首页> 外文期刊>Antiviral chemistry & chemotherapy >Characterization of human immunodeficiency virus type 1 resistant to modified cyclodextrin sulphate (mCDS71) in vitro.
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Characterization of human immunodeficiency virus type 1 resistant to modified cyclodextrin sulphate (mCDS71) in vitro.

机译:体外对修饰的硫酸环糊精(mCDS71)抗性的1型人类免疫缺陷病毒的特征。

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摘要

Drug resistance of human immunodeficiency virus type 1 (HIV) to modified cyclodextrin sulphate (mCDS71) has been analysed with respect to both the in vitro appearance of resistance to the compound and the mechanism of the acquisition of resistance. Resistant strains could be obtained in all three strains (NL432, KK-1 and A018) tested after serial passages in MT-4 cells with a gradual increase of the concentration of mCDS71. Cross-resistance both to mCDS71 and dextran sulphate 8000 was observed. As a result of sequencing analysis of the gp120 V3-C5 region of resistant strains, the mechanism of resistance can be explained in several ways: (i) substitution of sugar chain-binding amino acids, N and S; (ii) three to five amino acid deletion in V4 loop; and (iii) several mutations in V3 and V4 regions. The real cause of the resistance may be a combination of these three mechanisms. The results suggest that the target of mCDS71 is relatively widely distributed on the viral surface glycoprotein.
机译:已针对化合物的体外抗药性和获得抗药性的机理分析了人类1型免疫缺陷病毒(HIV)对修饰的环糊精硫酸盐(mCDS71)的抗药性。在MT-4细胞中连续传代后,随着mCDS71浓度的逐渐增加,可以在测试的所有三种菌株(NL432,KK-1和A018)中获得耐药菌株。观察到与mCDS71和硫酸葡聚糖8000的交叉抗性。对抗性菌株的gp120 V3-C5区进行测序分析的结果,可以用几种方式解释抗性的机理:(i)取代糖链结合氨基酸N和S; (ii)V4环中有3至5个氨基酸缺失; (iii)V3和V4区域的几个突变。抵抗的真正原因可能是这三种机制的组合。结果表明,mCDS71的靶标相对广泛地分布在病毒表面糖蛋白上。

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