Zanini Fabio, Puller Vadim, Brodin Johanna, Albert Jan, Neher Richard A
Max Planck Institute for Developmental Biology, Tübingen 72076, Germany.
Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Virus Evol. 2017 Mar 2;3(1):vex003. doi: 10.1093/ve/vex003. eCollection 2017 Jan.
Mutation rates and fitness costs of deleterious mutations are difficult to measure but essential for a quantitative understanding of evolution. Using whole genome deep sequencing data from longitudinal samples during untreated HIV-1 infection, we estimated mutation rates and fitness costs in HIV-1 from the dynamics of genetic variation. At approximately neutral sites, mutations accumulate with a rate of 1.2 × 10 per site per day, in agreement with the rate measured in cell cultures. We estimated the rate from G to A to be the largest, followed by the other transitions C to T, T to C, and A to G, while transversions are less frequent. At other sites, mutations tend to reduce virus replication. We estimated the fitness cost of mutations at every site in the HIV-1 genome using a model of mutation selection balance. About half of all non-synonymous mutations have large fitness costs (>10 percent), while most synonymous mutations have costs <1 percent. The cost of synonymous mutations is especially low in most of where we could not detect measurable costs for the majority of synonymous mutations. In contrast, we find high costs for synonymous mutations in important RNA structures and regulatory regions. The intra-patient fitness cost estimates are consistent across multiple patients, indicating that the deleterious part of the fitness landscape is universal and explains a large fraction of global HIV-1 group M diversity.
有害突变的突变率和适应度代价难以衡量,但对于定量理解进化过程至关重要。利用未经治疗的HIV-1感染期间纵向样本的全基因组深度测序数据,我们从遗传变异动态中估计了HIV-1的突变率和适应度代价。在大约中性位点,突变以每天每个位点1.2×10的速率积累,这与在细胞培养中测得的速率一致。我们估计从G到A的突变率最大,其次是其他转换C到T、T到C以及A到G,而颠换则较少见。在其他位点,突变往往会降低病毒复制。我们使用突变选择平衡模型估计了HIV-1基因组中每个位点突变的适应度代价。所有非同义突变中约有一半具有较大的适应度代价(>10%),而大多数同义突变的代价<1%。在大多数情况下,同义突变的代价特别低,我们无法检测到大多数同义突变的可测量代价。相比之下,我们发现在重要的RNA结构和调控区域中同义突变的代价很高。患者体内的适应度代价估计在多个患者中是一致的,这表明适应度景观的有害部分是普遍存在的,并且解释了全球HIV-1 M组多样性的很大一部分。