Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, Nuffield Department of Medicine, University of Oxford, United Kingdom.
Department of Statistics, University of Oxford, United Kingdom.
J Infect Dis. 2019 May 5;219(11):1722-1729. doi: 10.1093/infdis/jiy747.
Despite recent breakthroughs in treatment of hepatitis C virus (HCV) infection, we have limited understanding of how virus diversity generated within individuals impacts the evolution and spread of HCV variants at the population scale. Addressing this gap is important for identifying the main sources of disease transmission and evaluating the risk of drug-resistance mutations emerging and disseminating in a population.
We have undertaken a high-resolution analysis of HCV within-host evolution from 4 individuals coinfected with human immunodeficiency virus 1 (HIV-1). We used long-read, deep-sequenced data of full-length HCV envelope glycoprotein, longitudinally sampled from acute to chronic HCV infection to investigate the underlying viral population and evolutionary dynamics.
We found statistical support for population structure maintaining the within-host HCV genetic diversity in 3 out of 4 individuals. We also report the first population genetic estimate of the within-host recombination rate for HCV (0.28 × 10-7 recombination/site/year), which is considerably lower than that estimated for HIV-1 and the overall nucleotide substitution rate estimated during HCV infection.
Our findings indicate that population structure and strong genetic linkage shapes within-host HCV evolutionary dynamics. These results will guide the future investigation of potential HCV drug resistance adaptation during infection, and at the population scale.
尽管最近在丙型肝炎病毒 (HCV) 感染的治疗方面取得了突破,但我们对个体内部产生的病毒多样性如何影响 HCV 变异在人群中的进化和传播知之甚少。解决这一差距对于确定疾病传播的主要来源以及评估人群中耐药突变出现和传播的风险至关重要。
我们对 4 名同时感染人类免疫缺陷病毒 1 (HIV-1) 的个体的 HCV 个体内进化进行了高分辨率分析。我们使用来自急性到慢性 HCV 感染的全长 HCV 包膜糖蛋白的长读、深度测序数据,来研究潜在的病毒群体和进化动态。
我们发现有统计学证据表明,在 4 名个体中的 3 名中,群体结构维持了 HCV 个体内的遗传多样性。我们还报告了 HCV 个体内重组率的第一个群体遗传估计值(0.28×10-7 重组/位点/年),这明显低于 HIV-1 的估计值和 HCV 感染期间估计的总核苷酸替代率。
我们的研究结果表明,群体结构和强烈的遗传连锁塑造了 HCV 个体内的进化动态。这些结果将指导未来对感染过程中潜在的 HCV 耐药适应性以及在人群水平上的研究。