Cargando…

Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases

Flaviviruses, particularly Japanese encephalitis virus (JEV) and West Nile virus (WNV), are important causes of virus-induced central nervous system (CNS) disease in humans. We used microarray analysis to identify cellular genes that are differentially regulated following infection of the brain with...

Descripción completa

Detalles Bibliográficos
Autores principales: Clarke, Penny, Leser, J. Smith, Bowen, Richard A., Tyler, Kenneth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952157/
https://www.ncbi.nlm.nih.gov/pubmed/24618253
http://dx.doi.org/10.1128/mBio.00902-14
_version_ 1782307176301199360
author Clarke, Penny
Leser, J. Smith
Bowen, Richard A.
Tyler, Kenneth L.
author_facet Clarke, Penny
Leser, J. Smith
Bowen, Richard A.
Tyler, Kenneth L.
author_sort Clarke, Penny
collection PubMed
description Flaviviruses, particularly Japanese encephalitis virus (JEV) and West Nile virus (WNV), are important causes of virus-induced central nervous system (CNS) disease in humans. We used microarray analysis to identify cellular genes that are differentially regulated following infection of the brain with JEV (P3) or WNV (New York 99). Gene expression data for these flaviviruses were compared to those obtained following infection of the brain with reovirus (type 3 Dearing), an unrelated neurotropic virus. We found that a large number of genes were up-regulated by all three viruses (using the criteria of a change of >2-fold and a P value of <0.001), including genes associated with interferon signaling, the immune system, inflammation, and cell death/survival signaling. In addition, genes associated with glutamate signaling were down-regulated in infections with all three viruses (criteria, a >2-fold change and a P value of <0.001). These genes may serve as broad-spectrum therapeutic targets for virus-induced CNS disease. A distinct set of genes were up-regulated following flavivirus infection but not following infection with reovirus. These genes were associated with tRNA charging and may serve as therapeutic targets for flavivirus-induced CNS disease.
format Online
Article
Text
id pubmed-3952157
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher American Society of Microbiology
record_format MEDLINE/PubMed
spelling pubmed-39521572014-03-13 Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases Clarke, Penny Leser, J. Smith Bowen, Richard A. Tyler, Kenneth L. mBio Research Article Flaviviruses, particularly Japanese encephalitis virus (JEV) and West Nile virus (WNV), are important causes of virus-induced central nervous system (CNS) disease in humans. We used microarray analysis to identify cellular genes that are differentially regulated following infection of the brain with JEV (P3) or WNV (New York 99). Gene expression data for these flaviviruses were compared to those obtained following infection of the brain with reovirus (type 3 Dearing), an unrelated neurotropic virus. We found that a large number of genes were up-regulated by all three viruses (using the criteria of a change of >2-fold and a P value of <0.001), including genes associated with interferon signaling, the immune system, inflammation, and cell death/survival signaling. In addition, genes associated with glutamate signaling were down-regulated in infections with all three viruses (criteria, a >2-fold change and a P value of <0.001). These genes may serve as broad-spectrum therapeutic targets for virus-induced CNS disease. A distinct set of genes were up-regulated following flavivirus infection but not following infection with reovirus. These genes were associated with tRNA charging and may serve as therapeutic targets for flavivirus-induced CNS disease. American Society of Microbiology 2014-03-11 /pmc/articles/PMC3952157/ /pubmed/24618253 http://dx.doi.org/10.1128/mBio.00902-14 Text en Copyright © 2014 Clarke et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Clarke, Penny
Leser, J. Smith
Bowen, Richard A.
Tyler, Kenneth L.
Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title_full Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title_fullStr Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title_full_unstemmed Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title_short Virus-Induced Transcriptional Changes in the Brain Include the Differential Expression of Genes Associated with Interferon, Apoptosis, Interleukin 17 Receptor A, and Glutamate Signaling as Well as Flavivirus-Specific Upregulation of tRNA Synthetases
title_sort virus-induced transcriptional changes in the brain include the differential expression of genes associated with interferon, apoptosis, interleukin 17 receptor a, and glutamate signaling as well as flavivirus-specific upregulation of trna synthetases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952157/
https://www.ncbi.nlm.nih.gov/pubmed/24618253
http://dx.doi.org/10.1128/mBio.00902-14
work_keys_str_mv AT clarkepenny virusinducedtranscriptionalchangesinthebrainincludethedifferentialexpressionofgenesassociatedwithinterferonapoptosisinterleukin17receptoraandglutamatesignalingaswellasflavivirusspecificupregulationoftrnasynthetases
AT leserjsmith virusinducedtranscriptionalchangesinthebrainincludethedifferentialexpressionofgenesassociatedwithinterferonapoptosisinterleukin17receptoraandglutamatesignalingaswellasflavivirusspecificupregulationoftrnasynthetases
AT bowenricharda virusinducedtranscriptionalchangesinthebrainincludethedifferentialexpressionofgenesassociatedwithinterferonapoptosisinterleukin17receptoraandglutamatesignalingaswellasflavivirusspecificupregulationoftrnasynthetases
AT tylerkennethl virusinducedtranscriptionalchangesinthebrainincludethedifferentialexpressionofgenesassociatedwithinterferonapoptosisinterleukin17receptoraandglutamatesignalingaswellasflavivirusspecificupregulationoftrnasynthetases