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Analysis, Quantification, and Evolutionary Consequences of HIV-1 in Vitro Recombination

机译:HIV-1体外重组的分析,定量和进化结果

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HIV-1 recombination was studied in vitro by viral cocultivation of four combinations of strains of subtypes B, D, and F. Viral cocultivations were performed in MT-4 cells and maintained for 22 days. The parental and recombinant forms were quantified by a specific PCR system in an env fragment of 2500 nucleotides. On day 5, there was a close correlation between the proportion of recombination and the genetic distance between strains. In three of the four viral combinations studied, a steady increase in the proportion of recombinant genomes was observed over time. This rise coincided with the progressive loss of one of the parental strains, resulting in less diverse viral populations. Nucleotide sequencing of biological recombinant clones from the B/D cocultivation revealed a higher number of recombination events in pol than in env gene, and an increasing number of crossovers per clone with time.
机译:通过病毒共培养B,D和F型亚型的四种组合在体外研究了HIV-1重组。病毒共培养在MT-4细胞中进行,并维持22天。通过特异性PCR系统在2500个核苷酸的env片段中定量亲本和重组形式。在第5天,重组比例与菌株之间的遗传距离紧密相关。在研究的四个病毒组合中的三个中,随着时间的推移,观察到重组基因组比例的稳定增加。这种上升与其中一种亲本菌株的逐渐丧失相吻合,导致病毒种群的多样性降低。来自B / D共培养的生物重组克隆的核苷酸测序显示pol中重组事件的数量比env基因中重组事件的数量大,并且每个克隆的交叉次数随时间增加。

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