R 0 May Not Tell Us Everything: Transient Disease Dynamics of Some SIR Models Over Patchy Environments.

This paper examines the short-term or transient dynamics of SIR infectious disease models in patch environments. We employ reactivity of an equilibrium and amplification rates, concepts from ecology, to analyze how dispersals/travels between patches, spatial heterogeneity, and other disease-related parameters impact short-term dynamics. Our findings reveal that in certain scenarios, due to the impact of spatial heterogeneity and the dispersals, the short-term disease dynamics over a patch environment may disagree with the long-term disease dynamics that is typically reflected by the basic reproduction number. Such an inconsistence can mislead the public, public healthy agencies and governments when making public health policy and decisions, and hence, these findings are of practical importance.

Modelling the impact of precaution on disease dynamics and its evolution.

In this paper, we introduce the notion of practically susceptible population, which is a fraction of the biologically susceptible population. Assuming that the fraction depends on the severity of the epidemic and the public's level of precaution (as a response of the public to the epidemic), we propose a general framework model with the response level evolving with the epidemic. We firstly verify the well-posedness and confirm the disease's eventual vanishing for the framework model under the assumption that the basic reproduction number R 0 < 1 . For R 0 > 1 , we study how the behavioural response evolves with epidemics and how such an evolution impacts the disease dynamics. More specifically, when the precaution level is taken to be the instantaneous best response function in literature, we show that the endemic dynamic is convergence to the endemic equilibrium; while when the precaution level is the delayed best response, the endemic dynamic can be either convergence to the endemic equilibrium, or convergence to a positive periodic solution. Our derivation offers a justification/explanation for the best response used in some literature. By replacing "adopting the best response" with "adapting toward the best response", we also explore the adaptive long-term dynamics.

Wolbachia Dynamics in Mosquitoes with Incomplete CI and Imperfect Maternal Transmission by a DDE System.

In this paper, we propose a delay differential equation model to describe the Wolbachia infection dynamics in mosquitoes in which the key factor of cytoplasmic incompactibility (CI) is incorporated in a more natural way than those in the literature. By analyzing the dynamics of the model, we are able to obtain some information on the impact of four important parameters: the competition capabilities of the wild mosquitoes and infected mosquitoes, the maternal transmission level and the CI level. The analytic results show that there are ranges of parameters that support competition exclusion principle, and there are also ranges of parameters that allow co-persistence for both wild and infected mosquitoes. These ranges account for the scenarios of failure of invasion, invasion and suppressing the wild mosquitoes, and invasion and replacing the wild mosquitoes. We also discuss some possible future problems both in mathematics and in modeling.

Evolution and Adaptation of Anti-predation Response of Prey in a Two-Patchy Environment.

When perceiving a risk from predators, a prey may respond by reducing its reproduction and decreasing or increasing (depending on the species) its mobility. We formulate a patch model to investigate the aforementioned fear effect which is indirect, in contrast to the predation as a direct effect, of the predator on the prey population. We consider not only cost but also benefit of anti-predation response of the prey, and explore their trade-offs together as well as the impact of the fear effect mediated dispersals of the prey. In the case of constant response level, if there is no dispersal and for some given response functions, the model indicates the existence of an evolutionary stable strategy which is also a convergence stable strategy for the response level; and if there is dispersal, the analysis of the model shows that it will enhance the co-persistence of the prey on both patches. Considering the trait as another variable, we continue to study the evolution of anti-predation strategy for the model with dispersal, which leads to a three-dimensional system of ordinary differential equations. We perform some numerical simulations, which demonstrate global convergence to a positive equilibrium with the response level evolving towards a positive constant level, implying the existence of an optimal anti-predation response level.

Modeling the Potential Role of Engineered Symbiotic Bacteria in Malaria Control.

