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Development of improved vaccine cell lines against rotavirus
Rotavirus is a major cause of severe gastroenteritis among very young children. In developing countries, rotavirus is the major cause of mortality in children under five years old, causing up to 20% of all childhood deaths in countries with high diarrheal disease burden, with more than 90% of these...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332008/ https://www.ncbi.nlm.nih.gov/pubmed/28248921 http://dx.doi.org/10.1038/sdata.2017.21 |
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author | Wu, Weilin Orr-Burks, Nichole Karpilow, Jon Tripp, Ralph A. |
author_facet | Wu, Weilin Orr-Burks, Nichole Karpilow, Jon Tripp, Ralph A. |
author_sort | Wu, Weilin |
collection | PubMed |
description | Rotavirus is a major cause of severe gastroenteritis among very young children. In developing countries, rotavirus is the major cause of mortality in children under five years old, causing up to 20% of all childhood deaths in countries with high diarrheal disease burden, with more than 90% of these deaths occurring in Africa and Asia. Rotavirus vaccination mimics the first infection without causing illness, thus inducing strong and broad heterotypic immunity against prospective rotavirus infections. Two live vaccines are available, Rotarix and RotaTeq, but vaccination efforts are hampered by high production costs. Here, we present a dataset containing a genome-wide RNA interference (RNAi) screen that identified silencing events that enhanced rotavirus replication. Evaluated against several rotavirus vaccine strains, hits were validated in a Vero vaccine cell line as well as CRISPR/Cas9 generated cells permanently and stably lacking the genes that affect RV replication. Knockout cells were dramatically more permissive to RV replication and permitted an increase in rotavirus replication. These data show a means to improve manufacturing of rotavirus vaccine. |
format | Online Article Text |
id | pubmed-5332008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53320082017-03-03 Development of improved vaccine cell lines against rotavirus Wu, Weilin Orr-Burks, Nichole Karpilow, Jon Tripp, Ralph A. Sci Data Data Descriptor Rotavirus is a major cause of severe gastroenteritis among very young children. In developing countries, rotavirus is the major cause of mortality in children under five years old, causing up to 20% of all childhood deaths in countries with high diarrheal disease burden, with more than 90% of these deaths occurring in Africa and Asia. Rotavirus vaccination mimics the first infection without causing illness, thus inducing strong and broad heterotypic immunity against prospective rotavirus infections. Two live vaccines are available, Rotarix and RotaTeq, but vaccination efforts are hampered by high production costs. Here, we present a dataset containing a genome-wide RNA interference (RNAi) screen that identified silencing events that enhanced rotavirus replication. Evaluated against several rotavirus vaccine strains, hits were validated in a Vero vaccine cell line as well as CRISPR/Cas9 generated cells permanently and stably lacking the genes that affect RV replication. Knockout cells were dramatically more permissive to RV replication and permitted an increase in rotavirus replication. These data show a means to improve manufacturing of rotavirus vaccine. Nature Publishing Group 2017-03-01 /pmc/articles/PMC5332008/ /pubmed/28248921 http://dx.doi.org/10.1038/sdata.2017.21 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0 Metadata associated with this Data Descriptor is available at http://www.nature.com/sdata/ and is released under the CC0 waiver to maximize reuse. |
spellingShingle | Data Descriptor Wu, Weilin Orr-Burks, Nichole Karpilow, Jon Tripp, Ralph A. Development of improved vaccine cell lines against rotavirus |
title | Development of improved vaccine cell lines against rotavirus |
title_full | Development of improved vaccine cell lines against rotavirus |
title_fullStr | Development of improved vaccine cell lines against rotavirus |
title_full_unstemmed | Development of improved vaccine cell lines against rotavirus |
title_short | Development of improved vaccine cell lines against rotavirus |
title_sort | development of improved vaccine cell lines against rotavirus |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332008/ https://www.ncbi.nlm.nih.gov/pubmed/28248921 http://dx.doi.org/10.1038/sdata.2017.21 |
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