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Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques

Middle East respiratory syndrome coronavirus (MERS-CoV) has recently emerged in the Middle East. Since 2012, there have been approximately 2,100 confirmed cases, with a 35% case fatality rate. Disease severity has been linked to patient health status, as people with chronic diseases or an immunocomp...

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Autores principales: Prescott, Joseph, Falzarano, Darryl, de Wit, Emmie, Hardcastle, Kath, Feldmann, Friederike, Haddock, Elaine, Scott, Dana, Feldmann, Heinz, Munster, Vincent Jacobus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816332/
https://www.ncbi.nlm.nih.gov/pubmed/29483914
http://dx.doi.org/10.3389/fimmu.2018.00205
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author Prescott, Joseph
Falzarano, Darryl
de Wit, Emmie
Hardcastle, Kath
Feldmann, Friederike
Haddock, Elaine
Scott, Dana
Feldmann, Heinz
Munster, Vincent Jacobus
author_facet Prescott, Joseph
Falzarano, Darryl
de Wit, Emmie
Hardcastle, Kath
Feldmann, Friederike
Haddock, Elaine
Scott, Dana
Feldmann, Heinz
Munster, Vincent Jacobus
author_sort Prescott, Joseph
collection PubMed
description Middle East respiratory syndrome coronavirus (MERS-CoV) has recently emerged in the Middle East. Since 2012, there have been approximately 2,100 confirmed cases, with a 35% case fatality rate. Disease severity has been linked to patient health status, as people with chronic diseases or an immunocompromised status fare worse, although the mechanisms of disease have yet to be elucidated. We used the rhesus macaque model of mild MERS to investigate whether the immune response plays a role in the pathogenicity in relation to MERS-CoV shedding. Immunosuppressed macaques were inoculated with MERS-CoV and sampled daily for 6 days to assess their immune statues and to measure viral shedding and replication. Immunosuppressed macaques supported significantly higher levels of MERS-CoV replication in respiratory tissues and shed more virus, and virus disseminated to tissues outside of the respiratory tract, whereas viral RNA was confined to respiratory tissues in non-immunosuppressed animals. Despite increased viral replication, pathology in the lungs was significantly lower in immunosuppressed animals. The observation that the virus was less pathogenic in these animals suggests that disease has an immunopathogenic component and shows that inflammatory responses elicited by the virus contribute to disease.
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spelling pubmed-58163322018-02-26 Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques Prescott, Joseph Falzarano, Darryl de Wit, Emmie Hardcastle, Kath Feldmann, Friederike Haddock, Elaine Scott, Dana Feldmann, Heinz Munster, Vincent Jacobus Front Immunol Immunology Middle East respiratory syndrome coronavirus (MERS-CoV) has recently emerged in the Middle East. Since 2012, there have been approximately 2,100 confirmed cases, with a 35% case fatality rate. Disease severity has been linked to patient health status, as people with chronic diseases or an immunocompromised status fare worse, although the mechanisms of disease have yet to be elucidated. We used the rhesus macaque model of mild MERS to investigate whether the immune response plays a role in the pathogenicity in relation to MERS-CoV shedding. Immunosuppressed macaques were inoculated with MERS-CoV and sampled daily for 6 days to assess their immune statues and to measure viral shedding and replication. Immunosuppressed macaques supported significantly higher levels of MERS-CoV replication in respiratory tissues and shed more virus, and virus disseminated to tissues outside of the respiratory tract, whereas viral RNA was confined to respiratory tissues in non-immunosuppressed animals. Despite increased viral replication, pathology in the lungs was significantly lower in immunosuppressed animals. The observation that the virus was less pathogenic in these animals suggests that disease has an immunopathogenic component and shows that inflammatory responses elicited by the virus contribute to disease. Frontiers Media S.A. 2018-02-12 /pmc/articles/PMC5816332/ /pubmed/29483914 http://dx.doi.org/10.3389/fimmu.2018.00205 Text en Copyright © 2018 Prescott, Falzarano, de Wit, Hardcastle, Feldmann, Haddock, Scott, Feldmann and Munster. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Prescott, Joseph
Falzarano, Darryl
de Wit, Emmie
Hardcastle, Kath
Feldmann, Friederike
Haddock, Elaine
Scott, Dana
Feldmann, Heinz
Munster, Vincent Jacobus
Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title_full Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title_fullStr Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title_full_unstemmed Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title_short Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques
title_sort pathogenicity and viral shedding of mers-cov in immunocompromised rhesus macaques
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816332/
https://www.ncbi.nlm.nih.gov/pubmed/29483914
http://dx.doi.org/10.3389/fimmu.2018.00205
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