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杆状病毒生物农药的体外生产——用于生产和系统生物学研究的昆虫细胞克隆的自动化选择。

In vitro production of Helicoverpa baculovirus biopesticides--automated selection of insect cell clones for manufacturing and systems biology studies.

机构信息

Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, Brisbane 4072, Australia.

出版信息

J Virol Methods. 2011 Aug;175(2):197-205. doi: 10.1016/j.jviromet.2011.05.011. Epub 2011 May 17.

DOI:10.1016/j.jviromet.2011.05.011
PMID:21616093
Abstract

Baculovirus pesticides are increasingly being used as effective biological control agents against caterpillar pests worldwide. Increasing occlusion body (OB) yields per cell in culture is the main challenge to enable commercialization of in vitro production of baculovirus pesticides. Isolating clones from a heterogeneous cell population may allow development of a high virus producing cell clone. To date, the selection of insect clones has been based mainly on laborious cell serial dilution methods which create few viable clones. This work used an automated robotic clone picking system to establish over 250 insect clones of a Helicoverpa zea cell population to be screened for virus production. However, the higher producing clones only produced 10-30% higher OB yields than the original cell population. This study suggested that unless screening of thousands of clones is performed, obtaining a 2-fold increase in OB/cell yield compared to the parent population is unlikely. Nevertheless, it creates pure clones for manufacturing. In addition, two clones that were at least 2-3 times different in OB yields were isolated. Hence, this method can create a high contrast system (OB/cell yield basis), for comparative studies using a systems biology approach, which should inform a more targeted approach to engineer genetically a production cell line.

摘要

杆状病毒杀虫剂作为有效的生物防治制剂,在全球范围内被越来越多地用于防治鳞翅目害虫。提高细胞培养中每细胞的包埋体(OB)产量是实现杆状病毒杀虫剂体外生产商业化的主要挑战。从异质细胞群体中分离克隆可能有助于开发高产病毒的细胞克隆。迄今为止,昆虫克隆的选择主要基于费力的细胞连续稀释方法,该方法只能产生很少的存活克隆。本工作使用自动化机器人克隆挑选系统建立了超过 250 个 Heliothis zea 细胞群体的昆虫克隆,以筛选病毒生产。然而,高产生克隆的 OB 产量仅比原始细胞群体高 10-30%。本研究表明,除非筛选数千个克隆,否则与亲本群体相比,获得 OB/细胞产量增加 2 倍的可能性不大。尽管如此,它为生产创造了纯克隆。此外,还分离到了至少在 OB 产量上相差 2-3 倍的两个克隆。因此,该方法可以创建一个高对比度系统(基于 OB/细胞产量),用于使用系统生物学方法进行比较研究,这应该为基因工程生产细胞系提供更有针对性的方法。

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