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Alterations in the host transcriptome in vitro following Rift Valley fever virus infection

Rift Valley fever virus (RVFV) causes major outbreaks among livestock, characterized by “abortion storms” in which spontaneous abortion occurs in almost 100% of pregnant ruminants. Humans can also become infected with mild symptoms that can progress to more severe symptoms, such as hepatitis, enceph...

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Autores principales: Pinkham, Chelsea, Dahal, Bibha, de la Fuente, Cynthia L., Bracci, Nicole, Beitzel, Brett, Lindquist, Michael, Garrison, Aura, Schmaljohn, Connie, Palacios, Gustavo, Narayanan, Aarthi, Campbell, Catherine E., Kehn-Hall, Kylene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662566/
https://www.ncbi.nlm.nih.gov/pubmed/29085037
http://dx.doi.org/10.1038/s41598-017-14800-3
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author Pinkham, Chelsea
Dahal, Bibha
de la Fuente, Cynthia L.
Bracci, Nicole
Beitzel, Brett
Lindquist, Michael
Garrison, Aura
Schmaljohn, Connie
Palacios, Gustavo
Narayanan, Aarthi
Campbell, Catherine E.
Kehn-Hall, Kylene
author_facet Pinkham, Chelsea
Dahal, Bibha
de la Fuente, Cynthia L.
Bracci, Nicole
Beitzel, Brett
Lindquist, Michael
Garrison, Aura
Schmaljohn, Connie
Palacios, Gustavo
Narayanan, Aarthi
Campbell, Catherine E.
Kehn-Hall, Kylene
author_sort Pinkham, Chelsea
collection PubMed
description Rift Valley fever virus (RVFV) causes major outbreaks among livestock, characterized by “abortion storms” in which spontaneous abortion occurs in almost 100% of pregnant ruminants. Humans can also become infected with mild symptoms that can progress to more severe symptoms, such as hepatitis, encephalitis, and hemorrhagic fever. The goal of this study was to use RNA-sequencing (RNA-seq) to analyze the host transcriptome in response to RVFV infection. G2/M DNA damage checkpoint, ATM signaling, mitochondrial dysfunction, regulation of the antiviral response, and integrin-linked kinase (ILK) signaling were among the top altered canonical pathways with both the attenuated MP12 strain and the fully virulent ZH548 strain. Although several mRNA transcripts were highly upregulated, an increase at the protein level was not observed for the selected genes, which was at least partially due to the NSs dependent block in mRNA export. Inhibition of ILK signaling, which is involved in cell motility and cytoskeletal reorganization, resulted in reduced RVFV replication, indicating that this pathway is important for viral replication. Overall, this is the first global transcriptomic analysis of the human host response following RVFV infection, which could give insight into novel host responses that have not yet been explored.
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spelling pubmed-56625662017-11-08 Alterations in the host transcriptome in vitro following Rift Valley fever virus infection Pinkham, Chelsea Dahal, Bibha de la Fuente, Cynthia L. Bracci, Nicole Beitzel, Brett Lindquist, Michael Garrison, Aura Schmaljohn, Connie Palacios, Gustavo Narayanan, Aarthi Campbell, Catherine E. Kehn-Hall, Kylene Sci Rep Article Rift Valley fever virus (RVFV) causes major outbreaks among livestock, characterized by “abortion storms” in which spontaneous abortion occurs in almost 100% of pregnant ruminants. Humans can also become infected with mild symptoms that can progress to more severe symptoms, such as hepatitis, encephalitis, and hemorrhagic fever. The goal of this study was to use RNA-sequencing (RNA-seq) to analyze the host transcriptome in response to RVFV infection. G2/M DNA damage checkpoint, ATM signaling, mitochondrial dysfunction, regulation of the antiviral response, and integrin-linked kinase (ILK) signaling were among the top altered canonical pathways with both the attenuated MP12 strain and the fully virulent ZH548 strain. Although several mRNA transcripts were highly upregulated, an increase at the protein level was not observed for the selected genes, which was at least partially due to the NSs dependent block in mRNA export. Inhibition of ILK signaling, which is involved in cell motility and cytoskeletal reorganization, resulted in reduced RVFV replication, indicating that this pathway is important for viral replication. Overall, this is the first global transcriptomic analysis of the human host response following RVFV infection, which could give insight into novel host responses that have not yet been explored. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662566/ /pubmed/29085037 http://dx.doi.org/10.1038/s41598-017-14800-3 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pinkham, Chelsea
Dahal, Bibha
de la Fuente, Cynthia L.
Bracci, Nicole
Beitzel, Brett
Lindquist, Michael
Garrison, Aura
Schmaljohn, Connie
Palacios, Gustavo
Narayanan, Aarthi
Campbell, Catherine E.
Kehn-Hall, Kylene
Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title_full Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title_fullStr Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title_full_unstemmed Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title_short Alterations in the host transcriptome in vitro following Rift Valley fever virus infection
title_sort alterations in the host transcriptome in vitro following rift valley fever virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662566/
https://www.ncbi.nlm.nih.gov/pubmed/29085037
http://dx.doi.org/10.1038/s41598-017-14800-3
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