Virus cross-species transmission. Defining the immunological barriers to viral emergence

  • Funded by UK Research and Innovation (UKRI)
  • Total publications:15 publications

Grant number: MC_UU_00034/3

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Key facts

  • Disease

    Unspecified, Disease X
  • Start & end year

    2023
    2028
  • Known Financial Commitments (USD)

    $3,732,651.09
  • Funder

    UK Research and Innovation (UKRI)
  • Principal Investigator

    Massimo Palmarini
  • Research Location

    United Kingdom
  • Lead Research Institution

    University of Glasgow
  • 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

    Unspecified

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Humans are constantly exposed to a variety of animal viruses. Understanding why most of these viruses fail to spillover and thrive in human populations is crucial to devise optimal strategies to manage viral emergence. Our programme aims to understand diverse immunological barriers to virus cross-species transmission. Our hypothesis is that the genetic and immunological variability of each individual or species helps define susceptibility or resistance to virus cross-species transmission. Our first aim is to identify those genes that are activated immediately after virus infection (known as interferon-stimulated genes, ISGs) and block respiratory viruses. Our second aim is to create a risk assessment framework to identify those specific viral proteins (and specific amino acid residues within the proteins) that favour the spillover of avian influenza viruses into the human population. The third and last aim of the programme is to understand the antibody landscape in humans and selected animal species, in order to estimate the impact of cross-neutralising antibodies and, at the population level, cross-immunity on constraining viral emergence. At the end of this programme, we will be able to translate our discoveries by delivering actionable data that can support the risk assessment of the zoonotic potential of viruses.

Publicationslinked via Europe PMC

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View all publications at Europe PMC

Diverse behavioural responses of vampire bats to human disturbance revealed by state-space modelling of sparse GPS data

Ecology and evolutionary trajectories of morbilliviruses in Neotropical bats.

MITD1 is a brain-specific interferon-inducible factor that inhibits flavivirus replication.

Smallpox vaccination campaigns resulted in age-associated population cross-immunity against monkeypox virus.

Evolution of enhanced innate immune suppression by SARS-CoV-2 Omicron subvariants.

Resurrection of 2'-5'-oligoadenylate synthetase 1 (OAS1) from the ancestor of modern horseshoe bats blocks SARS-CoV-2 replication.

Phenotyping the virulence of SARS-CoV-2 variants in hamsters by digital pathology and machine learning.

SARS-CoV-2 variants evolve convergent strategies to remodel the host response.

Detection of antimicrobial-resistant Enterobacterales in insectivorous bats from Chile.