Branching process approach for epidemics in dynamic partnership network.

We study the spread of sexually transmitted infections (STIs) and other infectious diseases on a dynamic network by using a branching process approach. The nodes in the network represent the sexually active individuals, while connections represent sexual partnerships. This network is dynamic as partnerships are formed and broken over time and individuals enter and leave the sexually active population due to demography. We assume that individuals enter the sexually active network with a random number of partners, chosen according to a suitable distribution and that the maximal number of partners that an individual can have at a time is finite. We discuss two different branching process approximations for the initial stages of an outbreak of the STI. In the first approximation we ignore some dependencies between infected individuals. We compute the offspring mean of this approximating branching process and discuss its relation to the basic reproduction number [Formula: see text]. The second branching process approximation is asymptotically exact, but only defined if individuals can have at most one partner at a time. For this model we compute the probability of a minor outbreak of the epidemic starting with one or few initial cases. We illustrate complications caused by dependencies in the epidemic model by showing that if individuals have at most one partner at a time, the probabilities of extinction of the two approximating branching processes are different. This implies that ignoring dependencies in the epidemic model leads to a wrong prediction of the probability of a large outbreak. Finally, we analyse the first branching process approximation if the number of partners an individual can have at a given time is unbounded. In this model we show that the branching process approximation is asymptomatically exact as the population size goes to infinity.

Optimal control of a malaria model with asymptomatic class and superinfection.

In this paper, we introduce a malaria model with an asymptomatic class in human population and exposed classes in both human and vector populations. The model assumes that asymptomatic individuals can get re-infected and move to the symptomatic class. In the case of an incomplete treatment, symptomatic individuals move to the asymptomatic class. If successfully treated, the symptomatic individuals recover and move to the susceptible class. The basic reproduction number, R0, is computed using the next generation approach. The system has a disease-free equilibrium (DFE) which is locally asymptomatically stable when R0<1, and may have up to four endemic equilibria. The model exhibits backward bifurcation generated by two mechanisms; standard incidence and superinfection. If the model does not allow for superinfection or deaths due to the disease, then DFE is globally stable which suggests that backward bifurcation is no longer possible. Simulations suggest that total prevalence of malaria is the highest if all individuals show symptoms upon infection, but then undergoes an incomplete treatment and the lowest when all the individuals first move to the symptomatic class then treated successfully. Total prevalence is average if more individuals upon infection move to the asymptomatic class. We study optimal control strategies applied to bed-net use and treatment as main tools for reducing the total number of symptomatic and asymptomatic individuals. Simulations suggest that the optimal control strategies are very dynamic. Although they always lead to decrease in the symptomatic infectious individuals, they may lead to increase in the number of asymptomatic infectious individuals. This last scenario occurs if a large portion of newly infected individuals move to the symptomatic class but many of them do not complete treatment or if they all complete treatment but the superinfection rate of asymptomatic individuals is average.

Comment on "Transmission Model of Hepatitis B Virus with the Migration Effect".

Some consequences of erroneous results concerning eigenvalues in the recent literature of mathematical biology are highlighted. Furthermore, an improved stability criterion and the true value of the basic reproduction number is presented.

False mathematical reasoning in biology.

Some consequences of fallacious mathematical reasoning in the recent literature of mathematical biology are highlighted.