首页> 外文期刊>AIDS Research and Human Retroviruses >Accumulation of P(T/S)AP late domain duplications in HIV type 1 subtypes B, C, and F derived from individuals failing ARV therapy and ARV drug-naive patients.
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Accumulation of P(T/S)AP late domain duplications in HIV type 1 subtypes B, C, and F derived from individuals failing ARV therapy and ARV drug-naive patients.

机译:艾滋病毒1型B,C和F亚型中P(T / S)AP晚期结构域重复的积累,这些亚型来源于ARV治疗失败的患者和ARV初次使用药物的患者。

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摘要

HIV-1 budding requires short peptide motifs in p6(Gag), known as late domains, that promote the release of infectious virions. The primary late domain of HIV-1 is a Pro-(Thr/Ser)-Ala-Pro (hereafter referred to as a PTAP) motif. This motif may be completely or partially duplicated. In this work we analyzed p6(Gag) sequences from 547 isolates from drug-naive patients and 213 isolates from patients failing HAART therapy. Complete duplications within PTAP were selected during HAART therapy in all HIV-1 subtypes analyzed: B (p = 0.0338), F1 (p = 0.0294), and C (p = 0.0001). Nevertheless, the patterns of these duplications were different; subtype C isolates accumulated longer duplications and displayed a higher frequency of duplications in both treated (54%) and drug-naive isolates (23%). Accumulation of PTAP duplications within subtypes B, F1, and C during therapy suggests a potential role of the duplications in antiretroviral drug resistance.
机译:HIV-1出芽需要p6(Gag)中的短肽基序(称为后期结构域),以促进感染性病毒体的释放。 HIV-1的主要晚期区域是Pro-(Thr / Ser)-Ala-Pro(以下称为PTAP)基序。该主题可以完全或部分复制。在这项工作中,我们分析了547例来自单纯药物患者的分离株和213例HAART治疗失败的患者的分离株的p6(Gag)序列。在HAART治疗期间,在所有分析的HIV-1亚型中选择了PTAP内的完全重复:B(p = 0.0338),F1(p = 0.0294)和C(p = 0.0001)。然而,这些重复的模式是不同的。在治疗(54%)和未经药物治疗的分离株(23%)中,C型亚型分离株积累了更长的重复并显示出更高的重复频率。在治疗期间,B,F1和C型亚型中PTAP复制的积累表明,这些复制在抗逆转录病毒药物耐药性中具有潜在作用。

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