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DISSERTATION RESEARCH: Scaling within host interactions to epidemic patterns

DISSERTATION RESEARCH: Scaling within host interactions to epidemic patterns
论文研究:将宿主相互作用扩展到流行病模式
批准号:
1601353
负责人:
Volker Rudolf
金额:
$2.01万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-06-01 至 2019-02-28

项目摘要

项目成果

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中文摘要
翻译
寄生虫控制着几乎所有种群的动态,绝大多数宿主(包括人类)同时受到多种寄生虫物种的感染。多种寄生虫的感染是否会增加宿主人群中流行的风险?这项研究将建立一个预测联合感染如何影响宿主人群流行的一般框架。结果将有助于预测并发出现的寄生虫的后果,并将为帮助遏制威胁野生动物、动物种群、农作物和人类种群的流行病的战略提供依据。该项目将通过支持两个新的实验来扩展博士生的研究和培训,这两个实验将改进现有的数学模型。研究人员将通过关于传染病的讲座,以及参与实验设计和结果数据分析,让休斯顿公立学校的不同学生参与进来。当多种寄生虫感染宿主时,感染顺序可能起着重要作用,因为它可以决定传播率和宿主死亡率。到达顺序的影响--或优先效应--在单一宿主中得到了很好的记录,但很少被纳入预测和理解多寄生虫流行的经典模型中。该项目的目标是确定(1)感染的相对时间如何改变多寄生虫系统中的流行病,以及多重感染是否增加了流行病结局的差异,以及(2)测试是否可以用包含来自单一宿主数据的联合感染后果的机制模型来预测这种差异。这些目标将通过实验和模型的组合来实现。第一个实验将检查具有多个寄生虫到达顺序的多寄生虫流行以及双重感染和单感染人群。这将决定优先效应如何改变宿主人口一级的流行模式。将进行一系列单宿主感染实验,以参数化预测流行病模型,该模型解释宿主的感染历史以及该历史如何影响共同感染的寄生虫和宿主之间的相互作用。将模型预测与经验流行病进行比较,将检验在考虑宿主感染史时,是否可以从单个宿主数据预测自然人口中流行病模式的变化。该模型的预测能力将与不包括优先效应的传统模型进行比较。
英文摘要
Parasites regulate the dynamics of almost all populations, and the vast majority of hosts (including humans) are infected by multiple parasite species at the same time. Do infections by multiple parasite species increase the risk of epidemics in host populations? This research will establish a general framework that predicts how co-infections affect epidemics in host populations. Results will help predict the consequences of concurrent emerging parasites and will inform strategies to help curb epidemics that threaten wildlife, animal stocks, agricultural crops, and human populations. The project will extend the research and training of a doctoral student by supporting two new experiments that will improve existing mathematical models. The researchers will engage a diverse range of students in the Houston Public Schools through lectures on infectious disease and participation in the design of experiments and analysis of resulting data. When multiple parasites infect hosts, the order of infection likely plays an important role because it can determine transmission rates and host mortality. The effects of arrival order - or priority effects - are well documented within single hosts but rarely incorporated in classical models to predict and understand multi-parasite epidemics. The goal of this project is to determine (1) how the relative timing of infections alters epidemics in multi-parasite systems and whether multiple infections increase variation in outcome of epidemics, and (2) test whether this variation can be predicted with mechanistic models that incorporate the consequences of co-infection from single-host data. These goals will be accomplished using a combination of experiments and models. The first experiment will examine multi-parasite epidemics with multiple arrival orders of parasites and doubly infected and singly infected populations. This will determine how priority effects alter epidemic patterns at the host population level. A series of single host infection experiments will be conducted to parameterize a predictive epidemic model that accounts for the infection history of hosts and how this history influences interactions among co-infecting parasites and hosts. Comparing model predictions to empirical epidemics will test whether variation in epidemics patterns in natural populations can be predicted from individual host data when accounting for the infection history of hosts. The predictive power of this model will be compared to traditional models that do not include priority effects.
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