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Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam
BACKGROUND: HIV is characterized by high levels of genetic variability, including increased numbers of heterogeneous sequences of the envelope region. Therefore, studying genetic variability of HIV in relation to viral replication might facilitate prognosis of disease progression. METHODS: The study...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323269/ https://www.ncbi.nlm.nih.gov/pubmed/32637106 http://dx.doi.org/10.1177/2050312120937198 |
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author | Dang, Linh Vu Phuong Pham, Hung Viet Dinh, Thanh Thi Nguyen, Thu Hoai Vu, Quyen Thi Huyen Vu, Nhung Thi Phuong Le, Phuong Thi Bich Nguyen, Lam Van Le, Hai Thanh Vu, Phuong Thi Olson, Linus |
author_facet | Dang, Linh Vu Phuong Pham, Hung Viet Dinh, Thanh Thi Nguyen, Thu Hoai Vu, Quyen Thi Huyen Vu, Nhung Thi Phuong Le, Phuong Thi Bich Nguyen, Lam Van Le, Hai Thanh Vu, Phuong Thi Olson, Linus |
author_sort | Dang, Linh Vu Phuong |
collection | PubMed |
description | BACKGROUND: HIV is characterized by high levels of genetic variability, including increased numbers of heterogeneous sequences of the envelope region. Therefore, studying genetic variability of HIV in relation to viral replication might facilitate prognosis of disease progression. METHODS: The study was designed as cross-sectional; data and samples of participants collected and analyzed env genes were obtained from 23 children enrolled by Vietnam National Children’s Hospital. RESULTS: Substantial mutations in the C2 region were found in patients with high levels of viral replication while changes in the C3 region were mostly found in patients with low viral load. In the V1 region, we found profound amino acid modifications in patients with low HIV viral loads in contrast to the V2 sequence, where we identified single point mutations in patients with increased HIV viral load. The V3 region was relatively homogeneous, while profound deletions in the V4 region were detected in patients with increased viral replication. CONCLUSION: Our results suggest that genetic variations in different regions of the HIV envelope sequence, including both conserved C2 and C3 and variable V1/V2 and V4 regions, might be involved in increased viral infectivity and replication capacity. Such knowledge might help improve prediction of HIV progress and treatment in patients. |
format | Online Article Text |
id | pubmed-7323269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-73232692020-07-06 Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam Dang, Linh Vu Phuong Pham, Hung Viet Dinh, Thanh Thi Nguyen, Thu Hoai Vu, Quyen Thi Huyen Vu, Nhung Thi Phuong Le, Phuong Thi Bich Nguyen, Lam Van Le, Hai Thanh Vu, Phuong Thi Olson, Linus SAGE Open Med Original Article BACKGROUND: HIV is characterized by high levels of genetic variability, including increased numbers of heterogeneous sequences of the envelope region. Therefore, studying genetic variability of HIV in relation to viral replication might facilitate prognosis of disease progression. METHODS: The study was designed as cross-sectional; data and samples of participants collected and analyzed env genes were obtained from 23 children enrolled by Vietnam National Children’s Hospital. RESULTS: Substantial mutations in the C2 region were found in patients with high levels of viral replication while changes in the C3 region were mostly found in patients with low viral load. In the V1 region, we found profound amino acid modifications in patients with low HIV viral loads in contrast to the V2 sequence, where we identified single point mutations in patients with increased HIV viral load. The V3 region was relatively homogeneous, while profound deletions in the V4 region were detected in patients with increased viral replication. CONCLUSION: Our results suggest that genetic variations in different regions of the HIV envelope sequence, including both conserved C2 and C3 and variable V1/V2 and V4 regions, might be involved in increased viral infectivity and replication capacity. Such knowledge might help improve prediction of HIV progress and treatment in patients. SAGE Publications 2020-06-25 /pmc/articles/PMC7323269/ /pubmed/32637106 http://dx.doi.org/10.1177/2050312120937198 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Dang, Linh Vu Phuong Pham, Hung Viet Dinh, Thanh Thi Nguyen, Thu Hoai Vu, Quyen Thi Huyen Vu, Nhung Thi Phuong Le, Phuong Thi Bich Nguyen, Lam Van Le, Hai Thanh Vu, Phuong Thi Olson, Linus Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title | Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title_full | Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title_fullStr | Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title_full_unstemmed | Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title_short | Characterization of envelope sequence of HIV virus in children infected with HIV in Vietnam |
title_sort | characterization of envelope sequence of hiv virus in children infected with hiv in vietnam |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323269/ https://www.ncbi.nlm.nih.gov/pubmed/32637106 http://dx.doi.org/10.1177/2050312120937198 |
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