Janssens W, Laukkanen T, Salminen M O, Carr J K, Van der Auwera G, Heyndrickx L, van der Groen G, McCutchan F E
Department of Microbiology, Institute of Tropical Medicine, Antwerp, Belgium.
AIDS. 2000 Jul 28;14(11):1533-43. doi: 10.1097/00002030-200007280-00009.
To characterize near-full-length genomes of two HIV-1 subtype H strains. To extend sequence data to include full env and gag, and analyse and redefine, previously documented subtype H strains.
Near-full-length genomes of HIV-1 env subtype H strains VI991 and VI997 were amplified, cloned, sequenced, phylogenetically analysed and compared with a panel of 23 HIV-1 group M reference isolates. The mosaic nature of previously published subtype H strains VI557 and CA13 was reanalysed.
Peripheral blood mononuclear cells (PBMC) from individuals harbouring strains VI991 and VI997 were co-cultivated with PHA stimulated donor PBMC. Near-full-length genomes of VI991 and VI997, and gag and env genes of CA13 and VI557, were amplified by polymerase chain reaction, cloned and sequenced. Intersubtype recombination analyses were performed by similarity plot, bootscanning and phylogenetic analysis.
Near-full-length clones of HIV-1 VI991 and VI997 are representative of subtype H. They form a phylogenetic cluster with the only previously described subtype H representative HIV-1 90CF056.1, regardless of the genome region analysed. VI557 is redefined as a gag and env subtype H mosaic virus containing unclassified fragments. CA13 is a complex intersubtype recombinant between subtypes A, H and unclassified strains
Near-full-length genome analysis identified HIV-1 VI991 and VI997 as two new subtype H representatives. These reagents will allow defining and classifying non-recombinant as well as recombinant HIV-1, eventually helping to solve the puzzle of HIV-1 subtypes.
对两株HIV-1 H亚型毒株的近全长基因组进行特征分析。扩展序列数据以纳入完整的env和gag基因,并分析和重新定义先前记录的H亚型毒株。
对HIV-1 env H亚型毒株VI991和VI997的近全长基因组进行扩增、克隆、测序、系统发育分析,并与一组23株HIV-1 M组参考毒株进行比较。对先前发表的H亚型毒株VI557和CA13的镶嵌性质进行重新分析。
将携带毒株VI991和VI997个体的外周血单个核细胞(PBMC)与PHA刺激的供体PBMC共同培养。通过聚合酶链反应扩增VI991和VI997的近全长基因组以及CA13和VI557的gag和env基因,进行克隆和测序。通过相似性图、靴带扫描和系统发育分析进行亚型间重组分析。
HIV-1 VI991和VI997的近全长克隆代表H亚型。无论分析的基因组区域如何,它们与之前唯一描述的H亚型代表性毒株HIV-1 90CF056.1形成一个系统发育簇。VI557被重新定义为一种包含未分类片段的gag和env H亚型镶嵌病毒。CA13是A、H亚型和未分类毒株之间的复杂亚型间重组体。
近全长基因组分析确定HIV-1 VI991和VI997为两株新的H亚型代表毒株。这些试剂将有助于定义和分类非重组以及重组HIV-1,最终有助于解开HIV-1亚型之谜。