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In Vivo Investigation of Filovirus Glycoprotein-Mediated Infection in a BSL2 Setting
Journal article

In Vivo Investigation of Filovirus Glycoprotein-Mediated Infection in a BSL2 Setting

Paige T Richards, Jose Alberto Aguilar Briseño, Bethany A Brunton and Wendy Maury
Methods in molecular biology (Clifton, N.J.), Vol.2877, pp.183-198
2025
DOI: 10.1007/978-1-0716-4256-6_13
PMCID: PMC11727417
PMID: 39585622
url
https://pmc.ncbi.nlm.nih.gov/articles/PMC11727417/pdf/nihms-2043982.pdfView
Open Access

Abstract

Highly pathogenic viruses in the Filoviridae family are causative agents of filovirus disease (FVD). Ebola virus (EBOV) is one such member and, of all filoviruses, represents the largest threat to global public health. The study of FVD has been hampered by the lack of tools to study filovirus infection outside maximum containment laboratories. Recombinant vesicular stomatitis virus (VSV) lacking its native glycoprotein and expressing a filovirus glycoprotein (VSV-filo GP) has improved our understanding of GP-mediated host-cell interactions as well as adaptive and humoral immune responses in in vitro and in vivo studies. Furthermore, mouse models suitable for these studies are readily available. Here, we describe multiple injection routes for investigating filovirus GP-mediated infection and pathogenesis using VSV-filo GP and interferon α/β receptor-deficient (Ifnar ) mice as models. These tools can be safely used outside maximum containment laboratories, are cost effective, and easy to manipulate.
Animals Containment of Biohazards - methods Disease Models, Animal Ebolavirus - genetics Ebolavirus - pathogenicity Filoviridae - genetics Filoviridae - pathogenicity Filoviridae Infections - virology Glycoproteins - genetics Glycoproteins - metabolism Humans Mice Mice, Knockout Receptor, Interferon alpha-beta - deficiency Receptor, Interferon alpha-beta - genetics Receptor, Interferon alpha-beta - metabolism Vesiculovirus - genetics Vesiculovirus - physiology Viral Envelope Proteins - genetics Viral Envelope Proteins - metabolism

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