具有一般形式饱和接触率SEIS模型渐近分析

研究具有一般形式饱和接触率SEIS模型渐近性态,得到决定疾病绝灭和持续的阈值-基本再生数R0。当R0 ≤ 1时,仅存在无病平衡点P^0;当R0＞1时,除存在无病平衡点P^0外,还存在惟一的地方病平衡点P^＊。当R0＜1时,无病平衡点P^0全局渐近稳定;当R0＞1时,地方病平衡点P^＊局部渐近稳定。特别地,无因病死亡时,极限方程地方病平衡点P^-＊全局渐近稳定。     

Global dynamics of an SEIR epidemic model with saturating contact rate

Heesterbeek and Metz [J. Math. Biol. 31 (1993) 529] derived an expression for the saturating contact rate of individual contacts in an epidemiological model. In this paper, the SEIR model with this saturating contact rate is studied. The basic reproduction number R0 is proved to be a sharp threshold which completely determines the global dynamics and the outcome of the disease. If R0 < or =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 globally stable and the disease persists at an endemic equilibrium state if it initially exists. The contribution of the saturating contact rate to the basic reproduction number and the level of the endemic equilibrium is also analyzed.     

Dynamics of an SIQS epidemic model with transport-related infection and exit-entry screenings

Population dispersal, as a common phenomenon in human society, may cause the spreading of many diseases such as influenza, SARS, etc. which are easily transmitted from one region to other regions. Exit and entry screenings at the border are considered as effective ways for controlling the spread of disease. In this paper, the dynamics of an SIQS model are analyzed and the combined effects of transport-related infection enhancing and exit-entry screenings suppressing on disease spread are discussed. The basic reproduction number is computed and proved to be a threshold for disease control. If it is not greater than the unity, the disease free equilibrium is globally asymptotically stable. And there exists an endemic equilibrium which is locally asymptotically stable if the reproduction number is greater than unity. It is shown that the disease is endemic in the sense of permanence if and only if the endemic equilibrium exists. Exit screening and entry screening are shown to be helpful for disease eradication since they can always have the possibility to eradicate the disease endemic led by transport-related infection and furthermore have the possibility to eradicate disease even when the isolated cites are disease endemic.     

一类具有垂直传染和预防接种的传染病模型的稳定性

考虑了垂直传染和预防接种因素对传染病流行影响的SEIRS模型,主要研究了系统的平衡点及其稳定性,得出当预防接种水平超过某一个阈值时疾病可以根除,若接种水平低于阈值时疾病将流行.     

Spread of disease with transport-related infection and entry screening

An SIQS model is proposed to study the effect of transport-related infection and entry screening. If the basic reproduction number is below unity, the disease free equilibrium is locally asymptotically stable. There exists an endemic equilibrium which is locally asymptotically stable if the reproduction number is larger than unity. It is shown that the disease is endemic in the sense of permanence if and only if the endemic equilibrium exists. Entry screening is shown to be helpful for disease eradication since it can always have the possibility to eradicate the disease led by transport-related infection and furthermore have the possibility to eradicate disease even when the disease is endemic in both isolated cities.     

若干具有非线性传染力的传染病模型的稳定性分析

讨论了具有常数迁入和非线性传染力的三类传染病模型,即SIRI模型,SIRI框架下的DS模型及SIR框架下的DI模型。给出了它们基本再生数R0的表达式,证明了R0≤1时无病平衡点是全局稳定的,同时证明了如果地方病平衡点存在,则必是全局稳定的结果（从而必唯一）对第一和第三个模型还给出了R0＞1时地方病平衡点的存在唯一性。     

具有周期传染率的SIR传染病模型的周期解

考虑了具有周期传染率的SIR流行病模型,定义了基本再生数^-R0=β／（μ＋γ）,分析了该模型的动力学性态,证明了当^-R0〈1时无病平衡点是全局稳定的;^-R0〉1时,无病平衡点是不稳定的,模型至少存在一个周期解。对小振幅的周期传染率模型,给出了模型周期解的近似表达式,证明了该周期解的稳定性,最后做了数值模拟,结果显示周期解可能是全局稳定的。     

The Ross-Macdonald model in a patchy environment

We generalize to n patches the Ross-Macdonald model which describes the dynamics of malaria. We incorporate in our model the fact that some patches can be vector free. We assume that the hosts can migrate between patches, but not the vectors. The susceptible and infectious individuals have the same dispersal rate. We compute the basic reproduction ratio R(0). We prove that if R(0)1, then the disease-free equilibrium is globally asymptotically stable. When R(0)>1, we prove that there exists a unique endemic equilibrium, which is globally asymptotically stable on the biological domain minus the disease-free equilibrium.     

