Professional Documents
Culture Documents
A Coronavirus Disease (Covid-19) Mathematical Model With Asymptomatic and Symptomatic Groups.
A Coronavirus Disease (Covid-19) Mathematical Model With Asymptomatic and Symptomatic Groups.
Master of Science
In
APPLIED MATHEMATICS AND COMPUTING
By
SAROJ KUMAR PATRA(MAM20006)
Under the supervision of
DR. PRASANT NAYAK
May – 2022
2
CONTENTS
ABSRACT............................................................................................................................ 3
1.INTRODUCTION.............................................................................................................3
2.MODEL FORMULATION...............................................................................................4
4.CONCLUSION................................................................................................................15
5.REFERENCE..................................................................................................................16
3
ABSRACT
The goal of this paper's study is to use a mathematical model that uses both the Ordinary
Differential Equation (ODE) and the Fractional Differential Equation to characterize the
Coronavirus Disease 2019 (COVID-19) epidemic. For some years, the disease's
transmission has been on the rise over the world, with no end in sight. The numerical
simulation that was fitted to the model was based on data from COVID-19 cases in
Nigeria. We included the consideration of both asymptomatic and symptomatic sick
persons, as well as the fact that an exposed individual is either quarantined or moved to
one of the diseased classes, with the chance that a susceptible individual might also
migrate to the quarantined class. The disease-free equilibrium point (DFE) and the
endemic equilibrium point (EEP) were discovered to be the two equilibrium points in the
suggested model (E1). When the fundamental reproduction number, R0 < 1, the
equilibrium points (E0) are locally asymptotically stable, whereas (E1) is globally
asymptotically stable. The parameters in the R0 > 1 were subjected to a sensitivity
analysis, and the profile of each state variable was presented using the fitted values of the
parameters to demonstrate the disease's spread. The contact rate between susceptible
people and the rate of transfer of persons from exposed to symptomatically infected
classes are the most sensitive factors in the R0. Furthermore, R0≈ 1.7031 is determined as
the data's fundamental reproduction number.
1.INTRODUCTION
NO OF CASE NO OF DEATH
FIGURE 1
The following is how the paper is structured: In Section 2, we formulated the model as
well as the description of the model's parameters. We get the invariant area in Section 3.
We also compute the fundamental reproduction number and investigate its disease-free
equilibrium (DFE), local stability, endemic equilibrium existence, endemic equilibrium
local stability, and endemic equilibrium global stability. The importance of sensitivity
analysis and numerical simulation is also emphasized. Finally, in Section 6, we present
the paper's conclusion.
2.MODEL FORMULATION
In this study, a model of the coronavirus (COVID-19) illness with simple transmission
rates is investigated. Let N(t) be the total human population. This population is separated
into seven groups: susceptible people S(t), exposed people E(t), asymptotically infected
people IA (t), symptomatic infected people IS (t), quarantined people Q(t), and those who
have recovered/removed from COVID-19 R(t ). Taking this into account, the overall
population is N (t )=S (t )+ E (t)+Q(t)+ I A (t )+ I S (t)+ R(t ).
Natural human natality and death rates are represented by Λ and μ , respectively.
Susceptible individuals (S) become infected through sufficient contact with exposed
individuals (E) at a rate of or simply transfer to the confined class at a rate of. Individuals
who have been exposed (E) may migrate to the quarantined (Q) class first, or they may
get infected without symptoms (asymptomatic) (IA) or with symptoms (symptomatic) (I
S) at rates of, and, respectively. Individuals who have been quarantined (Q) may also be
proven infected with a test with symptoms (IS) or without symptoms (IA) at rates of ν and
ϑ , respectively. Asymptomatic infected people (IA) may recover at a rate of r1, whereas
symptomatic infected people (Is) may recover at a rate of r2.
5
Table 1
Paramete Description
r
τ Transfer rate of susceptible people to quarantine
β The frequency of contact between susceptible and exposed persons
δ Coronavirus mortality rate in the symptomatic infected person class
Γ Transfer of exposed persons to quarantine at a high rate
η Transfer rate of people from the exposed class to the symptomatic infected
class
ϑ The proportion of quarantined people in the class of asymptomatic infected
people
μ Rate of natural mortality
v Transfer rate of quarantined persons to the class of symptomatic infected
individuals
σ Transfer rate of exposed persons to asymptomatic ones
r1 The percentage of asymptomatic sick people who recover
r2 Individuals who are symptomatic and infected have a higher rate of
recovery.
