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Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis
One of the key events in viral encephalitis is the ability of virus to enter the central nervous system (CNS). Several encephalitic viruses, including La Crosse Virus (LACV), primarily induce encephalitis in children, but not adults. This phenomenon is also observed in LACV mouse models, where the v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195820/ https://www.ncbi.nlm.nih.gov/pubmed/37202395 http://dx.doi.org/10.1038/s41467-023-37833-x |
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author | Basu, Rahul Ganesan, Sundar Winkler, Clayton W. Anzick, Sarah L. Martens, Craig Peterson, Karin E. Fraser, Iain D. C. |
author_facet | Basu, Rahul Ganesan, Sundar Winkler, Clayton W. Anzick, Sarah L. Martens, Craig Peterson, Karin E. Fraser, Iain D. C. |
author_sort | Basu, Rahul |
collection | PubMed |
description | One of the key events in viral encephalitis is the ability of virus to enter the central nervous system (CNS). Several encephalitic viruses, including La Crosse Virus (LACV), primarily induce encephalitis in children, but not adults. This phenomenon is also observed in LACV mouse models, where the virus gains access to the CNS of weanling animals through vascular leakage of brain microvessels, likely through brain capillary endothelial cells (BCECs). To examine age and region-specific regulatory factors of vascular leakage, we used genome-wide transcriptomics and targeted siRNA screening to identify genes whose suppression affected viral pathogenesis in BCECs. Further analysis of two of these gene products, Connexin43 (Cx43/Gja1) and EphrinA2 (Efna2), showed a substantial effect on LACV pathogenesis. Induction of Cx43 by 4-phenylbutyric acid (4-PBA) inhibited neurological disease in weanling mice, while Efna2 deficiency increased disease in adult mice. Thus, we show that Efna2 and Cx43 expressed by BCECs are key mediators of LACV-induced neuroinvasion and neurological disease. |
format | Online Article Text |
id | pubmed-10195820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101958202023-05-20 Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis Basu, Rahul Ganesan, Sundar Winkler, Clayton W. Anzick, Sarah L. Martens, Craig Peterson, Karin E. Fraser, Iain D. C. Nat Commun Article One of the key events in viral encephalitis is the ability of virus to enter the central nervous system (CNS). Several encephalitic viruses, including La Crosse Virus (LACV), primarily induce encephalitis in children, but not adults. This phenomenon is also observed in LACV mouse models, where the virus gains access to the CNS of weanling animals through vascular leakage of brain microvessels, likely through brain capillary endothelial cells (BCECs). To examine age and region-specific regulatory factors of vascular leakage, we used genome-wide transcriptomics and targeted siRNA screening to identify genes whose suppression affected viral pathogenesis in BCECs. Further analysis of two of these gene products, Connexin43 (Cx43/Gja1) and EphrinA2 (Efna2), showed a substantial effect on LACV pathogenesis. Induction of Cx43 by 4-phenylbutyric acid (4-PBA) inhibited neurological disease in weanling mice, while Efna2 deficiency increased disease in adult mice. Thus, we show that Efna2 and Cx43 expressed by BCECs are key mediators of LACV-induced neuroinvasion and neurological disease. Nature Publishing Group UK 2023-05-18 /pmc/articles/PMC10195820/ /pubmed/37202395 http://dx.doi.org/10.1038/s41467-023-37833-x Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Basu, Rahul Ganesan, Sundar Winkler, Clayton W. Anzick, Sarah L. Martens, Craig Peterson, Karin E. Fraser, Iain D. C. Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title | Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title_full | Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title_fullStr | Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title_full_unstemmed | Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title_short | Identification of age-specific gene regulators of La Crosse virus neuroinvasion and pathogenesis |
title_sort | identification of age-specific gene regulators of la crosse virus neuroinvasion and pathogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195820/ https://www.ncbi.nlm.nih.gov/pubmed/37202395 http://dx.doi.org/10.1038/s41467-023-37833-x |
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