Disentangling the human vector relationship to disrupt dengue and chikungunya virus outbreaks in Kenya

理清人类媒介关系以阻止肯尼亚登革热和基孔肯雅病毒的爆发

• 批准号: 9927557
• 负责人: Angelle Desiree LaBeaud
• 金额: $ 67.66万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-05 至 2024-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9927557
• 关键词: Address; Aedes; Africa South of the Sahara; African; Antiviral Agents; Arbovirus Infections; Arboviruses; Behavior; Behavioral; Blood Circulation; Breeding; Cellular Phone; Characteristics; Chikungunya virus; Climate; Clinical; Communities; Country; Coupled; Culicidae; Data; Decision Making; Dengue; Dengue Infection; Dengue Virus; Detection; Diagnosis; Diagnostic; Disease; Disease Outbreaks; Entomology; Environmental Risk Factor; Epidemic; Etiology; Exposure to; Fever; Future; Goals; Habitats; Habits; High Prevalence; Human; Human Activities; Incidence; Infection; Influentials; Intervention; Kenya; Knowledge; Lead; Link; Location; Longitudinal Studies; Maintenance; Maps; Measurable; Measures; Modeling; Mosquito Control; Movement; Pathway Analysis; Pattern; Periodicity; Pharmaceutical Preparations; Policies; Policy Maker; Population; Prevention; Probability; Public Health; Research; Risk; Risk Behaviors; Seasonal Variations; Seasons; Sequence Analysis; Statistical Models; Syndrome; Time; Time Series Analysis; Viral; Viral Vaccines; Virus; Weather; arm; base; burden of illness; chikungunya; chikungunya infection; cohort; design; disability; evidence base; exposed human population; feeding; implementation trial; in silico; new technology; novel strategies; predictive modeling; prevent; programs; simulation; time use; transmission process; urban planning; vector

In sub-Saharan Africa, routine passive surveillance for dengue (DENV) and chikungunya (CHIKV) viruses detects only a fraction of their impact, given the high probability of misdiagnosis and unstudied levels of transmission across different landscapes and within different susceptible populations. Known and unknown entomologic, environmental, and behavioral factors differentially drive transmission in different habitats. The lack of systematic surveillance and accurate diagnostics coupled with low levels of clinical suspicion all lead to under-diagnosis in the African setting and the inability to prevent outbreaks. In this renewal proposal, our hypothesis is that ongoing endemic transmission leads to potential for outbreaks that is modified by measurable factors (human movement and behavior patterns, weather/climate, and viral importations/introductions), and that this transition is predictable and preventable. The objective of these studies is to detail the dominant factors that facilitate epidemic transmission at the human-vector interface and to identify opportunities to blockade them. In order to define key drivers of outbreaks, we plan to: 1) Measure mosquito abundance in space and time; 2) Better define human-vector exposure using novel technology; 3) Identify human attributes such as movement and behavior that contribute to increased exposure; 4) Understand if outbreaks are due to new viral introductions or endemic viral strains and; 5) Identify the most influential drivers of ongoing human transmission and outbreak initiation and then use modeling to compare the potential impact of intervention strategies. Using novel approaches, we address the following aims: 1) Define time periods of increased vector abundance and increased risk for human transmission to delineate thresholds for dengue and chikungunya epidemic transition; 2) Detail locations with increased vector abundance and increased risk for human transmission; 3) Identify whether documented infection clusters occur due to importation/introduction vs. endemic transmission; and 4) Model outbreaks for predictive impact to inform policy. This research is based on 15 years of collaborative longitudinal studies and involves cohorts in Mombasa (coastal) and Kisumu (western), Kenya, where there is year-round transmission and documented recent outbreaks of DENV and CHIKV. These studies will fill knowledge gaps about the persistence of CHIKV and DENV in local habitats and the factors that contribute to outbreak transmission in varied settings. The data will also answer fundamental questions about arboviral etiologies in fever syndromes, while providing best estimates of related disease burden and long-term sequelae.

在撒哈拉以南非洲，对登革热(DENV)和基孔肯雅(CHIKV)病毒的常规被动监测只能检测到其影响的一小部分，因为误诊的可能性很高，而且在不同地形和不同易感人群中的传播水平未经研究。已知和未知的昆虫学、环境和行为因素在不同的生境中以不同的方式驱动传播。缺乏系统的监测和准确的诊断，加上临床怀疑程度低，都导致非洲的诊断不足，无法预防疫情暴发。在这项更新建议中，我们的假设是，持续的地方性传播导致爆发的可能性被可测量的因素(人类活动和行为模式、天气/气候和病毒输入/引入)所改变，并且这种转变是可预测和可预防的。这些研究的目的是详细说明在人-病媒界面促进流行病传播的主导因素，并找出封锁这些因素的机会。为了确定暴发的关键驱动因素，我们计划：1)测量蚊子在空间和时间上的丰度；2)使用新技术更好地定义人类媒介暴露；3)确定导致暴露增加的人类属性，如运动和行为；4)了解暴发是由于新的病毒引入还是地方性病毒株；以及5)确定持续的人类传播和暴发引发的最具影响力的驱动因素，然后使用建模来比较干预策略的潜在影响。使用新的方法，我们解决以下目标：1)定义媒介丰度增加和人类传播风险增加的时间段，以划定登革热和基孔肯雅热疫情过渡的阈值；2)媒介丰度增加和人类传播风险增加的详细地点；3)确定有记录的感染聚集性是否由于输入/引入和地方性传播而发生；以及4)为预测影响建立疫情模型，以便为政策提供信息。这项研究基于15年的纵向合作研究，涉及肯尼亚蒙巴萨(沿海)和基苏木(西部)的队列，那里常年传播DENV和CHIKV，并记录了最近的疫情。这些研究将填补有关CHIKV和DENV在当地生境中的持久性以及在不同环境中导致暴发传播的因素的知识空白。这些数据还将回答有关发烧综合征的虫媒病毒病因的基本问题，同时提供对相关疾病负担和长期后遗症的最佳估计。