Defining Long Term Neurological Consequences Following Asymptomatic ZIKV Infection

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

Grant number: 1F31NS143386-01

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Key facts

  • Disease

    Zika virus disease, Congenital infection caused by Zika virus
  • Start & end year

    2025
    2028
  • Known Financial Commitments (USD)

    $39,298
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    GRADUATE STUDENT Evan DaPrano
  • Research Location

    United States of America
  • Lead Research Institution

    RUTGERS, THE STATE UNIV OF N.J.
  • 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

Project Summary Recent work has underscored the potential for chronic neurological consequences following systemic viral infections. Although mild and asymptomatic cases make up the vast majority of human viral infections, studies in this area to date have overwhelmingly focused on models of severe viral infection and encephalitis. Zika virus is an emerging flavivirus of global concern that is most known for its connection with congenital sequalae following infection in utero. However, despite possessing tropism for neurons, astrocytes, and neural progenitors, infection in healthy adults is asymptomatic in approximately 80% of cases. We have developed an immunocompetent mouse model of systemic ZIKV infection in which infected animals do not display any clinical illness or differences in weight gain, despite ZIKV being detectable in the brain. In this asymptomatic model, we demonstrate leukocyte recruitment into the brain and the establishment of brain tissue resident memory cells (TRMs) up to 32 weeks post infection. Transcriptomic and metabolomic approaches demonstrate dysfunction in pathways related to inflammation, neurodegeneration, and senescence in the postinfectious brain, while computationally driven behavioral approaches illustrate perturbed movement patterns in freely moving mice at 32 weeks post infection. Based on their deleterious role in other neurotropic infections, we propose that CD8 T cell residence in the brain contributes to the induction and maintenance of these deficits. We thus hypothesize that depletion of CD8 T cells during acute infection will prevent these phenotypes. Results from this proposal will define the neurologic consequences of asymptomatic ZIKV infection while describing roles for CD8 T cells in promoting neurologic sequelae in the postinfectious brain.