Department of Translational Medicine, Lund University, 205 02 Malmo, Sweden.
TB/HIV Department, Ethiopian Public Health Institute, Addis Ababa 1242, Ethiopia.
Viruses. 2022 Mar 30;14(4):729. doi: 10.3390/v14040729.
Dolutegravir-based antiretroviral therapy (ART) has been scaled up in many developing countries, including Ethiopia. However, subtype-dependent polymorphic differences might influence the occurrence of HIV-drug-resistance mutations (HIVDRMs). We analyzed the prevalence of pre-treatment integrase strand transfer inhibitor (INSTI) HIVDRMs and naturally occurring polymorphisms (NOPs) of the integrase gene, using plasma samples collected as part of the national HIVDR survey in Ethiopia in 2017. We included a total of 460 HIV-1 integrase gene sequences from INSTI-naïve (n = 373 ART-naïve and n = 87 ART-experienced) patients. No dolutegravir-associated HIVDRMs were detected, regardless of previous exposure to ART. However, we found E92G in one ART-naïve patient specimen and accessory mutations in 20/460 (4.3%) of the specimens. Moreover, among the 288 integrase amino acid positions of the subtype C, 187/288 (64.9%) were conserved (<1.0% variability). Analysis of the genetic barrier showed that the Q148H/K/R dolutegravir resistance pathway was less selected in subtype C. Docking analysis of the dolutegravir showed that protease- and reverse-transcriptase-associated HIVDRMs did not affect the native structure of the HIV-1 integrase. Our results support the implementation of a wide scale-up of dolutegravir-based regimes. However, the detection of polymorphisms contributing to INSTI warrants the continuous surveillance of INSTI resistance.
在包括埃塞俄比亚在内的许多发展中国家,已经扩大了基于多替拉韦的抗逆转录病毒疗法(ART)的应用。然而,亚型依赖性多态性差异可能会影响 HIV 耐药突变(HIVDRMs)的发生。我们分析了在 2017 年埃塞俄比亚全国 HIVDR 调查中收集的血浆样本中,整合酶抑制剂(INSTI)HIVDRMs 和整合酶基因天然发生的多态性(NOPs)的流行情况。我们共纳入了 460 例从未接受过 INSTI 治疗(n = 373 例未接受过 ART 治疗,n = 87 例接受过 ART 治疗)的 HIV-1 整合酶基因序列。无论先前是否接触过 ART,均未检测到与多替拉韦相关的 HIVDRMs。然而,我们在 1 例未接受过 ART 治疗的患者样本中发现了 E92G 突变,在 460 个样本中有 20 个(4.3%)发现了辅助突变。此外,在 C 亚型的 288 个整合酶氨基酸位置中,187/288(64.9%)是保守的(<1.0%的变异性)。遗传屏障分析表明,C 亚型中 Q148H/K/R 多替拉韦耐药途径的选择较少。对多替拉韦的对接分析表明,蛋白酶和逆转录酶相关的 HIVDRMs 不会影响 HIV-1 整合酶的天然结构。我们的研究结果支持广泛推广基于多替拉韦的治疗方案。然而,发现与 INSTI 相关的多态性需要对 INSTI 耐药性进行持续监测。