Mutation Frequencies in RNAi Targets in HIV-1 Genomes Obtained from Blood Plasma of Patients Receiving Anti-Retroviral Therapy

• Published in: Molecular biology (New York) Vol. 52; no. 4; pp. 510 - 513
• Main Authors: Kretova, O. V., Gorbacheva, M. A., Fedoseeva, D. M., Kravatsky, Y. V., Chechetkin, V. R., Tchurikov, N. A.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01.07.2018; Springer Nature B.V
• Subjects: Acquired immune deficiency syndrome; AIDS; Antiretroviral agents; Antiretroviral drugs; Antiretroviral therapy; Biochemistry; Biomedical and Life Sciences; Blood; Chemotherapy; Drug therapy; Gene therapy; Genomes; Genomics. Transcriptomics; HIV; Human Genetics; Human immunodeficiency virus; Life Sciences; Mutation; RNA-directed DNA polymerase; RNA-mediated interference; Transcription; HIV-1; mutations; RNA interference; ultra-deep sequencing; antiretroviral therapy; gene therapy; transitions; transversions
• ISSN: 0026-8933; 1608-3245
• DOI: 10.1134/S0026893318040118

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.