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SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity
Numerous viruses use specialized surface molecules called fusogens to enter host cells. Many of these viruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can infect the brain and are associated with severe neurological symptoms through poorly understood mechanisms. W...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246911/ https://www.ncbi.nlm.nih.gov/pubmed/37285437 http://dx.doi.org/10.1126/sciadv.adg2248 |
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author | Martínez-Mármol, Ramón Giordano-Santini, Rosina Kaulich, Eva Cho, Ann-Na Przybyla, Magdalena Riyadh, Md Asrafuzzaman Robinson, Emilija Chew, Keng Yih Amor, Rumelo Meunier, Frédéric A. Balistreri, Giuseppe Short, Kirsty R. Ke, Yazi D. Ittner, Lars M. Hilliard, Massimo A. |
author_facet | Martínez-Mármol, Ramón Giordano-Santini, Rosina Kaulich, Eva Cho, Ann-Na Przybyla, Magdalena Riyadh, Md Asrafuzzaman Robinson, Emilija Chew, Keng Yih Amor, Rumelo Meunier, Frédéric A. Balistreri, Giuseppe Short, Kirsty R. Ke, Yazi D. Ittner, Lars M. Hilliard, Massimo A. |
author_sort | Martínez-Mármol, Ramón |
collection | PubMed |
description | Numerous viruses use specialized surface molecules called fusogens to enter host cells. Many of these viruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can infect the brain and are associated with severe neurological symptoms through poorly understood mechanisms. We show that SARS-CoV-2 infection induces fusion between neurons and between neurons and glia in mouse and human brain organoids. We reveal that this is caused by the viral fusogen, as it is fully mimicked by the expression of the SARS-CoV-2 spike (S) protein or the unrelated fusogen p15 from the baboon orthoreovirus. We demonstrate that neuronal fusion is a progressive event, leads to the formation of multicellular syncytia, and causes the spread of large molecules and organelles. Last, using Ca(2+) imaging, we show that fusion severely compromises neuronal activity. These results provide mechanistic insights into how SARS-CoV-2 and other viruses affect the nervous system, alter its function, and cause neuropathology. |
format | Online Article Text |
id | pubmed-10246911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102469112023-06-08 SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity Martínez-Mármol, Ramón Giordano-Santini, Rosina Kaulich, Eva Cho, Ann-Na Przybyla, Magdalena Riyadh, Md Asrafuzzaman Robinson, Emilija Chew, Keng Yih Amor, Rumelo Meunier, Frédéric A. Balistreri, Giuseppe Short, Kirsty R. Ke, Yazi D. Ittner, Lars M. Hilliard, Massimo A. Sci Adv Neuroscience Numerous viruses use specialized surface molecules called fusogens to enter host cells. Many of these viruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can infect the brain and are associated with severe neurological symptoms through poorly understood mechanisms. We show that SARS-CoV-2 infection induces fusion between neurons and between neurons and glia in mouse and human brain organoids. We reveal that this is caused by the viral fusogen, as it is fully mimicked by the expression of the SARS-CoV-2 spike (S) protein or the unrelated fusogen p15 from the baboon orthoreovirus. We demonstrate that neuronal fusion is a progressive event, leads to the formation of multicellular syncytia, and causes the spread of large molecules and organelles. Last, using Ca(2+) imaging, we show that fusion severely compromises neuronal activity. These results provide mechanistic insights into how SARS-CoV-2 and other viruses affect the nervous system, alter its function, and cause neuropathology. American Association for the Advancement of Science 2023-06-07 /pmc/articles/PMC10246911/ /pubmed/37285437 http://dx.doi.org/10.1126/sciadv.adg2248 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Martínez-Mármol, Ramón Giordano-Santini, Rosina Kaulich, Eva Cho, Ann-Na Przybyla, Magdalena Riyadh, Md Asrafuzzaman Robinson, Emilija Chew, Keng Yih Amor, Rumelo Meunier, Frédéric A. Balistreri, Giuseppe Short, Kirsty R. Ke, Yazi D. Ittner, Lars M. Hilliard, Massimo A. SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title | SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title_full | SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title_fullStr | SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title_full_unstemmed | SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title_short | SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
title_sort | sars-cov-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246911/ https://www.ncbi.nlm.nih.gov/pubmed/37285437 http://dx.doi.org/10.1126/sciadv.adg2248 |
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