23 research outputs found

    Finite Element Analysis of Thermal-Diffusions Problem for Unbounded Elastic Medium Containing Spherical Cavity under DPL Model

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    In this work, the thermo-diffusions interaction in an unbounded material with spherical cavities in the context dual phase lag model is investigated. The finite element technique has been used to solve the problem. The bounding surface of the inner hole is loaded thermally by external heat flux and is traction-free. The delay times caused in the microstructural interactions, the requirement for thermal physics to take account of hyperbolic effects within the medium, and the phase lags of chemical potential and diffusing mass flux vector are interpreted. A comparison is made in the case of the presence and the absence of mass diffusions between coupled, Lord-Shulman and dual phase lag theories. The numerical results for the displacement, concentration, temperature, chemical potential and stress are presented numerically and graphically

    Effect of antibodies on pathogen dynamics with delays and two routes of infection

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    We study the global stability of pathogen dynamics models with saturated pathogen-susceptible and infected-susceptible incidence. The models incorporate antibody immune response and three types of discrete or distributed time delays. We first show that the solutions of the model are nonnegative and ultimately bounded. We determine two threshold parameters, the basic reproduction number and antibody response activation number. We establish the existence and stability of the steady states. We study the global stability analysis of models using Lyapunov method. The numerical simulations have shown that antibodies can reduce the pathogen progression

    Stability of CHIKV infection models with CHIKV-monocyte and infected-monocyte saturated incidences

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    We study the global stability of within-host Chikungunya virus (CHIKV) infection models with antibodies. We incorporate two modes of infections, attaching a CHIKV to a host monocyte, and contacting an infected monocyte with an uninfected monocyte. The CHIKV-monocyte and infected-monocyte incidence rates are given by saturation. In the second model we consider two classes of infected monocytes, latently infected monocytes and actively infected monocytes. The global stability analysis of the equilibria are established using Lyapunov method. We support our theoretical results by numerical simulations

    Stability of latent pathogen infection model with CTL immune response and saturated cellular infection

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    We propose a pathogen dynamics model with CTL immune response and both pathogenic and cellular infections. Both actively infected cells and latently infected cells are incorporated into the model. The infected-susceptible and pathogen-susceptible infection rates are given by saturated incidence. Three distributed time delays are considered. The existence and global stability of the equilibria are determined by two threshold parameters, the basic reproduction number and the CTL response activation number. The global stability of the three equilibria are proven using Lyapunov method. We solve the system of delay differential equations numerically to support the theoretical results

    Global Dynamics of an HTLV-I and SARS-CoV-2 Co-Infection Model with Diffusion

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    Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel respiratory virus that causes coronavirus disease 2019 (COVID-19). Symptoms of COVID-19 range from mild to severe illness. It was observed that disease progression in COVID-19 patients depends on their immune response, especially in elderly patients whose immune system suppression may put them at increased risk of infection. Human T-cell lymphotropic virus type-I (HTLV-I) attacks the CD4+ T cells (T cells) of the immune system and leads to immune dysfunction. Co-infection with HTLV-I and SARS-CoV-2 has been reported in recent studies. Modeling HTLV-I and SARS-CoV-2 co-infection can be a helpful tool to understand the in-host co-dynamics of these viruses. The aim of this study was to construct a model that characterizes the in-host dynamics of HTLV-I and SARS-CoV-2 co-infection. By considering the mobility of the viruses and cells, the model is represented by a system of partial differential equations (PDEs). The system contains two independent variables, time t and position x, and seven dependent variables for representing the densities of healthy epithelial cells (ECs), latent SARS-CoV-2-infected ECs, active SARS-CoV-2-infected ECs, SARS-CoV-2, healthy T cells, latent HTLV-I-infected T cells and active HTLV-I-infected T cells. We first studied the fundamental properties of the solutions of the system, then deduced all steady states and proved their global properties. We examined the global stability of the steady states by constructing appropriate Lyapunov functions. The analytical results were illustrated by performing numerical simulations. We discussed the effect of HTLV-I infection on COVID-19 progression. The results suggest that patients with HTLV-I have a weakened immune response; consequently, their risk of COVID-19 infection may be increased

    Global Dynamics of an HTLV-I and SARS-CoV-2 Co-Infection Model with Diffusion

    No full text
    Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel respiratory virus that causes coronavirus disease 2019 (COVID-19). Symptoms of COVID-19 range from mild to severe illness. It was observed that disease progression in COVID-19 patients depends on their immune response, especially in elderly patients whose immune system suppression may put them at increased risk of infection. Human T-cell lymphotropic virus type-I (HTLV-I) attacks the CD4+ T cells (T cells) of the immune system and leads to immune dysfunction. Co-infection with HTLV-I and SARS-CoV-2 has been reported in recent studies. Modeling HTLV-I and SARS-CoV-2 co-infection can be a helpful tool to understand the in-host co-dynamics of these viruses. The aim of this study was to construct a model that characterizes the in-host dynamics of HTLV-I and SARS-CoV-2 co-infection. By considering the mobility of the viruses and cells, the model is represented by a system of partial differential equations (PDEs). The system contains two independent variables, time t and position x, and seven dependent variables for representing the densities of healthy epithelial cells (ECs), latent SARS-CoV-2-infected ECs, active SARS-CoV-2-infected ECs, SARS-CoV-2, healthy T cells, latent HTLV-I-infected T cells and active HTLV-I-infected T cells. We first studied the fundamental properties of the solutions of the system, then deduced all steady states and proved their global properties. We examined the global stability of the steady states by constructing appropriate Lyapunov functions. The analytical results were illustrated by performing numerical simulations. We discussed the effect of HTLV-I infection on COVID-19 progression. The results suggest that patients with HTLV-I have a weakened immune response; consequently, their risk of COVID-19 infection may be increased
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