Rapid Risk Assessment Framework to Estimate Potential for Spillback at Human–Wildlife Interfaces

IF 3.5 2区 农林科学 Q2 INFECTIOUS DISEASES
Travis McDevitt-Galles, Tricia L. Fry, Katherine L. D. Richgels, Daniel A. Grear
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引用次数: 0

Abstract

More than 60% of emerging infectious diseases of humans have a wildlife origin, and when these diseases spread through human populations to new geographical areas, there is a considerable risk of spillback from humans to wildlife species. Spillback events can have severe consequences for wildlife populations, where the disease may cause morbidity and mortality, and human populations, where the establishment in wildlife may lead to prolonged transmission or new exposures in humans. Mitigating these consequences requires identifying the key risk factors that lead to human–wildlife transmission events and implementing risk-reducing actions, a challenge given that cross-species transmission events are rare and often data deficient. To identify potential species and locations that are most likely to lead to these rare events, we developed a spatially explicit, rapid risk assessment framework that incorporates three components of the spillback process: wildlife susceptibility, wildlife exposure, and pathogen introduction pressure. To demonstrate the broad applicability of our framework, we conducted a rapid risk assessment on two recent emerging zoonotic pathogens in humans, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and mpox, to determine the relative spillback risk to wild mammalian species in the continental United States. The rapid risk assessment identified both species and locations with higher than expected spillback risk, providing managers and researchers with valuable information to prioritize surveillance and risk-mitigation actions. Our framework represents a rapid and flexible approach to assess the risks of spillback to wildlife populations during rapidly evolving zoonotic disease outbreaks.

评估人类与野生动物交界面溢油可能性的快速风险评估框架
60%以上的人类新发传染病源于野生动物,当这些疾病通过人群传播到新的地理区域时,存在从人类向野生动物物种溢出的相当大的风险。外溢事件可对野生动物种群和人类种群造成严重后果,野生动物种群中的疾病可能导致发病和死亡,野生动物种群中的疾病可能导致长期传播或人类新的接触。减轻这些后果需要确定导致人类-野生动物传播事件的关键风险因素并实施降低风险的行动,这是一项挑战,因为跨物种传播事件很少,而且往往缺乏数据。为了确定最有可能导致这些罕见事件的潜在物种和地点,我们开发了一个空间明确的快速风险评估框架,该框架包含了溢出过程的三个组成部分:野生动物易感性、野生动物暴露和病原体引入压力。为了证明我们的框架的广泛适用性,我们对最近在人类中出现的两种人畜共患病原体进行了快速风险评估,即严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)和mpox,以确定对美国大陆野生哺乳动物物种的相对溢出风险。快速风险评估确定了溢漏风险高于预期的物种和地点,为管理人员和研究人员提供了有价值的信息,以确定监测和减轻风险行动的优先次序。我们的框架提供了一种快速和灵活的方法来评估在快速演变的人畜共患疾病暴发期间对野生动物种群溢出的风险。
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来源期刊
Transboundary and Emerging Diseases
Transboundary and Emerging Diseases 农林科学-传染病学
CiteScore
8.90
自引率
9.30%
发文量
350
审稿时长
1 months
期刊介绍: Transboundary and Emerging Diseases brings together in one place the latest research on infectious diseases considered to hold the greatest economic threat to animals and humans worldwide. The journal provides a venue for global research on their diagnosis, prevention and management, and for papers on public health, pathogenesis, epidemiology, statistical modeling, diagnostics, biosecurity issues, genomics, vaccine development and rapid communication of new outbreaks. Papers should include timely research approaches using state-of-the-art technologies. The editors encourage papers adopting a science-based approach on socio-economic and environmental factors influencing the management of the bio-security threat posed by these diseases, including risk analysis and disease spread modeling. Preference will be given to communications focusing on novel science-based approaches to controlling transboundary and emerging diseases. The following topics are generally considered out-of-scope, but decisions are made on a case-by-case basis (for example, studies on cryptic wildlife populations, and those on potential species extinctions): Pathogen discovery: a common pathogen newly recognised in a specific country, or a new pathogen or genetic sequence for which there is little context about — or insights regarding — its emergence or spread. Prevalence estimation surveys and risk factor studies based on survey (rather than longitudinal) methodology, except when such studies are unique. Surveys of knowledge, attitudes and practices are within scope. Diagnostic test development if not accompanied by robust sensitivity and specificity estimation from field studies. Studies focused only on laboratory methods in which relevance to disease emergence and spread is not obvious or can not be inferred (“pure research” type studies). Narrative literature reviews which do not generate new knowledge. Systematic and scoping reviews, and meta-analyses are within scope.
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