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Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro

BACKGROUND: HIV-1 produces defective mutants in the process of reproduction. The significance of the mutants has not been well investigated. METHODS: The plasmids of wild type (HIV-1(NL4–3)) and Env-defective (HIV-1(SG3)(ΔEnv)) HIV-1 were co-transfected into HEK293T cells. The progeny virus was coll...

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Autores principales: Wei, Huamian, Yu, Danwei, Geng, Xiuzhu, He, Yuxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401196/
https://www.ncbi.nlm.nih.gov/pubmed/32753067
http://dx.doi.org/10.1186/s12879-020-05288-w
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author Wei, Huamian
Yu, Danwei
Geng, Xiuzhu
He, Yuxian
author_facet Wei, Huamian
Yu, Danwei
Geng, Xiuzhu
He, Yuxian
author_sort Wei, Huamian
collection PubMed
description BACKGROUND: HIV-1 produces defective mutants in the process of reproduction. The significance of the mutants has not been well investigated. METHODS: The plasmids of wild type (HIV-1(NL4–3)) and Env-defective (HIV-1(SG3)(ΔEnv)) HIV-1 were co-transfected into HEK293T cells. The progeny virus was collected to infect MT4 cells. The env gene and near-full-length genome (NFLG) of HIV-1 were amplified and sequenced. The phylogenetic diversity, recombinant patterns and hotspots, and the functionality of HIV-1 Env were determined. RESULTS: A total of 42 env genes and 8 NFLGs were successfully amplified and sequenced. Five types of recombinant patterns of env were identified and the same recombinant sites were detected in different patterns. The recombination hotspots were found distributing mainly in conservative regions of env. The recombination between genes of HIV-1(NL4–3) and HIV-1(SG3)(Δenv) increased the variety of viral quasispecies and resulted in progeny viruses with relative lower infectious ability than that of HIV(NL4–3). The defective env genes as well as NFLG could be detected after 20 passages. CONCLUSION: The existence of the defective HIV-1 promotes the phylogenetic evolution of the virus, thus increasing the diversity of virus population. The role of defective genes may be converted from junk genes to useful materials and cannot be neglected in the study of HIV-1 reservoir.
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spelling pubmed-74011962020-08-06 Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro Wei, Huamian Yu, Danwei Geng, Xiuzhu He, Yuxian BMC Infect Dis Research Article BACKGROUND: HIV-1 produces defective mutants in the process of reproduction. The significance of the mutants has not been well investigated. METHODS: The plasmids of wild type (HIV-1(NL4–3)) and Env-defective (HIV-1(SG3)(ΔEnv)) HIV-1 were co-transfected into HEK293T cells. The progeny virus was collected to infect MT4 cells. The env gene and near-full-length genome (NFLG) of HIV-1 were amplified and sequenced. The phylogenetic diversity, recombinant patterns and hotspots, and the functionality of HIV-1 Env were determined. RESULTS: A total of 42 env genes and 8 NFLGs were successfully amplified and sequenced. Five types of recombinant patterns of env were identified and the same recombinant sites were detected in different patterns. The recombination hotspots were found distributing mainly in conservative regions of env. The recombination between genes of HIV-1(NL4–3) and HIV-1(SG3)(Δenv) increased the variety of viral quasispecies and resulted in progeny viruses with relative lower infectious ability than that of HIV(NL4–3). The defective env genes as well as NFLG could be detected after 20 passages. CONCLUSION: The existence of the defective HIV-1 promotes the phylogenetic evolution of the virus, thus increasing the diversity of virus population. The role of defective genes may be converted from junk genes to useful materials and cannot be neglected in the study of HIV-1 reservoir. BioMed Central 2020-08-04 /pmc/articles/PMC7401196/ /pubmed/32753067 http://dx.doi.org/10.1186/s12879-020-05288-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wei, Huamian
Yu, Danwei
Geng, Xiuzhu
He, Yuxian
Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title_full Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title_fullStr Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title_full_unstemmed Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title_short Defective HIV-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
title_sort defective hiv-1 envelope gene promotes the evolution of the infectious strain through recombination in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401196/
https://www.ncbi.nlm.nih.gov/pubmed/32753067
http://dx.doi.org/10.1186/s12879-020-05288-w
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