Taubenberger J K, Layne S P
Department of Cellular Pathology and Genetics, Division of Molecular Pathology, Armed Forces Institute of Pathology, Rockville, MD 20850-3125, USA.
Mol Diagn. 2001 Dec;6(4):291-305. doi: 10.1054/modi.2001.28063.
Influenza viruses continually circulate and cause yearly epidemics, which kill 20,000 people in an average year in the United States. Occasionally and unpredictably, pandemic influenza strains sweep the world, infecting 20% to 40% of the world's population in a single year. In 1918, the worst influenza pandemic on record caused 675,000 deaths in the United States and up to 40 million deaths worldwide. Despite the prevalence of this virus, molecular assays for influenza diagnosis, surveillance, vaccine strain selection, and research have lagged behind such assays for other common viral pathogens. The extreme genetic variability of influenza viruses makes the design of useful molecular-based assays challenging, but several different approaches have been successfully used. RT-PCR is effective for the initial diagnosis and has greater sensitivity than other available rapid assays. Molecular assays also can be used to subtype influenza isolates, and sequence analysis of hemagglutinin may assist greatly in surveillance studies and vaccine strain selection. RT-PCR for influenza also can be performed from tissue biopsy specimens for both retrospective diagnosis and research.
流感病毒持续传播并引发年度流行,在美国平均每年导致2万人死亡。偶尔且不可预测地,大流行性流感毒株会席卷全球,一年内感染全球20%至40%的人口。1918年,有记录以来最严重的流感大流行在美国导致67.5万人死亡,全球死亡人数高达4000万。尽管这种病毒很普遍,但用于流感诊断、监测、疫苗株选择和研究的分子检测方法落后于针对其他常见病毒病原体的此类检测方法。流感病毒极高的基因变异性使得设计有用的基于分子的检测方法具有挑战性,但已经成功使用了几种不同的方法。逆转录聚合酶链反应(RT-PCR)对初始诊断有效,并且比其他现有的快速检测方法具有更高的灵敏度。分子检测方法还可用于对流感分离株进行亚型分类,血凝素的序列分析可能对监测研究和疫苗株选择有很大帮助。用于流感的RT-PCR也可从组织活检标本中进行,用于回顾性诊断和研究。