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SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents

Coronavirus disease-19 (COVID-19) emerged in November, 2019 in China and rapidly became pandemic. As with other coronaviruses, a preponderance of evidence suggests the virus originated in horseshoe bats (Rhinolophus spp.) and likely underwent a recombination event in an intermediate host prior to en...

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Autores principales: Fagre, Anna, Lewis, Juliette, Eckley, Miles, Zhan, Shijun, Rocha, Savannah M, Sexton, Nicole R, Burke, Bradly, Geiss, Brian, Peersen, Olve, Kading, Rebekah, Rovnak, Joel, Ebel, Gregory D, Tjalkens, Ronald B, Aboellail, Tawfik, Schountz, Tony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418741/
https://www.ncbi.nlm.nih.gov/pubmed/32793912
http://dx.doi.org/10.1101/2020.08.07.241810
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author Fagre, Anna
Lewis, Juliette
Eckley, Miles
Zhan, Shijun
Rocha, Savannah M
Sexton, Nicole R
Burke, Bradly
Geiss, Brian
Peersen, Olve
Kading, Rebekah
Rovnak, Joel
Ebel, Gregory D
Tjalkens, Ronald B
Aboellail, Tawfik
Schountz, Tony
author_facet Fagre, Anna
Lewis, Juliette
Eckley, Miles
Zhan, Shijun
Rocha, Savannah M
Sexton, Nicole R
Burke, Bradly
Geiss, Brian
Peersen, Olve
Kading, Rebekah
Rovnak, Joel
Ebel, Gregory D
Tjalkens, Ronald B
Aboellail, Tawfik
Schountz, Tony
author_sort Fagre, Anna
collection PubMed
description Coronavirus disease-19 (COVID-19) emerged in November, 2019 in China and rapidly became pandemic. As with other coronaviruses, a preponderance of evidence suggests the virus originated in horseshoe bats (Rhinolophus spp.) and likely underwent a recombination event in an intermediate host prior to entry into human populations. A significant concern is that SARS-CoV-2 could become established in secondary reservoir hosts outside of Asia. To assess this potential, we challenged deer mice (Peromyscus maniculatus) with SARS-CoV-2 and found robust virus replication in the upper respiratory tract, lungs and intestines, with detectable viral RNA for up to 21 days in oral swabs and 14 days in lungs. Virus entry into the brain also occurred, likely via gustatory-olfactory-trigeminal pathway with eventual compromise to the blood brain barrier. Despite this, no conspicuous signs of disease were observed and no deer mice succumbed to infection. Expression of several innate immune response genes were elevated in the lungs, notably IFNα, Cxcl10, Oas2, Tbk1 and Pycard. Elevated CD4 and CD8β expression in the lungs was concomitant with Tbx21, IFNγ and IL-21 expression, suggesting a type I inflammatory immune response. Contact transmission occurred from infected to naive deer mice through two passages, showing sustained natural transmission. In the second deer mouse passage, an insertion of 4 amino acids occurred to fixation in the N-terminal domain of the spike protein that is predicted to form a solvent-accessible loop. Subsequent examination of the source virus from BEI Resources indicated the mutation was present at very low levels, demonstrating potent purifying selection for the insert during in vivo passage. Collectively, this work has determined that deer mice are a suitable animal model for the study of SARS-CoV-2 pathogenesis, and that they have the potential to serve as secondary reservoir hosts that could lead to periodic outbreaks of COVID-19 in North America.
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spelling pubmed-74187412020-08-13 SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents Fagre, Anna Lewis, Juliette Eckley, Miles Zhan, Shijun Rocha, Savannah M Sexton, Nicole R Burke, Bradly Geiss, Brian Peersen, Olve Kading, Rebekah Rovnak, Joel Ebel, Gregory D Tjalkens, Ronald B Aboellail, Tawfik Schountz, Tony bioRxiv Article Coronavirus disease-19 (COVID-19) emerged in November, 2019 in China and rapidly became pandemic. As with other coronaviruses, a preponderance of evidence suggests the virus originated in horseshoe bats (Rhinolophus spp.) and likely underwent a recombination event in an intermediate host prior to entry into human populations. A significant concern is that SARS-CoV-2 could become established in secondary reservoir hosts outside of Asia. To assess this potential, we challenged deer mice (Peromyscus maniculatus) with SARS-CoV-2 and found robust virus replication in the upper respiratory tract, lungs and intestines, with detectable viral RNA for up to 21 days in oral swabs and 14 days in lungs. Virus entry into the brain also occurred, likely via gustatory-olfactory-trigeminal pathway with eventual compromise to the blood brain barrier. Despite this, no conspicuous signs of disease were observed and no deer mice succumbed to infection. Expression of several innate immune response genes were elevated in the lungs, notably IFNα, Cxcl10, Oas2, Tbk1 and Pycard. Elevated CD4 and CD8β expression in the lungs was concomitant with Tbx21, IFNγ and IL-21 expression, suggesting a type I inflammatory immune response. Contact transmission occurred from infected to naive deer mice through two passages, showing sustained natural transmission. In the second deer mouse passage, an insertion of 4 amino acids occurred to fixation in the N-terminal domain of the spike protein that is predicted to form a solvent-accessible loop. Subsequent examination of the source virus from BEI Resources indicated the mutation was present at very low levels, demonstrating potent purifying selection for the insert during in vivo passage. Collectively, this work has determined that deer mice are a suitable animal model for the study of SARS-CoV-2 pathogenesis, and that they have the potential to serve as secondary reservoir hosts that could lead to periodic outbreaks of COVID-19 in North America. Cold Spring Harbor Laboratory 2020-08-07 /pmc/articles/PMC7418741/ /pubmed/32793912 http://dx.doi.org/10.1101/2020.08.07.241810 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Article
Fagre, Anna
Lewis, Juliette
Eckley, Miles
Zhan, Shijun
Rocha, Savannah M
Sexton, Nicole R
Burke, Bradly
Geiss, Brian
Peersen, Olve
Kading, Rebekah
Rovnak, Joel
Ebel, Gregory D
Tjalkens, Ronald B
Aboellail, Tawfik
Schountz, Tony
SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title_full SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title_fullStr SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title_full_unstemmed SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title_short SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for reverse zoonosis to New World rodents
title_sort sars-cov-2 infection, neuropathogenesis and transmission among deer mice: implications for reverse zoonosis to new world rodents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418741/
https://www.ncbi.nlm.nih.gov/pubmed/32793912
http://dx.doi.org/10.1101/2020.08.07.241810
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