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author Serrano, Geidy E.
Walker, Jessica E.
Arce, Richard
Glass, Michael J.
Vargas, Daisy
Sue, Lucia I.
Intorcia, Anthony J.
Nelson, Courtney M.
Oliver, Javon
Papa, Jaclyn
Russell, Aryck
Suszczewicz, Katsuko E.
Borja, Claryssa I.
Belden, Christine
Goldfarb, Danielle
Shprecher, David
Atri, Alireza
Adler, Charles H.
Shill, Holly A.
Driver-Dunckley, Erika
Mehta, Shyamal H.
Readhead, Benjamin
Huentelman, Matthew J.
Peters, Joseph L.
Alevritis, Ellie
Bimi, Christian
Mizgerd, Joseph P.
Reiman, Eric M.
Montine, Thomas J.
Desforges, Marc
Zehnder, James L.
Sahoo, Malaya K.
Zhang, Haiyu
Solis, Daniel
Pinsky, Benjamin A.
Deture, Michael
Dickson, Dennis W.
Beach, Thomas G.
author_facet Serrano, Geidy E.
Walker, Jessica E.
Arce, Richard
Glass, Michael J.
Vargas, Daisy
Sue, Lucia I.
Intorcia, Anthony J.
Nelson, Courtney M.
Oliver, Javon
Papa, Jaclyn
Russell, Aryck
Suszczewicz, Katsuko E.
Borja, Claryssa I.
Belden, Christine
Goldfarb, Danielle
Shprecher, David
Atri, Alireza
Adler, Charles H.
Shill, Holly A.
Driver-Dunckley, Erika
Mehta, Shyamal H.
Readhead, Benjamin
Huentelman, Matthew J.
Peters, Joseph L.
Alevritis, Ellie
Bimi, Christian
Mizgerd, Joseph P.
Reiman, Eric M.
Montine, Thomas J.
Desforges, Marc
Zehnder, James L.
Sahoo, Malaya K.
Zhang, Haiyu
Solis, Daniel
Pinsky, Benjamin A.
Deture, Michael
Dickson, Dennis W.
Beach, Thomas G.
author_sort Serrano, Geidy E.
collection PubMed
description The coronavirus SARS-CoV-2 (SCV2) causes acute respiratory distress, termed COVID-19 disease, with substantial morbidity and mortality. As SCV2 is related to previously-studied coronaviruses that have been shown to have the capability for brain invasion, it seems likely that SCV2 may be able to do so as well. To date, although there have been many clinical and autopsy-based reports that describe a broad range of SCV2-associated neurological conditions, it is unclear what fraction of these have been due to direct CNS invasion versus indirect effects caused by systemic reactions to critical illness. Still critically lacking is a comprehensive tissue-based survey of the CNS presence and specific neuropathology of SCV2 in humans. We conducted an extensive neuroanatomical survey of RT-PCR-detected SCV2 in 16 brain regions from 20 subjects who died of COVID-19 disease. Targeted areas were those with cranial nerve nuclei, including the olfactory bulb, medullary dorsal motor nucleus of the vagus nerve and the pontine trigeminal nerve nuclei, as well as areas possibly exposed to hematogenous entry, including the choroid plexus, leptomeninges, median eminence of the hypothalamus and area postrema of the medulla. Subjects ranged in age from 38 to 97 (mean 77) with 9 females and 11 males. Most subjects had typical age-related neuropathological findings. Two subjects had severe neuropathology, one with a large acute cerebral infarction and one with hemorrhagic encephalitis, that was unequivocally related to their COVID-19 disease while most of the 18 other subjects had non-specific histopathology including focal β-amyloid precursor protein white matter immunoreactivity and sparse perivascular mononuclear cell cuffing. Four subjects (20%) had SCV2 RNA in one or more brain regions including the olfactory bulb, amygdala, entorhinal area, temporal and frontal neocortex, dorsal medulla and leptomeninges. The subject with encephalitis was SCV2-positive in a histopathologically-affected area, the entorhinal cortex, while the subject with the large acute cerebral infarct was SCV2-negative in all brain regions. Like other human coronaviruses, SCV2 can inflict acute neuropathology in susceptible patients. Much remains to be understood, including what viral and host factors influence SCV2 brain invasion and whether it is cleared from the brain subsequent to the acute illness.
