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Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection

Powassan virus (POWV) is a tick-borne Flavivirus responsible for life-threatening encephalitis in North America and some regions of Russia. The ticks that have been reported to transmit the virus belong to the Ixodes species, and they feed on small-to-medium-sized mammals, such as Peromyscus leucopu...

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Autores principales: Mlera, Luwanika, Meade-White, Kimberly, Dahlstrom, Eric, Baur, Rachel, Kanakabandi, Kishore, Virtaneva, Kimmo, Porcella, Stephen F., Bloom, Marshall E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790856/
https://www.ncbi.nlm.nih.gov/pubmed/29147886
http://dx.doi.org/10.1007/s13365-017-0596-y
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author Mlera, Luwanika
Meade-White, Kimberly
Dahlstrom, Eric
Baur, Rachel
Kanakabandi, Kishore
Virtaneva, Kimmo
Porcella, Stephen F.
Bloom, Marshall E.
author_facet Mlera, Luwanika
Meade-White, Kimberly
Dahlstrom, Eric
Baur, Rachel
Kanakabandi, Kishore
Virtaneva, Kimmo
Porcella, Stephen F.
Bloom, Marshall E.
author_sort Mlera, Luwanika
collection PubMed
description Powassan virus (POWV) is a tick-borne Flavivirus responsible for life-threatening encephalitis in North America and some regions of Russia. The ticks that have been reported to transmit the virus belong to the Ixodes species, and they feed on small-to-medium-sized mammals, such as Peromyscus leucopus mice, skunks, and woodchucks. We previously developed a P. leucopus mouse model of POWV infection, and the model is characterized by a lack of clinical signs of disease following intraperitoneal or intracranial inoculation. However, intracranial inoculation results in mild subclinical encephalitis from 5 days post infection (dpi), but the encephalitis resolves by 28 dpi. We used RNA sequencing to profile the P. leucopus mouse brain transcriptome at different time points after intracranial challenge with POWV. At 24 h post infection, 42 genes were significantly differentially expressed and the number peaked to 232 at 7 dpi before declining to 31 at 28 dpi. Using Ingenuity Pathway Analysis, we determined that the genes that were significantly expressed from 1 to 15 dpi were mainly associated with interferon signaling. As a result, many interferon-stimulated genes (ISGs) were upregulated. Some of the ISGs include an array of TRIMs (genes encoding tripartite motif proteins). These results will be useful for the identification of POWV restriction factors.
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spelling pubmed-57908562018-02-05 Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection Mlera, Luwanika Meade-White, Kimberly Dahlstrom, Eric Baur, Rachel Kanakabandi, Kishore Virtaneva, Kimmo Porcella, Stephen F. Bloom, Marshall E. J Neurovirol Article Powassan virus (POWV) is a tick-borne Flavivirus responsible for life-threatening encephalitis in North America and some regions of Russia. The ticks that have been reported to transmit the virus belong to the Ixodes species, and they feed on small-to-medium-sized mammals, such as Peromyscus leucopus mice, skunks, and woodchucks. We previously developed a P. leucopus mouse model of POWV infection, and the model is characterized by a lack of clinical signs of disease following intraperitoneal or intracranial inoculation. However, intracranial inoculation results in mild subclinical encephalitis from 5 days post infection (dpi), but the encephalitis resolves by 28 dpi. We used RNA sequencing to profile the P. leucopus mouse brain transcriptome at different time points after intracranial challenge with POWV. At 24 h post infection, 42 genes were significantly differentially expressed and the number peaked to 232 at 7 dpi before declining to 31 at 28 dpi. Using Ingenuity Pathway Analysis, we determined that the genes that were significantly expressed from 1 to 15 dpi were mainly associated with interferon signaling. As a result, many interferon-stimulated genes (ISGs) were upregulated. Some of the ISGs include an array of TRIMs (genes encoding tripartite motif proteins). These results will be useful for the identification of POWV restriction factors. Springer International Publishing 2017-11-16 2018 /pmc/articles/PMC5790856/ /pubmed/29147886 http://dx.doi.org/10.1007/s13365-017-0596-y Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Mlera, Luwanika
Meade-White, Kimberly
Dahlstrom, Eric
Baur, Rachel
Kanakabandi, Kishore
Virtaneva, Kimmo
Porcella, Stephen F.
Bloom, Marshall E.
Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title_full Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title_fullStr Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title_full_unstemmed Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title_short Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection
title_sort peromyscus leucopus mouse brain transcriptome response to powassan virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790856/
https://www.ncbi.nlm.nih.gov/pubmed/29147886
http://dx.doi.org/10.1007/s13365-017-0596-y
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