[Genetic diversity of Vif protein in human immunodeficiency virus type 1 variants (Retroviridae: Orthoretrovirinae: Lentivirus: Human immunodeficiency virus-1) that circulated in the Moscow region in 2019-2020].

Q3 Medicine
A A Antonova, L A Protasova, K V Kim, I M Munchak, E N Mezhenskaya, E A Orlova-Morozova, A Y Pronin, A G Prilipov, A I Kuznetsova
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引用次数: 0

Abstract

Introduction: The Vif protein counteracts cellular deaminases, APOBEC3, which prevent viral replication. Vif is used for development of therapeutic agents. Natural polymorphisms in Vif can affect its functionality and may be associated with accelerated progression of HIV-infection to the AIDS. The study of Vif features in HIV-1 variants circulating in Russia has not been conducted previously.

The aim of the study: to study the genetic diversity of Vif in the HIV-1 variants that circulated in the Moscow region in 2019-2020.

Materials and methods: 234 whole blood samples obtained from HIV-infected patients without experience of therapy were analyzed. The study design included the following stages: extraction of proviral DNA, amplification of the vif gene, sequencing, identification of genetic variants, followed by a study of consensus sequences of the most common genetic variants of HIV-1, analysis of the conservation and genetic diversity of Vif-A6 (Vif protein of HIV-1 sub-subtype A6 variants) in patients with different stages of the disease, and assessment of genetic diversity of Vif-A6 in the Moscow region.

Results: A high degree of genetic diversity of vif gene was revealed. Consensus sequences of Vif in B and CRF63_02A6 variants were obtained for the first time. Characteristic substitutions in the consensus sequences were determined for the most common HIV-1 variants.

Conclusion: The limitation of this study is the small sample of B and CRF63_02A6. The results obtained may be of interest and may be taken into account in the development of therapeutic agents based on the Vif protein, as well as in the study of the pathogenicity of HIV-1 sub-subtype A6.

[2019-2020年在莫斯科地区流行的人类免疫缺陷病毒1型变异(逆转录病毒科:正转录病毒科:慢病毒:人类免疫缺陷病毒-1)中Vif蛋白的遗传多样性]。
Vif蛋白抵消细胞脱氨酶APOBEC3,防止病毒复制。Vif用于开发治疗剂。Vif的自然多态性可以影响其功能,并可能与hiv感染加速发展为艾滋病有关。在俄罗斯流行的HIV-1变异中,Vif特征的研究以前没有进行过。该研究的目的是:研究2019-2020年在莫斯科地区传播的HIV-1变异中Vif的遗传多样性。材料与方法:对未经治疗的hiv感染者234例全血标本进行分析。研究设计包括以下几个阶段:提取前病毒DNA,扩增vif基因,测序,鉴定遗传变异,然后研究HIV-1最常见遗传变异的共识序列,分析不同阶段疾病患者vif -A6 (HIV-1亚型A6变体的vif蛋白)的保守性和遗传多样性,以及评估莫斯科地区vif -A6的遗传多样性。结果:vif基因具有高度的遗传多样性。首次获得了Vif在B和CRF63_02A6变异中的一致序列。共识序列中的特征替换被确定为最常见的HIV-1变异。结论:本研究的局限性在于B和CRF63_02A6样本较少。获得的结果可能会引起人们的兴趣,并可能在基于Vif蛋白的治疗剂的开发以及HIV-1亚型A6的致病性研究中得到考虑。
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来源期刊
Voprosy virusologii
Voprosy virusologii Medicine-Infectious Diseases
CiteScore
2.00
自引率
0.00%
发文量
48
期刊介绍: The journal deals with advances in virology in Russia and abroad. It publishes papers dealing with investigations of viral diseases of man, animals and plants, the results of experimental research on different problems of general and special virology. The journal publishes materials are which promote introduction into practice of the achievements of the virological science in the eradication and incidence reduction of infectious diseases, as well as their diagnosis, treatment and prevention. The reader will find a description of new methods of investigation, new apparatus and devices.
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