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Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide

RNAi has been suggested for use in gene therapy of HIV/AIDS, but the main problem is that HIV-1 is highly variable and could escape attack from the small interfering RNAs (siRNAs) due to even single nucleotide substitutions in the potential targets. To exhaustively check the variability in selected...

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Autores principales: Kretova, Olga V., Fedoseeva, Daria M., Gorbacheva, Maria A., Gashnikova, Natalya M., Gashnikova, Maria P., Melnikova, Nataliya V., Chechetkin, Vladimir R., Kravatsky, Yuri V., Tchurikov, Nickolai A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537207/
https://www.ncbi.nlm.nih.gov/pubmed/28918033
http://dx.doi.org/10.1016/j.omtn.2017.07.010
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author Kretova, Olga V.
Fedoseeva, Daria M.
Gorbacheva, Maria A.
Gashnikova, Natalya M.
Gashnikova, Maria P.
Melnikova, Nataliya V.
Chechetkin, Vladimir R.
Kravatsky, Yuri V.
Tchurikov, Nickolai A.
author_facet Kretova, Olga V.
Fedoseeva, Daria M.
Gorbacheva, Maria A.
Gashnikova, Natalya M.
Gashnikova, Maria P.
Melnikova, Nataliya V.
Chechetkin, Vladimir R.
Kravatsky, Yuri V.
Tchurikov, Nickolai A.
author_sort Kretova, Olga V.
collection PubMed
description RNAi has been suggested for use in gene therapy of HIV/AIDS, but the main problem is that HIV-1 is highly variable and could escape attack from the small interfering RNAs (siRNAs) due to even single nucleotide substitutions in the potential targets. To exhaustively check the variability in selected RNA targets of HIV-1, we used ultra-deep sequencing of six regions of HIV-1 from the plasma of two independent cohorts of patients from Russia. Six RNAi targets were found that are invariable in 82%–97% of viruses in both cohorts and are located inside the domains specifying reverse transcriptase (RT), integrase, vpu, gp120, and p17. The analysis of mutation frequencies and their characteristics inside the targets suggests a likely role for APOBEC3G (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G, A3G) in G-to-A mutations and a predominant effect of RT biases in the detected variability of the virus. The lowest frequency of mutations was detected in the central part of all six targets. We also discovered that the identical RNAi targets are present in many HIV-1 strains from many countries and from all continents. The data are important for both the understanding of the patterns of HIV-1 mutability and properties of RT and for the development of gene therapy approaches using RNAi for the treatment of HIV/AIDS.
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spelling pubmed-55372072017-08-08 Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide Kretova, Olga V. Fedoseeva, Daria M. Gorbacheva, Maria A. Gashnikova, Natalya M. Gashnikova, Maria P. Melnikova, Nataliya V. Chechetkin, Vladimir R. Kravatsky, Yuri V. Tchurikov, Nickolai A. Mol Ther Nucleic Acids Original Article RNAi has been suggested for use in gene therapy of HIV/AIDS, but the main problem is that HIV-1 is highly variable and could escape attack from the small interfering RNAs (siRNAs) due to even single nucleotide substitutions in the potential targets. To exhaustively check the variability in selected RNA targets of HIV-1, we used ultra-deep sequencing of six regions of HIV-1 from the plasma of two independent cohorts of patients from Russia. Six RNAi targets were found that are invariable in 82%–97% of viruses in both cohorts and are located inside the domains specifying reverse transcriptase (RT), integrase, vpu, gp120, and p17. The analysis of mutation frequencies and their characteristics inside the targets suggests a likely role for APOBEC3G (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G, A3G) in G-to-A mutations and a predominant effect of RT biases in the detected variability of the virus. The lowest frequency of mutations was detected in the central part of all six targets. We also discovered that the identical RNAi targets are present in many HIV-1 strains from many countries and from all continents. The data are important for both the understanding of the patterns of HIV-1 mutability and properties of RT and for the development of gene therapy approaches using RNAi for the treatment of HIV/AIDS. American Society of Gene & Cell Therapy 2017-07-13 /pmc/articles/PMC5537207/ /pubmed/28918033 http://dx.doi.org/10.1016/j.omtn.2017.07.010 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Kretova, Olga V.
Fedoseeva, Daria M.
Gorbacheva, Maria A.
Gashnikova, Natalya M.
Gashnikova, Maria P.
Melnikova, Nataliya V.
Chechetkin, Vladimir R.
Kravatsky, Yuri V.
Tchurikov, Nickolai A.
Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title_full Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title_fullStr Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title_full_unstemmed Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title_short Six Highly Conserved Targets of RNAi Revealed in HIV-1-Infected Patients from Russia Are Also Present in Many HIV-1 Strains Worldwide
title_sort six highly conserved targets of rnai revealed in hiv-1-infected patients from russia are also present in many hiv-1 strains worldwide
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537207/
https://www.ncbi.nlm.nih.gov/pubmed/28918033
http://dx.doi.org/10.1016/j.omtn.2017.07.010
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