Next Article in Journal
SARS-CoV-2 in Namibian Dogs
Previous Article in Journal
Dynamics of Antibody and T Cell Immunity against SARS-CoV-2 Variants of Concern and the Impact of Booster Vaccinations in Previously Infected and Infection-Naïve Individuals
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Fractional Order Model Studying the Role of Negative and Positive Attitudes towards Vaccination

by
Isa Abdullahi Baba
1,2,
Fathalla A. Rihan
3,4,
Usa Wannasingha Humphries
1,* and
Badamasi Bashir Mikailu
2
1
Department of Mathematics, Faculty of Science, King Mongkuts University of Science and Technology Thonburi (KMUTT), Bangkok 10140, Thailand
2
Department of Mathematics, Bayero University Kano, Kano 700006, Nigeria
3
Department of Mathematical Sciences, College of Science, UAE University, Al Ain 15551, United Arab Emirates
4
Department of Mathematics, Faculty of Science, Helwan University, Cairo 11795, Egypt
*
Author to whom correspondence should be addressed.
Vaccines 2022, 10(12), 2135; https://doi.org/10.3390/vaccines10122135
Submission received: 19 November 2022 / Revised: 9 December 2022 / Accepted: 12 December 2022 / Published: 13 December 2022

Abstract

:
A fractional-order model consisting of a system of four equations in a Caputo–Fabrizio sense is constructed. This paper investigates the role of negative and positive attitudes towards vaccination in relation to infectious disease proliferation. Two equilibrium points, i.e., disease-free and endemic, are computed. Basic reproduction ratio is also deducted. The existence and uniqueness properties of the model are established. Stability analysis of the solutions of the model is carried out. Numerical simulations are carried out and the effects of negative and positive attitudes towards vaccination areclearly shown; the significance of the fractional-order from the biological point of view is also established. The positive effect of increasing awareness, which in turn increases positive attitudes towards vaccination, is also shown numerically.The results show that negative attitudes towards vaccination increase infectious disease proliferation and this can only be limited by mounting awareness campaigns in the population. It is also clear from our findings that the high vaccine hesitancy during the COVID-19 pandemicisan important problem, and further efforts should be madeto support people and give them correct information about vaccines.

1. Introduction

Scientific discoveries and their applications are what define modern societies. Recently, the emergence of anti-scientific attitudeshas led to a decrease in public trust in science [1]. Vaccines areamong the most significant discoveries in science, and have saved many lives. However, the increases anti-vaccine groups leads to vaccine rejection [2,3,4]. Hence, theseanti-vaccine groups increase the danger of infectious disease proliferation to themselves and to the entire society. Since the emergence ofthe COVID-19 pandemic and the serious problems it has caused, the study of the problemsleading to vaccine rejection is of paramount significance. Many people from different backgrounds are against vaccines, which consequently leads to reductions inpre-existing immunity [5].
Studying the causes of both negative and positive attitudes towards vaccination is therefore very significant as the purely scientific and applied perspectives are concerned. Several studies have investigated the causes of the increases in anti-vaccine groups and their focus has beengeared towards individual differencesmost of the time.For example, in [6] they claim that anti-vaccine attitudes are related tomoral purity concerns, and orthodox religiousness. In [7] they claim anti-vaccine attitudes have direct relationships withindividualistic/hierarchical worldviews and conspiratorial thinking.
Many models in theliterature have considered the vaccination decision-making process [8,9,10,11]. Most of these models are based on ordinary differential equations. In most of these models, the factors considered to affect the acceptance of vaccine are beliefs, fear, factual information, and rumors. Because of the hereditary properties and provision of a good description of the memory, fractional order derivatives and fractional integrals play important roles in mathematical modeling. This is why many researchers studyingreal-life phenomena use fractional order differential equations [12,13,14,15]. The Caputo–Fabrizio (CF) fractional-order derivative was developed in 2015. This fractional-order derivative is based on an exponential kernel and the details on the operator can be found in [16]. Many studies haveused the Caputo–Fabrizio derivative to model problems in various fields [17,18,19] and the Caputo–Fabrizio fractional derivative gives less noise than the Riemann–Liouville derivative [20]. Hence, in this research, the Caputo–Fabrizio fractional derivative was used.The Caputo-Fabrizio (CF) fractional operator used in this study is a particular case of the new generalized Hattaf fractional (GHF) operator presented in [21,22].
As for vaccine hesitancy, an investigation conducted in October 2020 [23] suggests that46%of French citizens are vaccine hesitant. Other countries exhibit percentages of opposition and hesitancy that exceed30%, i.e., 36%in Spain and the USA,35%in Italy,32%in South Africa, and31%in Japan and Germany. Globally, vaccinehesitancy and objection rates are as large as 27%.
Given these large percentages of hesitance and opposition to COVID-19 vaccines, [24] constructed a mathematical model that employs a behavioral epidemiology approach to study the implementation of a vaccination campaign for COVID-19. To this end, they adopt a strategy similar to the one used in [25]. In other words, they assume that the vaccination rate is a phenomenological function of the present and past information that the citizens have on the spread of the epidemic. Refs. [26,27,28,29] constructed a mathematical model in the context of SIR and SEIR infectious diseases, but thesemechanisticmodelsare based on evolutionary game theories which are reduced to the case of volatile opinion switching. Most of these models are either statistical or classical in nature, however in modeling hesitancy memory plays a vital role, hence the need for a fractional order model. Furthermore, the effect of awareness will be of paramount importance in reducing hesitancy. Our model is fractional in nature and also discusses the effect of awareness.
In our research, the main goal is to study the problem from a group processes viewpoint. In order to achieve this, we considered amathematical modeling approach. The target is to study the most significant parameters that lead to increases in anti-vaccine sentiments, and possibly study theeffects as they lead to increases in infectious disease proliferation using fractional order models. Present day social psychologists acknowledge that the most important procedure for group development is recognizing with the group and devotion to the group operation. Identity of a group can be seen from a cognitive-motivational perspective and the perspective of intergroup relations [8].
Here, we construct a model based on the Caputo–Fabrizio fractional derivative to study the role of negative and positive attitudes towards vaccination in relation to infectious disease proliferation. We divide the susceptible population into two:a pro-vaccination susceptible compartment and an anti-vaccination susceptible compartment. We also consider the possibility of changing compartments among the susceptible population, possibly due to change of mind.