Each of these classes may drop due to natural mortality μ, but the class of persons
infected with symptoms (IS) may also decrease due to disease death at the rate of δ.
Death as a result of the disease is not regarded in the infected class of persons without
symptoms (IA). This model does not account for the risk of reinfection following
recovery.
6
IA
R
S
IS
dS(t )
= Λ−(τ + μ) S (t )−βS (t) E(t )
dt
dE(t )
=βS (t) E(t )−(Γ + μ +η+σ ) E(t)
dt
dQ(t)
=τS(t)+ Γ E (t)−(μ+v +ϑ )Q(t)
dt
d I A (t )
=σE(t)+ϑQ (t )−( μ+r 1 ) I A (t)
dt
d I S ( t)
=ηE(t )+ vQ(t )−( δ + μ+r 2 ) I S (t)
dt
dR(t )
=r 1 I A (t)+r 2 I S (t )−μR(t)
dt
In the research of infectious illness models, reproduction number is critical [23]. This
section computes and displays the fundamental reproduction number and invariant area
for the suggested model , as well as investigates the
Setting the E=Q=I A=I S =R=0, parameters As a result, the disease-free equilibrium is
achieved. As a result, according to the system (2.1), the DFE point is supplied by
( τ +λ μ , 0,0,0,0,0) .
DFE=( S0 , 0,0,0,0,0 ) =
The predicted value of infection rate per time unit is given by R 0, which is the
fundamental reproduction number. The illness is spread across a vulnerable community
by an infected person. The article provides an equation involving the classifications of
exposed and infected population based on the system (2.1). In the infected classes, the
disease reproduction number R 0of the suggested model (2.1) is defined. [23,51] describes
this quantity as a threshold quantity. R0 <1 indicates that disease will reduce, but R0 >1
indicates that disease will continue within a community, and R0 =1 indicates that further
research is needed. R0 is calculated using the next generation matrix technique [23], which
has been employed by various authors.
dE (t)
¿ βS(t )E(t)−(Γ + μ+η+ σ) E(t )
dt
dQ (t)
¿ τS(t )+ Γ E (t)−( μ+ v+ ϑ )Q(t )
dt
d I A (t)
¿ σE (t)+ϑQ (t)−( μ+r 1 ) I A (t)
dt
d I S ( t)
¿ ηE(t)+ vQ(t)−( δ + μ+ r 2 ) I S (t)
dt
( )
βS(t ) E( t)
F= 0
0
0
and
( )
(Γ + μ+ η+σ ) E(t)
−τS(t )−Γ E(t )+(μ+ v+ ϑ )Q(t )
V=
−σE (t)−ϑQ (t )+ ( μ+r 1 ) I A (t)
−ηE(t)−vQ(t )+ ( δ + μ+ r 2 ) I S (t)
( )
βΛ
0 0 0
τ+ μ
F= 0 0 0 0
0 0 0 0
0 0 0 0
( )
Γ + μ+ η+σ 0 0 0
−Γ μ+v +ϑ 0 0
V=
−σ −ϑ μ+r 1 0
−η −v 0 δ+ μ+r 2
10
| |
( τ + μ) R0 −λ −( Γ + μ +η+σ ) 0 0 0 0
Γ + μ+η+ σ −λ 0 0 0 0
τ γ −(μ+ v+ ϑ )−λ 0 0 0
det ( J E −λI ) =
1
0 σ ϑ −( μ+r 1) −λ 0 0
0 η υ 0 −( δ + μ+r 2 ) −λ 0
0 0 0 r1 r2 −μ−λ
( )
βΛ
0 0 0
α (τ + μ)
−1
FV = 0 0 0 0 .
0 0 0 0
0 0 0 0
βΛ
So, ρ ( F V ) =
−1
=R 0, where α =Γ + μ+ η+σ .
α ( τ + μ)
Therefore,
βΛ
R0 = > 0.
