CAREER: The role of phenological mismatch and climate refugia in the ecology of infectious disease under global change

  • Funded by National Science Foundation (NSF)
  • Total publications:1 publications

Grant number: 2339209

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Key facts

  • Disease

    West Nile Virus Infection
  • Start & end year

    2024
    2029
  • Known Financial Commitments (USD)

    $977,779
  • Funder

    National Science Foundation (NSF)
  • Principal Investigator

    Andrew MacDonald
  • Research Location

    United States of America
  • Lead Research Institution

    University of California-Santa Barbara
  • Research Priority Alignment

    N/A
  • Research Category

    Animal and environmental research and research on diseases vectors

  • Research Subcategory

    Animal source and routes of transmission

  • Special Interest Tags

    Data Management and Data Sharing

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Global change, including climate and land use change, is shifting when and where species are active. For many infectious diseases, multiple species are involved in the amplification or dampening of disease risk and these species can be differentially affected by environmental conditions. For example, if the available suite of species upon which mosquito vectors of disease feed are not very effective at carrying the pathogen, disease risk may decrease even if mosquitoes are abundant. Alternatively, if the vector is active when effective hosts are abundant, disease risk likely increases more than otherwise expected. Thus, how disease risk will change will not only be determined by mosquito responses to environmental change, but how animal hosts of disease respond to these same processes. Using West Nile virus (WNV) in California's Central Valley as a case study, this project will investigate how seasonal activity of mosquito vectors and bird hosts will respond to environmental change, and whether and where activity of mosquitos and birds is likely to become more, or less synchronous as climate changes. More synchronous activity will likely increase disease transmission and human health risks. This project will also develop teaching materials and provide hands-on learning opportunities for underrepresented community college students in the Central Valley, develop outreach materials for communicating changing health risks to the public, and train undergraduates, graduate students and postdoctoral scholars in quantitative methods for predicting infectious disease dynamics. This project addresses three key questions at the interface of community ecology, global change ecology, and human health: 1) whether the degree of phenological synchrony between mosquito vectors and bird hosts predicts WNV activity, 2) how future scenarios of mosquito and bird host phenology might interact to change WNV prevalence and future transmission risk, and 3) how land use could modify phenological mismatch, creating climate refugia for vector-host interactions and pathogen transmission. This research will leverage a combination of machine learning-based species distribution modeling, causal inference statistical approaches, citizen science, and vector surveillance data. Together those approaches will be used to model mosquito and bird host phenology, its influence on West Nile virus infection rates in mosquitos, and potential future phenological mismatch. The project will also include field-based data collection for model validation, as well as associated public outreach and educational opportunities for underrepresented community college students in the Central Valley of California. This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

Publicationslinked via Europe PMC

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Remote sensing of temperature-dependent mosquito and viral traits predicts field surveillance-based disease risk.