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In this paper, we propose a time-delayed HIV/AIDS-PrEP model which takes into account the delay on pre-exposure prophylaxis (PrEP) distribution and adherence by uninfected persons that are in high risk of HIV infection, and analyze the impact of this delay on the number of individuals with HIV infection. We prove the existence and stability of two equilibrium points, for any positive time delay. After, an optimal control problem with state and control delays is proposed and analyzed, where the aim is to find the optimal strategy for PrEP implementation that minimizes the number of individuals with HIV infection, with minimal costs. Different scenarios are studied, for which the solutions derived from the Minimum Principle for Multiple Delayed Optimal Control Problems change depending on the values of the time delays and the weights constants associated with the number of HIV infected individuals and PrEP. We observe that changes on the weights constants can lead to a passage from bang-singular-bang to bang-bang extremal controls. [ABSTRACT FROM AUTHOR]

We improve a recent mathematical model for cholera by adding a time delay that represents the time between the instant at which an individual becomes infected and the instant at which he begins to have symptoms of cholera disease. We prove that the delayed cholera model is biologically meaningful and analyze the local asymptotic stability of the equilibrium points for positive time delays. An optimal control problem is proposed and analyzed, where the goal is to obtain optimal treatment strategies, through quarantine, that minimize the number of infective individuals and the bacterial concentration, as well as treatment costs. Necessary optimality conditions are applied to the delayed optimal control problem, with a L1 type cost functional. We show that the delayed cholera model fits better the cholera outbreak that occurred in the Department of Artibonite - Haiti, from 1 November 2010 to 1 May 2011, than the non-delayed model. Considering the data of the cholera outbreak in Haiti, we solve numerically the delayed optimal control problem and propose solutions for the outbreak control and eradication. [ABSTRACT FROM AUTHOR]

We propose a new mathematical model for the spread of Zika virus. Special attention is paid to the transmission of microcephaly. Numerical simulations show the accuracy of the model with respect to the Zika outbreak occurred in Brazil. [ABSTRACT FROM AUTHOR]

We propose and investigate a delayed model that studies the relationship between HIV and the immune system during the natural course of infection and in the context of antiviral treatment regimes. Sufficient criteria for local asymptotic stability of the infected and viral free equilibria are given. An optimal control problem with time delays both in state variables (incubation delay) and control (pharmacological delay) is then formulated and analyzed, where the objective consists to find the optimal treatment strategy that maximizes the number of uninfected CD4 +  T cells as well as cytotoxic T lymphocyte immune response cells, keeping the drug therapy as low as possible. Copyright © 2016 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

We propose a Caputo type fractional-order mathematical model for the transmission dynamics of tuberculosis (TB). Uniform asymptotic stability of the unique endemic equilibrium of the fractional-order TB model is proved, for any α ∈ (0,1). Numerical simulations for the stability of the endemic equilibrium are provided. [ABSTRACT FROM AUTHOR]

We propose a model for the human immunodeficiency virus type 1 (HIV-1) infection with intracellular delay and prove the local asymptotical stability of the equilibrium points. Then we introduce a control function representing the efficiency of reverse transcriptase inhibitors and consider the pharmacological delay associated to the control. Finally, we propose and analyze an optimal control problem with state and control delays. Through numerical simulations, extremal solutions are proposed for minimization of the virus concentration and treatment costs. [ABSTRACT FROM AUTHOR]

In this paper, we present a new result that allows for studying the global stability of the disease-free equilibrium point when the basic reproduction number is less than 1, in the fractional calculus context. The method only involves basic linear algebra and can be easily applied to study global asymptotic stability. After proving some auxiliary lemmas involving the Mittag–Leffler function, we present the main result of the paper. Under some assumptions, we prove that the disease-free equilibrium point of a fractional differential system is globally asymptotically stable. We then exemplify the procedure with some epidemiological models: a fractional-order SEIR model with classical incidence function, a fractional-order SIRS model with a general incidence function, and a fractional-order model for HIV/AIDS. [ABSTRACT FROM AUTHOR]