Suppr超能文献

HIV-1 整合酶 143、148 和 155 位氨基酸的替换在体内定义了对拉替拉韦耐药的不同遗传屏障。

Substitutions at amino acid positions 143, 148, and 155 of HIV-1 integrase define distinct genetic barriers to raltegravir resistance in vivo.

机构信息

Monogram Biosciences, South San Francisco, California, USA.

出版信息

J Virol. 2012 Jul;86(13):7249-55. doi: 10.1128/JVI.06618-11. Epub 2012 May 2.

Abstract

Mutations at amino acids 143, 148, and 155 in HIV-1 integrase (IN) define primary resistance pathways in subjects failing raltegravir (RAL)-containing treatments. Although each pathway appears to be genetically distinct, shifts in the predominant resistant virus population have been reported under continued drug pressure. To better understand this dynamic, we characterized the RAL susceptibility of 200 resistant viruses, and we performed sequential clonal analysis for selected cases. Patient viruses containing Y143R, Q148R, or Q148H mutations consistently exhibited larger reductions in RAL susceptibility than patient viruses containing N155H mutations. Sequential analyses of virus populations from three subjects revealed temporal shifts in subpopulations representing N155H, Y143R, or Q148H escape pathways. Evaluation of molecular clones isolated from different time points demonstrated that Y143R and Q148H variants exhibited larger reductions in RAL susceptibility and higher IN-mediated replication capacity (RC) than N155H variants within the same subject. Furthermore, shifts from the N155H pathway to either the Q148R or H pathway or the Y143R pathway were dependent on the amino acid substitution at position 148 and the secondary mutations in Y143R- or Q148R- or H-containing variants and correlated with reductions in RAL susceptibility and restorations in RC. Our observations in patient viruses were confirmed by analyzing site-directed mutations. In summary, viruses that acquire mutations defining the 143 or 148 escape pathways are less susceptible to RAL and exhibit greater RC than viruses containing 155 pathway mutations. These selective pressures result in the displacement of N155H variants by 143 or 148 variants under continued drug exposure.

摘要

HIV-1 整合酶(IN)中氨基酸 143、148 和 155 的突变定义了接受拉替拉韦(RAL)治疗的失败患者中的主要耐药途径。尽管每种途径似乎在遗传上是不同的,但在持续的药物压力下,主要耐药病毒群体的转变已经有报道。为了更好地理解这种动态变化,我们对 200 株耐药病毒进行了 RAL 敏感性特征分析,并对选定的病例进行了连续克隆分析。含有 Y143R、Q148R 或 Q148H 突变的患者病毒对 RAL 的敏感性降低幅度始终大于含有 N155H 突变的患者病毒。对来自三个患者的病毒群体进行的连续分析显示,N155H、Y143R 或 Q148H 逃逸途径的亚群在时间上发生了转变。对来自不同时间点分离的分子克隆的评估表明,与同一患者中的 N155H 变体相比,Y143R 和 Q148H 变体对 RAL 的敏感性降低幅度更大,并且具有更高的 IN 介导的复制能力(RC)。此外,从 N155H 途径到 Q148R 或 H 途径或 Y143R 途径的转变取决于位置 148 的氨基酸取代以及 Y143R-、Q148R-或 H- 包含变体中的次要突变,与 RAL 敏感性降低和 RC 恢复相关。对患者病毒的观察结果通过分析定点突变得到了证实。总之,获得定义 143 或 148 逃逸途径的突变的病毒对 RAL 的敏感性降低,并且比包含 155 途径突变的病毒具有更高的 RC。这些选择性压力导致在持续药物暴露下,N155H 变体被 143 或 148 变体取代。

相似文献

8
Impact of Y143 HIV-1 integrase mutations on resistance to raltegravir in vitro and in vivo.
Antimicrob Agents Chemother. 2010 Jan;54(1):491-501. doi: 10.1128/AAC.01075-09. Epub 2009 Nov 9.
9
HIV-1 Group O Resistance Against Integrase Inhibitors.
J Acquir Immune Defic Syndr. 2015 Sep 1;70(1):9-15. doi: 10.1097/QAI.0000000000000698.

引用本文的文献

4
HIV-1 Integrase Inhibitors That Are Active against Drug-Resistant Integrase Mutants.
Antimicrob Agents Chemother. 2020 Aug 20;64(9). doi: 10.1128/AAC.00611-20.
6
Management of Virologic Failure and HIV Drug Resistance.
Infect Dis Clin North Am. 2019 Sep;33(3):707-742. doi: 10.1016/j.idc.2019.05.004. Epub 2019 Jun 27.
7
Collaborative update of a rule-based expert system for HIV-1 genotypic resistance test interpretation.
PLoS One. 2017 Jul 28;12(7):e0181357. doi: 10.1371/journal.pone.0181357. eCollection 2017.
8
HIV drug resistance against strand transfer integrase inhibitors.
Retrovirology. 2017 Jun 5;14(1):36. doi: 10.1186/s12977-017-0360-7.
10
Lack of impact of pre-existing T97A HIV-1 integrase mutation on integrase strand transfer inhibitor resistance and treatment outcome.
PLoS One. 2017 Feb 17;12(2):e0172206. doi: 10.1371/journal.pone.0172206. eCollection 2017.

本文引用的文献

1
Switching between raltegravir resistance pathways analyzed by deep sequencing.
AIDS. 2011 Oct 23;25(16):1951-9. doi: 10.1097/QAD.0b013e32834b34de.
2
In Vitro antiretroviral properties of S/GSK1349572, a next-generation HIV integrase inhibitor.
Antimicrob Agents Chemother. 2011 Feb;55(2):813-21. doi: 10.1128/AAC.01209-10. Epub 2010 Nov 29.
3
Effect of raltegravir resistance mutations in HIV-1 integrase on viral fitness.
J Acquir Immune Defic Syndr. 2010 Oct;55(2):148-55. doi: 10.1097/QAI.0b013e3181e9a87a.
5
Evolution of integrase resistance during failure of integrase inhibitor-based antiretroviral therapy.
J Acquir Immune Defic Syndr. 2010 Aug;54(4):389-93. doi: 10.1097/QAI.0b013e3181c42ea4.
8
Natural polymorphisms of human immunodeficiency virus type 1 integrase and inherent susceptibilities to a panel of integrase inhibitors.
Antimicrob Agents Chemother. 2009 Oct;53(10):4275-82. doi: 10.1128/AAC.00397-09. Epub 2009 Aug 3.
10
Selection and analysis of HIV-1 integrase strand transfer inhibitor resistant mutant viruses.
Methods. 2009 Apr;47(4):277-82. doi: 10.1016/j.ymeth.2009.02.025. Epub 2009 Mar 13.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验