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水中SaV GⅣ的提取及荧光定量PCR检出方法研究 被引量:2

Extraction of SaV GⅣ in water sample and real-time QPCR detection method
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摘要 札幌病毒(Sapovirus/SaV)是引起急性腹泻的常见病毒,水体是SaV传播的主要途径之一。由于设备和检测水平的限制,水体中病毒的检出费时费力。本文利用分子诊断学中灵敏度高的水中病毒富集技术结合荧光定量PCR方法,对水中SaV GⅣ基因型快速检测方法进行了研究。获得了一套水中病毒富集、核酸提取及分子诊断学检出方法。对比了TaqMan探针法与SYBRGreen染料法在检测中的效果。初步建立了利用水中病毒分离装置富集SaV GⅣ病毒,应用TaqMan探针法与SYBRGreen染料法两种荧光定量PCR方法快速检出SaV GⅣ的分子诊断学方法。 Sapovirus( SaV) is a common cause of gastroenteritis. Water is one of the main media for the propagation of SaV. Because of a limitation in equipment and inspection ability,the detection of SaV in water is laborious. In this study,molecular diagnostics with highly sensitive nucleic acid extraction technology and a real-time quantitative PCR method were used for the rapid detection of SaV GⅣ in water. A rapid detection method for SaV GⅣ in water has been established.
出处 《黑龙江大学自然科学学报》 CAS 北大核心 2014年第4期504-510,共7页 Journal of Natural Science of Heilongjiang University
基金 黑龙江省财政基本科研业务费专项资助项目(CZ12BXHH08) 哈尔滨市应用技术研究与开发资助项目(2013RFQYJ072) 黑龙江省科学院国际科技合作交流项目
关键词 札幌病毒 实时定量PCR 水中病毒 分子诊断学 Sapovirus real-time QPCR virus in water molecular diagnostics
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