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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2022
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Hashimi, Marziah |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9774215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-97742152022-12-23 Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection 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 Res Sq Article 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. American Journal Experts 2022-12-12 /pmc/articles/PMC9774215/ /pubmed/36561186 http://dx.doi.org/10.21203/rs.3.rs-2340919/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article 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 Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title | Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title_full | Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title_fullStr | Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title_full_unstemmed | Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title_short | Antiviral response mechanisms in a Jamaican Fruit Bat intestinal organoid model of SARS-CoV-2 infection |
title_sort | antiviral response mechanisms in a jamaican fruit bat intestinal organoid model of sars-cov-2 infection |
topic | Article |
url | 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 |
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