De Baar Michel P, Abebe Almaz, Kliphuis Aletta, Tesfaye Girma, Goudsmit Jaap, Pollakis Georgios
Department of Human Retrovirology, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.
AIDS Res Hum Retroviruses. 2003 Oct;19(10):917-22. doi: 10.1089/088922203322493094.
While the Ethiopian HIV-1 epidemic is dominated by subtype C, two distinguishable cocirculating C genotypes have been identified based on sequences of the C2V3 envelope region. In this study we sequenced and analyzed the long terminal repeat (LTR) sequence from 22 Ethiopian HIV-1-positive individuals. The two phylogenetically distinguishable genotypes C (n = 13) and C' (n = 4) are separated by significant bootstrap values. Nucleotide differences between the two groups were identified in the NF-AT, TCF-1alpha, and SP1 transcription factor binding sites, whereas the NF-kappaB and NRE-core sequences were identical between the two groups. Five isolates that could not be classified C or C' were found to be recombinants within the LTR sequence upon boots can analysis. Comparison of all the LTR sequences with their corresponding C2V3 envelope sequence revealed four intersubtype C/C' recombinant isolates. Thus, the prevalence of C/C' recombinant viruses is well over 40%. Interestingly, the C2V3 envelope sequences of all recombinant viruses belonged to the genotype C', whereas every LTR sequence belonged to the genotype C. This result indicates that recombination between the two genotypes is unidirectional, possibly as the result of evolutionary pressure on the respective biological functions of the LTR promoter and the envelope protein.
虽然埃塞俄比亚的HIV-1流行以C亚型为主,但根据C2V3包膜区域的序列已鉴定出两种可区分的共同流行的C基因型。在本研究中,我们对22名埃塞俄比亚HIV-1阳性个体的长末端重复序列(LTR)进行了测序和分析。两种在系统发育上可区分的基因型C(n = 13)和C'(n = 4)通过显著的自展值分开。在NF-AT、TCF-1α和SP1转录因子结合位点鉴定出两组之间的核苷酸差异,而两组之间的NF-κB和NRE核心序列相同。在自展分析后发现,5株无法分类为C或C'的分离株在LTR序列内为重组体。将所有LTR序列与其相应的C2V3包膜序列进行比较,发现了4株C/C'亚型间重组分离株。因此,C/C'重组病毒的流行率远超过40%。有趣的是,所有重组病毒的C2V3包膜序列都属于C'基因型,而每个LTR序列都属于C基因型。这一结果表明,两种基因型之间的重组是单向的,这可能是LTR启动子和包膜蛋白各自生物学功能受到进化压力的结果。