2. Formulation of the Model

The model consists of a system of fractional order differential equations in the Caputo–Fabrizio sense with four compartments. The compartments are F ( t ) , A ( t ) , I ( t ) ,   and   R ( t ) , which stand for the pro-vaccine susceptible compartment, the anti-vaccine susceptible compartment, the infected compartment, and the recovered compartment, respectively. The model is given below:
D 0 C F t α F ( t ) = λ α F ( t ) I ( t ) + p [ μ 1 α I ( t ) + μ 2 α R ( t ) ] v α F ( t ) + γ α A ( t ) η α F ( t ) , D 0 C F t α A ( t ) = λ α A ( t ) I ( t ) + ( 1 p ) [ μ 1 α I ( t ) + μ 2 α R ( t ) ] γ α A ( t ) + η α F ( t ) , D 0 C F t α I ( t ) = λ α [ F ( t ) + A ( t ) ] I ( t ) ( β α + μ 1 α ) I ( t ) , D 0 C F t α R ( t ) = β α I ( t ) μ 2 α R ( t ) + v α F ( t ) ,
with the following initial conditions:
F ( 0 ) = a 1 , A ( 0 ) = a 2 , I ( 0 ) = a 3 , and   R ( 0 ) = a 4 .
Define N = F + A + I + R , to be the total population.
The meaning of the parameters involved in the model is given in Table 1 below.

3. Analysis of the Model

Here, existence and uniqueness analysis of the solution of the model iscarried out. Moreover, equilibria, basic reproduction number, and local stability analysis of the solution of the model are studied.

