Establishment of a Bat Resource for Infectious Disease Research

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 5U24AI165424-03

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Key facts

  • Disease

    COVID-19, Infection caused by Nipah virus
  • Start & end year

    2023.0
    2028.0
  • Known Financial Commitments (USD)

    $2,193,256
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    ASSOCIATE PROFESSOR William Schountz
  • Research Location

    United States of America
  • Lead Research Institution

    COLORADO STATE UNIVERSITY
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    N/A

  • 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

Bats are reservoirs, or suspected reservoirs, of many zoonotic viruses, including SARS, SARS2 and MERS coronaviruses, and Ebola, Sudan and Marburg viruses. Little is known about how these viruses circulate in their bat reservoirs, principally because of a lack of bat colonies that can be used for the development of experimental infection models. To address this deficiency, we have established a breeding colony of Jamaican fruit bats (Artibeus jamaicensis) and will establish a breeding colony of Egyptian fruit bats (Rousettus aegyptiacus) as a resource for investigators who study these viruses. Egyptian fruit bats are the principal natural reservoir of Marburg virus and Sosuga virus, both of which are human pathogens. Jamaican fruit bats are the best studied bat model for infectious diseases and we have demonstrated that they are a model organism for Ebola and Marburg virus infections. We will generate primary cell cultures and immortalized cell lines from various tissues from these species and freeze live bone marrow that will be useful for studying how these viruses infect bat cells, and how the viruses may modulate the innate immune responses. Recombinant cytokines will also be produced for the research community, including those for generating macrophages and dendritic cells (GM-CSF, Flt3L), T cells (IL-2, IL-7, IL-15) and for in vivo modulation of the adaptive immune response (IFNγ, IL-4). Moreover, we will generate monoclonal antibodies for use in cytokine detection assays and flow cytometry of immune cell subsets and in vivo neutralization. Finally, we will perform experimental infection studies of with ebolaviruses, Sosuga virus, and the SARS- related coronaviruses, BANAL-52 and BANAL-236, to study the infection kinetics, virus distribution and transcriptomic, proteomic and metabolomic profiles of bats during infection, and escalation and resolution of the immune response. Tissues, cells and sera from naïve and infected bats will be archived in a biobank that will be made available to the research community upon virus inactivation. The establishment of this resource will lead to a better understanding of how bats host highly pathogenic viruses without disease and may shed light on events that increase spillover risks to humans. In turn, this information could lead to development of mitigation strategies to prevent future virus spillover and uncover new strategies for therapeutic treatment of coronavirus and Nipah virus diseases.