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spelling pubmed-78994612021-02-23 Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease Serrano, Geidy E. Walker, Jessica E. Arce, Richard Glass, Michael J. Vargas, Daisy Sue, Lucia I. Intorcia, Anthony J. Nelson, Courtney M. Oliver, Javon Papa, Jaclyn Russell, Aryck Suszczewicz, Katsuko E. Borja, Claryssa I. Belden, Christine Goldfarb, Danielle Shprecher, David Atri, Alireza Adler, Charles H. Shill, Holly A. Driver-Dunckley, Erika Mehta, Shyamal H. Readhead, Benjamin Huentelman, Matthew J. Peters, Joseph L. Alevritis, Ellie Bimi, Christian Mizgerd, Joseph P. Reiman, Eric M. Montine, Thomas J. Desforges, Marc Zehnder, James L. Sahoo, Malaya K. Zhang, Haiyu Solis, Daniel Pinsky, Benjamin A. Deture, Michael Dickson, Dennis W. Beach, Thomas G. medRxiv Article The coronavirus SARS-CoV-2 (SCV2) causes acute respiratory distress, termed COVID-19 disease, with substantial morbidity and mortality. As SCV2 is related to previously-studied coronaviruses that have been shown to have the capability for brain invasion, it seems likely that SCV2 may be able to do so as well. To date, although there have been many clinical and autopsy-based reports that describe a broad range of SCV2-associated neurological conditions, it is unclear what fraction of these have been due to direct CNS invasion versus indirect effects caused by systemic reactions to critical illness. Still critically lacking is a comprehensive tissue-based survey of the CNS presence and specific neuropathology of SCV2 in humans. We conducted an extensive neuroanatomical survey of RT-PCR-detected SCV2 in 16 brain regions from 20 subjects who died of COVID-19 disease. Targeted areas were those with cranial nerve nuclei, including the olfactory bulb, medullary dorsal motor nucleus of the vagus nerve and the pontine trigeminal nerve nuclei, as well as areas possibly exposed to hematogenous entry, including the choroid plexus, leptomeninges, median eminence of the hypothalamus and area postrema of the medulla. Subjects ranged in age from 38 to 97 (mean 77) with 9 females and 11 males. Most subjects had typical age-related neuropathological findings. Two subjects had severe neuropathology, one with a large acute cerebral infarction and one with hemorrhagic encephalitis, that was unequivocally related to their COVID-19 disease while most of the 18 other subjects had non-specific histopathology including focal β-amyloid precursor protein white matter immunoreactivity and sparse perivascular mononuclear cell cuffing. Four subjects (20%) had SCV2 RNA in one or more brain regions including the olfactory bulb, amygdala, entorhinal area, temporal and frontal neocortex, dorsal medulla and leptomeninges. The subject with encephalitis was SCV2-positive in a histopathologically-affected area, the entorhinal cortex, while the subject with the large acute cerebral infarct was SCV2-negative in all brain regions. Like other human coronaviruses, SCV2 can inflict acute neuropathology in susceptible patients. Much remains to be understood, including what viral and host factors influence SCV2 brain invasion and whether it is cleared from the brain subsequent to the acute illness. Cold Spring Harbor Laboratory 2021-02-18 /pmc/articles/PMC7899461/ /pubmed/33619496 http://dx.doi.org/10.1101/2021.02.15.21251511 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Serrano, Geidy E.
Walker, Jessica E.
Arce, Richard
Glass, Michael J.
Vargas, Daisy
Sue, Lucia I.
Intorcia, Anthony J.
Nelson, Courtney M.
Oliver, Javon
Papa, Jaclyn
Russell, Aryck
Suszczewicz, Katsuko E.
Borja, Claryssa I.
Belden, Christine
Goldfarb, Danielle
Shprecher, David
Atri, Alireza
Adler, Charles H.
Shill, Holly A.
Driver-Dunckley, Erika
Mehta, Shyamal H.
Readhead, Benjamin
Huentelman, Matthew J.
Peters, Joseph L.
Alevritis, Ellie
Bimi, Christian
Mizgerd, Joseph P.
Reiman, Eric M.
Montine, Thomas J.
Desforges, Marc
Zehnder, James L.
Sahoo, Malaya K.
Zhang, Haiyu
Solis, Daniel
Pinsky, Benjamin A.
Deture, Michael
Dickson, Dennis W.
Beach, Thomas G.
Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title_full Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title_fullStr Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title_full_unstemmed Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title_short Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease
title_sort mapping of sars-cov-2 brain invasion and histopathology in covid-19 disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899461/
https://www.ncbi.nlm.nih.gov/pubmed/33619496
http://dx.doi.org/10.1101/2021.02.15.21251511
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