Articles

Dynamic analysis of a fractional-order SIRS model with time delay*

Xueyong Zhou
School of Mathematics and Statistics, Xinyang Normal University, China
Mengya Wang
School of Mathematics and Statistics, Xinyang Normal University, China

Dynamic analysis of a fractional-order SIRS model with time delay*

Nonlinear Analysis: Modelling and Control, vol. 27, núm. 2, pp. 368-384, 2022

Vilniaus Universitetas

Recepción: 18 Febrero 2021

Revisado: 24 Septiembre 2021

Publicación: 12 Febrero 2022

Abstract: Mathematical modeling plays a vital role in the epidemiology of infectious diseases. Policy makers can provide the effective interventions by the relevant results of the epidemic models. In this paper, we build a fractional-order SIRS epidemic model with time delay and logistic growth, and we discuss the dynamical behavior of the model, such as the local stability of the equilibria and the existence of Hopf bifurcation around the endemic equilibrium. We present the numerical simulations to verify the theoretical analysis.

Keywords: fractional calculus, epidemic model, stability, Hopf bifurcation, delay.

1 Introduction

Mathematical models of infectious disease are widely used by many researchers. The first epidemic model was presented by Bernoulli in 1760 [2]. Epidemic models have become a valuable tool for the analysis of dynamics of infectious disease in recent years. Many deterministic or stochastic epidemic models were presented and analyzed by previous researches [10, 13, 22, 26].

In [16], the authors proposed an SIRS model as follows:

where denote the susceptible number, the infected number and the recovered number of individuals at time , respectively. Parameters are nonnegative constants. is the recruitment rate of the population, is the disease transmission coefficient, is the death rate of the population, is the rate constant for recovery, is the death rate due to the disease, and is the rate constant for loss of immunity. Mena-Lorca and Hetheote discussed the dynamical behavior of this model.

In [8], Ranjith Kumar et al. considered an epidemic model with time delay and logistic growth of the susceptibles as follows:

where represents the number of susceptible and infected population, respectively. represents intrinsic birth rate constant, represents carrying capacity of susceptible, represents the force of infection or the rate of transmission, represents immigration coefficient of represents death coefficient of is the latent period of the disease. The locally asymptotical stability of the disease-free equilibrium and endemic equilibrium of system (1) were studied. Hopf bifurcation around the endemic equilibrium was addressed.

Taking into account the latent period of the disease (time delay) and logistic growth of the susceptibles, we can present the following SIRS epidemic model:

The meanings of parameters are same as in system (1). is the death rate of the population, is the death rate due to the disease, is the rate of disease recovery.

In recent years, many scholars have proposed the idea of using fractional-order model to study infectious disease model [1, 4, 7, 15, 17, 21, 24, 25]. Fractional-order model is an extension of integer-order model, and fractional-order model has certain advantages in describing processes with memory and heritability [12, 14, 20].

In [24], the author studied a class of SIR infectious disease model with Caputo fractional-order derivative

However, the above fractional-order system does not take into account the influence of the latent period of the disease, i.e., time delay. In fact, it takes a certain time for an infected person to show symptoms from being infected, so it is of great significance to discuss the influence of time-delay factors.

Based on the above analysis, the following SIRS model with Caputo fractional-order derivative and time delay will be studied in this paper:

where represent the number of susceptible, infected and removed persons at time , respectively; denotes the infection coefficient; represents the natural mortality rate; denotes the death rate of the disease; is the carrying capacity of susceptible population; is the state transition rate from the recovered to the susceptible one; is the state transition rate from the infected to the recovered one; denotes the latent period of the disease.

The initial value condition of model (2) is

In this paper, stability and bifurcation problems system of (2) will be studied by using the theory of fractional-order stability and delay differential equation. The remaining sections of the paper are organized as follows. Preliminaries, such as definition of fractional-order Caputo derivative and some useful lemmas, are given in Section 2. Some basic results, such as the existence and uniqueness, nonnegativity, positive invariance of the solutions for system (2), are presented in Section 3. The local asymptotic stability and bifurcation results for fractional-order epidemic model are derived in Section 4. Numerical examples are given in Section 5 to verify the obtained theoretical results. Finally, Section 6 contains conclusion.

