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来自西非绿猴(猕猴属埃塞俄比亚亚种)的猿猴免疫缺陷病毒的调控基因。

Regulatory genes of simian immunodeficiency viruses from west African green monkeys (Cercopithecus aethiops sabaeus).

作者信息

Jubier-Maurin V, Sarni-Manchado P, Veas F, Vidal N, Bibollet-Ruche F, Durand J P, Galat-Luong A, Cuny G

机构信息

Laboratoire Rétrovirus, Institute Français de Recherche Scientifique pour le Développment en Coopération (ORSTOM), Montpellier, France.

出版信息

J Virol. 1995 Nov;69(11):7349-53. doi: 10.1128/JVI.69.11.7349-7353.1995.

DOI:10.1128/JVI.69.11.7349-7353.1995
PMID:7474168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC189668/
Abstract

The high seroprevalence of simian immunodeficiency viruses (SIVs) in African green monkeys (AGMs) without immunological defects in their natural hosts has prompted consideration of SIV-infected AGMs as a model of apathogenic SIV infection. Study of the molecular mechanisms of SIVagm asymptomatic infection could thus provide clues for understanding the pathogenesis of human immunodeficiency viruses. Regulatory genes could be candidates for genetic control of SIVagm apathogenicity. We have characterized Vpr, Tat, Rev, and Nef genes of two SIVagm strains isolated from naturally infected sabaeus monkeys captured in Senegal. The results provide further evidence that SIVagm from West African green monkeys is the most divergent class of AGM viruses, with structural features in long terminal repeat sequences and Vpr and Tat genes that distinguish them from viruses isolated from other AGM species (vervet, grivet, and tantalus monkeys).

摘要

在自然宿主中无免疫缺陷的非洲绿猴(AGM)体内,猿猴免疫缺陷病毒(SIV)的血清阳性率很高,这促使人们将感染SIV的AGM视为无致病性SIV感染的模型。因此,对SIVagm无症状感染分子机制的研究可为理解人类免疫缺陷病毒的发病机制提供线索。调控基因可能是SIVagm无致病性遗传控制的候选基因。我们已经对从在塞内加尔捕获的自然感染的黑绿猴中分离出的两种SIVagm毒株的Vpr、Tat、Rev和Nef基因进行了表征。结果提供了进一步的证据,表明来自西非绿猴的SIVagm是AGM病毒中差异最大的一类,其长末端重复序列以及Vpr和Tat基因的结构特征使其与从其他AGM物种(绿猴、长尾猴和白臀长尾猴)分离出的病毒有所区别。

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本文引用的文献

1
Simian immunodeficiency viruses from central and western Africa: evidence for a new species-specific lentivirus in tantalus monkeys.来自中非和西非的猿猴免疫缺陷病毒:在草原猴中发现一种新的物种特异性慢病毒的证据。
J Virol. 1993 Mar;67(3):1227-35. doi: 10.1128/JVI.67.3.1227-1235.1993.
2
Electrostatic interactions modulate the RNA-binding and transactivation specificities of the human immunodeficiency virus and simian immunodeficiency virus Tat proteins.静电相互作用调节人类免疫缺陷病毒和猿猴免疫缺陷病毒Tat蛋白的RNA结合及反式激活特异性。
Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1571-5. doi: 10.1073/pnas.90.4.1571.
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A distinct African lentivirus from Sykes' monkeys.一种来自非洲绿猴的独特慢病毒。
J Virol. 1993 Mar;67(3):1517-28. doi: 10.1128/JVI.67.3.1517-1528.1993.
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Importance of vpr for infection of rhesus monkeys with simian immunodeficiency virus.Vpr对恒河猴感染猴免疫缺陷病毒的重要性。
J Virol. 1993 Feb;67(2):902-12. doi: 10.1128/JVI.67.2.902-912.1993.
5
The Vpr protein of human immunodeficiency virus type 1 influences nuclear localization of viral nucleic acids in nondividing host cells.人类免疫缺陷病毒1型的Vpr蛋白影响病毒核酸在非分裂宿主细胞中的核定位。
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7311-5. doi: 10.1073/pnas.91.15.7311.
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Mosaic genome structure of simian immunodeficiency virus from west African green monkeys.来自西非绿猴的猿猴免疫缺陷病毒的镶嵌基因组结构
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