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Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection

Bats are natural reservoirs for several zoonotic viruses, potentially due to an enhanced capacity to control viral infection. However, the mechanisms of antiviral responses in bats are poorly defined. Here we established a Jamaican fruit bat (JFB) intestinal organoid model of severe acute respirator...

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Detalles Bibliográficos
Autores principales: Hashimi, Marziah, Sebrell, Thomas, Hedges, Jodi, Snyder, Deann, Lyon, Katrina, Byrum, Stephanie, Mackintosh, Samuel G, Cherne, Michelle, Skwarchuk, David, Crowley, Dan, Robison, Amanda, Sidar, Barkan, Kunze, Anja, Loveday, Emma, Taylor, Matthew, Chang, Connie, Wilking, James, Walk, Seth, Schountz, Tony, Jutila, Mark, Bimczok, Diane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774215/
https://www.ncbi.nlm.nih.gov/pubmed/36561186
http://dx.doi.org/10.21203/rs.3.rs-2340919/v1
Descripción
Sumario:Bats are natural reservoirs for several zoonotic viruses, potentially due to an enhanced capacity to control viral infection. However, the mechanisms of antiviral responses in bats are poorly defined. Here we established a Jamaican fruit bat (JFB) intestinal organoid model of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. JFB organoids were susceptible to SARS-CoV-2 infection, with increased viral RNA and subgenomic RNA detected in cell lysates and supernatants. Gene expression of type I interferons and inflammatory cytokines was induced in response to SARS-CoV-2 but not in response to TLR agonists. Interestingly, SARS-CoV-2 did not lead to cytopathic effects in JFB organoids but caused enhanced organoid growth. Proteomic analyses revealed an increase in inflammatory signaling, cell turnover, cell repair, and SARS-CoV-2 infection pathways. Collectively, our findings suggest that primary JFB intestinal epithelial cells can mount a successful antiviral interferon response and that SARS-CoV-2 infection in JFB cells induces protective regenerative pathways.