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美洲型猪繁殖与呼吸综合征病毒荧光RT-PCR检测方法的建立

Development of real-time RT-PCR for the detection of North American type porcine reproductive and respiratory syndrome virus

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【作者】 范忠军柴虹陈继明吴延功孙承英王志亮

【Author】 FAN Zhong-jun2, CHAI Hong2, CHEN Ji-ming1, WU Yan-gong1, SUN Cheng-ying1, WANG Zhi-liang1* (1. National Animal Quarantine Institute, Ministry of Agriculture, Qingdao 226032, China; 2. Key Laboratory of Infectious Disease, Yangzhou University, Yangzhou 225009, China)

【机构】 扬州大学农业部畜禽传染病重点开放实验室农业部青岛动检所农业部青岛动检所 江苏扬州225009江苏扬州225009山东青岛266032

【摘要】 参照美洲型猪繁殖与呼吸综合征病毒(PRRSV)M基因序列,设计引物和探针,并建立其荧光RT-PCR检测方法,以检测严重危害我国养猪业的此型PRRSV。该法能检测到1 TCID50的PRRSV。用此法检测猪瘟病毒、乙脑病毒、伪狂犬病毒、马动脉炎病毒、圆环病毒Ⅱ型和MARC145细胞的RNA,结果均为阴性。对126份临床样品进行检测应用,检测结果(7份阳性,119份阴性)与病毒分离完全符合。此法中的阳性对照为体外转录的dsRNA,具有高度的稳定性,解决了此类检测方法所用的RNA阳性对照所普遍存在的易于降解的难题。

【Abstract】 A real-time RT-PCR assay for the detection of North American type porcine reproductive and respiratory syndrome virus (PPRSV) was developed using a pair of primers derived from the published sequences of the Matrix gene of PPRSV. This assay could detect 1 TCID50 of the virus with a high specificity. No products detected against RNAs of hog cholera virus, Japanese encephalitis B virus, porcine pseudorabies virus, equine arteritis virus, porcine circovirus virus ¢òand MARC145 cell. Testing on 126 clinical samples detected 7 positive virus infection, which was consistent with results of virus isolation. This assay used an in vitro transcribed dsRNA RNA as positive control, which provides a reliable alternative over conventional and less stable single stranded RNA control.

【基金】 国家十五攻关项目(编号:2003BA712A04-04)
  • 【文献出处】 中国预防兽医学报 ,Chinese Journal of Preventive Veterinary Medicine , 编辑部邮箱 ,2007年02期
  • 【分类号】S854.43
  • 【被引频次】23
  • 【下载频次】245
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