High-Density Microcarrier Cell Cultures for Influenza Virus Production

被引:36
作者
Bock, A. [1 ]
Schulze-Horsel, J. [1 ]
Schwarzer, J. [1 ]
Rapp, E. [1 ]
Genzel, Y. [1 ]
Reichl, U. [1 ,2 ]
机构
[1] Max Planck Inst Dynam Complex Tech Syst, D-39106 Magdeburg, Germany
[2] Univ Magdeburg, Chair Bioproc Engn, D-39106 Magdeburg, Germany
关键词
high-density cell culture; MDCK; microcarrier; influenza; vaccine; PERFUSION CULTURE; RECOMBINANT PROTEINS; VECTOR PRODUCTION; GLYCAN ANALYSIS; RABIES VACCINE; INSECT CELLS; MDCK CELLS; FREE MEDIA; SERUM; BACULOVIRUS;
D O I
10.1002/btpr.539
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Influenza virus A/PR/8/34 virus propagation in adherent Madin-Darby canine kidney cells in high-density microcarrier cultures is described. To improve virus yields, perfusion and repeated fed-batch modes were applied using cell-specific feed rates. Cell densities up to 1.1 x 10(7) cells/mL were achieved. Cell-specific virus yields in high-density cultures were at similar levels compared with standard, low-density cultivations. In the average 2,400 and 3,300 virions per cell were obtained for two variants of the virus strain A/PR/8/34, PR8-National Institute for Biological Standards and Control (NIBSC) and PR8-Robert Koch Institute, respectively. Maximum virus titer (HA activity = 1,778 HAU/100 mu L) for virus variant PR8-NIBSC was obtained for a cultivation infected before maximum cell concentration was reached. (C) 2011 American Institute of Chemical Engineers Biotechnol. Prog., 27: 241-250, 2011
引用
收藏
页码:241 / 250
页数:10
相关论文
共 46 条
[1]   Production of recombinant proteins by vaccinia virus in a microcarrier based mammalian cell perfusion bioreactor [J].
Bleckwenn, NA ;
Golding, H ;
Bentley, WE ;
Shiloach, J .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (06) :663-674
[2]   Growth Behavior of Number Distributed Adherent MDCK Cells for Optimization in Microcarrier Cultures [J].
Bock, Andreas ;
Sann, Heiner ;
Schulze-Horsel, Josef ;
Genzel, Yvonne ;
Reichl, Udo ;
Moehler, Lars .
BIOTECHNOLOGY PROGRESS, 2009, 25 (06) :1717-1731
[3]  
Burleson F.G., 1992, VIROLOGY LAB MANUAL
[4]  
BUTLER M, 1983, J CELL SCI, V61, P351
[5]   Optimisation of the cellular metabolism of glycosylation for recombinant proteins produced by mammalian cell systems [J].
Butler, M. .
CYTOTECHNOLOGY, 2006, 50 (1-3) :57-76
[6]  
Castilho Leda R, 2002, Adv Biochem Eng Biotechnol, V74, P129
[7]  
Chico E, 2000, BIOTECHNOL BIOENG, V70, P574, DOI 10.1002/1097-0290(20001205)70:5<574::AID-BIT12>3.0.CO
[8]  
2-Q
[9]   PLAQUE FORMATION BY INFLUENZA A2 VIRUS IN MONKEY KIDNEY CELLS [J].
CHOPPIN, PW .
VIROLOGY, 1962, 18 (02) :332-&
[10]   A perfusion culture system using a stirred ceramic membrane reactor for hyperproduction of IgG2a monoclonal antibody by hybridoma cells [J].
Dong, H ;
Tang, YJ ;
Ohashi, R ;
Hamel, JFP .
BIOTECHNOLOGY PROGRESS, 2005, 21 (01) :140-147