M., Alshomrani A.S. Positivity and boundedness preserving numerical algorithm for the solution of fractional nonlinear epidemic model of HIV/AIDS transmission. Chaos Solitons Fractals. 2020;134 [Google Scholar]
  • 28.Lambert J.D. John Wiley and Sons; Chichester, UK: 1991. Numerical methods for ordinary differential systems: The initial value problem. [Google Scholar]
  • 29.Moghadas S.M., Alexander M.E., Corbett B.D., Gumel A.B. A positivity-preserving mickens type discretization of an epidemic model. J Difference Equ Appl. 2003;9(11):1037–1051. [Google Scholar]
  • 30.E.Mickens R. World Scientific; River Edge, NJ, USA: 2000. Applications of nonstandard finite difference schemes. [Google Scholar]
  • 31.Mickens R.E. Dynamic consistency: a fundamental principle for constructing nonstandard finite difference schemes for differential equations. J Difference Equ Appl. 2005;11(7):645–653. [Google Scholar]
  • 32.Mickens R.E., Jordan P. A positivity-preserving nonstandard finite difference scheme for the damped wave equation. Numer Methods Partial Differential Equations. 2004;20(5) [Google Scholar]
  • 33.Mickens R.E., Jordan P. A new positivity-preserving nonstandard finite difference scheme for the DWE. Numer Methods Partial Differential Equations. 2005;21(5):976–985. [Google Scholar]
  • 34.Dimitrov D.T., Kojouharov H.V. Positive and elementary stable nonstandard numerical methods with applications to predator–prey models. J Comput Appl Math. 2006;189:98–108. [Google Scholar]
  • 35.Anguelov R., Lubuma J.M.-S. Contributions to the mathematics of the nonstandard finite difference method and applications. Numer Methods Partial Differential Equations. 2001;17(5):518–543. 14 Journal of Applied Mathematics. [Google Scholar]
  • 36.Moghadas S.M., Alexander M.E., Corbett B.D. A nonstandard numerical scheme for a generalized Gause-type predator–prey model. Physica D. 2004;188(1–2):134–151. [Google Scholar]
  • 37.Anguelov R., Lubuma J.M.-S. Nonstandard finite difference method by nonlocal approximation. Math Comput Simulation. 2003;61(3–6):465–475. [Google Scholar]
  • 38.Dimitrov D.T., Kojouharov H.V. Nonstandard finite-difference schemes for general two dimensional autonomous dynamical systems. Appl Math Lett. 2005;18(7):769–774. [Google Scholar]
  • 39.Chen-Charpentier B.M., Dimitrov D.T., Kojouharov H.V. Combined nonstandard numerical methods for ODEs with polynomial right-hand sides. Math Comput Simulation. 2006;73(1–4):105–113. [Google Scholar]
  • 40.Rafiq M., Ahmadian A., Raza A., Baleanu D., Ahsan M.S., Sathar M.H.A. Numerical controlmeasures of stochastic malaria epidemic model. Comput Mater Contin. 2020;65 p. 33-51. [Google Scholar]
  • 41.Khan M.A., Atangana A. Modeling the dynamics of novel coronavirus (2019-nCov) with fractional derivative. Alex Eng J. 2020 [Google Scholar]
  • 42.Moss R., Wood J., Brown D., Shearer F., Black A.J., Cheng A., McCaw J.M., McVernon J. Modelling the impact of COVID-19 in Australia to inform transmission reducing measures and health system preparedness. MedRxiv. 2020 doi: 10.3201/eid2612.202530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Liu M., Ning J., Du Y., Cao J., Zhang D., Wang J., Chen M. Modelling the evolution trajectory of COVID-19 in Wuhan, China: experience and suggestions. Public Health. 2020;183:76–80. doi: 10.1016/j.puhe.2020.05.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Aghdaoui H., Tilioua M., Nisar K.S., Khan I. A fractional epidemic model with Mittag-Leffler kernel for COVID-19. Math Biol Bioinform. 2021;16(1):39–56. [Google Scholar]
  • 45.Peter O.J., Shaikh A.S., Ibrahim M.O., Nisar K.S., Baleanu D., Khan I., Abioye A.I. Analysis and dynamics of fractional order mathematical model of COVID-19 in Nigeria using atangana-baleanu operator. Comput Mater Contin. 2021;66(2):1823–1848. [Google Scholar]
  • 46.Noor M.A., Raza A., Arif M.S., Rafiq M., Nisar K.S., Khan I., Abdelwahab S.F. Non-standard computational analysis of the stochastic COVID-19 pandemic model: An application of computational biology. Alex Eng J. 2021;61(1):619–630. [Google Scholar]
  • 47.Chatterjee A.N., Basir F.A., Almuqrin M.A., Mondal J., Khan I. SARS-CoV-2 infection with lytic and non-lytic immune responses: A fractional order optimal control theoretical study. Results Phys. 2021;26 doi: 10.1016/j.rinp.2021.104260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Almuqrin M.A., Goswami P., Sharma S., Khan I., Dubey R.S., Khan A. Fractional model of Ebola virus in population of bats in frame of Atangana-Baleanu fractional derivative. Results Phys. 2021;26 [Google Scholar]