Recent experimental study suggests that the engineered symbiotic bacteria Serratia AS1 may provide a novel, effective and sustainable biocontrol of malaria. These recombinant bacteria have been shown to be able to rapidly disseminate throughout mosquito populations and to efficiently inhibit development of malaria parasites in mosquitoes in controlled laboratory experiments. In this paper, we develop a climate-based malaria model which involves both vertical and horizontal transmissions of the engineered Serratia AS1 bacteria in mosquito population. We show that the dynamics of the model system is totally determined by the vector reproduction ratio [Formula: see text], and the basic reproduction ratio [Formula: see text]. If [Formula: see text], then the mosquito-free state is globally attractive. If [Formula: see text] and [Formula: see text], then the disease-free periodic solution is globally attractive. If [Formula: see text] and [Formula: see text], then the positive periodic solution is globally attractive. Numerically, we verify the obtained analytic result and evaluate the effects of releasing the engineered Serratia AS1 bacteria in field by conducting a case study for Douala, Cameroon. We find that ideally, by using Serratia AS1 alone, it takes at least 25 years to eliminate malaria from Douala. This implies that continued long-term investment is needed in the fight against malaria and confirms the necessity of integrating multiple control measures.

Threshold Dynamics of a Temperature-Dependent Stage-Structured Mosquito Population Model with Nested Delays.

Mosquito-borne diseases remain a significant threat to public health and economics. Since mosquitoes are quite sensitive to temperature, global warming may not only worsen the disease transmission case in current endemic areas but also facilitate mosquito population together with pathogens to establish in new regions. Therefore, understanding mosquito population dynamics under the impact of temperature is considerably important for making disease control policies. In this paper, we develop a stage-structured mosquito population model in the environment of a temperature-controlled experiment. The model turns out to be a system of periodic delay differential equations with periodic delays. We show that the basic reproduction number is a threshold parameter which determines whether the mosquito population goes to extinction or remains persistent. We then estimate the parameter values for Aedes aegypti, the mosquito that transmits dengue virus. We verify the analytic result by numerical simulations with the temperature data of Colombo, Sri Lanka where a dengue outbreak occurred in 2017.

Effect of impulsive controls in a model system for age-structured population over a patchy environment.

In this paper, a very general model of impulsive delay differential equations in n-patches is rigorously derived to describe the impulsive control of population of a single species over n-patches. The model allows an age structure consisting of immatures and matures, and also considers mobility and culling of both matures and immatures. Conditions are obtained for extinction and persistence of the model system under three special scenarios: (1) without impulsive control; (2) with impulsive culling of the immatures only; and (3) with impulsive culling of the matures only, respectively. In the case of persistence, the persistence level is also estimated for the systems in the case of identical n patches, by relating the issue to the dynamics of multi-dimensional maps. Two illustrative examples and their numerical simulations are given to show the effectiveness of the results. Based on the theoretical results, some strategies of impulsive culling are provided to eradicate the population of a pest species.

Modeling the Fear Effect in Predator-Prey Interactions with Adaptive Avoidance of Predators.

Recent field experiments on vertebrates showed that the mere presence of a predator would cause a dramatic change of prey demography. Fear of predators increases the survival probability of prey, but leads to a cost of prey reproduction. Based on the experimental findings, we propose a predator-prey model with the cost of fear and adaptive avoidance of predators. Mathematical analyses show that the fear effect can interplay with maturation delay between juvenile prey and adult prey in determining the long-term population dynamics. A positive equilibrium may lose stability with an intermediate value of delay and regain stability if the delay is large. Numerical simulations show that both strong adaptation of adult prey and the large cost of fear have destabilizing effect while large population of predators has a stabilizing effect on the predator-prey interactions. Numerical simulations also imply that adult prey demonstrates stronger anti-predator behaviors if the population of predators is larger and shows weaker anti-predator behaviors if the cost of fear is larger.

Impact of Spring Bird Migration on the Range Expansion of Ixodes scapularis Tick Population.

