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SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts

Vaccines are urgently needed to combat the global coronavirus disease 2019 (COVID-19) pandemic, and testing of candidate vaccines in an appropriate non-human primate (NHP) model is a critical step in the process. Infection of African green monkeys (AGM) with a low passage human isolate of SARS-CoV-2...

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Autores principales: Hartman, Amy L., Nambulli, Sham, McMillen, Cynthia M., White, Alexander G., Tilston-Lunel, Natasha Louise, Albe, Joseph R., Cottle, Emily, Dunn, Matthew D., Frye, L. James, Gilliland, Theron H., Olsen, Emily L., O’Malley, Katherine J., Schwarz, Madeline M., Tomko, Jaime A., Walker, Reagan C., Xia, Mengying, Hartman, Matthew S., Klein, Edwin, Scanga, Charles A., Flynn, JoAnne L., Klimstra, William B., McElroy, Anita K., Reed, Douglas S., Duprex, W. Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7535860/
https://www.ncbi.nlm.nih.gov/pubmed/32946524
http://dx.doi.org/10.1371/journal.ppat.1008903
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author Hartman, Amy L.
Nambulli, Sham
McMillen, Cynthia M.
White, Alexander G.
Tilston-Lunel, Natasha Louise
Albe, Joseph R.
Cottle, Emily
Dunn, Matthew D.
Frye, L. James
Gilliland, Theron H.
Olsen, Emily L.
O’Malley, Katherine J.
Schwarz, Madeline M.
Tomko, Jaime A.
Walker, Reagan C.
Xia, Mengying
Hartman, Matthew S.
Klein, Edwin
Scanga, Charles A.
Flynn, JoAnne L.
Klimstra, William B.
McElroy, Anita K.
Reed, Douglas S.
Duprex, W. Paul
author_facet Hartman, Amy L.
Nambulli, Sham
McMillen, Cynthia M.
White, Alexander G.
Tilston-Lunel, Natasha Louise
Albe, Joseph R.
Cottle, Emily
Dunn, Matthew D.
Frye, L. James
Gilliland, Theron H.
Olsen, Emily L.
O’Malley, Katherine J.
Schwarz, Madeline M.
Tomko, Jaime A.
Walker, Reagan C.
Xia, Mengying
Hartman, Matthew S.
Klein, Edwin
Scanga, Charles A.
Flynn, JoAnne L.
Klimstra, William B.
McElroy, Anita K.
Reed, Douglas S.
Duprex, W. Paul
author_sort Hartman, Amy L.
collection PubMed
description Vaccines are urgently needed to combat the global coronavirus disease 2019 (COVID-19) pandemic, and testing of candidate vaccines in an appropriate non-human primate (NHP) model is a critical step in the process. Infection of African green monkeys (AGM) with a low passage human isolate of SARS-CoV-2 by aerosol or mucosal exposure resulted in mild clinical infection with a transient decrease in lung tidal volume. Imaging with human clinical-grade (18)F-fluoro-2-deoxy-D-glucose positron emission tomography ((18)F-FDG PET) co-registered with computed tomography (CT) revealed pulmonary lesions at 4 days post-infection (dpi) that resolved over time. Infectious virus was shed from both respiratory and gastrointestinal (GI) tracts in all animals in a biphasic manner, first between 2–7 dpi followed by a recrudescence at 14–21 dpi. Viral RNA (vRNA) was found throughout both respiratory and gastrointestinal systems at necropsy with higher levels of vRNA found within the GI tract tissues. All animals seroconverted simultaneously for IgM and IgG, which has also been documented in human COVID-19 cases. Young AGM represent an species to study mild/subclinical COVID-19 disease and with possible insights into live virus shedding. Future vaccine evaluation can be performed in AGM with correlates of efficacy being lung lesions by PET/CT, virus shedding, and tissue viral load.
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spelling pubmed-75358602020-10-15 SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts Hartman, Amy L. Nambulli, Sham McMillen, Cynthia M. White, Alexander G. Tilston-Lunel, Natasha Louise Albe, Joseph R. Cottle, Emily Dunn, Matthew D. Frye, L. James Gilliland, Theron H. Olsen, Emily L. O’Malley, Katherine J. Schwarz, Madeline M. Tomko, Jaime A. Walker, Reagan C. Xia, Mengying Hartman, Matthew S. Klein, Edwin Scanga, Charles A. Flynn, JoAnne L. Klimstra, William B. McElroy, Anita K. Reed, Douglas S. Duprex, W. Paul PLoS Pathog Research Article Vaccines are urgently needed to combat the global coronavirus disease 2019 (COVID-19) pandemic, and testing of candidate vaccines in an appropriate non-human primate (NHP) model is a critical step in the process. Infection of African green monkeys (AGM) with a low passage human isolate of SARS-CoV-2 by aerosol or mucosal exposure resulted in mild clinical infection with a transient decrease in lung tidal volume. Imaging with human clinical-grade (18)F-fluoro-2-deoxy-D-glucose positron emission tomography ((18)F-FDG PET) co-registered with computed tomography (CT) revealed pulmonary lesions at 4 days post-infection (dpi) that resolved over time. Infectious virus was shed from both respiratory and gastrointestinal (GI) tracts in all animals in a biphasic manner, first between 2–7 dpi followed by a recrudescence at 14–21 dpi. Viral RNA (vRNA) was found throughout both respiratory and gastrointestinal systems at necropsy with higher levels of vRNA found within the GI tract tissues. All animals seroconverted simultaneously for IgM and IgG, which has also been documented in human COVID-19 cases. Young AGM represent an species to study mild/subclinical COVID-19 disease and with possible insights into live virus shedding. Future vaccine evaluation can be performed in AGM with correlates of efficacy being lung lesions by PET/CT, virus shedding, and tissue viral load. Public Library of Science 2020-09-18 /pmc/articles/PMC7535860/ /pubmed/32946524 http://dx.doi.org/10.1371/journal.ppat.1008903 Text en © 2020 Hartman et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hartman, Amy L.
Nambulli, Sham
McMillen, Cynthia M.
White, Alexander G.
Tilston-Lunel, Natasha Louise
Albe, Joseph R.
Cottle, Emily
Dunn, Matthew D.
Frye, L. James
Gilliland, Theron H.
Olsen, Emily L.
O’Malley, Katherine J.
Schwarz, Madeline M.
Tomko, Jaime A.
Walker, Reagan C.
Xia, Mengying
Hartman, Matthew S.
Klein, Edwin
Scanga, Charles A.
Flynn, JoAnne L.
Klimstra, William B.
McElroy, Anita K.
Reed, Douglas S.
Duprex, W. Paul
SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title_full SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title_fullStr SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title_full_unstemmed SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title_short SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
title_sort sars-cov-2 infection of african green monkeys results in mild respiratory disease discernible by pet/ct imaging and shedding of infectious virus from both respiratory and gastrointestinal tracts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7535860/
https://www.ncbi.nlm.nih.gov/pubmed/32946524
http://dx.doi.org/10.1371/journal.ppat.1008903
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