2 Preliminaries

In this section, we present the definition of Caputo fractional-order derivative, and some useful lemmas are recalled for next analysis.

Definition 1. (See [19].) The fractional integral of order for a function is defined as

where is the gamma function,

Definition 2. (See [19].) The Caputo fractional derivative of order for the function is defined by

where is a positive integer such that .

Furthermore, when

Lemma 1. (See [9].) Consider the following fractional-order differential system Caputo derivative:

where . The characteristic equation of system(4)is all of the roots of the characteristic equation have negative real parts, then the zero solution of the system is asymptotically stable.

Lemma 2. (See [5].) Consider the following fractional-order delay differential system with Caputo derivative:

were, then the characteristic equation of system(5)is. If all of the roots of the characteristic equation have negative real parts, then the zero solution of the system is asymptotically stable.

3 Basic results

In this section, we will discuss the existence and uniqueness of the solution for system (2). Furthermore, the solutions of system (2) with initial condition (3) are nonnegative and positively invariant.

Theorem 1. If is the continuous function of Banach space and in an initial condition, then system (2)has a unique solution where

Proof. Consider the mapping , where

For any

where . Hence, satisfies Lipschitz condition. From Lemma 5 in [11] we can obtain that system (2) has a unique solution .

Theorem 2. The solutions of system (2)with initial condition (3)are nonnegative.

Proof. Assume that is positively invariant. System (2) can be written in the vector form

Here , and

. For that, we investigate the direction of the vector field on each coordinate space and see whether the vector field points to the interior of . From (2) we have

From Theorem 1 in [18], Lemma 6 in [3] and Eq. (6) the vector field is interior of . The solution of (2) with initial condition , say in such a way, .

Theorem 3. The set is positively invariant with respect to system (2).

Proof. Let , be the solution of system (2) with initial condition (3). Set . From system (2) we can obtain

Hence,

Obviously, . Hence, when is positively invariant with respect to system (2).

4 Analysis of stability and Hopf bifurcation

The equilibria of system (2) are the points of intersections at which . It is straightforward to see that for system (2), there always exists a trivial equilibrium and a disease-free equilibrium . The basic reproduction number is defined as the average number of secondary infections produced when one infected individual is introduced into a host population, where everyone is susceptible [23]. Now, we use next-generation matrix method in [23] to obtain the basic reproduction number of system (2).

If , then when , the original system can be expressed as

Where

We can get

The next-generation matrix for model (2) is

The spectral radius . According to Theorem 2 in [23], the basic reproduction number of system (2) is

The basic reproduction number is affected by several factors including: the disease transmission coefficient , the carrying capacity of susceptible population , the natural death rate of the population , the death rate of the disease , the state transition rate from the infected to the recovered one .

Theorem 4. If , system (2)has a unique endemic equilibrium , there is no endemic equilibrium of system (2).

Proof. To obtain the endemic equilibrium of system (2), we need to impose the right side of system (2) to be equal to 0. In other words, the equilibrium should satisfy the following equations:

From above we can obtain

It is obvious that , when system (2) has a unique endemic equilibrium, and when, there is no endemic equilibrium of system (2).

In the following, we will discuss the locally asymptotical stability of the trivial equilibrium , the disease-free equilibrium , the endemic equilibrium for system (2) and the existence of Hopf bifurcation around the endemic equilibrium .

To discuss the locally asymptotical stability of system (2), we have to linearize it. Let us consider the following coordinate transformation:

where denotes any equilibrium of system (2). So we can obtain that the corresponding linearized system is of the form

Taking Laplace transform on both sides of (7), we get

Here are the Laplace transform of , respectively. The above system (8) can be written as follows:

where

and

Theorem 5. The trivial equilibrium is always unstable.

Proof. The characteristic matrix at is

The characteristic equation at the trivial equilibrium reduces to

Obviously, Eq. (9) has a positive root . Then the trivial equilibrium of system (2) is always unstable.