Many observational studies suggest that seasonal migratory birds play an important role in spreading Ixodes scapularis, a vector of Lyme disease, along their migratory flyways, and they are believed to be responsible for geographic range expansion of I. scapularis in Canada. However, the interplay between the dynamics of I. scapularis on land and migratory birds in the air is not well understood. In this study, we develop a periodic delay meta-population model which takes into consideration the local landscape for tick reproduction within patches and the times needed for ticks to be transported by birds between patches. Assuming that the tick population is endemic in the source region, we find that bird migration may boost an already established tick population at the subsequent region and thus increase the risk to humans, or bird migration may help ticks to establish in a region where the local landscape is not appropriate for ticks to survive in the absence of bird migration, imposing risks to public health. This theoretical study reveals that bird migration plays an important role in the geographic range expansion of I. scapularis, and therefore our findings may suggest some strategies for Lyme disease prevention and control.

A Mathematical Model for Biocontrol of the Invasive Weed Fallopia japonica.

We propose a mathematical model for biocontrol of the invasive weed Fallopia japonica using one of its co-evolved natural enemies, the Japanese sap-sucking psyllid Aphalara itadori. This insect sucks the sap from the stems of the plant thereby weakening it. Its diet is highly specific to F. japonica. We consider a single isolated knotweed stand, the plant's size being described by time-dependent variables for total stem and rhizome biomass. It is the larvae of A. itadori that damage the plant most, so the insect population is described in terms of variables for the numbers of larvae and adults, using a stage-structured modelling approach. The dynamics of the model depends mainly on a parameter h, which measures how long it takes for an insect to handle (digest) one unit of F. japonica stem biomass. If h is too large, then the model does not have a positive equilibrium and the plant biomass and insect numbers both grow together without bound, though at a lower rate than if the insects were absent. If h is sufficiently small, then the model possesses a positive equilibrium which appears to be locally stable. The results based on our model imply that satisfactory long-term control of the knotweed F. japonica using the insect A. itadori is only possible if the insect is able to consume and digest knotweed biomass sufficiently quickly; if it cannot, then the insect can only slow down the growth which is still unbounded.

Modelling the fear effect in predator-prey interactions.

A recent field manipulation on a terrestrial vertebrate showed that the fear of predators alone altered anti-predator defences to such an extent that it greatly reduced the reproduction of prey. Because fear can evidently affect the populations of terrestrial vertebrates, we proposed a predator-prey model incorporating the cost of fear into prey reproduction. Our mathematical analyses show that high levels of fear (or equivalently strong anti-predator responses) can stabilize the predator-prey system by excluding the existence of periodic solutions. However, relatively low levels of fear can induce multiple limit cycles via subcritical Hopf bifurcations, leading to a bi-stability phenomenon. Compared to classic predator-prey models which ignore the cost of fear where Hopf bifurcations are typically supercritical, Hopf bifurcations in our model can be both supercritical and subcritical by choosing different sets of parameters. We conducted numerical simulations to explore the relationships between fear effects and other biologically related parameters (e.g. birth/death rate of adult prey), which further demonstrate the impact that fear can have in predator-prey interactions. For example, we found that under the conditions of a Hopf bifurcation, an increase in the level of fear may alter the direction of Hopf bifurcation from supercritical to subcritical when the birth rate of prey increases accordingly. Our simulations also show that the prey is less sensitive in perceiving predation risk with increasing birth rate of prey or increasing death rate of predators, but demonstrate that animals will mount stronger anti-predator defences as the attack rate of predators increases.

Impact of Tenofovir gel as a PrEP on HIV infection: a mathematical model.

Pre-exposure prophylaxis (PrEP) has been considered as one of the promising interventions for HIV infection as experiments on various groups and sites have reported its significant effectiveness. This study evaluates the effectiveness of Tenofovir gel, one of the widely used PrEPs for women, through a mathematical model. Our model has excellent agreement with the experimental data on the use of Tenofovir gel as a PrEP in South African women. Using our model, we estimate both male-to-female and female-to-male transmission rates with and without Tenofovir gel protection. Through these estimates we demonstrate that the use of Tenofovir gel as a PrEP can significantly reduce the reproduction numbers, new infections, and HIV prevalence in South Africa. Our results further show that the effectiveness of Tenofovir gel largely depends on the level of adherence to the gel and the proportion of women under gel coverage. Even though Tenofovir gel alone may not be able to eradicate the disease as indicated by our estimates of the reproduction numbers, together with other interventions, such as condom use, it can serve as a strong weapon to fight against HIV epidemics.

