Lotfian Pantea, Levy M Susana, Coffin Rob, Ward John, Shamlou Parviz Ayazi
Department of Biochemical Engineering, University College London, Torrington Place, London WC1E 7JE, UK.
Biotechnol Appl Biochem. 2003 Dec;38(Pt 3):271-81. doi: 10.1042/BA20030074.
A new process route is proposed to increase the production yield of disabled herpes simplex virus type 1 (HSV-1 DIS). Infected baby-hamster kidney (BHK) cells were subjected to a range of shear rates between 3.69 x 10(3) s(-1) and 51.3 x 10(3) s(-1) in the gap between a pair of co-axial cylinders. Analysis of the supernatant fractions of sheared material established that optimal virus release was achieved by exposing the infected cells to a shear rate of 42.7 x 10(3) s(-1) for a period of 1 min. Compared with the current laboratory process, the titre of HSV-1 DIS was increased over 30-fold, from about 1 x 10(6) to 30 x 10(6) pfu (plaque-forming units)/ml. Evaluation of the supernatant fractions by flow cytometry, total protein assay, PAGE and dot-blot assays showed no evidence of cell disruption, supporting the hypothesis that shear-induced release of the cell-membrane-bound virus was achieved without compromising downstream purification. The proposed method is scalable, and since no additional chemicals are required, it provides an attractive option for enhanced recovery of virus particles for therapeutic applications.
提出了一种新的工艺路线以提高1型单纯疱疹病毒(HSV-1 DIS)失活病毒的产量。将感染的幼仓鼠肾(BHK)细胞置于一对同轴圆柱体之间的间隙中,使其承受3.69×10³ s⁻¹至51.3×10³ s⁻¹的一系列剪切速率。对剪切后物料的上清液部分进行分析表明,将感染细胞暴露于42.7×10³ s⁻¹的剪切速率下1分钟可实现最佳病毒释放。与当前的实验室工艺相比,HSV-1 DIS的滴度提高了30多倍,从约1×10⁶增加到30×10⁶ pfu(空斑形成单位)/毫升。通过流式细胞术、总蛋白测定、PAGE和斑点印迹测定对上清液部分进行评估,未发现细胞破裂的迹象,这支持了以下假设:在不影响下游纯化的情况下实现了剪切诱导的细胞膜结合病毒的释放。所提出的方法具有可扩展性,并且由于不需要额外的化学物质,它为增强用于治疗应用的病毒颗粒回收提供了一个有吸引力的选择。