Salaun J J
Ann Biol Clin (Paris). 1978;36(1):23-5.
The author describes here a simplified and economical plaque forming system for rabies virus study. It is achieved in three steps (cells preparation and infection, apply of overlay, staining). It presents more advantages than previous techniques: time as well as culture media and handling spearing, easy and durable reading. Cells prepared with di-ethyl-amino-ethyl-dextran are added to equal quantities of diluted virus (for titration) or to virus-serum mixing (for seroneutralization) and overlaid after 4 hours with a carboxymethylcellulose medium. Reading is carried out after 6 days incubation and staining with amido black. Plaques obtained are to 2-3 mm in diameter, regularly reproductible, clear and easy to read. This technique enables titration and seroneutralization and even a rabies virus cloning.
作者在此描述了一种用于狂犬病病毒研究的简化且经济的蚀斑形成系统。该系统通过三个步骤实现(细胞制备与感染、覆盖层应用、染色)。它比以前的技术具有更多优势:节省时间以及培养基和操作,易于且持久读取。用二乙氨基乙基葡聚糖制备的细胞加入等量稀释病毒(用于滴定)或病毒 - 血清混合物(用于血清中和)中,4小时后用羧甲基纤维素培养基覆盖。孵育6天后用酰胺黑染色并进行读取。获得的蚀斑直径为2 - 3毫米,可规律重现,清晰且易于读取。该技术能够进行滴定和血清中和,甚至实现狂犬病病毒克隆。