Fox M P, Otto M J, McKinlay M A
Antimicrob Agents Chemother. 1986 Jul;30(1):110-6. doi: 10.1128/AAC.30.1.110.
WIN 51711, a potent new antipicornavirus drug, has been shown to inhibit an early event in the replication cycle of human poliovirus type 2 and human rhinovirus type 2. WIN 51711 was not virucidal and had no measurable effect on the adsorption of [3H]uridine-labeled virions to cells. When virion penetration of the plasma membrane was determined through loss of sensitivity to neutralizing antisera, WIN 51711 had no effect on poliovirus penetration, but inhibited rhinovirus penetration by 40%. In the presence of WIN 51711, exposure of neutral red-encapsidated virus-infected cells to light at 3 h postinfection resulted in a 3-log reduction in the number of infectious centers, indicating that WIN 51711 maintained the viral RNA in the encapsidated state after penetrating the cell membrane. The inhibition of uncoating by WIN 51711 in the neutral red assay was found to be concentration dependent, with a concentration of 0.03 micrograms/ml resulting in a 90% inhibition of uncoating. Sucrose gradient sedimentation of lysates from whole cells infected with [3H]uridine-labeled poliovirus showed that poliovirions remained intact in the presence of WIN 51711, but were uncoated in the absence of drug. WIN 51711 also prevented thermal inactivation of poliovirus infectivity, indicating a direct stabilizing effect of this compound on virion capsid conformation.
WIN 51711是一种新型强效抗微小核糖核酸病毒药物,已被证明可抑制人2型脊髓灰质炎病毒和人2型鼻病毒复制周期中的早期事件。WIN 51711没有杀病毒作用,对[3H]尿苷标记的病毒粒子吸附到细胞上也没有可测量的影响。当通过对中和抗血清敏感性的丧失来测定病毒粒子对质膜的穿透时,WIN 51711对脊髓灰质炎病毒的穿透没有影响,但可抑制鼻病毒穿透40%。在WIN 51711存在的情况下,感染后3小时用中性红包封的病毒感染细胞经光照后,感染中心数量减少3个对数级,这表明WIN 51711在穿透细胞膜后使病毒RNA保持在包封状态。在中性红试验中发现WIN 51711对脱壳的抑制作用呈浓度依赖性,浓度为0.03微克/毫升时可导致90%的脱壳抑制。用[3H]尿苷标记的脊髓灰质炎病毒感染全细胞的裂解物经蔗糖梯度沉降显示,在WIN 51711存在的情况下脊髓灰质炎病毒粒子保持完整,但在无药物时则发生脱壳。WIN 51711还可防止脊髓灰质炎病毒感染性的热失活,表明该化合物对病毒粒子衣壳构象有直接稳定作用。