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HIV-1 Gag C-terminal amino acid substitutions emerging under selective pressure of protease inhibitors in patient populations infected with different HIV-1 subtypes

机译:在感染了不同HIV-1亚型的患者人群中在蛋白酶抑制剂的选择性压力下出现了HIV-1 Gag C末端氨基酸取代

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摘要

HIV-1 Gag amino acid substitutions associated with protease inhibitor (PI) treatment have mainly been reported in subtype B, while information on other subtypes is scarce. Using sequences from 11613 patients infected with different HIV-1 subtypes, we evaluated the prevalence of 93 Gag amino acid substitutions and their association with genotypic PI resistance. A significant association was found for 13 Gag substitutions, including A431V in both subtype B and CRF01_AE. K415R in subtype C and S451G in subtype B were newly identified. Most PI-associated Gag substitutions are located in the flexible C-terminal domain, revealing the key role this region plays in PI resistance.Electronic supplementary materialThe online version of this article (doi:10.1186/s12977-014-0079-7) contains supplementary material, which is available to authorized users.
机译:与蛋白酶抑制剂(PI)治疗相关的HIV-1 Gag氨基酸替代主要在B型中报道,而其他亚型的信息却很少。使用来自11613名感染了不同HIV-1亚型的患者的序列,我们评估了93个Gag氨基酸取代的患病率以及它们与基因型PI耐药性的关联。发现与13个Gag取代显着相关,包括B亚型和CRF01_AE中的A431V。新鉴定了C亚型的K415R和B亚型的S451G。大多数与PI相关的Gag取代位于柔性C端结构域中,揭示了该区域在PI抗性中发挥关键作用。电子补充材料本文的在线版本(doi:10.1186 / s12977-014-0079-7)包含补充信息资料,可供授权用户使用。

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