Fernàndez Guerau, Clotet Bonaventura, Martínez Miguel Angel
Fundacio irsiCaixa, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, 08916 Badalona, Barcelona, Spain.
J Virol. 2007 Mar;81(5):2485-96. doi: 10.1128/JVI.01594-06. Epub 2006 Dec 6.
Here we show, at a high resolution (1%), the human immunodeficiency virus type 1 (HIV-1) protease gene quasispecies landscape from three infected naïve individuals. A huge range of genetic configurations was found (67%, 71%, and 80% of the nucleotide clones from the three individuals, respectively, were different), and these configurations created a dense net that linked different parts of the viral population. Similarly, a vast diversity of different protease activities was also found. Importantly, 65% of the analyzed enzymes had detectable protease activity, and 11% of the minority individual variants showed similar or better fitness than the master (most abundant) enzyme, suggesting that the viral complexity in this genomic region does not exclusively depend on the enzyme's catalytic efficiency. Several high-fitness minority variants had only one substitution compared to the master sequence, supporting the possibility that the rugged HIV-1 protease quasispecies fitness landscape may be formed by a continuous network that can be traversed by single mutational steps without passing through defective or less-adapted proteins.
在此,我们以高分辨率(1%)展示了三名初治感染个体的人类免疫缺陷病毒1型(HIV-1)蛋白酶基因准种图谱。发现了范围广泛的基因构型(分别来自三名个体的核苷酸克隆中,67%、71%和80%是不同的),这些构型形成了一个密集网络,将病毒群体的不同部分连接起来。同样,还发现了多种多样的不同蛋白酶活性。重要的是,65%的分析酶具有可检测到的蛋白酶活性,11%的少数个体变体显示出与主要(最丰富)酶相似或更好的适应性,这表明该基因组区域的病毒复杂性并非完全取决于酶的催化效率。与主要序列相比,几个高适应性的少数变体仅有一个替换,这支持了崎岖的HIV-1蛋白酶准种适应性图谱可能由一个连续网络形成的可能性,该网络可通过单个突变步骤穿越,而无需经过有缺陷或适应性较差的蛋白质。