Theorem 6. If , then the disease-free equilibrium of system (2)is locally asymptotically stable for all

Proof. The characteristic matrix at is

Then the characteristic equation at the disease-free equilibrium is

When , the characteristic equation can be translated into

Let (10) can be rewritten as

Its characteristic roots are

Obviously, . Hence when the basic reproduction number . Hence, all the eigenvalues satisfy. According to Lemma 2, the disease-free equilibrium is locally asymptotically stable when .

When , since the first two factors of the left side of Eq. (10) do not contain time delay , we only need to consider the third factor

Assume , then is substituted in (11), we get

Separating the imaginary parts and real parts leads to

Squaring and adding both sides of this equation, we can obtain

Obviously, , then by our assumption that , Eq. (12) has no positive roots, which ensures that Eq. (10) has no purely imaginary roots if . According to Lemma 2, the equilibrium is locally asymptotically stable for any delay if . The proof is completed.

Next, we discuss the local stability and bifurcation results at the endemic equilibrium point . When , the endemic equilibrium point exists. The characteristic matrix at is

The associated characteristic equation of system (2) at can be described as

where

and

Case 1. When , Eq. (13) becomes

On the basis of Routh–Hurwitz theorem, the endemic equilibrium point is locally asymptotically stable if

Case 2. When , let be a root of Eq. (13). Substituting in (13), we obtain

where

Separating the real and imaginary parts of (14) yields

From Eq. (15) we have

It is obvious that , and

where

Let

Then let us discuss the distribution of roots of Eq. (13). It is imperative that the following lemma is useful and needed.

Lemma 3. For Eq. (13), the following results hold:

(i) If , then Eq. (13)has no root with zero real parts for all .

(ii) If , then Eq. (13)has a pair of purely imaginary roots , where

Let be the root of Eq. (13) such that whensatisfies Taking the derivative of Eq. (13) with respect to ,

In (16), consider the numerator and denominator terms described as

where

Then from Eq. (16) we have

Define , and based on the bifurcation theorem for functional differential equations [6], we have the following theorem.

Theorem 7. Assume . For system (2), the following results hold:

  1. 1. If , then the endemic equilibrium is locally asymptotically stable for
  2. 2. If and , then the endemic equilibrium is locally asymptotically stable for and
  3. 3. System (2) undergoes a Hopf bifurcation at the endemic equilibrium when .

5 Numerical simulations

In this section, several illustrative numerical examples are presented to confirm the the- oretical results and to examine the dynamical behavior of system (2). All the figures are plotted by using Matlab 2018a. From Section 4 we can find that delay and fractional order are the important factors, which affect the convergence speed of solutions. We select parameters as follows: with initial conditions . We can calculate. System (2) have three equilibria and . We only discuss the stability of .

From Fig. 1 we can see that the positive equilibrium of system (2) exhibits a Hopf bifurcation when bifurcation parameter passes the critical value when fixes.

  1. 1. . We can calculate from (15). Obviously,. From Theorem 4 we can obtain that is locally asymptotically stable (see Fig. 2).
  2. 2. . It is to see that . From Theorem 4 we can find that is unstable and Hopf bifurcation occurs (see Fig. 3).
  3. 3. . We can calculate . Then is locally asymptotically stable (see Fig. 3).

Bifurcation diagrams of system (2) showing the influence of τ for α = 0.98, where r = 0.15,
Figure 1
Bifurcation diagrams of system (2) showing the influence of τ for α = 0.98, where r = 0.15,

For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 0.8 and α = 0.98, the endemic equilibrium E∗ of system (2) is locally asymptotically stable.
Figure 2
For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 0.8 and α = 0.98, the endemic equilibrium E∗ of system (2) is locally asymptotically stable.

For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 12 and α = 0.98, the endemic equilibrium E∗ of system (2) is unstable.
Figure 3
For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 12 and α = 0.98, the endemic equilibrium E∗ of system (2) is unstable.