( Γ + μ+η+ σ )(τ + μ)
Proof. The Jacobian matrix with regard to the system (2.1) may be calculated as follows:
11
( )
−(τ + μ)−βE −βS 0 0 0 0
βE βS−( Γ +μ +η+σ ) 0 0 0 0
τ Γ −( μ+ v +θ) 0 0 0
J= ,
0 σ ϑ −( μ+r 1) 0 0
0 η v 0 −( δ + μ+r 2 ) 0
0 0 0 r1 r2 −μ
which implies
( )
−β Λ
−( τ + μ) 0 0 0 0
(τ + μ)
β Λ− βS−( Γ + μ+ η+ σ )
βE 0 0 0 0
(τ + μ)
J DFE= .
τ Γ −(μ+ v +θ) 0 0 0
0 σ ϑ −( μ+ r 1 ) 0 0
0 η v 0 −( δ+ μ+r 2 ) 0
0 0 0 r1 r2 −μ
( J DFE−λI ) =0, is the characteristic polynomial of the Jacobian matrix at DFE, where λ is
the eigenvalue and I is the 6 × 6 identity matrix. As a result, (( J DFE−λI ))'s is
λ 1=−( τ + μ)<0
λ2=−(μ+v+ϑ )< 0
λ 3=−( μ+ r 1) < 0
λ4 =−( δ + μ+r 2 )
λ5 =−μ<0
λ 6=( Γ +μ+η+ σ) ( R0 −1 ) <0 , provided that R0 <1
In this part, we'll look at whether or not there is an endemic equilibrium point. Let's
¿ ¿ ¿ ¿ ¿ ¿
consider it endemic equilibrium. by E1=¿ ( S , E ,Q , I A , I S , R ). For simplicity,
S(t )=S , E (t)=E ,Q(t )=Q , I A (t)=¿ I A , I S (t)=I S and R(t )=R , will be utilized in the
future. This endemic equilibrium always yields the following results:
¿ ¿ ¿
0 ¿ Λ−(τ + μ)S −β S E
¿ ¿ ¿
0 ¿ β S E −(Γ + μ+η+ σ )E
¿ ¿ ¿
0 ¿ τ S + Γ E −(μ+ v +ϑ )Q
0 ¿ σ E¿ +θ Q¿− ( μ +r 1 ) I ¿A
0 ¿ η E ¿ + v Q¿ −( δ + μ+r 2 ) I ¿S
¿ ¿ ¿
0 ¿ r 1 I A +r 2 I S −μ R
¿ Λ
S= ¿
Γ + μ+ β E
( τ+ μ)
E¿ = ( R0−1 )
β
τβ(Γ + μ+η+σ )+ Γ (τ + μ)
Q¿ = ( R0 −1 )
β ( μ+ v +ϑ )
We get the fourth Equation of (3.6) by substituting Eqs. (3.8) and (3.10).
¿ ( τ + μ)[σ (μ+ v+ ϑ )+ Γ ϑ ]
I A= ( R 0−1 ) .
β (μ+v +ϑ ) ( μ+r 1 )
In the fifth equation of (3.6), we get by combining Eqs. (3.8) and (3.10).
(τ + μ)[η( μ+ v+ ϑ )+ τβv( Γ +v + η+ σ )+ Γ ]
I ¿S= ( R 0−1 ) .