3.1. Existence and Uniqueness of a Solution of the Model

In this paper, a fixed-point result is applied to check the existence and uniqueness of the solution of the model. Let the system be re-written as
D 0 C F t α F ( t ) = F 1 ( t , F ) ,
D 0 C F t α A ( t ) = F 2 ( t , A ) ,  
D 0 C F t α I ( t ) = F 3 ( t , I ) ,
D 0 C F t α R ( t ) = F 4 ( t , R ) .  
Applying the Caputo–Fabrizio operator, the system becomes:
F ( t ) F ( 0 ) = 2 ( 1 α ) ( 2 α ) M ( α ) F 1 ( t , F ) + 2 α ( 2 α ) M ( α ) 0 t F 1 ( η , F ) d η ,
A ( t ) A ( 0 ) = 2 ( 1 α ) ( 2 α ) M ( α ) F 2 ( t , A ) + 2 α ( 2 α ) M ( α ) 0 t F 2 ( η , A ) d η ,
I ( t ) I ( 0 ) = 2 ( 1 α ) ( 2 α ) M ( α ) F 3 ( t , I ) + 2 α ( 2 α ) M ( α ) 0 t F 3 ( η , I ) d η ,
R ( t ) R ( 0 ) = 2 ( 1 α ) ( 2 α ) M ( α ) F 4 ( t , R ) + 2 α ( 2 α ) M ( α ) 0 t F 4 ( η , R ) d η .
Now, we need to prove F 1 , ,   F 4 satisfy Lipschitz continuity and contraction. See the theorem below:
Theorem 1.
F 1 is Lipschitz and if
0 λ α k 1 + v α + η α < 1 ,
it is a contraction.
Proof. 
F 1 ( t , F ) F 1 ( t , F 1 ) = λ α I ( t ) ( F ( t ) F 1 ( t ) ) ( v α + η α ) ( F ( t ) F 1 ( t ) ) λ α I ( t ) F ( t ) F 1 ( t ) + ( v α + η α ) F ( t ) F 1 ( t ) ( λ α k 1 + v α + η α ) F ( t ) F 1 ( t ) L 1 F ( t ) F 1 ( t ) ,
where L 1 = λ α k 1 + v α + η α a n d k 1 I ( t ) .
In the same way, we show the Lipschitz continuity and contraction for F 2 , ,   F 4 , where we obtain L 2 , ,   L 4 , respectively, as their Lipschitz constants.
In recursive form, let
q 1 n ( t ) = F n ( t ) F n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 1 ( t , F n 1 ) F 1 ( t , F n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 1 ( δ , F n 1 ) F 1 ( δ , F n 2 ) ) d δ ,
q 2 n ( t ) = A n ( t ) A n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 2 ( t , A n 1 ) F 2 ( t , A n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 2 ( δ , A n 1 ) F 2 ( δ , A n 2 ) ) d δ ,
q 3 n ( t ) = I n ( t ) I n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 3 ( t , I n 1 ) F 3 ( t , I n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 3 ( δ , I n 1 ) F 3 ( δ , I n 2 ) ) d δ ,
q 4 n ( t ) = R n ( t ) R n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 4 ( t , R n 1 ) F 4 ( t , R n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 4 ( δ , R n 1 ) F 4 ( δ , R n 2 ) ) d δ ,
with initial conditions:
F 0 ( t ) = F ( 0 ) , A 0 ( t ) = A ( 0 ) , I 0 ( t ) = I ( 0 ) a n d R 0 ( t ) = R ( 0 ) .
Taking norm of q 1 n , we have:
q 1 n ( t ) = F n ( t ) F n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 1 ( t , F n 1 ) F 1 ( t , F n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 1 ( δ , F n 1 ) F 1 ( δ , F n 2 ) ) d δ .
Applying triangular inequality, we have:
q 1 n ( t ) = F n ( t ) F n 1 ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 1 ( t , F n 1 ) F 1 ( t , F n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 1 ( δ , F n 1 ) F 1 ( δ , F n 2 ) ) d δ 2 ( 1 α ) ( 2 α ) M ( α ) L 1 F n ( t ) F n 1 ( t ) + 2 α ( 2 α ) M ( α ) L 1 0 t F n ( t ) F n 1 ( t ) d δ .
This implies:
q 1 n ( t ) 2 ( 1 α ) ( 2 α ) M ( α ) L 1 q 1 n 1 ( t ) + 2 α ( 2 α ) M ( α ) L 1 0 t q 1 n 1 ( t ) d δ .
Similarly,
q 2 n ( t ) 2 ( 1 α ) ( 2 α ) M ( α ) L 2 q 2 n 1 ( t ) + 2 α ( 2 α ) M ( α ) L 2 0 t q 2 n 1 ( t ) d δ ,
q 3 n ( t ) 2 ( 1 α ) ( 2 α ) M ( α ) L 3 q 3 n 1 ( t ) + 2 α ( 2 α ) M ( α ) L 3 0 t q 3 n 1 ( t ) d δ ,
q 4 n ( t ) 2 ( 1 α ) ( 2 α ) M ( α ) L 4 q 4 n 1 ( t ) + 2 α ( 2 α ) M ( α ) L 4 0 t q 4 n 1 ( t ) d δ .
Subsequently, we have:
F n ( t ) = i = 1 n q 1 i ( t ) ,   A n ( t ) = i = 1 n q 2 i ( t ) ,   I n ( t ) = i = 1 n q 3 i ( t ) ,   R n ( t ) = i = 1 n q 4 i ( t ) .    
To show the existence of the solution, we prove the following theorem:
Theorem 2.
The solution exists if there exist t 1 such that the following inequality is true,
2 ( 1 α ) ( 2 α ) M ( α ) L i + 2 α t 1 ( 2 α ) M ( α ) L i < 1 ,   i = 1 ,   ,   5 .  
Proof. 
Recursively, we have
q 1 n ( t ) F n ( 0 ) [ 2 ( 1 α ) ( 2 α ) M ( α ) L 1 + 2 α ( 2 α ) M ( α ) L 1 ] n ,  
q 2 n ( t ) A n ( 0 ) [ 2 ( 1 α ) ( 2 α ) M ( α ) L 2 + 2 α ( 2 α ) M ( α ) L 2 ] n ,
q 3 n ( t ) I n ( 0 ) [ 2 ( 1 α ) ( 2 α ) M ( α ) L 3 + 2 α ( 2 α ) M ( α ) L 3 ] n ,  
q 4 n ( t ) R n ( 0 ) [ 2 ( 1 α ) ( 2 α ) M ( α ) L 4 + 2 α ( 2 α ) M ( α ) L 4 ] n .  
Hence, solutions exist and are continuous. To show that the functions above construct the solutions, consider:
F ( t ) F ( 0 ) = F n ( t ) H 1 n ( t ) ,  
A ( t ) A ( 0 ) = A n ( t ) H 2 n ( t ) ,  
I ( t ) I ( 0 ) = I n ( t ) H 3 n ( t ) ,
R ( t ) R ( 0 ) = R n ( t ) K 4 n ( t ) .  
Hence,
H 1 n ( t ) = 2 ( 1 α ) ( 2 α ) M ( α ) ( F 1 ( t , F n 1 ) F 1 ( t , F n 2 ) ) + 2 α ( 2 α ) M ( α ) 0 t ( F 1 ( δ , F n 1 ) F 1 ( δ , F n 2 ) ) d δ 2 ( 1 α ) ( 2 α ) M ( α ) F 1 ( t , F n 1 ) F 1 ( t , F n 2 ) + 2 α ( 2 α ) M ( α ) 0 t ( F 1 ( δ , F n 1 ) F 1 ( δ , F n 2 ) ) d δ 2 ( 1 α ) ( 2 α ) M ( α ) L 1 F F n 1 + 2 α ( 2 α ) M ( α ) L 1 F F n 1 t .
Carrying out the procedure, we get
H 1 n ( t ) [ 2 ( 1 α ) ( 2 α ) M ( α ) + 2 α t ( 2 α ) M ( α ) ] n + 1 L 1 n + 1 h .
At t = t 1 , we get
H 1 n ( t ) [ 2 ( 1 α ) ( 2 α ) M ( α ) + 2 α t 1 ( 2 α ) M ( α ) ] n + 1 L 1 n + 1 h .
Taking limit as n , we get
H 1 n ( t ) 0 .
Similarly, we get
H 2 n ( t ) , H 3 n ( t ) ,   H 4 n ( t ) 0 .
Finally, to show uniqueness, assume there exists some solutions say, F 1 ( t ) , A 1 ( t ) ,   I 1 ( t )   and   R 1 ( t ) ,   then
F ( t ) F 1 ( t ) ( 1 2 ( 1 α ) ( 2 α ) M ( α ) L 1 2 α t ( 2 α ) M ( α ) L 1 ) 0 .
The following theorem completes the result.
Theorem 3.
If
( 1 2 ( 1 α ) ( 2 α ) M ( α ) L 1 2 α t ( 2 α ) M ( α ) L 1 ) > 0 ,
then the solution is unique.
Proof. 
Consider
F ( t ) F 1 ( t ) ( 1 2 ( 1 α ) ( 2 α ) M ( α ) L 1 2 α t ( 2 α ) M ( α ) L 1 ) 0 .
Since,
( 1 2 ( 1 α ) ( 2 α ) M ( α ) L 1 2 α t ( 2 α ) M ( α ) L 1 ) > 0 ,
then
F ( t ) F 1 ( t ) = 0 .
This implies,
F ( t ) = F 1 ( t ) .
This applies to the remaining functions.
Since R = N ( F + A + I ) , we can limit our analysis tothree compartments, { F , A , I } .

