Mutation Frequencies in RNAi Targets in HIV-1 Genomes Obtained from Blood Plasma of Patients Receiving Anti-Retroviral Therapy
- 作者: Kretova O.V.1, Gorbacheva M.A.1, Fedoseeva D.M.1, Kravatsky Y.V.1, Chechetkin V.R.1, Tchurikov N.A.1
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隶属关系:
- Engelhardt Institute of Molecular Biology
- 期: 卷 52, 编号 4 (2018)
- 页面: 510-513
- 栏目: Genomics. Transcriptomics
- URL: https://journals.rcsi.science/0026-8933/article/view/163585
- DOI: https://doi.org/10.1134/S0026893318040118
- ID: 163585
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详细
Gene therapy for AIDS based on RNA interference (RNAi) is currently looked upon as a promising alternative to conventional antiretroviral chemotherapy. The high variability of HIV-1 is the main challenge in developing new approaches to AIDS therapy. To date, about 18 million HIV-1 infected individuals receive antiretroviral therapy worldwide. As of 2017, about 44% of individuals with AIDS received antiretroviral therapy in Russia. Since the RNAs used for efficient RNAi and the corresponding targets in the viral transcript should be perfectly complementary to each other, it is necessary to continuously monitor the nucleotide sequences of clinical HIV-1 isolates obtained from blood and cells of naïve patients and patients receiving antiretroviral therapy. Comprehensive analysis of the mutation frequencies in the viral genome is only possible with deep sequencing approaches. The present paper reports on an analysis of the mutation frequencies in six 100 bp genome regions in clinical HIV-1 isolates obtained from blood plasma of four Russian AIDS patients who have been receiving antiretroviral therapy for several years. These regions contain efficient RNAi targets. The average frequencies of all possible transversions and transitions within the RNAi targets and in their proximity have been estimated. It has been demonstrated that reverse transcriptase inhibition decreases the frequency of a number of reverse mutations. It has been found that mutations in RNAi targets are rarer (5–75 times lower than the mutation frequency for different nucleotide substitutions) than in the adjacent sequences. Our findings speak in favor of these conservative targets for developing new approaches to gene therapy of AIDS.
作者简介
O. Kretova
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
M. Gorbacheva
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
D. Fedoseeva
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
Y. Kravatsky
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
V. Chechetkin
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
N. Tchurikov
Engelhardt Institute of Molecular Biology
编辑信件的主要联系方式.
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
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