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三株南非1型人类免疫缺陷病毒C亚型分离株的近全长基因组序列特征分析

Characterisation of near-full length genome sequences of three South African human immunodeficiency virus type 1 subtype C isolates.

作者信息

Hunt Gillian M, Papathanasopoulos Maria A, Gray Glenda E, Tiemessen Caroline T

机构信息

AIDS Virus Research Unit, National Institute for Communicable Diseases and Department of Virology, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Virus Genes. 2003 Jan;26(1):49-56. doi: 10.1023/a:1022378022104.

DOI:10.1023/a:1022378022104
PMID:12680693
Abstract

As subtype C is the most prevalent circulating human immunodeficiency virus type 1 (HIV-1) subtype internationally as well as locally in South Africa, more information on the biological nature and molecular characteristics of these viruses is required. Proviral DNA was isolated from primary cultures of three South African R5 isolates and the near-full length genome amplified by PCR. The resultant PCR product was cloned into the pCR-XL-TOPO vector and a representative clone from each isolate sequenced by primer walking. Phylogenetic analysis showed all three clones clustered within subtype C with a bootstrap value of 100%, and no recombination with other subtypes was identified by distance scan and bootscan analysis. Analysis of the potential coding regions revealed premature truncations of the second rev exon but no other potential structural distortions nor frameshift mutations in the open reading frames. All the clones contained three potential NF-kappaB binding sites, a feature unique to subtype C viruses. The tips of the V3 loops contained the GPGQ sequence motif characteristic of CCR5-utilising subtype C strains, as well as relatively low overall net positive charge characteristic of non-syncytium-inducing isolates. This information contributes to our overall knowledge of circulating strains in South Africa and to the making of effective vaccines and chemotherapeutic agents.

摘要

由于C亚型是国际上以及南非本地最普遍流行的人类免疫缺陷病毒1型(HIV-1)亚型,因此需要更多关于这些病毒生物学特性和分子特征的信息。从三个南非R5分离株的原代培养物中分离出前病毒DNA,并通过PCR扩增近乎全长的基因组。将所得的PCR产物克隆到pCR-XL-TOPO载体中,并通过引物步移法对每个分离株的一个代表性克隆进行测序。系统发育分析表明,所有三个克隆都聚集在C亚型内,自展值为100%,并且通过距离扫描和bootscan分析未发现与其他亚型的重组。对潜在编码区的分析显示,第二个rev外显子有过早截断,但在开放阅读框中未发现其他潜在的结构畸变或移码突变。所有克隆都含有三个潜在的NF-κB结合位点,这是C亚型病毒特有的特征。V3环的末端包含利用CCR5的C亚型毒株特有的GPGQ序列基序,以及非合胞体诱导分离株相对较低的总体净正电荷特征。这些信息有助于我们全面了解南非的流行毒株,并有助于开发有效的疫苗和化疗药物。

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