Malewicz B, Jenkin H M
J Clin Microbiol. 1979 May;9(5):609-14. doi: 10.1128/jcm.9.5.609-614.1979.
An improved plaque assay for dengue virus was developed utilizing baby hamster kidney (BHK-21) cells initially grown in shaker culture. Different media preparations were tested for uniform and fast formation of BHK-21 cell sheets. Several overlay formulas were tested to develop a rapid plaque assay in 6- and 24-well plastic plates. The best results were obtained utilizing Eagle minimal essential medium (pH 7.2 to 7.4) supplemented with 1 mg of NaHCO3 per ml and 5% newborn calf serum for the formation of cell monolayers after 8 to 24 h of incubation at 37 degrees C. Serum-free Eagle minimal essential medium supplemented with 1% methylcellulose and buffered with 10 mM N-2-hydroxyethyl piperazine-N'-2-ethanesulfonic acid (pH 7.4 to 7.6) was used as an overlay medium. This system allowed for plaque formation after 3 days of incubation of dengue type 2 virus and after 4 days for dengue type 1 and 4 viruses.
利用最初在摇瓶培养中生长的幼仓鼠肾(BHK-21)细胞,开发了一种改进的登革病毒蚀斑测定法。测试了不同的培养基制剂,以实现BHK-21细胞单层的均匀快速形成。测试了几种覆盖液配方,以开发在6孔和24孔塑料板中进行的快速蚀斑测定法。使用补充有每毫升1毫克碳酸氢钠和5%新生牛血清的伊格尔最低限度基本培养基(pH 7.2至7.4),在37℃孵育8至24小时后形成细胞单层,获得了最佳结果。补充有1%甲基纤维素并用10 mM N-2-羟乙基哌嗪-N'-2-乙磺酸缓冲(pH 7.4至7.6)的无血清伊格尔最低限度基本培养基用作覆盖液培养基。该系统在登革2型病毒孵育3天后以及登革1型和4型病毒孵育4天后允许蚀斑形成。