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高致病性猪繁殖与呼吸综合征病毒双重液相基因芯片检测方法的建立

陈茹 于晓璐 高小博 薛春宜 宋长绪 邱杨 刘志玲 王莹 段燕喻

动物医学进展2016,Vol.37Issue(6):1-6,6.
动物医学进展2016,Vol.37Issue(6):1-6,6.

高致病性猪繁殖与呼吸综合征病毒双重液相基因芯片检测方法的建立

Development of a Duplex xMAP Assay for Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus

陈茹 1于晓璐 2高小博 3薛春宜 4宋长绪 3邱杨 5刘志玲 1王莹 1段燕喻2

作者信息

  • 1. 广东出入境检验检疫局技术中心,广东广州 510623
  • 2. 广东省动植物与食品进出口技术措施研究重点实验室,广东广州 510623
  • 3. 中山大学生命科学大学院,广东广州 510275
  • 4. 国家卫生计生委科学技术研究所,北京 100081
  • 5. 广东省农业科学院动物卫生研究所,广东广州 510640
  • 折叠

摘要

Abstract

A duplex xMAP bead-based assay was developed for rapid detection of porcine reproductive and respiratory syndrome virus (PRRSV)and differentiation of highly pathogenic strains (HP-PRRSV).The xMAP assay could simultaneously detect two target sequences,including the GP2 envelope protein gene of PRRS and the Nsp2 gene conserved region specific for HP-PRRSV strains.The assay detected 12 PRRSV strains used in this study and identified 7 strains as HP-PRRSV,without cross-reactions with 12 non-tar-get swine pathogens.The lower detection limit of the assay on PRRSV,HP-PRRSV strains was deter-mined as below 0.5 TCID50 per reaction,respectively.The inter-assay and intra-assay variances (CV%) were both lower than 10%.The assay was applied to test 55 suspected field samples and compared with a commercialized single-plex real-time RT-PCR method.The detection results of the two methods were 98.2% (54/55 )in consistency.The study provided a novel molecular method for rapid diagnosis of PRRSV infection.

关键词

猪繁殖与呼吸综合征病毒/高致病性猪繁殖与呼吸综合征病毒/xMAP液相芯片

Key words

Porcine reproductive and respiratory syndrome virus (PRRSV)/highly pathogenic PRRSV (HP-PRRSV)/xMAP LiquiChip

分类

农业科技

引用本文复制引用

陈茹,于晓璐,高小博,薛春宜,宋长绪,邱杨,刘志玲,王莹,段燕喻..高致病性猪繁殖与呼吸综合征病毒双重液相基因芯片检测方法的建立[J].动物医学进展,2016,37(6):1-6,6.

基金项目

国家质量监督检验检疫总局科研项目(2013IK029);广东省农业攻关项目 ()

动物医学进展

OA北大核心CSTPCD

1007-5038

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