首页> 外文期刊>Veterinarni Medicina >Simultaneous detection of porcine pseudorabies virus, porcine parvovirus and porcine circovirus type 2 by multiplex real-time PCR and amplicon melting curve analysis using SYBR Green I
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Simultaneous detection of porcine pseudorabies virus, porcine parvovirus and porcine circovirus type 2 by multiplex real-time PCR and amplicon melting curve analysis using SYBR Green I

机译:使用Sybr Green I通过多重实时PCR和扩增熔化曲线分析同时检测猪伪毒性病毒,猪细小病毒和猪胃肠病毒型2型2

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摘要

Porcine parvovirus, porcine pseudorabies virus and porcine circovirus type 2 can cause reproductive failure in pigs, and swine are often simultaneously infected by combinations of the three viruses. We here report the development of a SYBR Green I-based multiplex real time PCR assay for simultaneous detection of porcine parvovirus, porcine pseudorabies virus and porcine circovirus type 2. Three pairs of specific primers were designed for the porcine parvovirus-VP2, porcine pseudorabies virus-gH and porcine circovirus type 2-ORF2 genes. Viral genomes were identified based on their distinctive melting temperatures in singleplex PCR reactions. The melting temperature was 74.5 °C for the 313 bp amplicon of porcine parvovirus-VP2 gene, 87.5 °C for the 355 bp amplicon of porcine pseudorabies virus-gH gene and 80.5 °C for the 171 bp amplicon of the porcine circovirus type 2-ORF2 gene, respectively. The detection limit of the method ranged from 0.01-0.03 TCID_(50)/ml for the three viruses. In addition, porcine parvovirus, porcine pseudorabies virus and porcine circovirus type 2 viral loads were measured in 100 field samples, and the result showed that the concordance between real-time PCR and conventional PCR was 60.42%. The sensitivity and specificity of real-time PCR were 100% and 100%, while those of conventional PCR were 40.83% and 72.22%, respectively.
机译:猪Parvovirus,猪伪毒性病毒和猪圆环病毒2型可能导致猪生殖失败,并且猪通常同时被三种病毒的组合感染。我们在这里报道了SYBR Green I基的多重实时PCR测定,用于同时检测猪细分病毒,猪伪毒性病毒和猪胃肠病毒型2.为猪Parvovirus-VP2,猪伪症病毒设计了三对特异性引物-gh和猪圆环病毒2- orf2基因。基于其独特的PCR反应中的独特熔化温度来鉴定病毒基因组。对于猪Parvovirus-VP2基因的313bp扩增子,猪尾癫痫病毒-GH基因的355bp扩增子的313bp扩增子和80.5℃的猪循环循环系统型2-5℃,熔融温度为74.5℃。分别是orf2基因。该方法的检测限为三种病毒的0.01-0.03 TCID_(50)/ mL。此外,在100场样品中测量猪剖腹产,猪伪毒性病毒和猪胃肠病毒2型病毒载量,结果表明,实时PCR与常规PCR之间的一致性为60.42%。实时PCR的敏感性和特异性为100%和100%,而常规PCR分别为40.83%和72.22%。

著录项

  • 来源
    《Veterinarni Medicina》 |2018年第8期|共9页
  • 作者单位

    College of Animal Science and Veterinary Medicine Henan Agricultural University;

    College of Animal Science and Veterinary Medicine Henan Agricultural University;

    Henan Province Product Quality Supervision and Inspection Center;

    Xuchang Entry-Exit Inspection and Quarantine Bureau;

    College of Animal Science and Veterinary Medicine Henan Agricultural University;

    College of Animal Science and Veterinary Medicine Henan Agricultural University;

    College of Animal Science and Veterinary Medicine Henan Agricultural University;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 畜牧、动物医学、狩猎、蚕、蜂;
  • 关键词

    pig; swine; specific primer;

    机译:猪;猪;特定底漆;

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