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High resolution melting curve analysis as a new tool for rapid identification of canine parvovirus type 2 strains

机译:高分辨率熔解曲线分析作为快速鉴定犬细小病毒2型毒株的新工具

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A high resolution melting (HRM) curve method was developed to identify canine parvovirus type 2 (CPV-2) strains by nested PCR. Two sets of primers, CPV-426F/426R and CPV-87R/87F, were designed that amplified a 52 bp and 53 bp product from the viral VP2 capsid gene. The region amplified by CPV-426F/426R included the A4062G and T4064A mutations in CPV-2a, CPV-2b and CPV-2c. The region amplified by CPV-87F/87R included the A3045T mutation in the vaccine strains of CPV-2 and CPV-2a, CPV-2b and CPV-2c. Faecal samples were obtained from 30 dogs that were CPV antigen-positive. The DNA was isolated from the faecal samples and PCR-amplified using the two sets of primers, and genotyped by HRM curve analysis. The PCR-HRM assay was able to distinguish single nucleotide polymorphisms between CPV-2a, CPV-2b and CPV-2c using CPV-426F/426R. CPV-2a was distinguished from CPV-2b and CPV-2c by differences in the melting temperature. CPV-2b and CPV-2c could be distinguished based on the shape of the melting curve after generating heteroduplexes using a CPV-2b reference sample. The vaccine strains of CPV-2 were identified using CPV-87F/87R. Conventional methods for genotyping CPV strains are labor intensive, expensive or time consuming; the present PCR-based HRM assay might be an attractive alternative. (C) 2014 Elsevier Ltd. All rights reserved.
机译:开发了一种高分辨率熔解(HRM)曲线方法,以通过嵌套PCR鉴定2型犬细小病毒(CPV-2)菌株。设计了两组引物CPV-426F / 426R和CPV-87R / 87F,它们从病毒VP2衣壳基因扩增了52 bp和53 bp的产物。通过CPV-426F / 426R扩增的区域包括CPV-2a,CPV-2b和CPV-2c中的A4062G和T4064A突变。通过CPV-87F / 87R扩增的区域在CPV-2和CPV-2a,CPV-2b和CPV-2c疫苗株中包括A3045T突变。从30只CPV抗原阳性的狗获得粪便样品。从粪便样品中分离DNA,并使用两组引物进行PCR扩增,并通过HRM曲线分析进行基因分型。 PCR-HRM分析能够使用CPV-426F / 426R区分CPV-2a,CPV-2b和CPV-2c之间的单核苷酸多态性。 CPV-2a与CPV-2b和CPV-2c的区别在于熔融温度的差异。在使用CPV-2b参考样品生成异源双链体后,可以根据熔解曲线的形状区分CPV-2b和CPV-2c。使用CPV-87F / 87R鉴定了CPV-2疫苗株。对CPV菌株进行基因分型的常规方法是劳动密集型,昂贵或费时的。目前基于PCR的HRM分析可能是一个有吸引力的选择。 (C)2014 Elsevier Ltd.保留所有权利。

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