KOPS - The Institutional Repository of the University of Konstanz

Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2

Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2

Cite This

Files in this item

Checksum: MD5:dc16a7ee607230c42c4c5c8cbfda906c

BULLEN, C. Korin, Helena T. HOGBERG, Asli BAHADIRLI-TALBOTT, William R. BISHAI, Thomas HARTUNG, Casey KEUTHAN, Monika M. LOONEY, Andrew PEKOSZ, Carolina J. ROMERO, Lena SMIRNOVA, 2020. Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2. In: Alternatives to Animal Experimentation : ALTEX. Springer Spektrum. 37(4), pp. 665-671. ISSN 1868-596X. eISSN 1868-8551. Available under: doi: 10.14573/altex.2006111

@article{Bullen2020Infec-52879, title={Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2}, year={2020}, doi={10.14573/altex.2006111}, number={4}, volume={37}, issn={1868-596X}, journal={Alternatives to Animal Experimentation : ALTEX}, pages={665--671}, author={Bullen, C. Korin and Hogberg, Helena T. and Bahadirli-Talbott, Asli and Bishai, William R. and Hartung, Thomas and Keuthan, Casey and Looney, Monika M. and Pekosz, Andrew and Romero, Carolina J. and Smirnova, Lena} }

<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/52879"> <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/"/> <dc:creator>Keuthan, Casey</dc:creator> <dc:creator>Bahadirli-Talbott, Asli</dc:creator> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/52879"/> <dcterms:issued>2020</dcterms:issued> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/52879/1/Bullen_2-o6k09vvixjpy1.pdf"/> <dc:contributor>Hartung, Thomas</dc:contributor> <dc:contributor>Bahadirli-Talbott, Asli</dc:contributor> <dc:contributor>Hogberg, Helena T.</dc:contributor> <dc:contributor>Pekosz, Andrew</dc:contributor> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/52879/1/Bullen_2-o6k09vvixjpy1.pdf"/> <dc:contributor>Bullen, C. Korin</dc:contributor> <dc:creator>Bishai, William R.</dc:creator> <dc:creator>Hartung, Thomas</dc:creator> <dc:creator>Looney, Monika M.</dc:creator> <dc:creator>Romero, Carolina J.</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2021-02-17T12:28:12Z</dc:date> <dcterms:title>Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2</dcterms:title> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Bullen, C. Korin</dc:creator> <dc:language>eng</dc:language> <dc:contributor>Romero, Carolina J.</dc:contributor> <dc:contributor>Keuthan, Casey</dc:contributor> <dc:creator>Hogberg, Helena T.</dc:creator> <dc:contributor>Looney, Monika M.</dc:contributor> <dcterms:abstract xml:lang="eng">Reports from Wuhan suggest that 36% of COVID-19 patients show neurological symptoms, and cases of viral encephalitis have been reported, suggesting that the virus is neurotropic under unknown circumstances. This is well established for other coronaviruses. In order to understand why some patients develop such symptoms and others do not, we address herein the infectability of the central nervous system (CNS). Reports that the ACE2 receptor – critical for virus entry into lung cells – is found in different neurons support this expectation. We employed a human induced pluripotent stem cell (iPSC)- derived BrainSphere model, which we used earlier for Zika, Dengue, HIV and John Cunningham virus infection studies. We detected the expression of the ACE2 receptor, but not TMPRSS2, in the model. Incubating the BrainSpheres for 6 hours with SARS-CoV-2 at a multiplicity of infection (MOI) of 0.1 led to infection of a fraction of neural cells with replication of the virus evident at 72 hpi. Virus particles were found in the neuronal cell body extending into apparent neurite structures. PCR measurements corroborated the replication of the virus, suggesting at least a tenfold increase in virus copies per total RNA. Leveraging state-of-the-art 3D organotypic cell culture, which has been shown to allow both virus infection and modeling of (developmental) neurotoxicity but is at the same time simple enough to be transferred and used in a BSL-3 environment, we demonstrate, for the first time, the potential critically important neurotropism of SARS-CoV-2.</dcterms:abstract> <dc:rights>Attribution 4.0 International</dc:rights> <dc:creator>Smirnova, Lena</dc:creator> <dc:contributor>Smirnova, Lena</dc:contributor> <dc:creator>Pekosz, Andrew</dc:creator> <dc:contributor>Bishai, William R.</dc:contributor> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2021-02-17T12:28:12Z</dcterms:available> </rdf:Description> </rdf:RDF>

Downloads since Feb 17, 2021 (Information about access statistics)

Bullen_2-o6k09vvixjpy1.pdf 30

This item appears in the following Collection(s)

Attribution 4.0 International Except where otherwise noted, this item's license is described as Attribution 4.0 International

Search KOPS


Browse

My Account