一个具非单调传染率的SEIR传染病模型的全局稳定性

本文研究一类描述某种严重疾病的传染数目变大时在心理上产生影响的非单调传染率的SEIR传染病模型.研究表明模型的动力行为和疾病的爆发完全由基本再生数R0决定.当R0≤1时,无病平衡点是全局稳定的,疾病消亡;当R0〉1时,地方病平衡点是全局稳定的,疾病持续且发展成地方病.     

An SIS patch model with variable transmission coefficients

In this paper, an SIS patch model with non-constant transmission coefficients is formulated to investigate the effect of media coverage and human movement on the spread of infectious diseases among patches. The basic reproduction number R₀ is determined. It is shown that the disease-free equilibrium is globally asymptotically stable if R₀?1, and the disease is uniformly persistent and there exists at least one endemic equilibrium if R₀>1. In particular, when the disease is non-fatal and the travel rates of susceptible and infectious individuals in each patch are the same, the endemic equilibrium is unique and is globally asymptotically stable as R₀>1. Numerical calculations are performed to illustrate some results for the case with two patches.     

Global dynamics of an epidemiological model with age of infection and disease relapse

In this paper, an epidemiological model with age of infection and disease relapse is investigated. The basic reproduction number for the model is identified, and it is shown to be a sharp threshold to completely determine the global dynamics of the model. By analysing the corresponding characteristic equations, the local stability of a disease-free steady state and an endemic steady state of the model is established. By means of suitable Lyapunov functionals and LaSalle's invariance principle, it is verified that if the basic reproduction number is less than unity, the disease-free steady state is globally asymptotically stable, and hence the disease dies out; if the basic reproduction number is greater than unity, the endemic steady state is globally asymptotically stable and the disease becomes endemic.     

Global stability of an SEIS epidemic model with recruitment and a varying total population size

This paper considers an SEIS epidemic model that incorporates constant recruitment, disease-caused death and disease latency. The incidence term is of the bilinear mass-action form. It is shown that the global dynamics is completely determined by the basic reproduction number R(0). If R(0)1, a unique endemic equilibrium is globally stable in the interior of the feasible region and the disease persists at the endemic equilibrium.     

Threshold dynamics in an SEIRS model with latency and temporary immunity

A disease transmission model of SEIRS type with distributed delays in latent and temporary immune periods is discussed. With general/particular probability distributions in both of these periods, we address the threshold property of the basic reproduction number \(R_0\) and the dynamical properties of the disease-free/endemic equilibrium points present in the model. More specifically, we 1. show the dependence of \(R_0\) on the probability distribution in the latent period and the independence of \(R_0\) from the distribution of the temporary immunity, 2. prove that the disease free equilibrium is always globally asymptotically stable when \(R_0<1\) , and 3. according to the choice of probability functions in the latent and temporary immune periods, establish that the disease always persists when \(R_0>1\) and an endemic equilibrium exists with different stability properties. In particular, the endemic steady state is at least locally asymptotically stable if the probability distribution in the temporary immunity is a decreasing exponential function when the duration of the latency stage is fixed or exponentially decreasing. It may become oscillatory under certain conditions when there exists a constant delay in the temporary immunity period. Numerical simulations are given to verify the theoretical predictions.     

Global stability of models of humoral immunity against multiple viral strains

We analyse, from a mathematical point of view, the global stability of equilibria for models describing the interaction between infectious agents and humoral immunity. We consider the models that contain the variables of pathogens explicitly. The first model considers the situation where only a single strain exists. For the single strain model, the disease steady state is globally asymptotically stable if the basic reproductive ratio is greater than one. The other models consider the situations where multiple strains exist. For the multi-strain models, the disease steady state is globally asymptotically stable. In the model that does not explicitly contain an immune variable, only one strain with the maximum basic reproductive ratio can survive at the steady state. However, in our models explicitly involving the immune system, multiple strains coexist at the steady state.     

