Department of Chemical Engineering, University of Queensland, 4072, St. Lucia, Qld., Australia.
Cytotechnology. 1996 Jan;22(1-3):217-24. doi: 10.1007/BF00353942.
The potential use of a wild-type Helicoverpa baculovirus as a biopesticide, using insect cell culture for its production, has been investigated. A Helicoverpa zea cell line was adapted to grow in suspension culture using a serum-free medium, SF900II and serum supplemented SF900II. The serum supplemented cells were infected with a wild-type nuclear polyhedrosis virus of Helicoverpa armigera (HaNPV), at different stages of growth, in conditioned and tresh medium, to determine the effect of cell density on polyhedra production. Cultures infected at low cell densities, produced similar yields of virus (20-40 PIB/cell), irrespective of medium conditions. However, in infections which occurred at high cell densities, there was a 16-fold improvement in cell specific yields, when the spent medium was renewed with fresh medium prior to infection. Results indicated that only 60-70% of the viable cells in a culture produced polyhedra as a result of infections.
已经研究了使用野生型杆状病毒作为生物农药的可能性,使用昆虫细胞培养来生产它。使用无血清培养基 SF900II 和补充有血清的 SF900II,将一种棉铃虫细胞系适应于悬浮培养。在不同的生长阶段,在条件培养基和新鲜培养基中用野生型核多角体病毒(HaNPV)感染补充有血清的细胞,以确定细胞密度对多角体产生的影响。在低细胞密度下感染的培养物产生相似的病毒产量(20-40 PIB/细胞),与培养基条件无关。然而,在高细胞密度下的感染中,在感染前用新鲜培养基替换用过的培养基,可以使细胞特异性产率提高 16 倍。结果表明,培养物中只有 60-70%的活细胞由于感染而产生多角体。