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