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Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis

Both monogenic diseases and viral infections can manifest in a broad spectrum of clinical phenotypes that range from asymptomatic to lethal, suggesting that other factors modulate disease severity. Here, we examine the interplay between the genetic neuronopathic Gaucher’s disease (nGD), and neuroinv...

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Autores principales: Melamed, Sharon, Avraham, Roy, Rothbard, Deborah E., Erez, Noam, Israely, Tomer, Klausner, Ziv, Futerman, Anthony H., Paran, Nir, Vitner, Einat B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443817/
https://www.ncbi.nlm.nih.gov/pubmed/32831144
http://dx.doi.org/10.1186/s40478-020-01020-6
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author Melamed, Sharon
Avraham, Roy
Rothbard, Deborah E.
Erez, Noam
Israely, Tomer
Klausner, Ziv
Futerman, Anthony H.
Paran, Nir
Vitner, Einat B.
author_facet Melamed, Sharon
Avraham, Roy
Rothbard, Deborah E.
Erez, Noam
Israely, Tomer
Klausner, Ziv
Futerman, Anthony H.
Paran, Nir
Vitner, Einat B.
author_sort Melamed, Sharon
collection PubMed
description Both monogenic diseases and viral infections can manifest in a broad spectrum of clinical phenotypes that range from asymptomatic to lethal, suggesting that other factors modulate disease severity. Here, we examine the interplay between the genetic neuronopathic Gaucher’s disease (nGD), and neuroinvasive Sindbis virus (SVNI) infection. Infection of nGD mice with SVNI had no influence on nGD severity. However, nGD mice were more resistant to SVNI infection. Significantly different inflammatory responses were seen in nGD brains when compared with SVNI brains: the inflammatory response in the nGD brains consisted of reactive astrocytes and microglia with no infiltrating macrophages, but the inflammatory response in the brains of SVNI-infected mice was characterized by infiltration of macrophages and altered activation of microglia and astrocytes. We suggest that the innate immune response activated in nGD confers resistance against viral infection of the CNS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-020-01020-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-74438172020-08-24 Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis Melamed, Sharon Avraham, Roy Rothbard, Deborah E. Erez, Noam Israely, Tomer Klausner, Ziv Futerman, Anthony H. Paran, Nir Vitner, Einat B. Acta Neuropathol Commun Research Both monogenic diseases and viral infections can manifest in a broad spectrum of clinical phenotypes that range from asymptomatic to lethal, suggesting that other factors modulate disease severity. Here, we examine the interplay between the genetic neuronopathic Gaucher’s disease (nGD), and neuroinvasive Sindbis virus (SVNI) infection. Infection of nGD mice with SVNI had no influence on nGD severity. However, nGD mice were more resistant to SVNI infection. Significantly different inflammatory responses were seen in nGD brains when compared with SVNI brains: the inflammatory response in the nGD brains consisted of reactive astrocytes and microglia with no infiltrating macrophages, but the inflammatory response in the brains of SVNI-infected mice was characterized by infiltration of macrophages and altered activation of microglia and astrocytes. We suggest that the innate immune response activated in nGD confers resistance against viral infection of the CNS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-020-01020-6) contains supplementary material, which is available to authorized users. BioMed Central 2020-08-24 /pmc/articles/PMC7443817/ /pubmed/32831144 http://dx.doi.org/10.1186/s40478-020-01020-6 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Melamed, Sharon
Avraham, Roy
Rothbard, Deborah E.
Erez, Noam
Israely, Tomer
Klausner, Ziv
Futerman, Anthony H.
Paran, Nir
Vitner, Einat B.
Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title_full Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title_fullStr Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title_full_unstemmed Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title_short Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
title_sort innate immune response in neuronopathic forms of gaucher disease confers resistance against viral-induced encephalitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443817/
https://www.ncbi.nlm.nih.gov/pubmed/32831144
http://dx.doi.org/10.1186/s40478-020-01020-6
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