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INSTIs and NNRTIs Potently Inhibit HIV-1 Polypurine Tract Mutants in a Single Round Infection Assay.整合酶抑制剂和非核苷类逆转录酶抑制剂在单次感染试验中能有效抑制 HIV-1 多聚嘌呤 tract 突变体。
Viruses. 2021 Dec 14;13(12):2501. doi: 10.3390/v13122501.
2
Specific mutations in the HIV-1 G-tract of the 3'-polypurine tract cause resistance to integrase strand transfer inhibitors.HIV-1 3'-多聚嘧啶 tract 中的 G-tract 中的特定突变导致对整合酶链转移抑制剂的耐药性。
J Antimicrob Chemother. 2022 Feb 23;77(3):574-577. doi: 10.1093/jac/dkab448.
3
Tax Induces the Recruitment of NF-κB to Unintegrated HIV-1 DNA To Rescue Viral Gene Expression and Replication.税收诱导 NF-κB 招募到未整合的 HIV-1 DNA 以挽救病毒基因表达和复制。
J Virol. 2021 Jun 10;95(13):e0028521. doi: 10.1128/JVI.00285-21.
4
Mutations in the HIV-1 3'-Polypurine Tract and Integrase Strand Transfer Inhibitor Resistance.HIV-1 3'-多聚嘌呤序列突变与整合酶链转移抑制剂耐药性
Antimicrob Agents Chemother. 2021 May 18;65(6). doi: 10.1128/AAC.02432-20.
5
Mechanistic Analysis of the Broad Antiretroviral Resistance Conferred by HIV-1 Envelope Glycoprotein Mutations.HIV-1 包膜糖蛋白突变赋予广泛抗逆转录病毒耐药性的机制分析。
mBio. 2021 Jan 12;12(1):e03134-20. doi: 10.1128/mBio.03134-20.
6
Reversal of Epigenetic Silencing Allows Robust HIV-1 Replication in the Absence of Integrase Function.逆转表观遗传沉默可使 HIV-1 在没有整合酶功能的情况下进行稳健复制。
mBio. 2020 Jun 2;11(3):e01038-20. doi: 10.1128/mBio.01038-20.
7
Human Immunodeficiency Virus Resistance to Dolutegravir: Are We Looking in the Wrong Place?人类免疫缺陷病毒对多替拉韦的耐药性:我们找错方向了吗?
J Infect Dis. 2018 Nov 5;218(12):2020. doi: 10.1093/infdis/jiy474.
8
Dolutegravir as maintenance monotherapy for HIV (DOMONO): a phase 2, randomised non-inferiority trial.多替拉韦作为 HIV 的维持单药治疗(DOMONO):一项 2 期、随机、非劣效性试验。
Lancet HIV. 2017 Dec;4(12):e547-e554. doi: 10.1016/S2352-3018(17)30152-2. Epub 2017 Oct 26.
9
Mutations Located outside the Integrase Gene Can Confer Resistance to HIV-1 Integrase Strand Transfer Inhibitors.突变位于整合酶基因之外可赋予 HIV-1 整合酶链转移抑制剂耐药性。
mBio. 2017 Sep 26;8(5):e00922-17. doi: 10.1128/mBio.00922-17.
10
Different Pathways Leading to Integrase Inhibitors Resistance.导致整合酶抑制剂耐药性的不同途径。
Front Microbiol. 2017 Jan 11;7:2165. doi: 10.3389/fmicb.2016.02165. eCollection 2016.

3'-PPT 突变导致 HIV-1 复制而不整合。

Mutations in the 3'-PPT Lead to HIV-1 Replication without Integration.

机构信息

LBPA, ENS Paris-Saclay, CNRS UMR8113, IDA FR3242, Université Paris-Saclay, Cachan, France.

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP) AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de virologie, Paris, France.

出版信息

J Virol. 2022 Jul 27;96(14):e0067622. doi: 10.1128/jvi.00676-22. Epub 2022 Jun 27.

DOI:10.1128/jvi.00676-22
PMID:35758669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9327692/
Abstract

Integration of the reverse-transcribed genome is a critical step of the retroviral life cycle. Strand-transfer inhibitors (INSTIs) used for antiretroviral therapy inhibit integration but can lead to resistance mutations in the integrase gene, the enzyme involved in this reaction. A significant proportion of INSTI treatment failures, particularly those with second-generation INSTIs, show no mutation in the integrase gene. Here, we show that replication of a selected dolutegravir-resistant virus with mutations in the 3'-PPT (polypurine tract) was effective, although no integrated viral DNA was detected, due to the accumulation of unintegrated viral DNA present as 1-LTR circles. Our results show that mutation in the 3'-PPT leads to 1-LTR circles and not linear DNA as classically reported. In conclusion, our data provide a molecular basis to explain a new mechanism of resistance to INSTIs, without mutation of the integrase gene and highlights the importance of unintegrated viral DNA in HIV-1 replication. Our work highlights the role of HIV-1 unintegrated viral DNA in viral replication. A virus, resistant to strand-transfer inhibitors, has been selected . This virus highlights a mutation in the 3'PPT region and not in the integrase gene. This mutation modifies the reverse transcription step leading to the accumulation of 1-LTR circles and not the linear DNA. This accumulation of 1-LTR circles leads to viral replication without integration of the viral genome.

摘要

逆转录基因组的整合是逆转录病毒生命周期的关键步骤。用于抗逆转录病毒治疗的整合酶抑制剂(INSTIs)抑制整合,但会导致整合酶基因发生耐药突变,该基因参与该反应。很大一部分 INSTI 治疗失败,特别是第二代 INSTIs,在整合酶基因中没有发现突变。在这里,我们表明,尽管由于存在未整合的病毒 DNA 作为 1-LTR 环而未检测到整合的病毒 DNA,但具有 3'-PPT(多嘌呤区)突变的选定的多替拉韦耐药病毒的复制是有效的。我们的结果表明,3'-PPT 中的突变导致 1-LTR 环而不是线性 DNA,如经典报道的那样。总之,我们的数据提供了一个分子基础来解释一种新的 INSTI 耐药机制,而无需整合酶基因的突变,并强调了未整合的病毒 DNA 在 HIV-1 复制中的重要性。我们的工作强调了 HIV-1 未整合病毒 DNA 在病毒复制中的作用。已经选择了一种对链转移抑制剂有抗性的病毒。该病毒突出了 3'PPT 区域而不是整合酶基因中的突变。该突变改变了反转录步骤,导致 1-LTR 环的积累而不是线性 DNA。这种 1-LTR 环的积累导致病毒复制而不整合病毒基因组。