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Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells

Chicken embryo fibroblast DF-1 cells are increasingly being used in the production of avian virus vaccines. However, the relatively low proliferative capacity does not meet the requirements of industrial production. In this study, we attempted to improve the proliferative capacity of DF-1 cells. The...

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Detalles Bibliográficos
Autores principales: Lin, Jia, Yi, Xiaoping, Zhuang, Yingping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070647/
https://www.ncbi.nlm.nih.gov/pubmed/35529190
http://dx.doi.org/10.1039/c9ra05128g
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author Lin, Jia
Yi, Xiaoping
Zhuang, Yingping
author_facet Lin, Jia
Yi, Xiaoping
Zhuang, Yingping
author_sort Lin, Jia
collection PubMed
description Chicken embryo fibroblast DF-1 cells are increasingly being used in the production of avian virus vaccines. However, the relatively low proliferative capacity does not meet the requirements of industrial production. In this study, we attempted to improve the proliferative capacity of DF-1 cells. The results of intracellular metabolomics showed that 28 types of metabolites could play roles in DF-1 cell growth based on the variance and timing analysis of intracellular metabolites from DF-1 cells grown in two media with distinct growth difference, DMEM/F12 (1 : 1) and DMEM. By examining the differences in the components in the two media, DOE was used to screen and optimize the growth medium for DF-1 cells. The maximum cell density was 40.72% higher, and the infectious bursal disease virus (IBDV) titer was 2.68 times higher, in the optimized medium than in the control. This study proposes a complete solution from metabolomics to media optimization.
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spelling pubmed-90706472022-05-05 Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells Lin, Jia Yi, Xiaoping Zhuang, Yingping RSC Adv Chemistry Chicken embryo fibroblast DF-1 cells are increasingly being used in the production of avian virus vaccines. However, the relatively low proliferative capacity does not meet the requirements of industrial production. In this study, we attempted to improve the proliferative capacity of DF-1 cells. The results of intracellular metabolomics showed that 28 types of metabolites could play roles in DF-1 cell growth based on the variance and timing analysis of intracellular metabolites from DF-1 cells grown in two media with distinct growth difference, DMEM/F12 (1 : 1) and DMEM. By examining the differences in the components in the two media, DOE was used to screen and optimize the growth medium for DF-1 cells. The maximum cell density was 40.72% higher, and the infectious bursal disease virus (IBDV) titer was 2.68 times higher, in the optimized medium than in the control. This study proposes a complete solution from metabolomics to media optimization. The Royal Society of Chemistry 2019-08-30 /pmc/articles/PMC9070647/ /pubmed/35529190 http://dx.doi.org/10.1039/c9ra05128g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Lin, Jia
Yi, Xiaoping
Zhuang, Yingping
Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title_full Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title_fullStr Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title_full_unstemmed Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title_short Medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast DF-1 cells
title_sort medium optimization based on comparative metabolomic analysis of chicken embryo fibroblast df-1 cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070647/
https://www.ncbi.nlm.nih.gov/pubmed/35529190
http://dx.doi.org/10.1039/c9ra05128g
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