Characterization of changes in PER.C6™ cellular metabolism during growth and propagation of a replication-deficient adenovirus vector

被引:25
作者
Maranga, L [1 ]
Aunins, JG [1 ]
Zhou, WC [1 ]
机构
[1] Merck & Co Inc, Merck Res Labs, Bioproc R&D, Fermentat & Cell Culture, W Point, PA 19486 USA
关键词
adenovirus; PER.C6; cells; cell metabolism; medium exchange;
D O I
10.1002/bit.20455
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
PER.C6 cells were cultivated for propagation of a replication-defective adenovirus vector in serum-free suspension bioreactors. Cellular metabolism during cell growth and adenovirus propagation was fully characterized using on-line and off-line methods. The energy metabolism was found to accelerate transiently after adenovirus infection with increases in glucose and oxygen consumption rates. Similar to other mammalian cells, glucose utilization was highly inefficient and a high lactate: glucose yield was observed, both before and after virus infection. A higher consumption of most of the essential amino acids was observed transiently after the infection, likely due to increased protein synthesis requirements for virus propagation. To improve virus propagation, a medium exchange strategy was implemented to increase PER.C6 cell concentration for infection. During cell growth, a 50% increase in glucose consumption and lactate production rates was observed after initiation of the medium exchange in comparison to the batch phase. This decrease in medium capacity only affected the central carbon metabolism and no increase in amino acid consumption was observed. In addition, even though cell concentrations of up to 10 x 10(6) cells/mL were reproducibly obtained by medium exchange, infections at cell concentrations higher than 1 x 10 cells/mL did not proportionally Improve volumetric adenovirus productivities. No measured nutrient limitation was observed at those high cell concentrations, indicating that adenovirus cell-specific productivity at higher cell concentrations is highly dependent on cell physiology. These results provide a better understanding of PER.C6 cellular metabolism and a basis for intensifying PER.C6 growth and adenovirus propagation. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:645 / 655
页数:11
相关论文
共 37 条
[1]  
BELLO LEONARD J., 1967, J VIROL, V1, P843
[2]   Induction of cell death by adenoviruses [J].
Braithwaite, AW ;
Russell, IA .
APOPTOSIS, 2001, 6 (05) :359-370
[3]  
Castilho Leda R, 2002, Adv Biochem Eng Biotechnol, V74, P129
[4]  
Côté J, 1998, BIOTECHNOL BIOENG, V59, P567, DOI 10.1002/(SICI)1097-0290(19980905)59:5<567::AID-BIT6>3.0.CO
[5]  
2-8
[6]   New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses [J].
Fallaux, FJ ;
Bout, A ;
Van der Velde, I ;
Van den Wollenberg, DJM ;
Hehir, KM ;
Keegan, J ;
Auger, C ;
Cramer, SJ ;
Van Ormondt, H ;
Van der Eb, AJ ;
Valerio, D ;
Hoeben, RC .
HUMAN GENE THERAPY, 1998, 9 (13) :1909-1917
[7]   On-line measurement of green fluorescent protein (GFP) fluorescence for the monitoring of recombinant adenovirus production [J].
Gilbert, PA ;
Garnier, A ;
Jacob, D ;
Kamen, A .
BIOTECHNOLOGY LETTERS, 2000, 22 (07) :561-567
[8]   CHARACTERISTICS OF A HUMAN CELL LINE TRANSFORMED BY DNA FROM HUMAN ADENOVIRUS TYPE-5 [J].
GRAHAM, FL ;
SMILEY, J ;
RUSSELL, WC ;
NAIRN, R .
JOURNAL OF GENERAL VIROLOGY, 1977, 36 (JUL) :59-72
[9]   Insights into adenoviral vector production kinetics in acoustic filter-based perf usion cultures [J].
Henry, O ;
Dormond, E ;
Perrier, M ;
Kamen, A .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 86 (07) :765-774
[10]   Comparison of manufacturing techniques for adenovirus production [J].
Iyer, P ;
Ostrove, JM ;
Vacante, D .
CYTOTECHNOLOGY, 1999, 30 (1-3) :169-172