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Investigation of cell culture conditions for optimal foot-and-mouth disease virus production
BACKGROUND: Foot-and-mouth disease is a highly contagious and economically devastating disease with endemic occurrence in many parts of the world. Vaccination is the method of choice to eradicate the disease and to limit the viral spread. The vaccine production process is based on mammalian cell cul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555971/ https://www.ncbi.nlm.nih.gov/pubmed/31174517 http://dx.doi.org/10.1186/s12896-019-0527-5 |
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author | Dill, Veronika Zimmer, Aline Beer, Martin Eschbaumer, Michael |
author_facet | Dill, Veronika Zimmer, Aline Beer, Martin Eschbaumer, Michael |
author_sort | Dill, Veronika |
collection | PubMed |
description | BACKGROUND: Foot-and-mouth disease is a highly contagious and economically devastating disease with endemic occurrence in many parts of the world. Vaccination is the method of choice to eradicate the disease and to limit the viral spread. The vaccine production process is based on mammalian cell culture, in which the viral yield varies in dependence of the composition of the culture media. For foot-and-mouth disease virus (FMDV), very little is known about the culture media components that are necessary to grow the virus to high titers in cell culture. RESULTS: This study examined the influence of increasing concentrations of glucose, glutamine, ammonium chloride and different cell densities on the yield of FMDV. While an excess of glucose or glutamine does not affect the viral yield, increasing cell density reduces the viral titer by a log(10) step at a cell density of 3 × 10(6) cells/mL. This can be mitigated by performing a 100% media exchange before infection of the cells. CONCLUSIONS: The reasons for the diminished viral growth, if no complete media exchange has been performed prior to infection, remain unclear and further studies are necessary to investigate the causes more deeply. For now, the results argue for a vaccine production process with 100% media exchange to reliably obtain high viral titers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0527-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6555971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65559712019-06-10 Investigation of cell culture conditions for optimal foot-and-mouth disease virus production Dill, Veronika Zimmer, Aline Beer, Martin Eschbaumer, Michael BMC Biotechnol Research Article BACKGROUND: Foot-and-mouth disease is a highly contagious and economically devastating disease with endemic occurrence in many parts of the world. Vaccination is the method of choice to eradicate the disease and to limit the viral spread. The vaccine production process is based on mammalian cell culture, in which the viral yield varies in dependence of the composition of the culture media. For foot-and-mouth disease virus (FMDV), very little is known about the culture media components that are necessary to grow the virus to high titers in cell culture. RESULTS: This study examined the influence of increasing concentrations of glucose, glutamine, ammonium chloride and different cell densities on the yield of FMDV. While an excess of glucose or glutamine does not affect the viral yield, increasing cell density reduces the viral titer by a log(10) step at a cell density of 3 × 10(6) cells/mL. This can be mitigated by performing a 100% media exchange before infection of the cells. CONCLUSIONS: The reasons for the diminished viral growth, if no complete media exchange has been performed prior to infection, remain unclear and further studies are necessary to investigate the causes more deeply. For now, the results argue for a vaccine production process with 100% media exchange to reliably obtain high viral titers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0527-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-07 /pmc/articles/PMC6555971/ /pubmed/31174517 http://dx.doi.org/10.1186/s12896-019-0527-5 Text en © The Author(s). 2019 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Dill, Veronika Zimmer, Aline Beer, Martin Eschbaumer, Michael Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title | Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title_full | Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title_fullStr | Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title_full_unstemmed | Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title_short | Investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
title_sort | investigation of cell culture conditions for optimal foot-and-mouth disease virus production |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555971/ https://www.ncbi.nlm.nih.gov/pubmed/31174517 http://dx.doi.org/10.1186/s12896-019-0527-5 |
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