Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
J Clin Microbiol. 2011 Jul;49(7):2602-9. doi: 10.1128/JCM.00277-11. Epub 2011 May 4.
Oseltamivir (Tamiflu), an oral neuraminidase inhibitor, has been widely used to treat pandemic 2009 (H1N1) influenza A. Although a majority of 2009 (H1N1) influenza A virus remains oseltamivir susceptible, the threat of resistance due to the His275Tyr mutation is highlighted by the limitations of alternative therapies and the potential for rapid, global fixation of this mutation in the circulating influenza A virus population. In order to better understand the emergence of resistance, we developed a rare-variant-sensitive high-resolution melting-curve analysis method (RVS-HRM) that is able to detect the His275Tyr oseltamivir resistance mutation to 0.5% in a background of susceptible virus. We applied RVS-HRM to clinical specimens from patients who developed oseltamivir resistance and demonstrated the ultrasensitive detection of influenza A virus N1 neuraminidase quasispecies. Interestingly, we were unable to detect the oseltamivir resistance mutation in pretreatment samples, suggesting that resistant virus does not reach even this very low detection threshold until exposed to selective drug pressure. Thus, patients naive to oseltamivir are most likely to be susceptible when this drug is used as a first-line treatment modality.
奥司他韦(达菲)是一种口服神经氨酸酶抑制剂,被广泛用于治疗大流行 2009 年(H1N1)甲型流感。尽管大多数 2009 年(H1N1)甲型流感病毒仍然对奥司他韦敏感,但由于 His275Tyr 突变导致的耐药性威胁,由于替代疗法的局限性以及这种突变在循环流感病毒种群中快速、全球固定的潜在可能性,这一突变突显了这一威胁。为了更好地了解耐药性的出现,我们开发了一种罕见变异敏感的高分辨率熔解曲线分析方法(RVS-HRM),该方法能够以 0.5%的背景检测到奥司他韦耐药的 His275Tyr 突变。我们将 RVS-HRM 应用于出现奥司他韦耐药的患者的临床标本,并证明了流感 A 病毒 N1 神经氨酸酶准种的超灵敏检测。有趣的是,我们无法在预处理样本中检测到奥司他韦耐药突变,这表明耐药病毒在接触到选择性药物压力之前,甚至无法达到如此低的检测阈值。因此,在将奥司他韦作为一线治疗方法时,未使用过奥司他韦的患者很可能仍然对其敏感。