Troyano-Hernáez Paloma, Reinosa Roberto, Holguín Africa
HIV-1 Molecular Epidemiology Laboratory, Department of Microbiology, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Hospital Universitario Ramón y Cajal, CIBER en Epidemiología y Salud Pública (CIBERESP), Red en Investigación Translacional en Infecciones Pediátricas (RITIP), Madrid, Spain.
Front Microbiol. 2022 Jul 14;13:866705. doi: 10.3389/fmicb.2022.866705. eCollection 2022.
The emergence and spread of new HIV-1 variants pose a challenge for the effectiveness of antiretrovirals (ARV) targeting Pol proteins. During viral evolution, non-synonymous mutations have fixed along the viral genome, leading to amino acid (aa) changes that can be variant-specific (V-markers). Those V-markers fixed in positions associated with drug resistance mutations (DRM), or R-markers, can impact drug susceptibility and resistance pathways. All available HIV-1 Pol sequences from ARV-naïve subjects were downloaded from the United States Los Alamos HIV Sequence Database, selecting 59,733 protease (PR), 6,437 retrotranscriptase (RT), and 6,059 integrase (IN) complete sequences ascribed to the four HIV-1 groups and group M subtypes and circulating recombinant forms (CRFs). Using a bioinformatics tool developed in our laboratory (EpiMolBio), we inferred the consensus sequences for each Pol protein and HIV-1 variant to analyze the aa conservation in Pol. We analyzed the Wu-Kabat protein variability coefficient (WK) in PR, RT, and IN group M to study the susceptibility of each site to evolutionary replacements. We identified as V-markers the variant-specific aa changes present in >75% of the sequences in variants with >5 available sequences, considering R-markers those V-markers that corresponded to DRM according to the IAS-USA2019 and Stanford-Database 9.0. The mean aa conservation of HIV-1 and group M consensus was 82.60%/93.11% in PR, 88.81%/94.07% in RT, and 90.98%/96.02% in IN. The median group M WK was 10 in PR, 4 in RT, and 5 in IN. The residues involved in binding or catalytic sites showed a variability <0.5%. We identified 106 V-markers: 31 in PR, 28 in RT, and 47 in IN, present in 11, 12, and 13 variants, respectively. Among them, eight (7.5%) were R-markers, present in five variants, being minor DRM with little potential effect on ARV susceptibility. We present a thorough analysis of Pol variability among all HIV-1 variants circulating to date. The relatively high aa conservation observed in Pol proteins across HIV-1 variants highlights their critical role in the viral cycle. However, further studies are needed to understand the V-markers' impact on the Pol proteins structure, viral cycle, or treatment strategies, and periodic variability surveillance studies are also required to understand PR, RT, and IN evolution.
新型HIV-1变体的出现和传播对靶向Pol蛋白的抗逆转录病毒药物(ARV)的有效性构成了挑战。在病毒进化过程中,非同义突变在病毒基因组中固定下来,导致氨基酸(aa)变化,这些变化可能是变体特异性的(V标记)。那些固定在与耐药突变(DRM)或R标记相关位置的V标记,会影响药物敏感性和耐药途径。从美国洛斯阿拉莫斯HIV序列数据库下载了所有来自未接受过ARV治疗的受试者的HIV-1 Pol序列,选择了59733条蛋白酶(PR)、6437条逆转录酶(RT)和6059条整合酶(IN)完整序列,这些序列归属于四种HIV-1组、M组亚型和循环重组形式(CRF)。使用我们实验室开发的生物信息学工具(EpiMolBio),我们推断了每种Pol蛋白和HIV-1变体的共有序列,以分析Pol中的氨基酸保守性。我们分析了M组PR、RT和IN中的Wu-Kabat蛋白变异性系数(WK),以研究每个位点对进化替代的敏感性。我们将在具有>5条可用序列的变体中>75%的序列中出现的变体特异性氨基酸变化确定为V标记,根据IAS-USA2019和斯坦福数据库9.0,将那些与DRM相对应的V标记视为R标记。HIV-1和M组共有的氨基酸保守性平均值在PR中为82.60%/93.11%,在RT中为88.81%/94.07%,在IN中为90.98%/96.02%。M组WK的中位数在PR中为10,在RT中为4,在IN中为5。参与结合或催化位点的残基变异性<0.5%。我们确定了106个V标记:PR中有31个,RT中有28个,IN中有47个,分别存在于11、12和13个变体中。其中,8个(7.5%)是R标记,存在于5个变体中,是对ARV敏感性影响较小的次要DRM。我们对迄今为止流行的所有HIV-1变体中的Pol变异性进行了全面分析。在所有HIV-1变体的Pol蛋白中观察到的相对较高的氨基酸保守性突出了它们在病毒周期中的关键作用。然而,需要进一步研究以了解V标记对Pol蛋白结构、病毒周期或治疗策略的影响,还需要定期进行变异性监测研究以了解PR、RT和IN的进化。