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Development of a Reverse Transcription-Loop-Mediated Isothermal Amplification Assay for Detection of Pandemic (H1N1) 2009 Virus as a Novel Molecular Method for Diagnosis of Pandemic Influenza in Resource-Limited Settings▿

机译:用于检测大流行性流感(H1N1)2009病毒的逆转录-循环介导的等温扩增测定方法的开发,该方法是一种在资源有限的环境中诊断大流行性流感的新型分子方法▿

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摘要

This paper reports on the development of a one-step, real-time reverse transcription-loop-mediated isothermal amplification (RT-LAMP) assay targeting the hemagglutinin (HA) gene for the rapid molecular-based detection of pandemic (H1N1) 2009 virus. The detection limit of the pandemic (H1N1) 2009 virus HA-specific RT-LAMP assay was same as that of the currently used real-time reverse transcription-PCR method. The assay detected the pandemic (H1N1) 2009 virus HA gene in 136 RNA samples extracted from nasopharyngeal swab specimens from Japanese and Vietnamese patients. No cross-reactive amplification with the RNA of other seasonal influenza viruses was observed, and the detection of specific viral genome targets in clinical specimens was achieved in less than 40 min. The sensitivity and specificity of the pandemic (H1N1) 2009 virus HA-specific RT-LAMP assay obtained in this study were 97.8% and 100%, respectively. Use of the (H1N1) 2009 virus HA-specific RT-LAMP assay will enable the faster and easier diagnosis of pandemic (H1N1) 2009 virus infection, especially in resource-limited situations in developing countries.
机译:本文报道了针对血凝素(HA)基因的一步法实时逆转录环介导的等温扩增(RT-LAMP)分析技术的开发,该技术可用于基于分子的大流行(H1N1)2009病毒的快速检测。大流行(H1N1)2009病毒HA特异性RT-LAMP测定的检出限与当前使用的实时逆转录PCR方法的检出限相同。该检测方法在从日本和越南患者的鼻咽拭子样本中提取的136个RNA样本中检测到了2009年大流行(H1N1)病毒HA基因。没有观察到与其他季节性流感病毒的RNA发生交叉反应扩增,并且在不到40分钟的时间内就完成了对临床标本中特定病毒基因组靶标的检测。这项研究中获得的2009年H1N1大流行性流感病毒HA特异性RT-LAMP检测的灵敏度和特异性分别为97.8%和100%。使用(H1N1)2009病毒HA特异的RT-LAMP分析将能够更快,更轻松地诊断2009年大流行(H1N1)病毒感染,尤其是在发展中国家资源有限的情况下。

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