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首页> 外文期刊>Veterinary Microbiology >Evaluation of a multiplex real-time RT-PCR for quantitative and differential detection of wild-type viruses and C-strain vaccine of Classical swine fever virus
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Evaluation of a multiplex real-time RT-PCR for quantitative and differential detection of wild-type viruses and C-strain vaccine of Classical swine fever virus

机译:多重实时RT-PCR定量和差异检测野生型病毒和经典猪瘟病毒C株疫苗的评估

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Classical swine fever virus (CSFV) is the causative agent of classical swine fever (CSF), one of OIE listed diseases. Most of the currently available detection methods do not allow discrimination between wild-type CSF viruses and the vaccine strains. This study was designed to develop a multiplex real-time RT-PCR for the quantitative and differential detection of wild-type viruses and C-strain vaccine widely used in China. CSFV specific primers and two differently labeled TaqMan probes for the differentiation of wild-type viruses from C-strain vaccine were designed in the 5'-untranslated region of the viral genome of CSFV. The two TaqMan probes specifically hybridize wild-type viruses of different subgroups and C-strain vaccine, respectively, in the multiplex real-time RT-PCR, with no cross-reaction to a number of non-CSFV porcine viruses. The sensitivity of the assay for detecting wild-type and C-strain-type vaccine viruses was determined to be 41.8 and 81.5copies/muL viral RNA, respectively. Completely correct differentiation of wild-type viruses from C-strain vaccine was achieved when testing reference strains and characterized field isolates of CSFV in China. The multiplex real-time RT-PCR was able to detect the viral RNA in the whole blood samples of experimentally infected pigs as early as 2 days post-infection, 3 to 4 days prior to the onset of clinical signs in co-housed pigs. The agreements between the multiplex real-time RT-PCR and a multiplex RT-nested PCR for detection of wild-type and C-strain-type viruses were 96.9% and 100%, respectively, when detecting 106 different field samples. There is a positive correlation between the titers of C-strain vaccines titrated in rabbits and RNA copies quantitated by the multiplex real-time RT-PCR. The novel assay described here is rapid and sensitive, and is useful for differentiating field strains and C-strain of CSFV in China.
机译:经典猪瘟病毒(CSFV)是经典猪瘟(CSF)的病原体,它是OIE列出的疾病之一。当前大多数可用的检测方法都不允许区分野生型CSF病毒和疫苗株。本研究旨在开发用于实时定量和差异检测野生型病毒和在中国广泛使用的C株疫苗的多重实时RT-PCR。在CSFV病毒基因组的5'-非翻译区中设计了CSFV特异性引物和两种不同标记的TaqMan探针,用于从C株疫苗中分化出野生型病毒。两种TaqMan探针在多重实时RT-PCR中分别特异性杂交不同亚组的野生型病毒和C株疫苗,并且与多种非CSFV猪病毒没有交叉反应。确定用于检测野生型和C株型疫苗病毒的测定的灵敏度分别为41.8和81.5个拷贝/μL病毒RNA。当在中国测试参考菌株并鉴定了猪瘟病毒的野外分离株时,就可以从C株疫苗中完全正确区分野生型病毒。多重实时RT-PCR能够最早在感染后2天,共同饲养的猪出现临床症状之前的3至4天检测实验感染的猪的全血样品中的病毒RNA。当检测106个不同的现场样品时,用于检测野生型和C株型病毒的多重实时RT-PCR和多重RT巢式PCR之间的协议分别为96.9%和100%。在兔中滴定的C株疫苗的滴度与通过多重实时RT-PCR定量的RNA拷贝之间存在正相关。本文所述的新方法快速,灵敏,可用于区分中国CSFV的野毒株和C株。

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