Global analysis of an SIS model with an infective vector on complex networks

In this paper, a modified SIS model with an infective vector on complex networks is proposed and analyzed, which incorporates some infectious diseases that are not only transmitted by a vector, but also spread by direct contacts between human beings. We treat direct human contacts as a social network and assume spatially homogeneous mixing between vector and human populations. By mathematical analysis, we obtain the basic reproduction number R₀ and study the effects of various immunization schemes. For the network model, we prove that if R₀<1, the disease-free equilibrium is globally asymptotically stable, otherwise there exists an unique endemic equilibrium such that it is globally attractive. Our theoretical results are confirmed by numerical simulations and suggest a promising way for the control of infectious diseases.     

Global stability of a SEIR epidemic model with infectious force in latent, infected and immune period

In this paper, we studied the global dynamics of a SEIR epidemic model in which the latent and immune state were infective. The basic reproductive rate, R₀, is derived. If R₀  1, the disease-free equilibrium is globally stable and the disease always dies out. If R₀ > 1, there exists a unique endemic equilibrium which is locally stable. Furthermore, we proved the global stability of the unique endemic equilibrium when ₁ = ₂ = 0 and the disease persists at an endemic equilibrium state if it initially exists.     

Mathematical analysis of a two-patch model of tuberculosis disease with staged progression

The spread of tuberculosis is studied through a two-patch epidemiological system SE₁ ? E_nI which incorporates migrations from one patch to another just by susceptible individuals. Our model is consider with bilinear incidence and migration between two patches, where infected and infectious individuals cannot migrate from one patch to another, due to medical reasons. The existence and uniqueness of the associated endemic equilibria are discussed. Quadratic forms and Lyapunov functions are used to show that when the basic reproduction ratio is less than one, the disease-free equilibrium (DFE) is globally asymptotically stable, and when it is greater than one there exists in each case a unique endemic equilibrium (boundary equilibria and endemic equilibrium) which is globally asymptotically stable. Numerical simulation results are provided to illustrate the theoretical results.     

Hopf bifurcation in epidemic models with a latent period and nonpermanent immunity

In this paper, some SEIRS epidemiological models with vaccination and temporary immunity are considered. First of all, previously published work is reviewed. In the next section, a general model with a constant contact rate and a density-dependent death rate is examined. The model is reformulated in terms of the proportions of susceptible, incubating, infectious, and immune individuals. Next the equilibrium and stability properties of this model are examined, assuming that the average duration of immunity exceeds the infectious period. There is a threshold parameter R_o and the disease can persist if and only if R_o exceeds one. The disease-free equilibrium always exists and is locally stable if R_o < 1 and unstable if R_o > 1. Conditions are derived for the global stability of the disease-free equilibrium. For R_o > 1, the endemic equilibrium is unique and locally asymptotically stable.For the full model dealing with numbers of individuals, there are two critical contact rates. These give conditions for the disease, respectively, to drive a population which would otherwise persist at a finite level or explode to extinction and to cause a population that would otherwise explode to be regulated at a finite level. If the contact rate β(N) is a monotone increasing function of the population size, then we find that there are now three threshold parameters which determine whether or not the disease can persist proportionally. Moreover, the endemic equilibrium need no longer be locally asymptotically stable. Instead stable limit cycles can arise by supercritical Hopf bifurcation from the endemic equilibrium as this equilibrium loses its stability. This is confirmed numerically.     

Global stability of a DS–DI epidemic model with age of infection

A model with differential susceptibility, differential infectivity (DS–DI), and age of infection is formulated in this paper. The susceptibles are divided into n groups according to their susceptibilities. The infectives are divided into m groups according to their infectivities. The total population size is assumed constant. Formula for the reproductive number is derived so that if the reproduction number is less than one, the infection-free equilibrium is locally stable, and unstable otherwise. Furthermore, if the reproductive number is less than one, the infection-free equilibrium is globally asymptotically stable. If the reproductive number is greater than one, it is shown that there exists a unique endemic equilibrium which is globally asymptotically stable. This result is obtained through a Lyapunov function.     

On global stability of the intra-host dynamics of malaria and the immune system

In this paper we consider an intra-host model for the dynamics of malaria. The model describes the dynamics of the blood stage malaria parasites and their interaction with host cells, in particular red blood cells (RBC) and immune effectors. We establish the equilibrium points of the system and analyze their stability using the theory of competitive systems, compound matrices and stability of periodic orbits. We established that the disease-free equilibrium is globally stable if and only if the basic reproduction number satisfies R₀?1 and the parasite will be cleared out of the host. If R₀>1, a unique endemic equilibrium is globally stable and the parasites persist at the endemic steady state. In the presence of the immune response, the numerical analysis of the model shows that the endemic equilibrium is unstable.     

