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来自非洲绿猴的猿猴免疫缺陷病毒和2型人类免疫缺陷病毒的突变分析。

Mutational analysis of simian immunodeficiency virus from African green monkeys and human immunodeficiency virus type 2.

作者信息

Shibata R, Adachi A, Sakai H, Ishimoto A, Miura T, Hayami M

机构信息

Institute for Virus Research, Kyoto University, Japan.

出版信息

J Med Primatol. 1990;19(3-4):217-25.

PMID:2231682
Abstract

We constructed ten mutants of simian immunodeficiency virus isolated from African green monkey (SIVAGM), and nine mutants of human immunodeficiency virus type 2 (HIV-2) in vitro. Their infectivity, cytopathogenicity, transactivation potential, virus RNA, and protein synthesis were examined by transfection and infection experiments. Mutations in three structural (gag, pol, env) and two regulator (tat, rev) genes abolished the infectivity of both viruses, but vpx, vpr (HIV-2), and nef were dispensable and mutant viruses were indistinguishable phenotypically from wild type virus. A vif mutant of HIV-2 showed poor infectivity in cell-free condition, whereas SIVAGM mutants grew equally well with wild type virus. In transient transfection assays, rev mutants derived from both viruses produced mainly small mRNA species and no detectable virus proteins and particles. Transactivation potential of tat mutants originated from both viruses was about three- to ten-fold less than that of respective wild type DNAs, generating small amounts of virus.

摘要

我们在体外构建了从非洲绿猴分离出的猿猴免疫缺陷病毒(SIVAGM)的十个突变体以及人类免疫缺陷病毒2型(HIV-2)的九个突变体。通过转染和感染实验检测了它们的感染性、细胞致病性、反式激活潜能、病毒RNA及蛋白质合成。三个结构基因(gag、pol、env)和两个调节基因(tat、rev)中的突变消除了两种病毒的感染性,但vpx、vpr(HIV-2)和nef是可有可无的,突变病毒在表型上与野生型病毒无法区分。HIV-2的一个vif突变体在无细胞条件下感染性较差,而SIVAGM突变体与野生型病毒生长情况相同。在瞬时转染实验中,两种病毒的rev突变体主要产生小的mRNA种类,未检测到病毒蛋白和病毒颗粒。两种病毒的tat突变体的反式激活潜能比各自的野生型DNA低约三到十倍,产生少量病毒。

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