For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 12 and α = 0.90, the endemic equilibrium E∗ of system (2) is locally asymptotically stable.
Figure 4
For the following parameter values r = 0.15, K = 90, β = 0.007, ρ = 0.004, µ = 0.035, δ = 0.1, σ = 0.2, τ = 12 and α = 0.90, the endemic equilibrium E∗ of system (2) is locally asymptotically stable.

6 Conclusion

In this work, we studied a fractional-order SIRS epidemic model with delay and logistic growth of the susceptibles. The dynamical behavior of system (2) is studied. Local stability of the equilibria for system (2) and Hopf bifurcation are analyzed. The trivial equilibrium of system (2) is always unstable. The disease-free equilibrium of system (2) is locally asymptotically stable for all when . When , the endemic equilibrium is locally asymptotically stable. According to Theorem 4, when and the last two conditions of Theorem 7 satisfied, the stability of the endemic equilibrium changes at Hopf bifurcation point . Our findings illustrate that using the time delay as bifurcation parameter, one can conclude that the positive equilibrium loses its stability, and Hopf bifurcation occurs when time delay increases. The numerical simulations shown in Figs. 1 and 2 verified the effectiveness of the obtained theoretical results. From Fig. 3 we can speculate that the positive equilibrium loses its stability and Hopf bifurcation occurs when is used as bifurcation parameter. It will be considered in future work.

Modeling of epidemic diseases by delayed fractional-order differential equations has more advantages and consistency rather than classical integer-order mathematical modeling. Our model takes into account several factors (time delay, Logistic growth, fractional order, etc.), which is more realistic. The model is thought to contribute valuable insight for public health, which is useful for some the prediction and control measures for some diseases.

References

1 E. Ahmed, A.S. Elgazzar, On fractional order differential equations model for nonlocal epidemics, Physica A, 379(2):607–614, 2007, https://doi.org/10.1016/j.physa. 2007.01.010.

2 D. Bernoulli, Essai d’une nouvelle analyse de la mortalité causée par la petite vérole et des avantages de l’inoculum pour la prévenir, in Mémoires de Mathématiques et de Physique, Académie Royale des Sciences, Paris, 1760, pp. 1–45.

3 A. Boukhouima, K. Hattaf, N. Yousfi, Dynamics of a fractional order HIV infection model with specific functional response and cure rate, Int. J. Differ. Equ., 2017:8372140, 2017, https://doi.org/10.1155/2017/8372140.

4 E. Demirci, A. Unal, N. Özalp, A fractional order SEIR model with density dependent death rate, Hacet. J. Math. Stat., 40(2):287–295, 2011.

5 W. Deng, C. Li, J. Lü, Stability analysis of linear fractional diferential system with multiple time delays, Nonlinear Dyn., 48:409–416, 2007, https://doi.org/10.1007/ s11071-006-9094-0.

6 J.K. Hale, Theory of Functional Differential Equations, Springer, Berlin, 1977.

7 J. Jia, X. Huang, Y. Li, J. Cao, A. Alsaedi, Global stabilization of fractional-order memristor- based neural networks with time delay, IEEE Trans. Neural Networks Learn. Syst., 31(3):997– 1009, 2020,https://doi.org/10.1109/TNNLS.2019.2915353.

8 G. Ranjith Kumar, K. Lakshmi Narayan, B. Ravindra Reddy, Stability and Hopf bifurcation analysis of SIR epidemic model with time delay, ARPN Journal of Engineering and Applied Sciences, 11(3):1419–1423, 2016.

9 C.P. Li, Z.G. Zhao, Asymptotical stability analysis of linear fractional diferential systems, J. Shanghai Jiaotong Univ. (Engl. Ed.), 13(3):197–206, 2009, https://doi.org/10. 1007/s11741-009-0302-1.

10 F. Li, X.-Q. Zhao, A periodic SEIRS epidemic model with a time-dependent latent period, J. Math. Biol., 78(5):1553–1579, 2019, https://doi.org/10.1007/s00285-018- 1319-6.

11 H.-L. Li, L. Zhang, C. Hu, Y.-L. Jiang, Z. Teng, Dynamical analysis of a fractional-order predator-prey model incorporating a prey refuge, J. Appl. Math. Comput., 54:435–449, 2017, https://doi.org/10.1007/s12190-016-1017-8.