Global behavior of a multi-group SIS epidemic model with age structure

We study global dynamics of a system of partial differential equations. The system is motivated by modelling the transmission dynamics of infectious diseases in a population with multiple groups and age-dependent transition rates. Existence and uniqueness of a positive (endemic) equilibrium are established under the quasi-irreducibility assumption, which is weaker than irreducibility, on the function representing the force of infection. We give a classification of initial values from which corresponding solutions converge to either the disease-free or the endemic equilibrium. The stability of each equilibrium is linked to the dominant eigenvalue s(A), where A is the infinitesimal generator of a “quasi-irreducible” semigroup generated by the model equations. In particular, we show that if s(A)<0 then the disease-free equilibrium is globally stable; if s(A)>0 then the unique endemic equilibrium is globally stable.     

Dynamical behavior of a virus dynamics model with CTL immune response

In this paper, the dynamical behavior of a virus dynamics model with CTL immune response is studied. Sufficient conditions for the asymptotical stability of a disease-free equilibrium, an immune-free equilibrium and an endemic equilibrium are obtained. We prove that there exists a threshold value of the infection rate b beyond which the endemic equilibrium bifurcates from the immune-free one. Still for increasing b values, the endemic equilibrium bifurcates towards a periodic solution. We further analyze the orbital stability of the periodic orbits arising from bifurcation by applying Poore’s condition. Numerical simulation with some hypothetical sets of data has been done to support the analytical findings.     

Global stability of multigroup epidemic model with group mixing and nonlinear incidence rates

In this paper, we introduce a basic reproduction number for a multigroup SEIR model with nonlinear incidence of infection and nonlinear removal functions between compartments. Then, we establish that global dynamics are completely determined by the basic reproduction number R₀. It shows that, the basic reproduction number R₀ is a global threshold parameter in the sense that if it is less than or equal to one, the disease free equilibrium is globally stable and the disease dies out; whereas if it is larger than one, there is a unique endemic equilibrium which is globally stable and thus the disease persists in the population. Finally, two numerical examples are also included to illustrate the effectiveness of the proposed result.     

Global stability of multi-group SEIR epidemic models with distributed delays and nonlinear transmission

The dynamics of multi-group SEIR epidemic models with distributed and infinite delay and nonlinear transmission are investigated. We derive the basic reproduction number R₀ and establish that the global dynamics are completely determined by the values of R₀: if R₀≤1, then the disease-free equilibrium is globally asymptotically stable; if R₀>1, then there exists a unique endemic equilibrium which is globally asymptotically stable. Our results contain those for single-group SEIR models with distributed and infinite delays. In the proof of global stability of the endemic equilibrium, we exploit a graph-theoretical approach to the method of Lyapunov functionals. The biological significance of the results is also discussed.     

Global stability of multi-group epidemic models with distributed delays

We investigate a class of multi-group epidemic models with distributed delays. We establish that the global dynamics are completely determined by the basic reproduction number R₀. More specifically, we prove that, if R₀?1, then the disease-free equilibrium is globally asymptotically stable; if R₀>1, then there exists a unique endemic equilibrium and it is globally asymptotically stable. Our proof of global stability of the endemic equilibrium utilizes a graph-theoretical approach to the method of Lyapunov functionals.     

Global analysis of a vector-host epidemic model with nonlinear incidences

In this paper, an epidemic model with nonlinear incidences is proposed to describe the dynamics of diseases spread by vectors (mosquitoes), such as malaria, yellow fever, dengue and so on. The constant human recruitment rate and exponential natural death, as well as vector population with asymptotically constant population, are incorporated into the model. The stability of the system is analyzed for the disease-free and endemic equilibria. The stability of the system can be controlled by the threshold number R₀. It is shown that if R₀ is less than one, the disease free equilibrium is globally asymptotically stable and in such a case the endemic equilibrium does not exist; if R₀ is greater than one, then the disease persists and the unique endemic equilibrium is globally asymptotically stable. Our results imply that the threshold condition of the system provides important guidelines for accessing control of the vector diseases, and the spread of vector epidemic in an efficient way can be prevented. The contribution of the nonlinear saturating incidence to the basic reproduction number and the level of the endemic equilibrium are also analyzed, respectively.     

具有常数输入的SEIR模型的稳定性分析

讨论了易感者类和潜伏者类均为常数输入,潜伏期、染病期和恢复期均具有传染力,且传染率为一般传染率的SEIR传染病模型.利用Hurwitz判据证明了地方病平衡点的局部渐近稳定性,进一步利用复合矩阵理论得到了地方病平衡点全局渐近稳定的充分条件.     

