RAPID: Comparative genomics of SARS-CoV-2 susceptibility and immune defense in mammals

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

Grant number: 2029774

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $199,767
  • Funder

    National Science Foundation (NSF)
  • Principal Investigator

    Elinor Karlsson
  • Research Location

    United States of America
  • Lead Research Institution

    University of Massachusetts Medical School
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen morphology, shedding & natural history

  • 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

Biological Sciences - The goal of this project is to compare genomes of hundreds of mammal species, finding differences in DNA that distinguish species resistant to SARS-CoV-2 from those that are very susceptible. This information is needed to understand how the current SARS-CoV-2 virus spread to humans and to identify potential host animals (e.g., pet, livestock, and pest species) that may be susceptible to SARS-CoV-2 in the USA. SARS-CoV-2, the cause of the COVID-19 pandemic, can infect diverse species of animals. There is a variation in susceptibility to and severity of disease between species. This variation suggests that some species have genetic differences that dictate susceptibility to COVID-19. This work will identify how coronaviruses adapt to new host species, information that will help predict and control future coronavirus outbreaks. Funding will support training a graduate student in research, thereby training the next generation of the bioeconomy workforce.

This project will investigate how the host genome shapes host-pathogen interactions, and how coronaviruses like SARS-CoV-2 evolve to exploit new hosts. The researchers will compare existing genomic data for hundreds of mammals using three complementary approaches: (1) Measure structural and sequence homology in two host proteins, ACE2 and TMPRSS2, necessary for infection in humans; (2) Analyze existing RNA-seq datasets to (a) identify species with co-expression of ACE2 and TMPRSS2, and potentially other proteases implicated in infection, in the same tissue, and (b) search for incidental coronaviral sequence data from diverse mammalian species; (3) Test for variants in evolutionarily conserved elements that are correlated with species susceptibility, using forward genomics. With these analyses, the researchers will identify species with potential as reservoirs for SARS-CoV-2 viral spillback into humans, and those that are promising systems for investigating SARS-CoV-2 evolution, host defenses, and host-pathogen interactions. This RAPID award is made by the Physiological and Structural Systems Cluster in the BIO Division of Integrative Organismal Systems, using funds from the Coronavirus Aid, Relief, and Economic Security (CARES) Act.

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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Broad host range of SARS-CoV-2 predicted by comparative and structural analysis of ACE2 in vertebrates.