12 D. Liu, J. Li, Y. Xu, Principal resonance responses of SDOF systems with small fractional derivative damping under narrow-band random parametric excitation, Commun. Nonlinear Sci. Numer. Simul., 19(10):3642–3652, 2014,https://doi.org/10.1016/j.cnsns. 2014.03.018.

13 Q. Liu, D. Jiang, T. Hayat, A. Alsaedi, Dynamics of a stochastic multigroup SIQR epidemic model with standard incidence rates, J. Franklin Inst., 356(5):2960–2993, 2019, https://doi.org/10.1016/j.jfranklin.2019.01.038.

14 J.A.T. Machado, M.E. Mata, Pseudo phase plane and fractional calculus modeling of western global economic downturn, Commun. Nonlinear Sci. Numer. Simul., 22(1–3):396–406, 2015, https://doi.org/10.1016/j.cnsns.2014.08.032.

15 F. Mansal, N. Sene, Analysis of fractional fishery model with reserve area in the context of time-fractional order derivative, Chaos Solitons Fractals, 140:110200, 2020, https://doi.org/10.1016/j.chaos.2020.110200.

16 J. Mena-Lorca, H.W. Hetheote, Dynamic models of infectious diseases as regulators of population sizes, J. Math. Biol., 30(7):693–716, 1992, https://doi.org/10.1007/ BF00173264.

17 B. Meng, X. Wang, Z. Zhang, Z. Wang, Necessary and sufficient conditions for normalization and sliding mode control of singular fractional-order systems with uncertainties, Sci. China, Inf. Sci., 63(5):152202, 2020,https://doi.org/10.1007/s11432-019-1521-5.

18 Z.M. Odibat, N.T. Shawagfeh, Generalized Taylor’s formula, Appl. Math. Computation, 186(1):286–293, 2007, https://doi.org/10.1016/j.amc.2006.07.102.

19 I. Podlubny, Fractional Differential Equations, Academic Press, New York, 1999.

20 K. Razminia, A. Razminia, J.A.T. Machado, Analysis of diffusion process in fractured reservoirs using fractional derivative approach, Commun. Nonlinear Sci. Numer. Simul., 19(9): 3161–3170, 2014,https://doi.org/10.1016/j.cnsns.2014.01.025.

21 F.A. Rihan, Q.M. Al-Mdallal, H.J. AlSakaji, A. Hashish, A fractional-order epidemic model with time-delay and nonlinear incidence rate, Chaos Solitons Fractals, 126:97–105, 2019, https://doi.org/10.1016/j.chaos.2019.05.039.

22 F.A. Rihan, C. Rajivganthi, Dynamics of fractional-order delay differential model of prey- predator system with Holling-type III and infection among predators, Chaos Solitons Fractals, 141:110365, 2020,https://doi.org/10.1016/j.chaos.2020.110365.

23 P. van den Driessche, J. Watmough, Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission, Math. Biosci., 180:29–48, 2007, https://doi.org/10.1016/S0025-5564(02)00108-6.

24 X. Wang, Z. Wang, X. Huang, Y. Li, Dynamic analysis of a delayed fractional-order SIR model with saturated incidence and treatment functions, Int. J. Bifurcation Chaos Appl. Sci. Eng., 28(14):1850180, 2018,https://doi.org/10.1142/S0218127418501808.

25 Z. Wang, X.H. Wang, J.W. Xia, H. Shen, B. Meng, Adaptive sliding mode output tracking control based-FODOB for a class of uncertain fractional-order nonlinear time-delayed systems, Sci. China, Technol. Sci., 63:1854–1862, 2020,https://doi.org/10.1007/s11431- 019-1476-4.

26 F. Zhang, T. Zhao, H. Liu, Y. Chen, Backward bifurcation in a stage-structured epidemic model, Appl. Math. Lett., 89:85–90, 2019, https://doi.org/10.1016/j.aml.2018.10. 001.

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