Literature DB >> 19003369

The new medium MDSS2N, free of any animal protein supports cell growth and production of various viruses.

O W Merten1, H Kallel, J C Manuguerra, M Tardy-Panit, R Crainic, F Delpeyroux, S Van der Werf, P Perrin.   

Abstract

The development of media free of serum and animal or human proteins is of utmost importance for increasing the safety of biologicals produced for therapy and vaccination. In order to reduce the risk of contamination, we have modified the serum free medium MDSS2, a very efficient serum free medium for the production of various biologicals including experimental vaccines using different cell lines (Merten et al., 1994), by replacing the animal derived products by plant extracts. The new serum and animal protein free medium (MDSS2N) can be efficiently used for biomass production of various cell lines. These cells grow equally well or better in this new serum-free medium than in the old formulation (MDSS2):* BHK-21/BRS cells, adapted to MDSS2N, showed an overall specific growth rate of 0.0197 h-1 (mu_max = 0.0510+/-0.0058 h-1), whereas those cultivated in MDSS2 grew with an average specific growth rate of 0.0179 h-1 (mu_max = 0.0305+/-0.0177 h-1).* Vero cells grew with an average specific growth rate of 0.0159 h-1 and 0.0153 h-1 in MDSS2 and MDSS2N, respectively. Very similar growth rates were obtained in microcarrier cultures in stirred tank reactors: the specific growth rates were 0.0161 h-1 and 0.0166 h-1 for MDSS2 and MDSS2N cultures, respectively.* For MDCK cells, when cultured on microcarriers in bioreactors, a higher average specific growth rate was observed in MDSS2N than in MDSS2; values of 0.0248 h-1 and 0.0168 h-1, respectively, were obtained.The capacity of MDSS2N to support the production of different viruses was equally evaluated and it could be established that for certain viruses there are no or insignificant differences between MDSS2N and MDSS2 (influenza and polio virus), whereas, the production of rabies virus is somewhat reduced in MDSS2N when compared to MDSS2. The use of MDSS2N for cell culture and the production of various viruses is discussed.

Entities:  

Year:  1999        PMID: 19003369      PMCID: PMC3449943          DOI: 10.1023/A:1008021317639

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  22 in total

1.  Evaluation of the serum-free medium MDSS2 for the production of poliovirus on vero cells in bioreactors.

Authors:  O W Merten; R Wu; E Couvé; R Crainic
Journal:  Cytotechnology       Date:  1997-11       Impact factor: 2.058

2.  Peptone, a low-cost growth-promoting nutrient for intensive animal cell culture.

Authors:  D C Jan; S J Jones; A N Emery; M al-Rubeai
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

3.  Thousand litre scale microcarrier culture of Vero cells for killed polio virus vaccine. Promising results.

Authors:  B Montagnon; J C Vincent-Falquet; B Fanget
Journal:  Dev Biol Stand       Date:  1983

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Authors:  L Keay
Journal:  Methods Cell Biol       Date:  1978       Impact factor: 1.441

5.  The large-scale cultivation of VERO cells in micro-carrier culture for virus vaccine production. Preliminary results for killed poliovirus vaccine.

Authors:  B J Montagnon; B Fanget; A J Nicolas
Journal:  Dev Biol Stand       Date:  1981

6.  Production of influenza virus in serum-free mammalian cell cultures.

Authors:  O W Merten; J C Manuguerra; C Hannoun; S van der Werf
Journal:  Dev Biol Stand       Date:  1999

7.  Recombinant Human Albumin in Cell Culture: Evaluation of Growth-Promoting Potential for NRK and SCC-9 Cells In Vitro.

Authors:  J Keenan; M Dooley; D Pearson; M Clynes
Journal:  Cytotechnology       Date:  1997-09       Impact factor: 2.058

8.  Serum-free growth medium for the cultivation of a wide spectrum of mammalian cells in stirred bioreactors.

Authors:  V Jäger; J Lehmann; P Friedl
Journal:  Cytotechnology       Date:  1988-11       Impact factor: 2.058

9.  Optimisation of hybridoma cell growth and monoclonal antibody secretion in a chemically defined, serum- and protein-free culture medium.

Authors:  Y J Schneider
Journal:  J Immunol Methods       Date:  1989-01-06       Impact factor: 2.303

10.  Role of iron chelators in growth-promoting effect on mouse hybridoma cells in a chemically defined medium.

Authors:  N Yabe; M Kato; Y Matsuya; I Yamane; M Iizuka; H Takayoshi; K Suzuki
Journal:  In Vitro Cell Dev Biol       Date:  1987-12
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  7 in total

1.  The role of recombinant proteins in the development of serum-free media.

Authors:  Joanne Keenan; Dermot Pearson; Martin Clynes
Journal:  Cytotechnology       Date:  2006-08-05       Impact factor: 2.058

2.  Semliki Forest Virus replicon particles production in serum-free medium BHK-21 cell cultures and their use to express different proteins.

Authors:  Sandra Fernanda Suárez-Patiño; Thaissa Consoni Bernardino; Eutimio Gustavo Fernández Núñez; Renato Mancini Astray; Carlos Augusto Pereira; Hugo R Soares; Ana S Coroadinha; Soraia Attie Calil Jorge
Journal:  Cytotechnology       Date:  2019-08-17       Impact factor: 2.058

3.  BHK 21 C13 cells for Aujeszky's disease virus production using the multiple harvest process.

Authors:  Visnja Gaurina Srcek; Stanislav Cajavec; Davor Sladić; Zlatko Kniewald
Journal:  Cytotechnology       Date:  2004-07       Impact factor: 2.058

4.  Characterisation of BHK-21 cells engineered to secrete human insulin.

Authors:  Patrick Gammell; Lorraine O'Driscoll; Martin Clynes
Journal:  Cytotechnology       Date:  2003-01       Impact factor: 2.058

5.  Evaluation of recombinant human transferrin (DeltaFerrin(TM)) as an iron chelator in serum-free media for mammalian cell culture.

Authors:  Joanne Keenan; Dermot Pearson; Lorraine O'Driscoll; Patrick Gammell; Martin Clynes
Journal:  Cytotechnology       Date:  2006-08-03       Impact factor: 2.058

6.  Production of inactivated influenza H5N1 vaccines from MDCK cells in serum-free medium.

Authors:  Alan Yung-Chih Hu; Yu-Fen Tseng; Tsai-Chuan Weng; Chien-Chun Liao; Johnson Wu; Ai-Hsiang Chou; Hsin-Ju Chao; Anna Gu; Janice Chen; Su-Chen Lin; Chia-Hsin Hsiao; Suh-Chin Wu; Pele Chong
Journal:  PLoS One       Date:  2011-01-24       Impact factor: 3.240

7.  Growth characteristics of canine pathogenic viruses in MDCK cells cultured in RPMI 1640 medium without animal protein.

Authors:  Masami Mochizuki
Journal:  Vaccine       Date:  2005-10-25       Impact factor: 3.641

  7 in total

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