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Isolation and characterization of NMSO3-resistant mutants of respiratory syncytial virus.

机译:呼吸道合胞病毒耐NMSO3突变体的分离和鉴定。

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We obtained two mutant strains of respiratory syncytial virus (RSV) which showed resistance against NMSO3 after 15 and 33 passages, respectively, in HEp-2 cells in the presence of 6.8 microM of NMSO3. The EC50 values of NMSO3 for the resistant virus strains were 0.48 and 0.93 microM, that is 4.8-9.3 times higher than that of the parent strain (EC50 = 0.1 microM). The most resistant strain also showed resistance against heparin but was sensitive to dextran sulfate and a polyoxotungstate, PM-523. In order to determine whether the acquisition of resistance to NMSO3 was the result of the accumulation of genetic changes of virus, we sequenced the G- and F-protein genes. In comparison with the standard type of RSV strains, we identified changes of 10 amino acids in the G protein including those at the central conserved segment. However, we did not observe any particular changes in the amino acid sequence of the F-protein of the resistant strains. From these results, we conclude that NMSO3 inhibits the G-protein interaction to the receptor. The mutations in the G-protein may result in the observed phenotypic resistance of RSV towards NMSO3.
机译:我们获得了两种呼吸道合胞病毒(RSV)突变株,它们分别在6.8 microM NMSO3存在下的HEp-2细胞中分别经过15和33代后显示出对NMSO3的抗性。抗性病毒株的NMSO3 EC50值分别为0.48和0.93 microM,比亲本株(EC50 = 0.1 microM)高4.8-9.3倍。耐药性最高的菌株还显示出对肝素的耐药性,但对硫酸葡聚糖和多氧钨酸盐PM-523敏感。为了确定对NMSO3的抗性获得是否是病毒遗传变化积累的结果,我们对G蛋白和F蛋白基因进行了测序。与标准型的RSV菌株相比,我们确定了G蛋白中10个氨基酸的变化,包括中央保守区段的变化。然而,我们没有观察到抗性菌株F蛋白的氨基酸序列有任何特别的变化。从这些结果,我们得出结论,NMSO3抑制了G蛋白与受体的相互作用。 G蛋白的突变可能导致观察到的RSV对NMSO3的表型抗性。

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