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猕猴和白眉猴的猴免疫缺陷病毒感染:不同分离株体内和体外特性之间的相关性

SIVsmm infection of macaque and mangabey monkeys: correlation between in vivo and in vitro properties of different isolates.

作者信息

Fultz P N, Anderson D C, McClure H M, Dewhurst S, Mullins J I

机构信息

Yerkes Regional Primate Research Center, Atlanta, GA.

出版信息

Dev Biol Stand. 1990;72:253-8.

PMID:1980901
Abstract

Simian immunodeficiency virus from sooty mangabey monkeys (SIVsmm), a lentivirus closely related to SIV from macaques and the human immunodeficiency virus type 2 (HIV-2), is pathogenic for various species of macaques but is nonpathogenic for mangabeys. Comparison of in vivo and in vitro responses of macaques and mangabeys or their lymphocytes, respectively, to SIVsmm infection indicated that lack of disease in mangabeys apparently was not due to effective control of virus expression by the immune system because SIVsmm-infected, asymptomatic mangabeys have high viral loads. Failure of mangabeys to develop disease may be related to the fact that the prototype SIVsmm (SMM-9) replicated in, but was not cytopathic for, mangabey CD4+ cells. In contrast, replication of SMM-9 in peripheral blood mononuclear cells from pigtailed macaques resulted in specific loss of CD4+ cells and induction of an AIDS-like disease. A variant of SMM-9, designated SMM-PBj14, was identified, however, that was extremely cytopathic for mangabey CD4+ cells and also induced acute lethal disease in both macaques and mangabeys. Acute disease was associated with extensive lymphoid hyperplasia, which was correlated in vitro with induction of proliferation of PBMC in SMM-PBj14-infected cultures. Infectious molecular clones of SMM-PBj14 exhibited the same in vitro and in vivo properties as SMM-PBj14. Future analysis of chimeric viruses may lead to the identification of specific regions of the viral genome that influence the various in vivo and in vitro properties of these SIVsmm isolates.

摘要

来自乌黑白眉猴的猴免疫缺陷病毒(SIVsmm)是一种慢病毒,与来自猕猴的SIV及人类免疫缺陷病毒2型(HIV-2)密切相关,它对多种猕猴具有致病性,但对黑白眉猴无致病性。分别比较猕猴和黑白眉猴或其淋巴细胞对SIVsmm感染的体内和体外反应表明,黑白眉猴不发病显然不是由于免疫系统对病毒表达的有效控制,因为感染SIVsmm且无症状的黑白眉猴病毒载量很高。黑白眉猴不发病可能与以下事实有关:原型SIVsmm(SMM-9)能在黑白眉猴CD4+细胞中复制,但不具有细胞病变效应。相比之下,SMM-9在猪尾猕猴的外周血单核细胞中复制会导致CD4+细胞特异性丧失并引发类似艾滋病的疾病。然而,已鉴定出一种SMM-9的变体,命名为SMM-PBj14,它对黑白眉猴CD4+细胞具有极强的细胞病变效应,并且在猕猴和黑白眉猴中都会引发急性致死性疾病。急性疾病与广泛的淋巴组织增生有关,这在体外与SMM-PBj14感染培养物中PBMC增殖的诱导相关。SMM-PBj14的感染性分子克隆在体外和体内表现出与SMM-PBj14相同的特性。对嵌合病毒的进一步分析可能会鉴定出病毒基因组中影响这些SIVsmm分离株各种体内和体外特性的特定区域。

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引用本文的文献

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Engineered CD4- and CXCR4-using simian immunodeficiency virus from African green monkeys is neutralization sensitive and replicates in nonstimulated lymphocytes.利用来自非洲绿猴的猿猴免疫缺陷病毒构建的CD4和CXCR4对中和敏感,且能在未受刺激的淋巴细胞中复制。
J Virol. 2002 Nov;76(21):10627-36. doi: 10.1128/jvi.76.21.10627-10636.2002.
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Characteristics of a pathogenic molecular clone of an end-stage serum-derived variant of simian immunodeficiency virus (SIV(F359)).
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J Virol. 2001 Oct;75(19):9328-38. doi: 10.1128/JVI.75.19.9328-9338.2001.
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Normal T-cell turnover in sooty mangabeys harboring active simian immunodeficiency virus infection.携带活跃猴免疫缺陷病毒感染的黑猩猩的正常T细胞更新。
J Virol. 2000 Feb;74(3):1209-23. doi: 10.1128/jvi.74.3.1209-1223.2000.
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Diverse host responses and outcomes following simian immunodeficiency virus SIVmac239 infection in sooty mangabeys and rhesus macaques.在乌黑白眉猴和恒河猴中感染猿猴免疫缺陷病毒SIVmac239后出现的多种宿主反应和结果。
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The U3 promoter and the nef gene of simian immunodeficiency virus (SIV) smmPBj1.9 do not confer acute pathogenicity upon SIVagm.猿猴免疫缺陷病毒(SIV)smmPBj1.9的U3启动子和nef基因不会赋予SIVagm急性致病性。
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Molecular and biological analyses of quasispecies during evolution of a virulent simian immunodeficiency virus, SIVsmmPBj14.毒性猿猴免疫缺陷病毒SIVsmmPBj14进化过程中准种的分子与生物学分析
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