3.2. Equilibria and Basic Reproduction Number

The equilibrium solutions are obtained by equating the equations in the model to zero and solving the system simultaneously. We obtain two equilibrium solutions:
  • Disease-free equilibrium ( E 0 )
    E 0 = { F 0 ,   A 0 , I 0 } = { λ α μ 2 α N [ γ α + β α + ( 1 p ) v α ] μ 2 α + λ α v α , [ η α + ( 1 p ) v α ] μ 2 α N [ γ α + β α + ( 1 p ) v α ] μ 2 α + λ α v α , 0 } .
  • Endemic equilibrium ( E 1 )
    E 1 = { F 1 , A 1 , I 1 } ,
    where
    F 1 = μ 2 α ( λ α N β α + μ 1 α 1 ) v λ α β α + μ 1 α β α + μ 2 α v α I 1 ,
    A 1 = β α + μ 1 α λ α [ μ 2 α ( λ α N β α + μ 1 α 1 ) v λ α β α + μ 1 α β α + μ 2 α v α I 1 ] ,
    and I 1 is obtained by solving the following quadratic equation,
    I 1 = a + a 2 b c 2 b ,
    where
    a = λ α μ 2 α ( λ α N β α + μ 1 α 1 ) v λ α β α + μ 1 α + p ( μ 1 α μ 2 α ) + β α + μ 2 α v α ( γ α + η α + v α ) , b = λ α ( β α + μ 2 α v α ) ,   a n d c = γ α ( β α + μ 1 α ) λ α μ 2 α ( λ α N β α + μ 1 α 1 ) v λ α β α + μ 1 α [ γ α + η α + ( 1 p ) v α ] .
Clearly, we can see that the endemic equilibrium exists only if,
( λ α N β α + μ 1 α ) [ γ α + η α + ( 1 p ) v α ] μ 2 α [ γ α + η α + ( 1 p ) v α ] μ 2 α + γ α v α > 1 .
Define ( λ α N β α + μ 1 α ) [ γ α + η α + ( 1 p ) v α ] μ 2 α [ γ α + η α + ( 1 p ) v α ] μ 2 α + γ α v α = R 0 , where R 0 is the basic reproduction number.

