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Anatomical barriers against SARS-CoV-2 neuroinvasion at vulnerable interfaces visualized in deceased COVID-19 patientsopen access

Authors
Khan, MonaClijsters, MarnickChoi, SuminBackaert, WoutClaerhout, MichielCouvreur, FloorVan Breda, LaureBourgeois, FlorenceSpeleman, KatoKlein, SamVan Laethem, JohanVerstappen, GillDereli, Ayse SumeyraYoo, Seung-JunZhou, HaiDan Do, Thuc NguyenJochmans, DirkLaenen, LiesDebaveye, YvesDe Munter, PaulGunst, JanJorissen, MarkLagrou, KatrienMeersseman, PhilippeNeyts, JohanThal, Dietmar RudolfTopsakal, VedatVandenbriele, ChristopheWauters, JoostMombaerts, PeterVan Gerven, Laura
Issue Date
Dec-2022
Publisher
Cell Press
Keywords
blood-brain barrier; brain parenchyma; Coronavirus; COVID-19; Delta; frontal lobe; glia limitans perivascularis; leptomeninges; neuroinvasion; neurotropism; olfactory; olfactory bulb; olfactory sensory neuron; Omicron; perineurial olfactory nerve fibroblast; RNAscope; SARS-CoV-2; Virchow-Robin space
Citation
Neuron, v.110, no.23, pp.3919 - 3935.e1–e6
Indexed
SCIE
SCOPUS
Journal Title
Neuron
Volume
110
Number
23
Start Page
3919
End Page
3935.e1–e6
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185144
DOI
10.1016/j.neuron.2022.11.007
ISSN
0896-6273
Abstract
Can SARS-CoV-2 hitchhike on the olfactory projection and take a direct and short route from the nose into the brain? We reasoned that the neurotropic or neuroinvasive capacity of the virus, if it exists, should be most easily detectable in individuals who died in an acute phase of the infection. Here, we applied a postmortem bedside surgical procedure for the rapid procurement of tissue, blood, and cerebrospinal fluid samples from deceased COVID-19 patients infected with the Delta, Omicron BA.1, or Omicron BA.2 variants. Confocal imaging of sections stained with fluorescence RNAscope and immunohistochemistry afforded the light-microscopic visualization of extracellular SARS-CoV-2 virions in tissues. We failed to find evidence for viral invasion of the parenchyma of the olfactory bulb and the frontal lobe of the brain. Instead, we identified anatomical barriers at vulnerable interfaces, exemplified by perineurial olfactory nerve fibroblasts enwrapping olfactory axon fascicles in the lamina propria of the olfactory mucosa.
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