β ( μ+ v+ ϑ )(δ + μ+ r)
When Eqs. (3.11) and (3.12) are combined in the sixth equation of (3.6), the result is
R
¿
¿
μ[
1 [ (τ+ μ)[σ (μ+v +θ)+ Γ ϑ ]r 1
β ( μ+ v+ ϑ )(μ +r )
¿ ¿
13
Theorem :The system (2.1) has a single endemic equilibrium point, which is defined by
| |
( τ + μ) R0 −λ −( Γ + μ +η+σ ) 0 0 0 0
Γ + μ+η+ σ −λ 0 0 0 0
τ γ −(μ+ v+ ϑ )−λ 0 0 0
det ( J E −λI ) =
1
0 σ ϑ −( μ+r 1) −λ 0 0
0 η υ 0 −( δ + μ+r 2 ) −λ 0
0 0 0 r1 r2 −μ−λ
¿¿
E1=¿ ( γ + μ +η+σ
β
, p ( R −1 ) , q ( R −1 ) ,r ( R −1 ) , s ( R −1 ) ,
0 0 0 0
( r r 1 +s r 2 )
μ )
( R0 −1 ) ,
(τ + μ)
p ¿
β
τβ( γ + μ+ η+σ )+ Γ ( τ + μ)
q ¿
β (μ +v +ϑ )
( τ + μ)[σ (μ+ v+ ϑ )+ Γ ϑ ]
r ¿
β(μ +v +ϑ ) ( μ+r 1 )
(τ + μ)[η(μ+v +ϑ )+ τβv( Γ +v +η+ σ )+ Γ ]
s ¿
β ( μ+v +ϑ ) ( δ + μ+r 2 )
14
Proof. The Jacobian matrix with regard to the system (2.1) is provided by:
( )
−(τ + μ)−βE −βS 0 0 0 0
βE βS−( Γ +μ +η+σ ) 0 0 0 0
τ Γ −( μ+ v +ϑ ) 0 0 0
J= ,
0 σ ϑ −( μ+ r 1 ) 0 0
0 η 0 0 −( δ+ μ+r 2 ) 0
0 0 0 r1 r2 −μ
which implies,
( )
−(τ + μ)R 0 −(Γ + μ+ η+ σ ) 0 0 0 0
Γ + μ+η+ σ 0 0 0 0 0
τ Γ −( μ+v +ϑ ) 0 0 0
JE = 1
0 σ ϑ −( μ+r 1 ) 0 0
0 η v 0 −( δ+ μ +r 2 ) 0
0 0 0 r1 r2 −μ
The Jacobian matrix's characteristic polynomial at E1 is given by det ( J Z −λI )=0 . where
1
λ1=−(μ+ v +θ)< 0
λ 2=−( μ+r 1 ) < 0
λ 3=−( δ + μ+r 2 ) < 0
λ4 =−μ<0
The quadratic λ 2+(τ + μ) Sso λ+ ¿ has all positive phrases, hence its origins must all be
negative. Meanings λ 5,6< 0.
Due to the breakout of the COVID-19 pandemic, the entire globe has been enduring a
huge and unprecedented global catastrophe since the beginning of 2020. Acute
respiratory distress syndrome (ARDS) is a severe and occasionally deadly respiratory
condition caused by the virus. Such a contagious disease with such a massive social and
economic impact has never been seen before, at least in recent memory. COVID-19
evolved from a strain of a new coronavirus that has quickly spread over the
world, beginning in Wuhan, China and infecting a huge number of individuals. The
spread of this disease has a complicated time dependency that is influenced not only by
the number of sick persons, but also by factors such as the total population of the country,
various standards and policies adopted by the nation at a given moment, and many others.
It is difficult to predict the size of the population that may be affected by this pandemic
and the typical time required for its control due to a lack of previous experience in
controlling a similar pandemic with such a high impact in the recent past due to a lack of
previous experience in controlling a similar pandemic with such a high impact.
The aforementioned dilemma necessitates computer modelling to gain a
quantitative knowledge of the time evolution of this complicated and non-linear process.
Statistical and mathematical examination of provided data can give useful insights into
the virus's spread pattern and thus aid in the implementation of various social
interventions to stop the virus from spreading as rapidly as feasible. Furthermore,
assessing reported epidemic data is critical for studying the underlying factors that
contribute to disease propagation and making forecasts about future trends. This allows
diverse groups to organise their measures toward limiting the spread more efficiently.
16
4.CONCLUSION
Both the ordinary differential equation (ODE) and the fractional differential equation
were used in the mathematical study. It is critical for health practitioners and the rest of
the globe to comprehend and foresee sick persons in order to plan for citizens' health
concerns and to manage the spread rate with limited supplies. The simulation's data is
based on the spread of illness in India. The model's positivity is established, and the
model's fundamental reproduction number, R0 , is obtained. When R0 <1, the disease-free
equilibrium is found to be locally asymptotically stable; otherwise, it is unstable. The
system's conduct further proved India's existing position. Both classical differential
equations show that the sickness is deteriorating, with a high rate of recovery.
As a result, it's simple to see how, in addition to quarantine and testing, a restriction on
social interaction in India might help reduce the number of infected people. In the fight
against the pandemic, it should be of particular significance to everyone that exposure as
a consequence of contact with infected persons, particularly those who are asymptomatic
(IA), be limited.
17
5.REFERENCE
11. Asif M, Khan ZA, Haider N, Al-Mdallal Q. Numerical simulation for solution of
seir models by meshless and finite difference methods. Chaos Solitons Fract
2020;141: 110340.
