Global Dynamics of a Virus Dynamical Model with Cell-to-Cell Transmission and Cure Rate

The cure effect of a virus model with both cell-to-cell transmission and cell-to-virus transmission is studied. By the method of next generation matrix, the basic reproduction number is obtained. The locally asymptotic stability of the virus-free equilibrium and the endemic equilibrium is considered by investigating the characteristic equation of the model. The globally asymptotic stability of the virus-free equilibrium is proved by constructing suitable Lyapunov function, and the sufficient condition for the globally asymptotic stability of the endemic equilibrium is obtained by constructing suitable Lyapunov function and using LaSalle invariance principal.


Introduction and Model Formulation
Since tobacco mosaic virus, the first virus of the world discovered by Beijerinck in 1898 [1], more and more viruses have been discovered by biologists, biomedical scientists, and medical scientists and more than 5,000 viruses have been recorded in detail [2]. However, according to a recent study, there are at least 32,0000 viruses waiting to be discovered in the spread between mammalian species. Identifying diseases caused by these viruses, especially those that can infect people, perhaps can help us to prevent epidemic disease [3]. At the early stage of the study, it is generally accepted that because of the specificity of viruses, virus can only infect certain plant or animal species; however, more and more cases associated with emerging zoonoses have appeared, and with a deeper understanding of the virus, we found that most viruses can infect humans, such as Human Immunodeficiency Virus (HIV), Prions, Influenza Virus, Rabies Virus, Ebola Virus, and Middle East Respiratory Syndrome Coronavirus (MERSV) [3][4][5][6].
Generally, the basic process of viral infection and virus replication occurs in six main steps: attachment, penetration, uncoating, replication, assembly, and release [7]. After the whole replicative cycle, free viruses begin to diffuse and infect new host cell. Therefore, investigating the processes of viral growth and destruction of host cells so as to gain the insights into the evolutionary processes of virus and cell in body is very important. To this end, mathematical models and analysis are powerful tools.
Since mathematical models and method of mathematical analysis were used to study the dynamics of the virus, lots of models have been established to explain the evolution of the uninfected target cells, infected cells, and the free virus. In these models, early works belonged to Nowak et al. [8], Nowak and May [9], Perelson and Nelson [10], and Perelson et al. [11]. The general class of models that have been studied [8][9][10][11][12] have a form similar to 2 Computational and Mathematical Methods in Medicine where , , and V represent the concentrations of uninfected target cells, infected cells, and virus, respectively. For explanations of other parameters we refer to literature [12]. This model describes the processes of virus invading the target cells and the release of the virus due to the infected cell apoptosis. In the model, the authors use V to represent the interaction between uninfected target and virus V, which obey the principle of mass action. Based on model (1), more authors used nonlinear functions to describe the rate constant characterizing infection of cells, for example, V/( + ) in [13], V/(1 + V) in [14,15], V/(1 + + V) in [16], and V/(1+ + V+ V) in [17], and for details of more general nonlinear incidence rate functions please see [18][19][20]. Notice that there exists a potentially possible cure rate of the infected cells to the susceptible host cells in the infection process of some virus, such as Hepatitis B Virus (HBV) [21][22][23][24][25] and HIV [26][27][28][29][30][31][32]; recently, Hattaf et al. [19] adopted a general nonlinear incidence rate function with the form ( , , V)V and introduced cure rate (denoted by ) into the following model: (2) In model (2), ( , , V) satisfies the following hypotheses: ( 1 ) (0, , V) = 0, for all ≥ 0.
Motivated by the works [18][19][20]48], we propose a virus dynamical model with both cell-to-virus infection and cellto-cell transmission and cure rate as follows: where , , and V denote the number of host cells, infected cells, and free virus, respectively. And , , and are the death rates of them, respectively. Free virus is produced by infected cells at a rate . Λ represents the regeneration rate of host cells. is the cure rate. ( , V) = ( + V) represents the total infection rate of host cells, which is divided into two parts and V . The former represents the part where infected cells infect host cells by direct contact, and the latter means that host cells are infected by the free virus. For more detail, please see [48]. In the present model, we can see ( , 0) = ̸ ≡ 0, for all ≥ 0 and ≥ 0, and ( , V) / = ≥ 0 for all ≥ 0, ≥ 0, and V ≥ 0, which do not satisfy conditions ( 3 ) in model (2) and conditions ( 1 ) and ( 3 ) in model (3). For biological considerations, we will study system (4) in the closed set = {( , , V) ∈ 3 The main goal of the present paper is to investigate the globally asymptotic stability of the equilibria of (4). This work is structured as follows. In Section 1, we give the motivation and study the background of the model. In Section 2, the existence of virus-free equilibrium and the endemic equilibrium is shown based on the basic reproduction number. And the local stability of the two equilibria is discussed in Section 3. We focus on the globally asymptotic stability of the two equilibria in Section 4. Finally, a brief conclusion and discussion are given in Section 5.

Basic Reproduction Number and Equilibria
The basic reproduction number [49,50] of model (4) is given as Based on the basic reproduction number R, we have Theorem 1.
Computational and Mathematical Methods in Medicine 3

Local Stability of the Two Equilibria
In this section, we shall show the local stability of equilibria 0 and 1 . (4), we have the following conclusion:

Global Stability of the Two Equilibria
In this section, we study the global behaviors of model (4) by constructing Lyapunov functions. Firstly, we show the global stability of 0 .
Theorem 3. If R < 1, the virus-free equilibrium 0 is globally asymptotically stable.
Next, we study the global stability of the endemic equilibrium 1 . Proof. If R > 1, we define a Lyapunov function 2 ( ) as follows: It follows from (4) and (15) Since the arithmetic mean is greater than or equal to the geometric mean, it follows that The above equality holds only for = * , = * , and V = V * . Clearly, if R > 1 and * − * * − * > 0, then 2 ( )/ ≤ 0. Note that * − * * − * ≥ 0 can be formulated as Computational and Mathematical Methods in Medicine 7 Since 2 ( )/ = 0 if and only if = * , = * , and V = V * , by LaSalle invariance principle [52], the equilibrium 1 is globally asymptotically stable.

Conclusion and Discussion
In this paper, we considered the cure effect of a virus model with both cell-to-cell transmission and cell-to-virus transmission. By the method of next generation matrix, the basic reproduction number R is obtained. Firstly the locally asymptotic stability of the virus-free equilibrium and the endemic equilibrium is considered. Then, the globally asymptotic stability of the virus-free equilibrium is proved by constructing suitable Lyapunov function, and the sufficient condition for the globally asymptotic stability of the endemic equilibrium is obtained by constructing suitable Lyapunov function and using LaSalle invariance principal. By analyzing the condition for the globally asymptotic stability of the endemic equilibrium, we have that if = 0, from Theorem 4, the conditions R > 1 can ensure the global stability of the equilibrium 1 , While if > 0, by the numerical simulations (see Figures 1 and 2), we find that R ≤ 1 + in Theorem 4 is not necessary and can be dropped.