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

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 d...

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Autores principales: Barreras, Paula, Pamies, David, Monaco, Maria Chiara, Muñoz, Laura S., Zhong, Xiali, Major, Eugene O., Hogberg, Helena T., Hartung, Thomas, Pardo, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892818/
https://www.ncbi.nlm.nih.gov/pubmed/35239145
http://dx.doi.org/10.1007/s13365-022-01062-7
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author Barreras, Paula
Pamies, David
Monaco, Maria Chiara
Muñoz, Laura S.
Zhong, Xiali
Major, Eugene O.
Hogberg, Helena T.
Hartung, Thomas
Pardo, Carlos A.
author_facet Barreras, Paula
Pamies, David
Monaco, Maria Chiara
Muñoz, Laura S.
Zhong, Xiali
Major, Eugene O.
Hogberg, Helena T.
Hartung, Thomas
Pardo, Carlos A.
author_sort Barreras, Paula
collection PubMed
description 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.
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spelling pubmed-88928182022-03-04 A human-derived 3D brain organoid model to study JC virus infection Barreras, Paula Pamies, David Monaco, Maria Chiara Muñoz, Laura S. Zhong, Xiali Major, Eugene O. Hogberg, Helena T. Hartung, Thomas Pardo, Carlos A. J Neurovirol Article 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. Springer International Publishing 2022-03-03 2022 /pmc/articles/PMC8892818/ /pubmed/35239145 http://dx.doi.org/10.1007/s13365-022-01062-7 Text en © Journal of NeuroVirology, Inc. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Barreras, Paula
Pamies, David
Monaco, Maria Chiara
Muñoz, Laura S.
Zhong, Xiali
Major, Eugene O.
Hogberg, Helena T.
Hartung, Thomas
Pardo, Carlos A.
A human-derived 3D brain organoid model to study JC virus infection
title A human-derived 3D brain organoid model to study JC virus infection
title_full A human-derived 3D brain organoid model to study JC virus infection
title_fullStr A human-derived 3D brain organoid model to study JC virus infection
title_full_unstemmed A human-derived 3D brain organoid model to study JC virus infection
title_short A human-derived 3D brain organoid model to study JC virus infection
title_sort human-derived 3d brain organoid model to study jc virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892818/
https://www.ncbi.nlm.nih.gov/pubmed/35239145
http://dx.doi.org/10.1007/s13365-022-01062-7
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