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In this paper, we investigate the qualitative behaviors of three viral infection models with two types of cocirculating target cells. The models take into account both antibodies and latently infected cells. The incidence rate is represented by bilinear, saturation and general function. For the first two models, we have derived two threshold parameters, R0 and R1 which completely determined the global properties of the models. Lyapunov functions are constructed and LaSalle's invariance principle is applied to prove the global asymptotic stability of all equilibria of the models. For the third model, we have established a set of conditions on the general incidence rate function which are sufficient for the global stability of the equilibria of the model. Theoretical results have been checked by numerical simulations. [ABSTRACT FROM AUTHOR]

In this paper, we study the global properties of two mathematical models which describe the interaction of the human immunodeficiency virus (HIV) with two classes of target cells, CD4+ T cells and macrophages. The incidence rate of virus infection is given by the Crowley-Martin functional response. The first model has two types of discrete delays while the second one incorporates two types of distributed delays to describe the time needed for infection of cell and virus replication. The basic reproduction number R0 is identified which completely determines the global dynamics of the models. By constructing suitable Lyapunov functionals, we have proven that if R0 ≤ 1 then the uninfected steady state is globally asymptotically stable (GAS), and if R0 > 1 then the infected steady state exists and it is GAS. [ABSTRACT FROM AUTHOR]

In this paper, we study the global analysis of virus dynamics models with discrete delay and with distributed delay. The models describe the interaction of the HIV with two classes of target cells, CD4+ T cells and macrophages. The incidence rate of virus infection is given by the Beddington-DeAngelis functional response. The models have two types of discrete time delay or distributed delay describing the time needed for infection of cell and virus replication. The basic reproduction number R0 is identified which completely determines the global dynamics of the models. By constructing suitable Lyapunov functionals, we have proven that if R0 ≤ 1 then the uninfected steady state is globally asymptotically stable (GAS), and if R0 > 1 then the infected steady state exists and it is GAS. [ABSTRACT FROM AUTHOR]