Variability of VPU protein in HIV-1 sub-subtype A6 in patients with different stages of HIV infection

The aim of the study: to compare the genetic diversity of the Vpu protein in HIV-1 in the people living with HIV (PLWH) with different stages of the disease. Materials and methods. An analysis was carried out of 259 clinical samples of whole blood from HIV-infected patients with no experience of taking antiretroviral therapy, who were observed at the Center for the Prevention and Control of AIDS and Infectious Diseases, Moscow, Russia. The analysis included the following stages: extraction of proviral DNA, amplification of the region of the virus genome containing the vpu gene, sequencing of amplification products, genotyping, comparison of conservation and amino acid substitutions in the Vpu protein sequences in PLWH with different stages of the disease. Results and discussion. In 255 out of 259 (98.4%) clinical samples, a sub-subtype A6 virus variant was identified. The consensus sequence of the Vpu sub-subtype A6 protein was obtained, which contained 81 amino acids. No significant differences in the conservation of Vpu protein sequences were found between HIV-1 variants obtained from patients with different stages of the disease. Amino acid substitution P3A was significantly more common in PLWH with the second stage of HIV infection. Conclusion. The results obtained highlight the issue of the influence of non-structural proteins of HIV-1 on the course of the disease and indicate directions for possible research in the future.

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Publication Details

Journal
HIV Infection and Immunosuppressive Disorders
Published
2024-09-05
DOI
https://doi.org/10.22328/2077-9828-2024-16-2-40-50
Citations
4
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
1.17
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article

Variability of VPU protein in HIV-1 sub-subtype A6 in patients with different stages of HIV infection

А. Г. Прилипов, Elena Kazennova, K. V. Kim, Anna Kuznetsovа et al.
4 citations
HIV Infection and Immunosuppressive Disorders
HIV Research and Treatment
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article

Variability of VPU protein in HIV-1 sub-subtype A6 in patients with different stages of HIV infection

А. Г. Прилипов, Elena Kazennova, K. V. Kim, Anna Kuznetsovа, Ekaterina Ozhmegova, А. С. Туманов, Anastasiia Antonova, Elena Orlova‐Morozova, Aleksey Lebedev, A Yu Pronin, Ya. M. Munchak
article en
4 citations

Abstract

The aim of the study: to compare the genetic diversity of the Vpu protein in HIV-1 in the people living with HIV (PLWH) with different stages of the disease. Materials and methods. An analysis was carried out of 259 clinical samples of whole blood from HIV-infected patients with no experience of taking antiretroviral therapy, who were observed at the Center for the Prevention and Control of AIDS and Infectious Diseases, Moscow, Russia. The analysis included the following stages: extraction of proviral DNA, amplification of the region of the virus genome containing the vpu gene, sequencing of amplification products, genotyping, comparison of conservation and amino acid substitutions in the Vpu protein sequences in PLWH with different stages of the disease. Results and discussion. In 255 out of 259 (98.4%) clinical samples, a sub-subtype A6 virus variant was identified. The consensus sequence of the Vpu sub-subtype A6 protein was obtained, which contained 81 amino acids. No significant differences in the conservation of Vpu protein sequences were found between HIV-1 variants obtained from patients with different stages of the disease. Amino acid substitution P3A was significantly more common in PLWH with the second stage of HIV infection. Conclusion. The results obtained highlight the issue of the influence of non-structural proteins of HIV-1 on the course of the disease and indicate directions for possible research in the future.

HIV Infection and Immunosuppressive DisordersVol. 16(2)
Gamalei Institute of Epidemiology and Microbiology (RU), Regional Center for Prevention and Control of AIDS and Infectious Diseases (RU)
Openalex Percentile: Top 22%
HIV Research and Treatment
1.17
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