The effects of human movement on the persistence of vector-borne diseases

With the recent resurgence of vector-borne diseases due to urbanization and development there is an urgent need to understand the dynamics of vector-borne diseases in rapidly changing urban environments. For example, many empirical studies have produced the disturbing finding that diseases continue to persist in modern city centers with zero or low rates of transmission. We develop spatial models of vector-borne disease dynamics on a network of patches to examine how the movement of humans in heterogeneous environments affects transmission. We show that the movement of humans between patches is sufficient to maintain disease persistence in patches with zero transmission. We construct two classes of models using different approaches: (i) Lagrangian models that mimic human commuting behavior and (ii) Eulerian models that mimic human migration. We determine the basic reproduction number R₀ for both modeling approaches. We show that for both approaches that if the disease-free equilibrium is stable (R₀<1) then it is globally stable and if the disease-free equilibrium is unstable (R₀>1) then there exists a unique positive (endemic) equilibrium that is globally stable among positive solutions. Finally, we prove in general that Lagrangian and Eulerian modeling approaches are not equivalent. The modeling approaches presented provide a framework to explore spatial vector-borne disease dynamics and control in heterogeneous environments. As an example, we consider two patches in which the disease dies out in both patches when there is no movement between them. Numerical simulations demonstrate that the disease becomes endemic in both patches when humans move between the two patches.     

Impact of group mixing on disease dynamics

A general mathematical model is proposed to study the impact of group mixing in a heterogeneous host population on the spread of a disease that confers temporary immunity upon recovery. The model contains general distribution functions that account for the probabilities that individuals remain in the recovered class after recovery. For this model, the basic reproduction number R₀ is identified. It is shown that if R₀<1, then the disease dies out in the sense that the disease free equilibrium is globally asymptotically stable; whereas if R₀>1, this equilibrium becomes unstable. In this latter case, depending on the distribution functions and the group mixing strengths, the disease either persists at a constant endemic level or exhibits sustained oscillatory behavior.     

Global dynamics of a SEIR model with varying total population size

A SEIR model for the transmission of an infectious disease that spreads in a population through direct contact of the hosts is studied. The force of infection is of proportionate mixing type. A threshold sigma is identified which determines the outcome of the disease; if sigma < or = 1, the infected fraction of the population disappears so the disease dies out, while of sigma > 1, the infected fraction persists and a unique endemic equilibrium state is shown, under a mild restriction on the parameters, to be globally asymptotically stable in the interior of the feasible region. Two other threshold parameters sigma' and sigma are also identified; they determine the dynamics of the population sizes in the cases when the disease dies out and when it is endemic, respectively.     

Stability in a two host epidemic model

An epidemic model is derived for a two host infectious disease. It is shown that if a non-trivial equilibrium solution exists, it is globally stable. This result is also proved for a similar one host model.     

An SIR pairwise epidemic model with infection age and demography

The demography and infection age play an important role in the spread of slowly progressive diseases. To investigate their effects on the disease spreading, we propose a pairwise epidemic model with infection age and demography on dynamic networks. The basic reproduction number of this model is derived. It is proved that there is a disease-free equilibrium which is globally asymptotically stable if the basic reproduction number is less that unity. Besides, sensitivity analysis is performed and shows that increasing the variance in recovery time and decreasing the variance in infection time can effectively control the diseases. The complex interaction between the death rate and equilibrium prevalence suggests that it is imperative to correctly estimate the parameters of demography in order to assess the disease transmission dynamics accurately. Moreover, numerical simulations show that the endemic equilibrium is globally asymptotically stable.     

A Within-Host Virus Model with Periodic Multidrug Therapy

This paper is devoted to the investigation of the effects of periodic drug treatment on a standard within-host virus model. We first introduce the basic reproduction ratio for the model, and then show that the infection free equilibrium is globally asymptotically stable, and the disease eventually disappears if $\mathcal{R}_{0} < 1$ , while there exists at least one positive periodic state and the disease persists when $\mathcal{R}_{0}>1$ . We also consider an optimization problem by shifting the phase of these drug efficacy functions. It turns out that shifting the phase can certainly affect the stability of the infection free steady state. A numerical study is performed to illustrate our analytic results.