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Establishment of a Real-time Fluorescent Quantitative RTPCR Method for Detecting NP Gene of Class Ⅰ Newcastle Disease Virus(NDV)

机译:实时荧光定量RTPCR方法检测Ⅰ类新城疫病毒NP基因

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Newcastle disease( ND) is one of the most serious infectious diseases that infect the poultry industry.There is only one serotype of Newcastle disease virus( NDV),but NDVs can be divided into two distinct classes( class Ⅰ,and class Ⅱ) according to their genetic relationship.To develop a method for rapid quantitative detection of class Ⅰ NDV,a pair of primers and a TaqM an probe were designed and synthesized according to the conservative sequence of NP gene of class Ⅰ NDV.The positive recombinant plasmid harboring NP gene of JS-18-05 isolate was used as a positive template to establish the standard curve.A real-time fluorescent quantitative RT-PCR method was established for rapid detection of class Ⅰ NDV with strong specificity,high sensitivity and good repeatability.The established method exhibited a good linear relationship within the concentration of 102 to 108 copies of NDV,by which 1 μl of 10 copy of NDV nucleic acid could be detected in the initial template.Compared with conventional virus isolation methods,the established method had similar sensitivity and led to the same results in detecting33 class Ⅰ,class Ⅱ NDV isolates.The study provided the basis for rapid quantitative detection of class Ⅰ NDVs and further clarification of their pathogenicity and pathogenic mechanism in poultry.
机译:新城疫(ND)是一种影响禽业的最严重的传染病。新城疫病毒(NDV)只有一种血清型,但是根据新城疫病毒的分类,新城疫可以分为两类(Ⅰ类和Ⅱ类)。为了建立一种快速定量检测Ⅰ类NDV的方法,根据Ⅰ类NDV的NP基因的保守序列,设计并合成了一对引物和TaqM a探针。以JS-18-05分离株基因为阳性模板建立标准曲线,建立了实时荧光定量RT-PCR方法,特异性强,灵敏度高,重复性好,可快速检测Ⅰ类NDV。所建立的方法在NDV浓度为102至108拷贝之间表现出良好的线性关系,从而可以在初始模板中检测到10拷贝NDV核酸中的1μl。最终的病毒分离方法,所建立的方法具有相似的灵敏度,并且在检测33种Ⅰ,Ⅱ类NDV分离株中得到相同的结果。该研究为快速定量检测Ⅰ类NDVs以及进一步阐明它们的致病性和致病机理提供了基础。家禽。

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