Department of Computational & Systems Biology, Center for Vaccine Research, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
J Infect Dis. 2012 Nov 15;206(10):1504-11. doi: 10.1093/infdis/jis571. Epub 2012 Sep 10.
A small proportion (1%-1.5%) of 2009 pandemic influenza A/H1N1 virus strains (A[H1N1]pdm09) are oseltamivir resistant, almost exclusively because of a H275Y mutation in the neuraminidase protein. However, many individuals infected with resistant strains had not received antivirals. Whether drug-resistant viruses are initially present as minor variants in untreated individuals before they emerge as the dominant strain in a virus population is of great importance for predicting the speed at which resistance will arise. To address this issue, we used ultra-deep sequencing of viral populations from serial nasopharyngeal specimens from an immunocompromised child and from 2 individuals in a household outbreak. We observed that the Y275 mutation was present as a minor variant in infected hosts before the onset of therapy. We also found evidence for the transmission of this drug-resistant variant with drug-susceptible viruses. These observations provide important information on the relative fitness of the Y275 mutation in the absence of oseltamivir treatment.
少数(1%-1.5%)2009 年大流行流感 A/H1N1 病毒株(A[H1N1]pdm09)对奥司他韦具有耐药性,几乎完全是由于神经氨酸酶蛋白中的 H275Y 突变所致。然而,许多感染耐药株的个体并未接受抗病毒药物治疗。在耐药病毒作为次要变异体出现在病毒群体中的主要菌株之前,它们是否最初存在于未经治疗的个体中,对于预测耐药性出现的速度非常重要。为了解决这个问题,我们使用了来自免疫功能低下儿童的连续鼻咽标本和家庭暴发中的 2 个人的病毒群的超深度测序。我们观察到,在开始治疗之前,Y275 突变作为受感染宿主中的一个次要变体存在。我们还发现了这种耐药变异体与敏感药物病毒传播的证据。这些观察结果为在没有奥司他韦治疗的情况下 Y275 突变的相对适应性提供了重要信息。