  • 49.Ahmad W., Abbas M. Effect of quarantine on transmission dynamics of Ebola virus epidemic: a mathematical analysis. Eur Phys J Plus. 2021;136(4) 1-33. [Google Scholar]
  • 50.Hale H.K. John Wiley and Sons; New York, NY, USA: 1969. Ordinary differential equations. [Google Scholar]
  • 51.Perko L. 3rd ed. Springer; New York, NY, USA: 2001. Differential equation and dynamical systems. [Google Scholar]
  • 52.Onuorah M.O., Nasir M.O., Ojo M.S., Ademu A. A deterministic mathematical model for Ebola virus incorporating the vector population. Int J Math Trends Technol (IJMTT) 2016;30 [Google Scholar]
  • 53.LaSalle J.P. SIAM; Philadelphia, PA: 1976. The stability of dynamical systems. [Google Scholar]
  • 54.Lakshmikantam V., Martynyuk A.A. Lyapunov’s direct method in stability theory (review) Int Appl Mech. 1992;28:135–144. [Google Scholar]
  • 55.Berge T., Lubuma J.M.-S. A simple mathematical model foe Ebola Virus in Africa. J Biol Dyn. 2017;11(1):42–74. doi: 10.1080/17513758.2016.1229817. [DOI] [PubMed] [Google Scholar]
  • 56.Potluri R., Kumar A., Maheshwari V., Smith C., Mathieu V.O., Luhn K., et al. Impact of prophylactic vaccination strategies on Ebola virus transmission: A modeling analysis. PLoS ONE. 2020;15(4) doi: 10.1371/journal.pone.0230406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Area I., Ndairou F., Nieto J.J. Ebola model and optimal control with vaccination constraints. J Ind Manag Optim. 2018;14(2):427–446. [Google Scholar]
  • 58.Wilder-Smith A., Freedman D.O. Isolation, quarantine, social distancing and community containment: pivotal role for old-style public health measures in the novel coronavirus (2019- ncov) outbreak. J Travel Med. 2020;27(2):taaa020. doi: 10.1093/jtm/taaa020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Liu P.-Y., He S., Rong L.-B., Tang S.-Y. The effect of control measures on COVID-19 transmission in Italy: Comparison with Guangdong province in China. Infect Dis Poverty. 2020;9:130. doi: 10.1186/s40249-020-00730-2. (1-13) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Sarkar K., Khajanchi S., Nieto J.J. Modeling and forecasting the COVID-19 pandemic in India. Chaos Solitons Fractals. 2020;139 doi: 10.1016/j.chaos.2020.110049. (1-16) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Ngonghala C.N., Iboi E., Eikenberry S., Scotch M., MacIntyre C.R., Bonds M.H., Gumel A.B. Mathematical assessment of the impact of non-pharmaceutical interventions on curtailing the 2019 novel Coronavirus. Math Biosci. 2020;325 doi: 10.1016/j.mbs.2020.108364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Madubueze C.E., Dachollom S., Onwubuya I.O. Controlling the spread of COVID-19: Optimal control analysis. Comput Math Methods Med. 2020;2020 doi: 10.1155/2020/6862516. (1-14) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Barbosa Libotte G., Sergio Lobato F., Mendes Platt G., Silva Neto A.J. Determination of an optimal control strategy for vaccine administration in COVID-19 pandemic treatment. Comput Methods Programs Biomed. 2020;196 doi: 10.1016/j.cmpb.2020.105664. (1-13) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Tian H., Liu Y., Li Y., Wu C.-H., Chen B., Kraemer M.U., Li B., Cai J., Xu B., Yang Q., et al. An investigation of transmission control measures during the first 50 days of the COVID- 19 epidemic in China. Science. 2020;368:638–642. doi: 10.1126/science.abb6105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Jeyanathan M., Afkhami S., Smaill F., Miller M.S., Lichty B.D., Xing Z. Immunological considerations for COVID-19 vaccine strategies. Nat Rev Immunol. 2020;20:615–632. doi: 10.1038/s41577-020-00434-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Leroy E.M., Kumulungui B., Pourrut X., Rouquet P., Hassanin A., Yaba P., Delicat A., Paweska J.T., Gonzalez J.-P., Swanepoel R. Fruit bats as reservoirs of Ebola virus. Nature. 2005;438:575–576. doi: 10.1038/438575a. [DOI] [PubMed] [Google Scholar]
  • 67.Butt A.I.K., Abbas M., Ahmad W. A mathematical analysis of an isothermal tube drawing process. Alex Eng J. 2020;59 p. 3419-3429. [Google Scholar]
  • 68.Alexander M.E., Bowman C., Moghadas S.M., Summers R., Gumel A.B., Sahai B.M. A vaccination model for transmission dynamics of influenza. SIAM J Appl Dyn Syst. 2004;3:503–524. [Google Scholar]
  • 69.Butt A.I.K., Ahmad W., Ahmad N. Numerical based approach to develop analytical solution of a steady-state melt-spinning model. Br J Math Comput Sci. 2016;18(4):1–9. [Google Scholar]

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