3.3. Local Stability Analysis of the Solution of the Model

Consider the following Jacobian matrix from (1),
J = [ λ α I v α η α Υ α λ α F + p μ 1 α η α λ α I Υ α λ α A + ( 1 p ) μ 1 α λ α I λ α I λ α ( F + A ) ( β α + μ 1 α ) ] .
Theorem 4.
The disease-free equilibrium is locally asymptotically stable if R 0 < 1 .
Proof. 
Consider (29) at E 0 , we get
J ( E 0 ) = [ v α η α Υ α λ α F 0 + p μ 1 α η α Υ α λ α A 0 + ( 1 p ) μ 1 α 0 0 λ α ( F 0 + A 0 ) ( β α + μ 1 α ) ] .  
The characteristics polynomial of (30) is
[ η α Υ α + ( ( v α + η α ) λ ) ( Υ α λ ) ] ( λ α ( F 0 + A 0 ) ( β α + μ 1 α ) λ ) = 0 .
Therefore,
λ 1 = λ α ( F 0 + A 0 ) ( β α + μ 1 α ) .
λ 2   and   λ 3 can be found by solving η α Υ α + ( ( v α + η α ) λ ) ( Υ α λ ) = 0 .
It is clear that λ 1 < 0 ,   i f λ α ( F 0 + A 0 ) ( β α + μ 1 α ) < 0 .
This implies that λ α ( F 0 + A 0 ) ( β α + μ 1 α ) < 1 .
Substituting the values of F 0   and   A 0 , we get
( λ α N β α + μ 1 α ) [ γ α + η α + ( 1 p ) v α ] μ 2 α [ γ α + η α + ( 1 p ) v α ] μ 2 α + γ α v α = R 0 < 1 .
Simplifying η α Υ α + ( ( v α + η α ) λ ) ( Υ α λ ) = 0 , we get
λ 2 + ( v α + η α + Υ α ) λ + v α Υ α = 0 .
Using the Routh–Hurwitz criterion, P ( s ) = s 2 + a 1 s + a 2 has both roots with negative real parts iff both coefficeints, a i > 0 ,   i = 0 , 1 , 2 . Here,
a 0 = 1 > 0 ,   a 1 = ( v α + η α + Υ α ) > 0 ,   a d a 2 = v α Υ α > 0 .
Hence, E 0 is locally asymptotically stable if R 0 < 1 .
Theorem 5.
The endemic equilibrium is locally asymptotically stable if R 0 > 1 , and the following conditions are satisfied;
i )   p μ 1 α λ α I 1 + Υ α + λ α I 1 + β α + μ 1 α η α + ( λ α ) 2 I 1 F 1 + λ α ( F 1 + A 1 ) > 1 ,   a n d i i ) 2 λ α 2 I 1 A 1 + η α λ α F 1 + A 1 β α + μ 1 α + p μ 1 α λ α I 1 η α λ α + Υ α + λ α I 1 λ α 2 λ α I 1 + 1 I 1 F 1 + 2 1 p μ 1 α λ α I 1 + λ α F 1 + A 1 β α + μ 1 α Υ α + λ α I 1 > 1 .
Proof. 
Consider (29) at E 1 , we get
J E 1 = λ α I 1 v α η α Υ α λ α F 1 + p μ 1 α η α λ α I 1 Υ α λ α A 1 + 1 p μ 1 α λ α I 1 λ α I 1 λ α F 1 + A 1 β α + μ 1 α .  
The characteristics polynomial of (31) is
[ λ 2 + λ η α λ α 2 I 1 F 1 + p μ 1 α λ α I 1 + Υ α + λ α I 1 λ α F 1 + A 1 + β α + μ 1 α + ( 2 λ α 2 I 1 A 1 + η α λ α F 1 + A 1 β α + μ 1 α + p μ 1 α λ α I 1 η α λ α + Υ α + λ α I 1 λ α 2 λ α I 1 + 1 I 1 F 1 + 2 1 p μ 1 α λ α I 1 + λ α F 1 + A 1 β α + μ 1 α Υ α + λ α I 1 ) ] [ λ α I 1 v α η α ] = 0 .
Therefore,
λ 1 = λ α I 1 v α η α .
Clearly, λ 1 < 0 , if I 1 0 , and I 1 0 if R 0 > 1 .
Applying the Routh–Hurwitz criterion to,
λ 2 + λ η α λ α 2 I 1 F 1 + p μ 1 α λ α I 1 + Υ α + λ α I 1 λ α F 1 + A 1 + β α + μ 1 α + ( 2 λ α 2 I 1 A 1 + η α λ α F 1 + A 1 β α + μ 1 α + p μ 1 α λ α I 1 η α λ α + Υ α + λ α I 1 λ α 2 λ α I 1 + 1 I 1 F 1 + 2 1 p μ 1 α λ α I 1 + λ α F 1 + A 1 β α + μ 1 α Υ α + λ α I 1 ) = 0 ,
we see that the remaining Eigen values are negative if,
p μ 1 α λ α I 1 + Υ α + λ α I 1 + β α + μ 1 α η α + ( λ α ) 2 I 1 F 1 + λ α ( F 1 + A 1 ) > 1 ,
and
2 λ α 2 I 1 A 1 + η α λ α F 1 + A 1 β α + μ 1 α + p μ 1 α λ α I 1 η α λ α + Υ α + λ α I 1 λ α 2 λ α I 1 + 1 I 1 F 1 + 2 1 p μ 1 α λ α I 1 + λ α F 1 + A 1 β α + μ 1 α Υ α + λ α I 1 > 1 .  