Repulsion effect on superinfecting virions by infected cells.

In this paper, the repulsion effect of superinfecting virion by infected cells is studied by a reaction diffusion equation model for virus infection dynamics. In this model, the diffusion of virus depends not only on its concentration gradient but also on the concentration of infected cells. The basic reproduction number, linear stability of steady states, spreading speed and existence of traveling wave solutions for the model are discussed. It is shown that viruses spread more rapidly with the repulsion effect of infected cells on superinfecting virions, than with random diffusion only. For our model, the spreading speed of free virus is not consistent with the minimal traveling wave speed. With our general model, numerical computations of the spreading speed show that the repulsion of superinfecting virion promotes the spread of virus, which confirms, not only qualitatively but also quantitatively, the experimental result of Doceul et al. (Science 327:873-876, 2010).

Modeling the role of altruism of antibiotic-resistant bacteria.

Based on the new findings in a recent experimental study (Lee et al., Nature 467, 82-86, 2010) that antibiotic resistant mutants of bacteria produce indoles to protect the wild strain bacteria, we propose a mathematical model to describe the evolution of the wild strain, resistant strain and indoles with limited nutrient. We distinguish two cases: (i) mutation is negligible and a resistant strain preexists; (ii) mutation is not negligible. For (i), we establish conditions for co-persistence of both strains, which indicate that the wild strain can survive with the help from the altruistic resistant strain, whereas it dies out in the absence of such a benefit. This consolidates the experimental findings in Lee et al. (Nature 467:82-86 2010). Further analysis and simulations also reveal some new phenomena not reported in Lee et al. (Nature 467:82-86 2010), that is, periodic oscillations of the populations may occur within certain range of the parameters, and there exists bistability in the sense that a stable positive periodic solution coexists with a stable positive equilibrium.

Transmission dynamics for vector-borne diseases in a patchy environment.

In this paper, a mathematical model is derived to describe the transmission and spread of vector-borne diseases over a patchy environment. The model incorporates into the classic Ross-MacDonald model two factors: disease latencies in both hosts and vectors, and dispersal of hosts between patches. The basic reproduction number R(0) is identified by the theory of the next generation operator for structured disease models. The dynamics of the model is investigated in terms of R(0). It is shown that the disease free equilibrium is asymptotically stable if R(0) > 1, and it is unstable if R(0) > 1; in the latter case, the disease is endemic in the sense that the variables for the infected compartments are uniformly persistent. For the case of two patches, more explicit formulas for R(0) are derived by which, impacts of the dispersal rates on disease dynamics are also explored. Some numerical computations for R(0) in terms of dispersal rates are performed which show visually that the impacts could be very complicated: in certain range of the parameters, R(0) is increasing with respect to a dispersal rate while in some other range, it can be decreasing with respect to the same dispersal rate. The results can be useful to health organizations at various levels for setting guidelines or making policies for travels, as far as malaria epidemics is concerned.

Population dynamics of a stoichiometric aquatic tri-trophic level model with fear effect.

In this paper, a stoichiometric aquatic tri-trophic level model is proposed and analyzed, which incorporates the effect of light and phosphorus, as well as the fear effect in predator-prey interactions. The analysis of the model includes the dissipativity and the existence and stability of equilibria. The influence of environmental factors and fear effect on the dynamics of the system is particularly investigated. The key findings reveal that the coexistence of populations is positively influenced by an appropriate level of light intensity and/or the dissolved phosphorus input concentration; however, excessive levels of phosphorus input can disrupt the system, leading to chaotic behaviors. Furthermore, it is found that the fear effect can stabilize the system and promote the chances of population coexistence.

On the treatment of melanoma: A mathematical model of oncolytic virotherapy.

