Gyarmati Péter, Conze Tim, Zohari Siamak, LeBlanc Neil, Nilsson Mats, Landegren Ulf, Banér Johan, Belák Sándor
Joint Research and Development Division, Department of Virology, National Veterinary Institute and Swedish University of Agricultural Sciences, Ulls väg 2B, SE-751 89 Uppsala, Sweden.
J Clin Microbiol. 2008 May;46(5):1747-51. doi: 10.1128/JCM.02292-07. Epub 2008 Mar 19.
A subtyping assay for both the hemagglutinin (HA) and neuraminidase (NA) surface antigens of the avian influenza virus (AIV) has been developed. The method uses padlock probe chemistry combined with a microarray output for detection. The outstanding feature of this assay is its capability to designate both the HA and the NA of an AIV sample from a single reaction mixture. A panel of 77 influenza virus strains was tested representing the entire assortment of the two antigens. One hundred percent (77/77) of the samples tested were identified as AIV, and 97% (75/77) were subtyped correctly in accordance with previous examinations performed by classical diagnostic methods. Testing of heterologous pathogens verified the specificity of the assay. This assay is a convenient and practical tool for the study of AIVs, providing important HA and NA data more rapidly than conventional methods.
已经开发出一种针对禽流感病毒(AIV)血凝素(HA)和神经氨酸酶(NA)表面抗原的亚型分析方法。该方法采用锁式探针化学技术并结合微阵列输出进行检测。此分析方法的突出特点是能够从单一反应混合物中确定AIV样本的HA和NA。对一组代表这两种抗原全部种类的77株流感病毒进行了测试。所测试的样本中有100%(77/77)被鉴定为AIV,并且97%(75/77)根据先前通过经典诊断方法进行的检测被正确分型。对异源病原体的测试验证了该分析方法的特异性。该分析方法是研究AIV的一种便捷实用工具,比传统方法能更快地提供重要的HA和NA数据。