4. Numerical Simulation

The numerical method used in this paper is similar to that of [21] and numerical simulations are carried out. Parameter values are given as, Λ = 0.6 day 1 , β = 0.5 day 1 , μ 1 = 0.001 day 1 , μ 2 = 0.0195 day 1 , v = 0.0005 day 1 ,   γ = 0.1 day 1 ,   η = 0.05 day 1 ,   α = 0.2 1.0 ( dimentioneless ) , p   = 0.5 ( dimentioneless ) .
The dynamics of the model are depicted in Figure 1. It is clear that none of the populations go to zero. The infected population and the recovered population simultaneously reach their peak at around 50 h, which is approximately two days.
Figure 2 compares the population of infected individuals with the pro-vaccine population. It can be seen that, in the absence of the pro-vaccine population, the infected population increases. This is because the remaining people in the population are against the vaccine and hence a large portion of the population will not be vaccinated. This leads to the proliferation of the disease.
Figure 3 compares the population of infected individuals with the anti-vaccine population. It can be seen that, in the absence of the anti-vaccine population, the infected population decreases. This is because the remaining people in the population are in support of the vaccine and hence a large portion of the population will be vaccinated. This leads to curtailing of the disease.
Figure 4 shows that increase in the level of awareness lead to decreases in the population of infected individuals. This is because as the level of awareness increases, the number of pro-vaccine individuals increases. This leads to increases in the number of vaccinated individuals, which in turn leads to decreases in the population of infected individuals.
Figure 5 shows the influence of the variation in the fractional-order α on the biological behavior of the infected population. It is clear from this figure that the population has an increasing effect when α is increased from 0.2   to   1 .

5. Conclusions

In this paper, we studied a fractional-order model consisting of a system of four equations in the Caputo–Fabrizio sense. Our aim was to study the role of negative and positive attitudes towards vaccination in relation to infectious disease proliferation. The compartments of the model were the pro-vaccine susceptible compartment, the anti-vaccine susceptible compartment, the infected compartment, and the recovered compartment. We obtained two equilibrium solutions, i.e., disease free and endemic. We were also able to obtain the basic reproduction ratio. This paper studied the existence and uniqueness properties of the model in detail. Numerical simulations were carried out to support the analytic results. The effect of negative and positive attitudes towards vaccination was clearly shown. Furthermore, the significance of the fractional-order from the biological point of view was established. It was shown that increases in the level of awareness lead to decreases in the population of infected individuals. This is because as the level of awareness increases, the number of pro-vaccine individuals increases. This leads to increases in the number of vaccinated individuals, which in turn leads to decreases in the population of infected individuals.
The limitation of this study is that there is a need for real data collection to validate the model, and people’s opinions need to be heard and incorporated into the model for further analysis.

Author Contributions

I.A.B., U.W.H., F.A.R. and B.B.M. have directly participated in the planning, execution, and analysis of this study. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

