Department of Mathematical Sciences, Clemson University, South Carolina, United States.
School of Human Evolution and Social Change; Simon A. Levin Mathematical Computational and Modeling Science Center, Arizona State University, Tempe, Arizona, United States.
Math Biosci. 2019 Mar;309:42-65. doi: 10.1016/j.mbs.2019.01.003. Epub 2019 Jan 16.
Stochastic epidemic models, generally more realistic than deterministic counterparts, have often been seen too complex for rigorous mathematical analysis because of level of details it requires to comprehensively capture the dynamics of diseases. This problem further becomes intense when complexity of diseases increases as in the case of vector-borne diseases (VBD). The VBDs are human illnesses caused by pathogens transmitted among humans by intermediate species, which are primarily arthropods. In this study, a stochastic VBD model is developed and novel mathematical methods are described and evaluated to systematically analyze the model and understand its complex dynamics. The VBD model incorporates some relevant features of the VBD transmission process including demographical, ecological and social mechanisms, and different host and vector dynamic scales. The analysis is based on dimensional reductions and model simplifications via scaling limit theorems. The results suggest that the dynamics of the stochastic VBD depends on a threshold quantity R, the initial size of infectives, and the type of scaling in terms of host population size. The quantity R for deterministic counterpart of the model is interpreted as a threshold condition for infection persistence as is mentioned in the literature for many infectious disease models. Different scalings yield different approximations of the model, and in particular, if vectors have much faster dynamics, the effect of the vector dynamics on the host population averages out, which largely reduces the dimension of the model. Specific scenarios are also studied using simulations for some fixed sets of parameters to draw conclusions on dynamics.
随机传染病模型通常比确定性模型更具现实性,但由于其需要全面捕捉疾病动态所需的细节水平,因此通常过于复杂而无法进行严格的数学分析。当疾病的复杂性增加时,例如在虫媒传染病 (VBD) 的情况下,这个问题就更加严重了。VBD 是由病原体通过中间物种在人类之间传播引起的人类疾病,这些中间物种主要是节肢动物。在这项研究中,开发了一种随机 VBD 模型,并描述和评估了新的数学方法,以系统地分析该模型并理解其复杂的动态。VBD 模型包含了 VBD 传播过程的一些相关特征,包括人口统计学、生态学和社会机制,以及不同的宿主和媒介动态尺度。分析基于通过标度极限定理进行维度减少和模型简化。结果表明,随机 VBD 的动态取决于一个阈值量 R、感染性初始大小以及宿主种群规模方面的标度类型。模型的确定性对应物的数量 R 被解释为感染持续存在的阈值条件,这在许多传染病模型的文献中都有提到。不同的标度产生不同的模型近似,特别是如果媒介的动态速度快得多,则媒介动态对宿主种群的影响平均化,这大大降低了模型的维度。还使用模拟针对一些固定参数集研究了特定场景,以得出关于动态的结论。