首页> 外文期刊>Taiwan Veterinary Journal >DETECTION AND DIFFERENTIATION OF THE VACCINE STRAIN AND FIELD ISOLATES OF DUCK HEPATITIS A VIRUS TYPE 1 USING REAL-TIME RT-PCR AND HIGH RESOLUTIONMELTING ASSAYS
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DETECTION AND DIFFERENTIATION OF THE VACCINE STRAIN AND FIELD ISOLATES OF DUCK HEPATITIS A VIRUS TYPE 1 USING REAL-TIME RT-PCR AND HIGH RESOLUTIONMELTING ASSAYS

机译:实时RT-PCR和高分辨熔解法检测和鉴定1型鸭肝炎疫苗株和野外分离株

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摘要

Duck hepatitis A virus type 1 (DHAV-1) infection is a highly contagious and fatal disease of young ducklings. A live attenuated vaccine strain designated as 5886 has been used in Taiwan for the control of DHAV-1. Although several molecular biologicalmethods are reported for diagnosis of DHAV-1 infection, none of them is able to discriminate between the vaccine strain and field viruses of DHAV-1. In the present study, a real-time reverse transcriptase polymerase chain reaction (RT-PCR) and high resolution melting (HRM) assay was developed for rapid detection and differentiation between the vaccine strain and field viruses of DHAV-1. This assay is highly specific for DHAV-1 and the detection limit is about 100 copies of the viral RNA. Experiments using fecal samples collected from ducklings experimentally infected with DHAV-1 showed that DHAV-1 could be detected in fecal samples as early as 6 h post-infection. In summary, a real-time RT-PCR and HRM assay is developed in this study and this assay could be valuable for diagnosis and surveillance of DHAV-1 infection in the field.
机译:鸭甲型肝炎病毒1型(DHAV-1)感染是一种高度传染性和致命性的雏鸭疾病。台湾已使用一种名为5886的减毒活疫苗株控制DHAV-1。尽管据报道有几种分子生物学方法可诊断DHAV-1感染,但它们均不能区分DHAV-1疫苗株和野病毒。在本研究中,开发了实时逆转录聚合酶链反应(RT-PCR)和高分辨率熔解(HRM)测定法,用于快速检测和区分DHAV-1疫苗株和野病毒。该测定法对DHAV-1具有高度特异性,检出限约为100份病毒RNA。使用从实验性感染DHAV-1的小鸭中收集的粪便样品进行的实验表明,最早在感染后6 h便可以在粪便样品中检测到DHAV-1。总而言之,本研究开发了一种实时RT-PCR和HRM检测方法,该检测方法对于现场诊断和监测DHAV-1感染可能是有价值的。

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