This research was supported by King Mongkut’s University of Science and Technology Thonburi’s Postdoctoral Fellowship.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Picon, N.C. The Sleep of Neoliberal Reason: Denialism, Conspiracies and Storytelling on Crises through Ventajas de viajarentren. Humanities 2022, 11, 64. [Google Scholar] [CrossRef]
  2. Larson, H.J.; Jarrett, C.; Eckersberger, E.; Smith, D.M.D.; Paterson, P. Understanding Vaccine Hesitancy around Vaccines and Vaccination from a Global Perspective: A Systematic Review of Published Literature, 2007–2012. Vaccine 2014, 32, 2150–2159. [Google Scholar] [CrossRef] [PubMed]
  3. Lin, C.; Tu, P.; Beitsch, L.M. Confidence and Receptivity for COVID-19 Vaccines: A Rapid Systematic Review. Vaccines 2021, 9, 16. [Google Scholar] [CrossRef] [PubMed]
  4. Piedrahita-Valdés, H.; Piedrahita-Castillo, D.; Bermejo-Higuera, J.; Guillem-Saiz, P.; Bermejo-Higuera, J.R.; Guillem-Saiz, J.; Sicilia-Montalvo, J.A.; Machío-Regidor, F. Vaccine Hesitancy on Social Media: Sentiment Analysis from June 2011 to April 2019. Vaccines 2021, 9, 28. [Google Scholar] [CrossRef] [PubMed]
  5. Reiter, P.L.; Pennell, M.L.; Katz, M.L. Acceptability of a COVID-19 vaccine among adults in the United States: How many people would get vaccinated? Vaccine 2020, 38, 6500–6507. [Google Scholar] [CrossRef]
  6. Bonte, J. The Continuum of Attitudes towards Vaccination A Qualitative Analysis of Arguments Used in Pro-, Anti-and Hesitant Tweets. Master’s Thesis, Utrecht University, Utrecht, The Netherlands, 2022. [Google Scholar]
  7. Lee, S.K.; Sun, J.; Jang, S.; Connelly, S. Misinformation of COVID-19 vaccines and vaccine hesitancy. Sci. Rep. 2022, 12, 1–11. [Google Scholar] [CrossRef]
  8. Crocetti, E.; Albarello, F.; Meeus, W.; Rubini, M. Identities: A developmental social-psychological perspective. Eur. Rev. Soc. Psychol. 2022, 1, 1–41. [Google Scholar] [CrossRef]
  9. Deml, M.J.; Buhl, A.; Huber, B.M.; Burton-Jeangros, C.; Tarr, P.E. Trust, affect, and choice in parents’ vaccination decision-making and health-care provider selection in Switzerland. Sociol. Health Illn. 2022, 44, 41–58. [Google Scholar] [CrossRef]
  10. Smith, S.E.; Sivertsen, N.; Lines, L.; De Bellis, A. Decision making in vaccine hesitant parents and pregnant women—An integrative review. Int. J. Nurs. Stud. Adv. 2022, 4, 100062. [Google Scholar] [CrossRef]
  11. de Waure, C.; Calabrò, G.E.; Ricciardi, W. Recommendations to drive a value-based decision-making on vaccination. Expert Rev. Vaccines 2022, 21, 289–296. [Google Scholar] [CrossRef]
  12. Karaagac, B.; Owolabi, K.M.; Pindza, E. Analysis and new simulations of fractional Noyes-Field model using Mittag-Leffler kernel. Sci. Afr. 2022, 17, e01384. [Google Scholar] [CrossRef]
  13. Georgiev, S.; Vulkov, L. Numerical Coefficient Reconstruction of Time-Depending Integer-and Fractional-Order SIR Models for Economic Analysis of COVID-19. Mathematics 2022, 10, 4247. [Google Scholar] [CrossRef]
  14. Afreen, A.; Raheem, A. Study of a nonlinear system of fractional differential equations with deviated arguments via Adomian decomposition method. Int. J. Appl. Comput. Math. 2022, 8, 1–7. [Google Scholar] [CrossRef]
  15. Vignesh, D.; Banerjee, S. Dynamical analysis of a fractional discrete-time vocal system. Nonlinear Dyn. 2022, 1, 1–5. [Google Scholar] [CrossRef]
  16. Baleanu, D.; Jajarmi, A.; Sajjadi, S.S.; Mozyrska, D. A new fractional model and optimal control of a tumor-immune surveillance with non-singular derivative operator. Chaos Interdiscip. J. Nonlinear Sci. 2019, 29, 083127. [Google Scholar] [CrossRef]
  17. Abouelregal, A.E.; Akgöz, B.; Civalek, Ö. Nonlocal thermoelastic vibration of a solid medium subjected to a pulsed heat flux via Caputo–Fabrizio fractional derivative heat conduction. Appl. Phys. A 2022, 128, 1–3. [Google Scholar] [CrossRef]
  18. Naeem, M.; Rezazadeh, H.; Khammash, A.A.; Shah, R.; Zaland, S. Analysis of the fuzzy fractional-order solitary wave solutions for the KdV equation in the sense of Caputo-Fabrizio derivative. J. Math. 2022, 2022, 3688916. [Google Scholar] [CrossRef]
  19. Edessa, G.K. Existence and Uniqueness Solution of the Model of Enzyme Kinetics in the Sense of Caputo–Fabrizio Fractional Derivative. Int. J. Differ. Equ. 2022, 2022, 1345919. [Google Scholar] [CrossRef]
