Hall Richard J, Peacey Matthew, Ralston Jacqui C, de Joux Danielle J, Bocacao Judy, Nicol Mackenzie, Ziki Molly, Gunn Wendy, Wang Jing, Huang Q Sue
WHO National Influenza Centre, Institute of Environmental Science & Research, National Centre for Biosecurity & Infectious Disease, New Zealand .
Western Pac Surveill Response J. 2012 Oct 30;3(4):71-7. doi: 10.5365/WPSAR.2012.3.3.002. Print 2012 Oct.
Oseltamivir (Tamiflu®) is an important pharmaceutical intervention against the influenza virus. The importance of surveillance for resistance to oseltamivir has been highlighted by two global events: the emergence of an oseltamivir-resistant seasonal influenza A(H1N1) virus in 2008, and emergence of the influenza A(H1N1)pdm09 virus in 2009. Oseltamivir is a prescription medicine in New Zealand, but more timely access has been provided since 2007 by allowing pharmacies to directly dispense oseltamivir to patients with influenza-like illness.
To determine the frequency of oseltamivir-resistance in the context of a medicine reclassification in 2007, the importation of an oseltamivir-resistant seasonal influenza virus in 2008, and the emergence of a pandemic in 2009.
A total of 1795 influenza viruses were tested for oseltamivir-resistance using a fluorometric neuraminidase inhibition assay. Viruses were collected as part of a sentinel influenza surveillance programme between the years 2006 and 2010.
All influenza B, influenza A(H3N2) and influenza A(H1N1)pdm09 viruses tested between 2006 and 2010 were shown to be sensitive to oseltamivir. Seasonal influenza A(H1N1) viruses from 2008 and 2009 were resistant to oseltamivir. Sequencing of the neuraminidase gene showed that the resistant viruses contained an H275Y mutation, and S247N was also identified in the neuraminidase gene of one seasonal influenza A(H1N1) virus that exhibited enhanced resistance.
No evidence was found to suggest that increased access to oseltamivir has promoted resistance. A probable importation event was documented for the global 2008 oseltamivir-resistant seasonal A(H1N1) virus nine months after it was first reported in Europe in January 2008.
奥司他韦(达菲®)是对抗流感病毒的一种重要药物干预手段。两项全球事件凸显了监测奥司他韦耐药性的重要性:2008年出现了对奥司他韦耐药的季节性甲型H1N1流感病毒,以及2009年出现了甲型H1N1pdm09流感病毒。在新西兰,奥司他韦是一种处方药,但自2007年以来,通过允许药店直接向患有流感样疾病的患者配发奥司他韦,患者能更及时地获得该药。
在2007年药品重新分类、2008年输入对奥司他韦耐药的季节性流感病毒以及2009年出现大流行的背景下,确定奥司他韦耐药性的发生频率。
使用荧光神经氨酸酶抑制试验对总共1795株流感病毒进行奥司他韦耐药性检测。这些病毒是在2006年至2010年期间作为流感哨点监测计划的一部分收集的。
2006年至2010年期间检测的所有乙型流感病毒、甲型H3N2流感病毒和甲型H1N1pdm09流感病毒对奥司他韦均敏感。2008年和2009年的季节性甲型H1N1流感病毒对奥司他韦耐药。神经氨酸酶基因测序显示,耐药病毒含有H275Y突变,并且在一株表现出增强耐药性的季节性甲型H1N