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一种加纳1型艾滋病毒A/G亚型间重组CRF02_AG全长分子DNA克隆的分离与鉴定,该克隆在有限宿主范围内具有复制能力。

Isolation and characterization of a full-length molecular DNA clone of Ghanaian HIV type 1 intersubtype A/G recombinant CRF02_AG, which is replication competent in a restricted host range.

作者信息

Kusagawa S, Takebe Y, Yang R, Motomura K, Ampofo W, Brandful J, Koyanagi Y, Yamamoto N, Sata T, Ishikawa K, Nagai Y, Tatsumi M

机构信息

AIDS Research Center, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.

出版信息

AIDS Res Hum Retroviruses. 2001 May 1;17(7):649-55. doi: 10.1089/088922201300119761.

Abstract

We have isolated a replication-competent, full-length molecular clone of HIV-1 CRF02_AG, designated p97GH-AG1, by reconstituting two separately amplified genomic regions of an HIV-1 provirus of a 1997 Ghanaian isolate. The phylogenetic and recombination breakpoint analyses revealed that 97GH-AG1 had an A/G recombinant structure similar to that of prototype Nigerian isolate IbNG. The 17-nucleotide insertion downstream of the primer-binding site appeared to be a common sequence signature specific to most CRF02_AG strains, including 97GH-AG1. 97GH-AG1 showed an R5 phenotype and exerted productive infection in both HOS and NP2 cell infectivity assays, whereas it failed to show a detectable level of progeny production in peripheral blood mononuclear cells (PBMCs). The data may suggest the presence of unknown determinant(s) that dictate efficient replication in PBMCs, but that are not required for replication in immortalized cell lines.

摘要

我们通过重组1997年加纳分离株的HIV-1前病毒的两个分别扩增的基因组区域,分离出了一种具有复制能力的HIV-1 CRF02_AG全长分子克隆,命名为p97GH-AG1。系统发育和重组断点分析表明,97GH-AG1具有与尼日利亚原型分离株IbNG相似的A/G重组结构。引物结合位点下游的17个核苷酸插入似乎是大多数CRF02_AG菌株(包括97GH-AG1)特有的常见序列特征。97GH-AG1表现出R5表型,并且在HOS和NP2细胞感染性试验中均产生了有效感染,然而,它在外周血单核细胞(PBMC)中未能显示出可检测水平的子代产生。这些数据可能表明存在未知的决定因素,这些因素决定了在PBMC中的有效复制,但在永生化细胞系中复制时并非必需。

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