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VereFlu™: an integrated multiplex RT-PCR and microarray assay for rapid detection and identification of human influenza A and B viruses using lab-on-chip technology

机译:VereFlu™:集成的多重RT-PCR和微阵列分析可通过芯片实验室技术快速检测和鉴定人类甲型和乙型流感病毒

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摘要

Threatening sporadic outbreaks of avian influenza and the H1N1 pandemic of 2009 highlight the need for rapid and accurate detection and typing of influenza viruses. In this paper, we describe the validation of the VereFlu™ Lab-on-Chip Influenza Assay, which is based on the integration of two technologies: multiplex reverse transcription (RT)-PCR followed by microarray amplicon detection. This assay simultaneously detects five influenza virus subtypes, including the 2009 pandemic influenza A (H1N1), seasonal H1N1, H3N2, H5N1 and influenza B virus. The VereFlu™ assay was clinically validated in Singapore and compared against reference methods of real-time PCR, virus detection by immunofluorescence of cell cultures and sequencing. A sensitivity and specificity of 96.8% and 92.8%, respectively, was demonstrated for pandemic H1N1; 95.7% and 100%, respectively, for seasonal H1N1; 91.2% and 97.6%, respectively, for seasonal H3N2; 95.2% and 100%, respectively, for influenza B. Additional evaluations carried out at the World Health Organization (WHO) Collaborating Centre, Melbourne, Australia, confirmed that the test was able to reliably detect H5N1. This portable, fast time-to-answer (3 hours) device is particularly suited for diagnostic applications of detection, differentiation and identification of human influenza virus subtypes.
机译:威胁性的零星禽流感爆发和2009年的H1N1大流行凸显了对快速,准确地检测和分类流感病毒的需求。在本文中,我们描述了VereFlu™芯片实验室流感检测方法的验证,该方法基于两种技术的集成:多重逆转录(RT)-PCR,然后进行微阵列扩增子检测。此测定法同时检测五种流感病毒亚型,包括2009年甲型大流行性流感(H1N1),季节性H1N1,H3N2,H5N1和B型流感病毒。 VereFlu™测定法在新加坡进行了临床验证,并与实时PCR,通过细胞培养物的免疫荧光检测病毒和测序的参考方法进行了比较。大流行H1N1的敏感性和特异性分别为96.8%和92.8%。季节性H1N1分别为95.7%和100%;季节性H3N2分别为91.2%和97.6%;乙型流感分别为95.2%和100%。在澳大利亚墨尔本的世界卫生组织(WHO)合作中心进行的其他评估证实,该测试能够可靠地检测H5N1。这种便携式的快速应答时间(3小时)设备特别适用于检测,区分和识别人类流感病毒亚型的诊断应用。

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