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Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier

Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to t...

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Autores principales: Khou, Cécile, Díaz-Salinas, Marco Aurelio, da Costa, Anaelle, Préhaud, Christophe, Jeannin, Patricia, Afonso, Philippe V., Vignuzzi, Marco, Lafon, Monique, Pardigon, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177624/
https://www.ncbi.nlm.nih.gov/pubmed/34086776
http://dx.doi.org/10.1371/journal.pone.0252595
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author Khou, Cécile
Díaz-Salinas, Marco Aurelio
da Costa, Anaelle
Préhaud, Christophe
Jeannin, Patricia
Afonso, Philippe V.
Vignuzzi, Marco
Lafon, Monique
Pardigon, Nathalie
author_facet Khou, Cécile
Díaz-Salinas, Marco Aurelio
da Costa, Anaelle
Préhaud, Christophe
Jeannin, Patricia
Afonso, Philippe V.
Vignuzzi, Marco
Lafon, Monique
Pardigon, Nathalie
author_sort Khou, Cécile
collection PubMed
description Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to the central nervous system (CNS). However, what happens at early times of JEV contact with the BBB is poorly understood. In the present work, we evaluated the ability of both a virulent and a vaccine strain of JEV (JEV RP9 and SA14-14-2, respectively) to cross an in vitro human BBB model. Using this system, we demonstrated that both JEV RP9 and SA14-14-2 are able to cross the BBB without disrupting it at early times post viral addition. Furthermore, we find that almost 10 times more RP9 infectious particles than SA14-14 cross the model BBB, indicating this BBB model discriminates between the virulent RP9 and the vaccine SA14-14-2 strains of JEV. Beyond contributing to the understanding of early events in JEV neuroinvasion, we demonstrate this in vitro BBB model can be used as a system to study the viral determinants of JEV neuroinvasiveness and the molecular mechanisms by which this flavivirus crosses the BBB during early times of neuroinvasion.
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spelling pubmed-81776242021-06-07 Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier Khou, Cécile Díaz-Salinas, Marco Aurelio da Costa, Anaelle Préhaud, Christophe Jeannin, Patricia Afonso, Philippe V. Vignuzzi, Marco Lafon, Monique Pardigon, Nathalie PLoS One Research Article Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to the central nervous system (CNS). However, what happens at early times of JEV contact with the BBB is poorly understood. In the present work, we evaluated the ability of both a virulent and a vaccine strain of JEV (JEV RP9 and SA14-14-2, respectively) to cross an in vitro human BBB model. Using this system, we demonstrated that both JEV RP9 and SA14-14-2 are able to cross the BBB without disrupting it at early times post viral addition. Furthermore, we find that almost 10 times more RP9 infectious particles than SA14-14 cross the model BBB, indicating this BBB model discriminates between the virulent RP9 and the vaccine SA14-14-2 strains of JEV. Beyond contributing to the understanding of early events in JEV neuroinvasion, we demonstrate this in vitro BBB model can be used as a system to study the viral determinants of JEV neuroinvasiveness and the molecular mechanisms by which this flavivirus crosses the BBB during early times of neuroinvasion. Public Library of Science 2021-06-04 /pmc/articles/PMC8177624/ /pubmed/34086776 http://dx.doi.org/10.1371/journal.pone.0252595 Text en © 2021 Khou et al 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 author and source are credited.
spellingShingle Research Article
Khou, Cécile
Díaz-Salinas, Marco Aurelio
da Costa, Anaelle
Préhaud, Christophe
Jeannin, Patricia
Afonso, Philippe V.
Vignuzzi, Marco
Lafon, Monique
Pardigon, Nathalie
Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title_full Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title_fullStr Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title_full_unstemmed Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title_short Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
title_sort comparative analysis of neuroinvasion by japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177624/
https://www.ncbi.nlm.nih.gov/pubmed/34086776
http://dx.doi.org/10.1371/journal.pone.0252595
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