Department of Chemical Engineering, The University of Queensland, 4072, St Lucia, Australia.
Cytotechnology. 1996 Jan;20(1-3):209-19. doi: 10.1007/BF00350401.
Infection of insect cells with baculovirus is a potentially attractive means for producing both viral insecticides and recombinant proteins. The continuation of mathematical modelling studies such as those reviewed in this paper are essential in order to realise the full potential of the system. Through mathematical models it is possible to predict complex behaviours such as those observed when infecting cells at low MOI or when propagating virus in a continuous culture system. A purely empirical analysis of the same phenomena is very difficult if not impossible.The present three models are - despite their complexity and the effort that has gone into developing them - all first generation models. They summarise, to a large extent, our present quantitative understanding of the interaction between baculovirus and insect cells, when looked upon as a black box system. The binding and initial infection processes are still quantitatively poorly understood and further work in this area is much needed. On the longer term, a second generation of models is likely to consider interior processes such as viral DNA and RNA accumulation in much more detail using a structured model of the infection cycle.
杆状病毒感染昆虫细胞是生产病毒杀虫剂和重组蛋白的一种极具吸引力的方法。为了充分发挥该系统的潜力,继续进行数学模型研究是至关重要的。通过数学模型,可以预测复杂的行为,例如在低 MOI 感染细胞或在连续培养系统中繁殖病毒时观察到的行为。如果不是不可能的话,对相同现象进行纯粹的经验分析是非常困难的。目前的三个模型 - 尽管它们很复杂,并且在开发它们方面付出了很多努力 - 都是第一代模型。它们在很大程度上总结了我们目前对杆状病毒与昆虫细胞之间相互作用的定量理解,将其视为一个黑盒系统。结合和初始感染过程在定量上仍未得到很好的理解,因此需要在这方面进行更多的工作。从长远来看,第二代模型可能会使用感染周期的结构模型更详细地考虑内部过程,例如病毒 DNA 和 RNA 的积累。