具有免疫接种且总人口规模变化的SIR传染病模型的稳定性

讨论一类具有预防免疫接种且有效接触率依赖于总人口的SIR传染病模型,给出了决定疾病灭绝和持续生存的基本再生数σ的表达式,在一定条件下证明了疾病消除平衡点的全局稳定性,得到了唯一地方病平衡点的存在性和局部渐近稳定性条件.最后研究了具有双线性传染率和标准传染率的两个具体模型,并证明了当σ>1时该模型地方病平衡点的全局渐近稳定性.     

Complicated endemics of an SIRS model with a generalized incidence under preventive vaccination and treatment controls

In this paper, we propose and study an SIRS epidemic model that incorporates: a generalized incidence rate function describing mechanisms of the disease transmission; a preventive vaccination in the susceptible individuals; and different treatment control strategies depending on the infective population. We provide rigorous mathematical results combined with numerical simulations of the proposed model including: treatment control strategies can determine whether there is an endemic outbreak or not and the number of endemic equilibrium during endemic outbreaks, in addition to the effects of the basic reproduction number; the large value of the preventive vaccination rate can reduce or control the spread of disease; and the large value of the psychological or inhibitory effects in the incidence rate function can decrease the infective population. Some of our interesting findings are that the treatment strategies incorporated in our SIRS model are responsible for backward or forward bifurcations and multiple endemic equilibria; and the infective population decreases with respect to the maximal capacity of treatment. Our results may provide us useful biological insights on population managements for disease that can be modeled through SIRS compartments.     

具有预防接种免疫力的双线性传染率SIR流行病模型全局稳定性

研究一类具有预防接种免疫力的双线性传染率 SIR流行病模型全局稳定性 ,找到了决定疾病灭绝和持续生存的阈值——基本再生数 R0 .当 R0 ≤ 1时 ,仅存在无病平衡态 E0 ;当 R0 >1时 ,存在唯一的地方病平衡态 E* 和无病平衡态 E0 .利用 Hurwitz判据及 Liapunov-Lasalle不变集原理可以得知 :当 R0 <1时 ,无病平衡态 E0 全局渐近稳定 ;当 R0 >1时 ,地方病平衡态 E*全局渐近稳定 ,无病平衡态 E0 不稳定 ;当 R0 =1时 ,计算机数值模拟结果显示 ,无病平衡态 E0 有可能是稳定的     

一类SIRS传染病模型

This paper considers an SIRS epidemic model that incorporates constant immigration rate, a general population-size dependent contact rate and proportional transfer rate from the infective class to susceptible class. A threshold parameter a is identified. If σ≤1, the disease-free equilibrium is globally stable. If σ＞1, a unique endemic equilibrium is locally asymptotically stable. For two important special cases of mass action incidence and standard incidence,global stability of the endemic equilibrium is proved provided the threshold is larger than unity. Some previous results are extended and improved.     

Analysis of an SVEIS epidemic model with partial temporary immunity and saturation incidence rate

In this paper, an SVEIS epidemic model for an infectious disease that spreads in the host population through horizontal transmission is investigated. The role that temporary immunity (natural, disease induced, vaccination induced) plays in the spread of disease, is incorporated in the model. The total host population is bounded and the incidence term is of the Holling-type II form. It is shown that the model exhibits two equilibria, namely, the disease-free equilibrium and the endemic equilibrium. The global dynamics are completely determined by the basic reproduction number R₀. If R₀<1, the disease-free equilibrium is globally stable which leads to the eradication of disease from population. If R₀>1, a unique endemic equilibrium exists and is globally stable in the feasible region under certain conditions. Further, the transcritical bifurcation at R₀=1 is explored by projecting the flow onto the extended center manifold. We use the geometric approach for ordinary differential equations which is based on the use of higher-order generalization of Bendixson’s criterion. Further, we obtain the threshold vaccination coverage required to eradicate the disease. Finally, taking biologically relevant parametric values, numerical simulations are performed to illustrate and verify the analytical results.     

Global stability of delay multigroup epidemic models with group mixing and nonlinear incidence rates

In this paper, we present a new delay multigroup SEIR model with group mixing and nonlinear incidence rates and investigate its global stability. We establish that the global dynamics of the models are completely determined by the basic reproduction number R₀. It is shown that, if R₀?1, then the disease free equilibrium is globally asymptotically stable and the disease dies out; if R₀>1, there exists a unique endemic equilibrium that is globally asymptotically stable and thus the disease persists in the population. Finally, a numerical example is also discussed to illustrate the effectiveness of the results.