  20. Baba, I.A.; Rihan, F.A. A fractional–order model with different strains of COVID-19. Phys. A Stat. Mech. Its Appl. 2022, 603, 127813. [Google Scholar] [CrossRef]
  21. Hattaf, K. On the stability and numerical scheme of fractional differential equations with application to biology. Computation 2022, 10, 97. [Google Scholar] [CrossRef]
  22. Hattaf, K. A new generalized definition of fractional derivative with non-singular kernel. Computation 2020, 8, 49. [Google Scholar] [CrossRef]
  23. IPSOS. Global Attitudes on a COVID-19 Vaccine–Ipsos Survey for The World Economic Forum. 2020. Available online: https://www.ipsos.com/sites/default/files/ct/news/documents/2020-11/global-attitudes-on-a-covid-19-vaccine-oct-2020.pdf (accessed on 1 November 2022).
  24. Buonomo, B.; Della Marca, R.; d’Onofrio, A.; Groppi, M. A behavioural modelling approach to assess the impact of COVID-19 vaccine hesitancy. J. Theor. Biol. 2022, 534, 110973. [Google Scholar] [CrossRef]
  25. d’Onofrio, A.; Manfredi, P.; Salinelli, E. Vaccinating behaviour, information, and the dynamics of SIR vaccine preventable diseases. Theor. Popul. Biol. 2007, 71, 301–317. [Google Scholar] [CrossRef]
  26. Bauch, C.T. Imitation dynamics predict vaccinating behaviour. Proc. R. Soc. B Biol. Sci. 2005, 272, 1669–1675. [Google Scholar] [CrossRef] [Green Version]
  27. d’Onofrio, A.; Manfredi, P.; Poletti, P. The interplay of public intervention and private choices in determining the outcome of vaccination programmes. PLoS ONE 2012, 7, e45653. [Google Scholar] [CrossRef] [Green Version]
  28. Della Marca, R.; d’Onofrio, A. Volatile opinions and optimal control of vaccine awareness campaigns: Chaotic behaviour of the forward-backward sweep algorithm vs. heuristic direct optimization. Commun. Nonlinear Sci. Numer. Simul. 2021, 98, 105768. [Google Scholar] [CrossRef]
  29. Wang, Z.; Bauch, C.T.; Bhattacharyya, S.; d’Onofrio, A.; Manfredi, P.; Perc, M.; Perra, N.; Salathé, M.; Zhao, D. Statistical physics of vaccination. Phys. Rep. 2016, 664, 1–13. [Google Scholar] [CrossRef]
Figure 1. Dynamics of the model.
Figure 1. Dynamics of the model.
Vaccines 10 02135 g001
Figure 2. Effect of eliminating the pro-vaccine population.
Figure 2. Effect of eliminating the pro-vaccine population.
Vaccines 10 02135 g002
Figure 3. Effect of eliminating the anti-vaccine population.
Figure 3. Effect of eliminating the anti-vaccine population.
Vaccines 10 02135 g003
Figure 4. Effect of increasing awareness level.
Figure 4. Effect of increasing awareness level.
Vaccines 10 02135 g004
Figure 5. Dynamics of the infected population for various values of α.
Figure 5. Dynamics of the infected population for various values of α.
Vaccines 10 02135 g005
Table 1. Meaning of parameters.
Table 1. Meaning of parameters.
Variable/ParameterMeaning
FFor-Vaccination susceptible compartment
AAgainst-Vaccination susceptible compartment
IInfected compartment
RRecovered compartment
ΛInfection rate
βRecovery rate
μ 1 Death rate of I
μ 2 Death rate of R
v Immunization rate of For-Vaccination compartment
γMigration rate from Against-Vaccination to For-Vaccination compartment through awareness
ηMigration rate from For-Vaccination to Against-Vaccination compartment through receiving false information about vaccines
αFractional order 0 < α 1
p Probability term 0 p 1
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Baba, I.A.; Rihan, F.A.; Humphries, U.W.; Mikailu, B.B. A Fractional Order Model Studying the Role of Negative and Positive Attitudes towards Vaccination. Vaccines 2022, 10, 2135. https://doi.org/10.3390/vaccines10122135

AMA Style

Baba IA, Rihan FA, Humphries UW, Mikailu BB. A Fractional Order Model Studying the Role of Negative and Positive Attitudes towards Vaccination. Vaccines. 2022; 10(12):2135. https://doi.org/10.3390/vaccines10122135

Chicago/Turabian Style

Baba, Isa Abdullahi, Fathalla A. Rihan, Usa Wannasingha Humphries, and Badamasi Bashir Mikailu. 2022. "A Fractional Order Model Studying the Role of Negative and Positive Attitudes towards Vaccination" Vaccines 10, no. 12: 2135. https://doi.org/10.3390/vaccines10122135

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop