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SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the value of pursuing different vaccine strategies. Vaccines based on whole viruses, a widely used vaccine technology, depend on efficient virus production. This study aimed to establish SARS-CoV-2 production...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310283/ https://www.ncbi.nlm.nih.gov/pubmed/34209694 http://dx.doi.org/10.3390/vaccines9070706 |
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author | Offersgaard, Anna Duarte Hernandez, Carlos Rene Pihl, Anne Finne Costa, Rui Venkatesan, Nandini Prabhakar Lin, Xiangliang Van Pham, Long Feng, Shan Fahnøe, Ulrik Scheel, Troels Kasper Høyer Ramirez, Santseharay Reichl, Udo Bukh, Jens Genzel, Yvonne Gottwein, Judith Margarete |
author_facet | Offersgaard, Anna Duarte Hernandez, Carlos Rene Pihl, Anne Finne Costa, Rui Venkatesan, Nandini Prabhakar Lin, Xiangliang Van Pham, Long Feng, Shan Fahnøe, Ulrik Scheel, Troels Kasper Høyer Ramirez, Santseharay Reichl, Udo Bukh, Jens Genzel, Yvonne Gottwein, Judith Margarete |
author_sort | Offersgaard, Anna |
collection | PubMed |
description | The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the value of pursuing different vaccine strategies. Vaccines based on whole viruses, a widely used vaccine technology, depend on efficient virus production. This study aimed to establish SARS-CoV-2 production in the scalable packed-bed CelCradle(TM) 500-AP bioreactor. CelCradle(TM) 500-AP bottles with 0.5 L working volume and 5.5 g BioNOC™ II carriers were seeded with 1.5 × 10(8) Vero (WHO) cells, approved for vaccine production, in animal component-free medium and infected at a multiplicity of infection of 0.006 at a total cell number of 2.2–2.5 × 10(9) cells/bottle seven days post cell seeding. Among several tested conditions, two harvests per day and a virus production temperature of 33 °C resulted in the highest virus yield with a peak SARS-CoV-2 infectivity titer of 7.3 log(10) 50% tissue culture infectious dose (TCID(50))/mL at 72 h post-infection. Six harvests had titers of ≥6.5 log(10) TCID(50)/mL, and a total of 10.5 log(10) TCID(50) were produced in ~5 L. While trypsin was reported to enhance virus spread in cell culture, addition of 0.5% recombinant trypsin after infection did not improve virus yields. Overall, we demonstrated successful animal component-free production of SARS-CoV-2 in well-characterized Vero (WHO) cells in a scalable packed-bed bioreactor. |
format | Online Article Text |
id | pubmed-8310283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83102832021-07-25 SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor Offersgaard, Anna Duarte Hernandez, Carlos Rene Pihl, Anne Finne Costa, Rui Venkatesan, Nandini Prabhakar Lin, Xiangliang Van Pham, Long Feng, Shan Fahnøe, Ulrik Scheel, Troels Kasper Høyer Ramirez, Santseharay Reichl, Udo Bukh, Jens Genzel, Yvonne Gottwein, Judith Margarete Vaccines (Basel) Article The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the value of pursuing different vaccine strategies. Vaccines based on whole viruses, a widely used vaccine technology, depend on efficient virus production. This study aimed to establish SARS-CoV-2 production in the scalable packed-bed CelCradle(TM) 500-AP bioreactor. CelCradle(TM) 500-AP bottles with 0.5 L working volume and 5.5 g BioNOC™ II carriers were seeded with 1.5 × 10(8) Vero (WHO) cells, approved for vaccine production, in animal component-free medium and infected at a multiplicity of infection of 0.006 at a total cell number of 2.2–2.5 × 10(9) cells/bottle seven days post cell seeding. Among several tested conditions, two harvests per day and a virus production temperature of 33 °C resulted in the highest virus yield with a peak SARS-CoV-2 infectivity titer of 7.3 log(10) 50% tissue culture infectious dose (TCID(50))/mL at 72 h post-infection. Six harvests had titers of ≥6.5 log(10) TCID(50)/mL, and a total of 10.5 log(10) TCID(50) were produced in ~5 L. While trypsin was reported to enhance virus spread in cell culture, addition of 0.5% recombinant trypsin after infection did not improve virus yields. Overall, we demonstrated successful animal component-free production of SARS-CoV-2 in well-characterized Vero (WHO) cells in a scalable packed-bed bioreactor. MDPI 2021-06-29 /pmc/articles/PMC8310283/ /pubmed/34209694 http://dx.doi.org/10.3390/vaccines9070706 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Offersgaard, Anna Duarte Hernandez, Carlos Rene Pihl, Anne Finne Costa, Rui Venkatesan, Nandini Prabhakar Lin, Xiangliang Van Pham, Long Feng, Shan Fahnøe, Ulrik Scheel, Troels Kasper Høyer Ramirez, Santseharay Reichl, Udo Bukh, Jens Genzel, Yvonne Gottwein, Judith Margarete SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title | SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title_full | SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title_fullStr | SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title_full_unstemmed | SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title_short | SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor |
title_sort | sars-cov-2 production in a scalable high cell density bioreactor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310283/ https://www.ncbi.nlm.nih.gov/pubmed/34209694 http://dx.doi.org/10.3390/vaccines9070706 |
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