A human-derived 3D brain organoid model to study JC virus infection

dc.contributor.authorBarreras, Paula
dc.contributor.authorPamies, David
dc.contributor.authorMonaco, Maria Chiara
dc.contributor.authorMuñoz, Laura S.
dc.contributor.authorZhong, Xiali
dc.contributor.authorMajor, Eugene O.
dc.contributor.authorHogberg, Helena T.
dc.contributor.authorHartung, Thomas
dc.contributor.authorPardo, Carlos A.
dc.date.accessioned2022-03-28T15:17:14Z
dc.date.available2022-03-28T15:17:14Z
dc.date.issued2022-02
dc.description.abstractProgressive multifocal leukoencephalopathy (PML) is a frequent neurological complication in immunosuppressed patients. PML is caused by the JC virus (JCV), a neurotropic DNA polyomavirus that infects oligodendrocytes and astrocytes, causing inflammation and demyelination which lead to neurological dysfunction. The pathogenesis of PML is poorly understood due to the lack of in vitro or animal models to study mechanisms of disease as the virus most efficiently infects only human cells. We developed a human-derived brain organotypic system (also called brain organoid) to model JCV infection. The model was developed by using human-induced pluripotent stem cells (iPSC) and culturing them in 3D to generate an organotypic model containing neurons, astrocytes, and oligodendrocytes which recapitulates aspects of the environment of the human brain. We infected the brain organoids with the JCV MAD4 strain or cerebrospinal fluid of a patient with PML. The organoids were assessed for evidence of infection by qPCR, immunofluorescence, and electron microscopy at 1, 2, and 3 weeks post-exposure. JCV infection in both JCV MAD4 strain and PML CSF-exposed brain organoids was confirmed by immunocytochemical studies demonstrating viral antigens and electron microscopy showing virion particles in the nuclear compartment of oligodendrocytes and astrocytes. No evidence of neuronal infection was visualized. Infection was also demonstrated by JCV qPCR in the virus-exposed organoids and their media. In conclusion, the brain organoid model of JCV infection establishes a human model suitable for studying the mechanisms of JCV infection and pathogenesis of PML and may facilitate the exploration of therapeutic approaches.eng
dc.description.versionpublishedeng
dc.identifier.doi10.1007/s13365-022-01062-7eng
dc.identifier.pmid35239145eng
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/57023
dc.language.isoengeng
dc.subjectJCV · JC virus · Organoid · In vitro model · Human cells · Microphysiological systemeng
dc.subject.ddc570eng
dc.titleA human-derived 3D brain organoid model to study JC virus infectioneng
dc.typeJOURNAL_ARTICLEeng
dspace.entity.typePublication
kops.citation.bibtex
@article{Barreras2022-02human-57023,
  year={2022},
  doi={10.1007/s13365-022-01062-7},
  title={A human-derived 3D brain organoid model to study JC virus infection},
  number={1},
  volume={28},
  issn={1355-0284},
  journal={Journal of neurovirology},
  pages={17--26},
  author={Barreras, Paula and Pamies, David and Monaco, Maria Chiara and Muñoz, Laura S. and Zhong, Xiali and Major, Eugene O. and Hogberg, Helena T. and Hartung, Thomas and Pardo, Carlos A.}
}
kops.citation.iso690BARRERAS, Paula, David PAMIES, Maria Chiara MONACO, Laura S. MUÑOZ, Xiali ZHONG, Eugene O. MAJOR, Helena T. HOGBERG, Thomas HARTUNG, Carlos A. PARDO, 2022. A human-derived 3D brain organoid model to study JC virus infection. In: Journal of neurovirology. Springer Nature. 2022, 28(1), pp. 17-26. ISSN 1355-0284. eISSN 1538-2443. Available under: doi: 10.1007/s13365-022-01062-7deu
kops.citation.iso690BARRERAS, Paula, David PAMIES, Maria Chiara MONACO, Laura S. MUÑOZ, Xiali ZHONG, Eugene O. MAJOR, Helena T. HOGBERG, Thomas HARTUNG, Carlos A. PARDO, 2022. A human-derived 3D brain organoid model to study JC virus infection. In: Journal of neurovirology. Springer Nature. 2022, 28(1), pp. 17-26. ISSN 1355-0284. eISSN 1538-2443. Available under: doi: 10.1007/s13365-022-01062-7eng
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    <dcterms:abstract xml:lang="eng">Progressive multifocal leukoencephalopathy (PML) is a frequent neurological complication in immunosuppressed patients. PML is caused by the JC virus (JCV), a neurotropic DNA polyomavirus that infects oligodendrocytes and astrocytes, causing inflammation and demyelination which lead to neurological dysfunction. The pathogenesis of PML is poorly understood due to the lack of in vitro or animal models to study mechanisms of disease as the virus most efficiently infects only human cells. We developed a human-derived brain organotypic system (also called brain organoid) to model JCV infection. The model was developed by using human-induced pluripotent stem cells (iPSC) and culturing them in 3D to generate an organotypic model containing neurons, astrocytes, and oligodendrocytes which recapitulates aspects of the environment of the human brain. We infected the brain organoids with the JCV MAD4 strain or cerebrospinal fluid of a patient with PML. The organoids were assessed for evidence of infection by qPCR, immunofluorescence, and electron microscopy at 1, 2, and 3 weeks post-exposure. JCV infection in both JCV MAD4 strain and PML CSF-exposed brain organoids was confirmed by immunocytochemical studies demonstrating viral antigens and electron microscopy showing virion particles in the nuclear compartment of oligodendrocytes and astrocytes. No evidence of neuronal infection was visualized. Infection was also demonstrated by JCV qPCR in the virus-exposed organoids and their media. In conclusion, the brain organoid model of JCV infection establishes a human model suitable for studying the mechanisms of JCV infection and pathogenesis of PML and may facilitate the exploration of therapeutic approaches.</dcterms:abstract>
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kops.sourcefieldJournal of neurovirology. Springer Nature. 2022, <b>28</b>(1), pp. 17-26. ISSN 1355-0284. eISSN 1538-2443. Available under: doi: 10.1007/s13365-022-01062-7deu
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kops.sourcefield.plainJournal of neurovirology. Springer Nature. 2022, 28(1), pp. 17-26. ISSN 1355-0284. eISSN 1538-2443. Available under: doi: 10.1007/s13365-022-01062-7eng
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