We develop and analyze a mathematical model of oncolytic virotherapy in the treatment of melanoma. We begin with a special, local case of the model, in which we consider the dynamics of the tumour cells in the presence of an oncolytic virus at the primary tumour site. We then consider the more general regional model, in which we incorporate a linear network of lymph nodes through which the tumour cells and the oncolytic virus may spread. The modelling also considers the impact of hypoxia on the disease dynamics. The modelling takes into account both the effects of hypoxia on tumour growth and spreading, as well as the impact of hypoxia on oncolytic virotherapy as a treatment modality. We find that oxygen-rich environments are favourable for the use of adenoviruses as oncolytic agents, potentially suggesting the use of complementary external oxygenation as a key aspect of treatment. Furthermore, the delicate balance between a virus' infection capabilities and its oncolytic capabilities should be considered when engineering an oncolytic virus. If the virus is too potent at killing tumour cells while not being sufficiently effective at infecting them, the infected tumour cells are destroyed faster than they are able to infect additional tumour cells, leading less favourable clinical results. Numerical simulations are performed in order to support the analytic results and to further investigate the impact of various parameters on the outcomes of treatment. Our modelling provides further evidence indicating the importance of three key factors in treatment outcomes: tumour microenvironment oxygen concentration, viral infection rates, and viral oncolysis rates. The numerical results also provide some estimates on these key model parameters which may be useful in the engineering of oncolytic adenoviruses.

Threshold dynamics of an infective disease model with a fixed latent period and non-local infections.

In this paper, we derive and analyze an infectious disease model containing a fixed latency and non-local infection caused by the mobility of the latent individuals in a continuous bounded domain. The model is given by a spatially non-local reaction-diffusion system carrying a discrete delay associated with the zero-flux condition on the boundary. By applying some existing abstract results in dynamical systems theory, we prove the existence of a global attractor for the model system. By appealing to the theory of monotone dynamical systems and uniform persistence, we show that the model has the global threshold dynamics which can be described either by the principal eigenvalue of a linear non-local scalar reaction diffusion equation or equivalently by the basic reproduction number R0 for the model. Such threshold dynamics predicts whether the disease will die out or persist. We identify the next generation operator, the spectral radius of which defines basic reproduction number. When all model parameters are constants, we are able to find explicitly the principal eigenvalue and R0. In addition to computing the spectral radius of the next generation operator, we also discuss an alternative way to compute R0.

A new perspective on infection forces with demonstration by a DDE infectious disease model.

In this paper, we revisit the notion of infection force from a new angle which can offer a new perspective to motivate and justify some infection force functions. Our approach can not only explain many existing infection force functions in the literature, it can also motivate new forms of infection force functions, particularly infection forces depending on disease surveillance of the past. As a demonstration, we propose an SIRS model with delay. We comprehensively investigate the disease dynamics represented by this model, particularly focusing on the local bifurcation caused by the delay and another parameter that reflects the weight of the past epidemics in the infection force. We confirm Hopf bifurcations both theoretically and numerically. The results show that, depending on how recent the disease surveillance data are, their assigned weight may have a different impact on disease control measures.

Re-examination of the impact of some non-pharmaceutical interventions and media coverage on the COVID-19 outbreak in Wuhan.

In this paper, based on the classic Kermack-McKendrick SIR model, we propose an ordinary differential equation model to re-examine the COVID-19 epidemics in Wuhan where this disease initially broke out. The focus is on the impact of all those major non-pharmaceutical interventions (NPIs) implemented by the local public healthy authorities and government during the epidemics. We use the data publicly available and the nonlinear least-squares solver lsqnonlin built in MATLAB to estimate the model parameters. Then we explore the impact of those NPIs, particularly the timings of these interventions, on the epidemics. The results can help people review the responses to the outbreak of the COVID-19 in Wuhan, while the proposed model also offers a framework for studying epidemics of COVID-19 and/or other similar diseases in other places, and accordingly helping people better prepare for possible future outbreaks of similar diseases.