SARS-CoV-2-Host Interactions: Implications for Secondary Bacterial Co-infections [Funder: Carleton University COVID-19 Rapid Research Response Grants]

Grant number: unknown

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Key facts

  • Disease

    COVID-19
  • Funder

    Other Funders (Canada)
  • Principal Investigator

    Edana Cassol, Joerg Overhage
  • Research Location

    Canada
  • Lead Research Institution

    Carleton University
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Respiratory viral infections - including human corona viruses - have been shown to predispose patients to bacterial co-infections, which can lead to increased disease severity and mortality. Up to 50% of patients with COVID-19 pneumonia have secondary bacterial infections, but it is unclear if these super infections contribute to disease. In this study, we will use in vitro and in vivo models to investigate if and how SARS-CoV-2 (causative agent of COVID-19) reprograms host immune responses to bacteria. We will also evaluate if this reprogramming drives excessive inflammation and increased lung destruction and damage. These studies will provide critical insights into the ability of SARS-CoV-2 to modulate the host immune responses and may identify new opportunities to inhibit inflammatory damage and prevent the development of secondary bacterial pneumonias in those most at risk.