Cargando…
Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin
Tick-borne encephalitis virus (TBEV), a member of the genus Flavivirus (Flaviviridae), is a causative agent of a severe neuroinfection. Recently, several flaviviruses have been shown to interact with host protein synthesis. In order to determine whether TBEV interacts with this host process in its n...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785130/ https://www.ncbi.nlm.nih.gov/pubmed/31560682 http://dx.doi.org/10.1371/journal.pntd.0007745 |
_version_ | 1783457840555360256 |
---|---|
author | Selinger, Martin Tykalová, Hana Štěrba, Ján Věchtová, Pavlína Vavrušková, Zuzana Lieskovská, Jaroslava Kohl, Alain Schnettler, Esther Grubhoffer, Libor |
author_facet | Selinger, Martin Tykalová, Hana Štěrba, Ján Věchtová, Pavlína Vavrušková, Zuzana Lieskovská, Jaroslava Kohl, Alain Schnettler, Esther Grubhoffer, Libor |
author_sort | Selinger, Martin |
collection | PubMed |
description | Tick-borne encephalitis virus (TBEV), a member of the genus Flavivirus (Flaviviridae), is a causative agent of a severe neuroinfection. Recently, several flaviviruses have been shown to interact with host protein synthesis. In order to determine whether TBEV interacts with this host process in its natural target cells, we analysed de novo protein synthesis in a human cell line derived from cerebellar medulloblastoma (DAOY HTB-186). We observed a significant decrease in the rate of host protein synthesis, including the housekeeping genes HPRT1 and GAPDH and the known interferon-stimulated gene viperin. In addition, TBEV infection resulted in a specific decrease of RNA polymerase I (POLR1) transcripts, 18S and 28S rRNAs and their precursor, 45-47S pre-rRNA, but had no effect on the POLR3 transcribed 5S rRNA levels. To our knowledge, this is the first report of flavivirus-induced decrease of specifically POLR1 rRNA transcripts accompanied by host translational shut-off. |
format | Online Article Text |
id | pubmed-6785130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67851302019-10-18 Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin Selinger, Martin Tykalová, Hana Štěrba, Ján Věchtová, Pavlína Vavrušková, Zuzana Lieskovská, Jaroslava Kohl, Alain Schnettler, Esther Grubhoffer, Libor PLoS Negl Trop Dis Research Article Tick-borne encephalitis virus (TBEV), a member of the genus Flavivirus (Flaviviridae), is a causative agent of a severe neuroinfection. Recently, several flaviviruses have been shown to interact with host protein synthesis. In order to determine whether TBEV interacts with this host process in its natural target cells, we analysed de novo protein synthesis in a human cell line derived from cerebellar medulloblastoma (DAOY HTB-186). We observed a significant decrease in the rate of host protein synthesis, including the housekeeping genes HPRT1 and GAPDH and the known interferon-stimulated gene viperin. In addition, TBEV infection resulted in a specific decrease of RNA polymerase I (POLR1) transcripts, 18S and 28S rRNAs and their precursor, 45-47S pre-rRNA, but had no effect on the POLR3 transcribed 5S rRNA levels. To our knowledge, this is the first report of flavivirus-induced decrease of specifically POLR1 rRNA transcripts accompanied by host translational shut-off. Public Library of Science 2019-09-27 /pmc/articles/PMC6785130/ /pubmed/31560682 http://dx.doi.org/10.1371/journal.pntd.0007745 Text en © 2019 Selinger et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Selinger, Martin Tykalová, Hana Štěrba, Ján Věchtová, Pavlína Vavrušková, Zuzana Lieskovská, Jaroslava Kohl, Alain Schnettler, Esther Grubhoffer, Libor Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title | Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title_full | Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title_fullStr | Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title_full_unstemmed | Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title_short | Tick-borne encephalitis virus inhibits rRNA synthesis and host protein production in human cells of neural origin |
title_sort | tick-borne encephalitis virus inhibits rrna synthesis and host protein production in human cells of neural origin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785130/ https://www.ncbi.nlm.nih.gov/pubmed/31560682 http://dx.doi.org/10.1371/journal.pntd.0007745 |
work_keys_str_mv | AT selingermartin tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT tykalovahana tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT sterbajan tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT vechtovapavlina tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT vavruskovazuzana tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT lieskovskajaroslava tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT kohlalain tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT schnettleresther tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin AT grubhofferlibor tickborneencephalitisvirusinhibitsrrnasynthesisandhostproteinproductioninhumancellsofneuralorigin |