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Virological characterization of HIV-2 vpx gene mutants in various cell systems.

作者信息

Nomaguchi Masako, Doi Naoya, Adachi Akio

机构信息

Department of Microbiology, Institute of Health Biosciences, The University of Tokushima Graduate School, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.

Department of Microbiology, Institute of Health Biosciences, The University of Tokushima Graduate School, 3-18-15 Kuramoto, Tokushima 770-8503, Japan; Japanese Foundation for AIDS Prevention, Chiyoda-ku, Tokyo 101-0061, Japan.

出版信息

Microbes Infect. 2014 Aug;16(8):695-701. doi: 10.1016/j.micinf.2014.06.004. Epub 2014 Jun 21.

DOI:10.1016/j.micinf.2014.06.004
PMID:24956595
Abstract

Requirement of intrinsically disordered protein Vpx for HIV-2 replication is cell-type dependent. To define Vpx-dependent conditions, replication ability of HIV-2 vpx mutants was analyzed in various cell lines that differ in cellular type, differentiation state and/or expression level of anti-HIV-1 SAMHD1 degraded by Vpx. Induction of Vpx-sensitive anti-HIV-2 state was not always associated with SAMHD1 expression. Compared with our previous data in lymphocytic cells, growth-defectiveness of the vpx mutants in differentiated THP-1 cells, a newly established multi-cycle infection system, was considerably different. Taken together, our results suggest that Vpx plays cell-type dependent role through its undetermined structure and/or function.

摘要

相似文献

1
Virological characterization of HIV-2 vpx gene mutants in various cell systems.
Microbes Infect. 2014 Aug;16(8):695-701. doi: 10.1016/j.micinf.2014.06.004. Epub 2014 Jun 21.
2
Degradation of SAMHD1 by Vpx Is Independent of Uncoating.Vpx介导的SAMHD1降解与脱壳无关。
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A novel DCAF1-binding motif required for Vpx-mediated degradation of nuclear SAMHD1 and Vpr-induced G2 arrest.一种新型 DCAF1 结合基序,对于 Vpx 介导的核 SAMHD1 降解和 Vpr 诱导的 G2 期阻滞是必需的。
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5
The efficiency of Vpx-mediated SAMHD1 antagonism does not correlate with the potency of viral control in HIV-2-infected individuals.Vpx 介导的 SAMHD1 拮抗作用的效率与 HIV-2 感染者中病毒控制的效力不相关。
Retrovirology. 2013 Mar 5;10:27. doi: 10.1186/1742-4690-10-27.
6
Evolutionary toggling of Vpx/Vpr specificity results in divergent recognition of the restriction factor SAMHD1.进化开关 VPx/Vpr 的特异性导致对限制因子 SAMHD1 的不同识别。
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7
HIV-2 Vpx neutralizes host restriction factor SAMHD1 to promote viral pathogenesis.HIV-2 Vpx 中和宿主限制因子 SAMHD1 以促进病毒发病机制。
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Functional region mapping of HIV-2 Vpx protein.
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9
Vpx and Vpr proteins of HIV-2 up-regulate the viral infectivity by a distinct mechanism in lymphocytic cells.HIV-2的Vpx和Vpr蛋白通过一种独特的机制上调淋巴细胞中的病毒感染性。
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HIV-2 Depletes CD4 T Cells through Pyroptosis despite Vpx-Dependent Degradation of SAMHD1.尽管 HIV-2 通过 Vpx 依赖性降解 SAMHD1 导致 CD4 T 细胞耗竭,但仍会导致细胞焦亡。
J Virol. 2019 Nov 26;93(24). doi: 10.1128/JVI.00666-19. Print 2019 Dec 15.

引用本文的文献

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Aromatic Side Chain at Position 412 of SERINC5 Exerts Restriction Activity toward HIV-1 and Other Retroviruses.SERINC5 第 412 位的芳香侧链对 HIV-1 和其他逆转录病毒具有限制活性。
J Virol. 2021 Aug 25;95(18):e0063421. doi: 10.1128/JVI.00634-21.
3
PIM kinases facilitate lentiviral evasion from SAMHD1 restriction via Vpx phosphorylation.
PIM 激酶通过 Vpx 磷酸化促进慢病毒逃避 SAMHD1 的限制。
Nat Commun. 2019 Apr 23;10(1):1844. doi: 10.1038/s41467-019-09867-7.
4
Introduction of H2C2-type zinc-binding residues into HIV-2 Vpr increases its expression level.将H2C2型锌结合残基引入HIV-2 Vpr可提高其表达水平。
FEBS Open Bio. 2017 Dec 19;8(1):146-153. doi: 10.1002/2211-5463.12358. eCollection 2018 Jan.
5
Expression Profiles of Vpx/Vpr Proteins Are Co-related with the Primate Lentiviral Lineage.Vpx/Vpr蛋白的表达谱与灵长类慢病毒谱系相关。
Front Microbiol. 2016 Aug 3;7:1211. doi: 10.3389/fmicb.2016.01211. eCollection 2016.