Pagano J S, McCutchan J H, Vaheri A
J Virol. 1967 Oct;1(5):891-7. doi: 10.1128/JVI.1.5.891-897.1967.
The enhancement by diethylaminoethyl-dextran (DEAE-D) of the infectivity of poliovirus ribonucleic acid (RNA) for cell cultures was demonstrated by infective-center as well as by plaque assays, both in nonprimate (L) and primate cell systems (MK, HeLa, LLC-MK(2)). The sensitivity of plaque assays was greatly improved by using a tris (hydroxymethyl)aminomethane-buffered synthetic medium (basal medium Eagle) and freshly confluent cell monolayers. Enhancement of nucleic acid infectivity was directly dependent on the molecular weight of the DEAE-D. Two observations bearing on the action of DEAE-D appeared important: ribonuclease activity was reduced by DEAE-D, and cells pretreated with DEAE-D remained susceptible to infection with RNA in isotonic medium. Appreciable susceptibility of the treated cells persisted for at least 2 hr; the susceptible state could be reversed at will by an application of heparin. Enhancement of nucleic acid infectivity was independent of an effect of DEAE-D on intact virus and agar inhibitors.
通过感染中心试验以及蚀斑试验,在非灵长类(L)和灵长类细胞系统(MK、HeLa、LLC-MK₂)中均证实了二乙氨基乙基葡聚糖(DEAE-D)可增强脊髓灰质炎病毒核糖核酸(RNA)对细胞培养物的感染性。使用三(羟甲基)氨基甲烷缓冲的合成培养基(伊格尔基础培养基)和刚汇合的细胞单层,蚀斑试验的灵敏度得到了极大提高。核酸感染性的增强直接取决于DEAE-D的分子量。关于DEAE-D作用的两项观察结果显得很重要:DEAE-D可降低核糖核酸酶活性,并且用DEAE-D预处理的细胞在等渗培养基中仍易被RNA感染。处理过的细胞的明显易感性至少持续2小时;通过应用肝素可随意逆转这种易感状态。核酸感染性的增强与DEAE-D对完整病毒和琼脂抑制剂的作用无关。