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Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia

Tat, the trans-activator of transcription, is a multifunctional HIV-1 protein that can induce chronic inflammation and the development of somatic diseases in HIV-infected patients. Natural polymorphisms in Tat can impact the propagation of the inflammatory signal. Currently, Tat is considered an obj...

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Autores principales: Kuznetsova, Anna, Kim, Kristina, Tumanov, Alexander, Munchak, Iana, Antonova, Anastasiia, Lebedev, Aleksey, Ozhmegova, Ekaterina, Orlova-Morozova, Elena, Drobyshevskaya, Elena, Pronin, Alexander, Prilipov, Aleksey, Kazennova, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675479/
https://www.ncbi.nlm.nih.gov/pubmed/38005889
http://dx.doi.org/10.3390/v15112212
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author Kuznetsova, Anna
Kim, Kristina
Tumanov, Alexander
Munchak, Iana
Antonova, Anastasiia
Lebedev, Aleksey
Ozhmegova, Ekaterina
Orlova-Morozova, Elena
Drobyshevskaya, Elena
Pronin, Alexander
Prilipov, Aleksey
Kazennova, Elena
author_facet Kuznetsova, Anna
Kim, Kristina
Tumanov, Alexander
Munchak, Iana
Antonova, Anastasiia
Lebedev, Aleksey
Ozhmegova, Ekaterina
Orlova-Morozova, Elena
Drobyshevskaya, Elena
Pronin, Alexander
Prilipov, Aleksey
Kazennova, Elena
author_sort Kuznetsova, Anna
collection PubMed
description Tat, the trans-activator of transcription, is a multifunctional HIV-1 protein that can induce chronic inflammation and the development of somatic diseases in HIV-infected patients. Natural polymorphisms in Tat can impact the propagation of the inflammatory signal. Currently, Tat is considered an object for creating new therapeutic agents. Therefore, the identification of Tat protein features in various HIV-1 variants is a relevant task. The purpose of the study was to characterize the genetic variations of Tat-A6 in virus variants circulating in the Moscow Region. The authors analyzed 252 clinical samples from people living with HIV (PLWH) with different stages of HIV infection. Nested PCR for two fragments (tat1, tat2) with subsequent sequencing, subtyping, and statistical analysis was conducted. The authors received 252 sequences for tat1 and 189 for tat2. HIV-1 sub-subtype A6 was identified in 250 samples. The received results indicated the features of Tat1-A6 in variants of viruses circulating in the Moscow Region. In PLWH with different stages of HIV infection, C31S in Tat1-A6 was detected with different occurrence rates. It was demonstrated that Tat2-A6, instead of a functional significant (78)RGD(80) motif, had a (78)QRD(80) motif. Herewith, G79R in Tat2-A6 was defined as characteristic amino acid substitution for sub-subtype A6. Tat2-A6 in variants of viruses circulating in the Moscow Region demonstrated high conservatism.
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spelling pubmed-106754792023-11-04 Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia Kuznetsova, Anna Kim, Kristina Tumanov, Alexander Munchak, Iana Antonova, Anastasiia Lebedev, Aleksey Ozhmegova, Ekaterina Orlova-Morozova, Elena Drobyshevskaya, Elena Pronin, Alexander Prilipov, Aleksey Kazennova, Elena Viruses Article Tat, the trans-activator of transcription, is a multifunctional HIV-1 protein that can induce chronic inflammation and the development of somatic diseases in HIV-infected patients. Natural polymorphisms in Tat can impact the propagation of the inflammatory signal. Currently, Tat is considered an object for creating new therapeutic agents. Therefore, the identification of Tat protein features in various HIV-1 variants is a relevant task. The purpose of the study was to characterize the genetic variations of Tat-A6 in virus variants circulating in the Moscow Region. The authors analyzed 252 clinical samples from people living with HIV (PLWH) with different stages of HIV infection. Nested PCR for two fragments (tat1, tat2) with subsequent sequencing, subtyping, and statistical analysis was conducted. The authors received 252 sequences for tat1 and 189 for tat2. HIV-1 sub-subtype A6 was identified in 250 samples. The received results indicated the features of Tat1-A6 in variants of viruses circulating in the Moscow Region. In PLWH with different stages of HIV infection, C31S in Tat1-A6 was detected with different occurrence rates. It was demonstrated that Tat2-A6, instead of a functional significant (78)RGD(80) motif, had a (78)QRD(80) motif. Herewith, G79R in Tat2-A6 was defined as characteristic amino acid substitution for sub-subtype A6. Tat2-A6 in variants of viruses circulating in the Moscow Region demonstrated high conservatism. MDPI 2023-11-04 /pmc/articles/PMC10675479/ /pubmed/38005889 http://dx.doi.org/10.3390/v15112212 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kuznetsova, Anna
Kim, Kristina
Tumanov, Alexander
Munchak, Iana
Antonova, Anastasiia
Lebedev, Aleksey
Ozhmegova, Ekaterina
Orlova-Morozova, Elena
Drobyshevskaya, Elena
Pronin, Alexander
Prilipov, Aleksey
Kazennova, Elena
Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title_full Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title_fullStr Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title_full_unstemmed Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title_short Features of Tat Protein in HIV-1 Sub-Subtype A6 Variants Circulating in the Moscow Region, Russia
title_sort features of tat protein in hiv-1 sub-subtype a6 variants circulating in the moscow region, russia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675479/
https://www.ncbi.nlm.nih.gov/pubmed/38005889
http://dx.doi.org/10.3390/v15112212
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