Dewindt B, van Eemeren K, Andries K
Department of Virology, Janssen Research Foundation, Beerse, Belgium.
Antiviral Res. 1994 Sep;25(1):67-72. doi: 10.1016/0166-3542(94)90094-9.
The effect of four structurally diverse capsid-binding compounds on the adsorption of seven human rhinoviruses (HRV), representative for both receptor and antiviral groupings was studied using infective center assays. Antiviral compounds studied included a pyridazinamine (R 61837), an isoxazole (WIN 51711), a flavan (4',6-dichloroflavan) and a chalcone (Ro-09410). Minor receptor viruses studied were HRV 1A, HRV 2 and HRV 29 (antiviral group B), major receptor viruses were HRV 9, HRV 39 and HRV 14, HRV 35 (antiviral group B and A, respectively). The adsorption of four out of the seven serotypes was inhibited by some antiviral compounds, but not by others, indicating that the conformational alterations induced by antiviral compounds can vary considerably within a given serotype, depending on the chemical nature of the antiviral compound used. A correlation between inhibition of adsorption and receptor grouping or antiviral grouping could not be found.
使用感染中心测定法研究了四种结构不同的衣壳结合化合物对七种人类鼻病毒(HRV)吸附的影响,这七种病毒分别代表受体和抗病毒分组。所研究的抗病毒化合物包括一种哒嗪胺(R 61837)、一种异恶唑(WIN 51711)、一种黄烷(4',6-二氯黄烷)和一种查耳酮(Ro-09410)。所研究的次要受体病毒为HRV 1A、HRV 2和HRV 29(抗病毒B组),主要受体病毒为HRV 9、HRV 39和HRV 14、HRV 35(分别为抗病毒B组和A组)。七种血清型中的四种血清型的吸附受到一些抗病毒化合物的抑制,但不受其他化合物的抑制,这表明抗病毒化合物诱导的构象改变在给定血清型内可能有很大差异,这取决于所用抗病毒化合物的化学性质。未发现吸附抑制与受体分组或抗病毒分组之间存在相关性。