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Isolation and characterization of simian immunodeficiency viruses from two subspecies of African green monkeys.

作者信息

Allan J S, Kanda P, Kennedy R C, Cobb E K, Anthony M, Eichberg J W

机构信息

Department of Virology and Immunology, Southwest Foundation for Biomedical Research, San Antonio, TX 78284.

出版信息

AIDS Res Hum Retroviruses. 1990 Mar;6(3):275-85. doi: 10.1089/aid.1990.6.275.

DOI:10.1089/aid.1990.6.275
PMID:2340199
Abstract

Cercopithecus aethiops (African Green monkey), a nonhuman primate species distributed throughout subsaharan Africa, has been shown to have high seroprevalence rates of antibodies to simian immunodeficiency virus (SIV), and therefore, has been proposed as a natural reservoir for immunodeficiency viruses. Our laboratories have isolated SIV-like viruses from two East African subspecies of C. aethiops designated grivet and vervet monkeys. Analysis of the structural proteins based on the molecular weights and immunologic cross-reactivity to the prototypic SIV(MAC), HIV-1, and HIV-2 isolates suggests that these viruses are distinctly different. Heterogeneity was observed in the molecular weights of the gag, pol, and env gene products between SIV isolates from vervets [SIV(AGM(VER))] and grivets [SIV(AGM(GRI))]. Phenotypically, SIV(AGM(VER)) isolates were distinguishable from SIV(AGM(GRI)) isolates by the apparent size difference of the major core antigen p24. All SIV(AGM(GRI)) and SIV(AGM(VER)) isolates were found to encode a transmembrane protein of approximately 40 kD (gp40) in contrast to gp32 of SIV(MAC). Furthermore, the transmembrane protein was shown to be encoded by the entire env open reading frame, unlike gp32 of SIC(MAC) or gp36 of SIV(AGM(TYO-1)). These data indicate that viruses from C. aethiops share common features with SIV(MAC) and HIV-1, but represent diverse SIV-like viruses which may vary according to subspecies and geographic location.

摘要

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引用本文的文献

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Plasmacytoid Dendritic Cell Infection and Sensing Capacity during Pathogenic and Nonpathogenic Simian Immunodeficiency Virus Infection.致病性和非致病性猿猴免疫缺陷病毒感染期间浆细胞样树突状细胞的感染与感知能力
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2
Simian immunodeficiency virus SIVagm from African green monkeys does not antagonize endogenous levels of African green monkey tetherin/BST-2.来自非洲绿猴的猿猴免疫缺陷病毒SIVagm不会拮抗非洲绿猴内源性水平的束缚素/BST-2。
J Virol. 2009 Nov;83(22):11673-81. doi: 10.1128/JVI.00569-09. Epub 2009 Sep 2.
3
Gag p27-specific B- and T-cell responses in Simian immunodeficiency virus SIVagm-infected African green monkeys.
猿猴免疫缺陷病毒SIVagm感染的非洲绿猴中针对Gag p27的B细胞和T细胞反应
J Virol. 2009 Mar;83(6):2770-7. doi: 10.1128/JVI.01841-08. Epub 2008 Dec 24.
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A challenge to the ancient origin of SIVagm based on African green monkey mitochondrial genomes.基于非洲绿猴线粒体基因组对猴免疫缺陷病毒(SIVagm)古老起源的挑战。
PLoS Pathog. 2007 Jul;3(7):e95. doi: 10.1371/journal.ppat.0030095.
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Evolution of the uniquely adaptable lentiviral envelope in a natural reservoir host.天然储存宿主中独特适应性慢病毒包膜的进化。
Retrovirology. 2006 Mar 20;3:19. doi: 10.1186/1742-4690-3-19.
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Simian immunodeficiency virus replicates to high levels in naturally infected African green monkeys without inducing immunologic or neurologic disease.猿猴免疫缺陷病毒在自然感染的非洲绿猴体内可大量复制,却不会引发免疫或神经疾病。
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