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Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate
African green monkey (AGM)-derived Vero cells have been utilized to produce various human vaccines. The Vero cell genome harbors a variety of simian endogenous type D retrovirus (SERV) sequences. In this study, a transcriptome analysis showed that DNA hypomethylation released the epigenetic repressi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766633/ https://www.ncbi.nlm.nih.gov/pubmed/29330501 http://dx.doi.org/10.1038/s41598-017-18934-2 |
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author | Sakuma, Chisato Sekizuka, Tsuyoshi Kuroda, Makoto Kasai, Fumio Saito, Kyoko Ikeda, Masaki Yamaji, Toshiyuki Osada, Naoki Hanada, Kentaro |
author_facet | Sakuma, Chisato Sekizuka, Tsuyoshi Kuroda, Makoto Kasai, Fumio Saito, Kyoko Ikeda, Masaki Yamaji, Toshiyuki Osada, Naoki Hanada, Kentaro |
author_sort | Sakuma, Chisato |
collection | PubMed |
description | African green monkey (AGM)-derived Vero cells have been utilized to produce various human vaccines. The Vero cell genome harbors a variety of simian endogenous type D retrovirus (SERV) sequences. In this study, a transcriptome analysis showed that DNA hypomethylation released the epigenetic repression of SERVs in Vero cells. Moreover, comparative genomic analysis of three Vero cell sublines and an AGM reference revealed that the genomes of the sublines have ~80 SERV integrations. Among them, ~60 integrations are present within all three cell sublines and absent from the reference sequence. At least several of these integrations consist of complete SERV proviruses. These results strongly suggest that SERVs integrated in the genome of Vero cells did not retrotranspose after the establishment of the cell lineage as far as cells were maintained under standard culture and passage conditions, providing a scientific basis for controlling the quality of pharmaceutical cell substrates and their derived biologics. |
format | Online Article Text |
id | pubmed-5766633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57666332018-01-25 Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate Sakuma, Chisato Sekizuka, Tsuyoshi Kuroda, Makoto Kasai, Fumio Saito, Kyoko Ikeda, Masaki Yamaji, Toshiyuki Osada, Naoki Hanada, Kentaro Sci Rep Article African green monkey (AGM)-derived Vero cells have been utilized to produce various human vaccines. The Vero cell genome harbors a variety of simian endogenous type D retrovirus (SERV) sequences. In this study, a transcriptome analysis showed that DNA hypomethylation released the epigenetic repression of SERVs in Vero cells. Moreover, comparative genomic analysis of three Vero cell sublines and an AGM reference revealed that the genomes of the sublines have ~80 SERV integrations. Among them, ~60 integrations are present within all three cell sublines and absent from the reference sequence. At least several of these integrations consist of complete SERV proviruses. These results strongly suggest that SERVs integrated in the genome of Vero cells did not retrotranspose after the establishment of the cell lineage as far as cells were maintained under standard culture and passage conditions, providing a scientific basis for controlling the quality of pharmaceutical cell substrates and their derived biologics. Nature Publishing Group UK 2018-01-12 /pmc/articles/PMC5766633/ /pubmed/29330501 http://dx.doi.org/10.1038/s41598-017-18934-2 Text en © The Author(s) 2018 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 Sakuma, Chisato Sekizuka, Tsuyoshi Kuroda, Makoto Kasai, Fumio Saito, Kyoko Ikeda, Masaki Yamaji, Toshiyuki Osada, Naoki Hanada, Kentaro Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title | Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title_full | Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title_fullStr | Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title_full_unstemmed | Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title_short | Novel endogenous simian retroviral integrations in Vero cells: implications for quality control of a human vaccine cell substrate |
title_sort | novel endogenous simian retroviral integrations in vero cells: implications for quality control of a human vaccine cell substrate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766633/ https://www.ncbi.nlm.nih.gov/pubmed/29330501 http://dx.doi.org/10.1038/s41598-017-18934-2 |
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