Lukashevich I S, Vasiuchkov A D, Mar'iankova R F, Votiakov V I
Vopr Virusol. 1982 Jan-Feb(1):57-61.
The method of Porterfield and Allison was adapted for titration of the infectious activity of Lassa virus by the plaque formation in Vero cells. The virus was cloned, and the effect of the time of adsorption, pH, temperature, as well as polycations (DEAD-dextran, protamine sulphate) dimethylsuphoxide (DMSO), and trypsin added during adsorption or into the agar overlay on the effectiveness of plaque production by Lassa virus (virus titres, plaque size) were studied. The optimal adsorption time was found to be 1 1/2-2 hours, pH 8.0. The number of plaques produced by the virus was approximately similar at 35 degrees C. The substances under study did not enhance the efficacy of plaque formation, on the contrary, DMSO and high concentrations of polycations decreased plaque size.
波特菲尔德和艾利森的方法经调整后,用于通过在Vero细胞中形成噬斑来滴定拉沙病毒的感染活性。该病毒被克隆,并研究了吸附时间、pH值、温度以及在吸附期间或加入到琼脂覆盖层中的聚阳离子(DEAD-葡聚糖、硫酸鱼精蛋白)、二甲基亚砜(DMSO)和胰蛋白酶对拉沙病毒产生噬斑的有效性(病毒滴度、噬斑大小)的影响。发现最佳吸附时间为1.5 - 2小时,pH值为8.0。在35摄氏度时,该病毒产生的噬斑数量大致相似。所研究的物质并未提高噬斑形成的效率,相反,DMSO和高浓度的聚阳离子减小了噬斑大小。