12. Atangana A. Derivative with a new parameter: theory, methods and applications.
Academic Press; 2015.
13. Atangana A. Fractional operators with constant and variable order with
application to geo-hydrology. Academic Press; 2017.
14. Atangana A. Modelling the spread of covid-19 with new fractal-fractional
operators: Can the lockdown save mankind before vaccination? Chaos Solitons
Fract 2020;136:109860.
15. Atangana A, Baleanu D. New fractional derivatives with nonlocal and non-
singular kernel: theory and application to heat transfer model. Therm Sci
2016;20(2): 763–9.
16. Baba IA, Nasidi BA. Fractional order epidemic model for the dynamics of novel
covid-19. Alexandria Eng J 2020.
17. Bailey NT, Sendov B, Tsanev R. Mathematical models in biology and medicine.
In IFIP-TC4 working conference on mathematical models in biology and
medicine (1972: Varna, Bulgaria). North-Holland Pub. Co.; 1974.
18. Baleanu D, Jajarmi A, Hajipour M. On the nonlinear dynamical systems within
the generalized fractional derivatives with Mittag–Leffler kernel. Nonlinear Dyn
2018; 94(1):397–414.
19. Baud D, Qi X, Nielsen-Saines K, Musso D, Pomar L, Favre G. Real estimates of
mortality following covid-19 infection. Lancet Infect Dis 2020.
20. Chen S-B, Rashid S, Noor MA, Hammouch Z, Chu Y-M. New fractional
approaches for n-polynomial p-convexity with applications in special function
theory. Adv Differ Equ 2020;2020(1):1–31.
21. Danane J, Allali K, Hammouch Z. Mathematical analysis of a fractional
differential model of hbv infection with antibody immune response. Chaos
Solitons Fract 2020; 136:109787.
19
22. Diekmann O, Heesterbeek JAP, Metz JA. On the definition and the computation
of the basic reproduction ratio r0 in models for infectious diseases in
heterogeneous populations. J Math Biol 1990;28(4):365–82.
23. Diethelm K. A fractional calculus based model for the simulation of an outbreak
of dengue fever. Nonlinear Dyn 2013;71(4):613–9.
24. Dourado-Neto D, Teruel D, Reichardt K, Nielsen D, Frizzone J, Bacchi O.
Principles of crop modeling and simulation: I. uses of mathematical models in
agricultural science. Sci Agricola 1998;55(SPE):46–50.
25. Edelstein-Keshet L. Mathematical models in biology. SIAM; 2005.
26. Gomez-Aguilar J, Cordova-Fraga T, Abdeljawad T, Khan A, Khan H. Analysis of
fractal-fractional malaria transmission model. Fractals 2020.
27. Goufo EFD, Khan Y, Chaudhry QA. Hiv and shifting epicenters for covid-19, an
alert for some countries. Chaos Solitons Fract 2020;139:110030.
28. Hajji MA, Al-Mdallal Q. Numerical simulations of a delay model for immune
system-tumor interaction. Sultan Qaboos Univ J Sci [SQUJS] 2018;23(1):19–31.
29. Khan H, G´omez-Aguilar J, Alkhazzan A, Khan A. A fractional order hiv-tb
coinfection model with nonsingular Mittag-Leffler law. Math Methods Appl Sci
2020;43(6):3786–806.
30. Khan MA, Atangana A. Modeling the dynamics of novel coronavirus (2019-ncov)
with fractional derivative. Alexandria Eng J 2020.
31. Kilbas A, Srivastava H, Trujillo J. Theory and applications of fractional derivatial
equations. North-Holland Mathematics Studies 2006;204.
32. Koo JR, Cook AR, Park M, Sun Y, Sun H, Lim JT, Tam C, Dickens BL.
Interventions to mitigate early spread of sars-cov-2 in singapore: a modelling
study. Lancet Infect Dis 2020.
33. Linton NM, Kobayashi T, Yang Y, Hayashi K, Akhmetzhanov AR, Jung S-M,
Yuan B, Kinoshita R, Nishiura H. Incubation period and other epidemiological
characteristics of 2019 novel coronavirus infections with right truncation: a
statistical analysis of publicly available case data. J Clin Med 2020;9(2):538.