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猪伪狂犬病PCR检测方法的建立与应用
引用本文:孙德刚,吴发兴,李晓成,黄保续,王洪斌,张燕霞. 猪伪狂犬病PCR检测方法的建立与应用[J]. 中国动物检疫, 2007, 24(2): 29-30
作者姓名:孙德刚  吴发兴  李晓成  黄保续  王洪斌  张燕霞
作者单位:1. 中国动物卫生与流行病学中心,山东青岛,266032;东北农业大学,黑龙江哈尔滨,150030
2. 中国动物卫生与流行病学中心,山东青岛,266032
3. 东北农业大学,黑龙江哈尔滨,150030
摘    要:根据Genbank中PRV gD基因序列设计引物建立了检测猪场狂犬病的PCR方法并对某省25份猪伪狂犬病疑似病料进行检测,结果在2S份病料中,检出伪狂犬阳性病料7份,阳性率接近30%。通过检测结果及特异性和敏感性实验发现此检测方法敏感度很高。这种检测方法适合科学研究、临床诊断以及流行病学调查。

关 键 词:伪狂犬病病毒  检测
文章编号:1005-944X(2007)02-0029-02

Establishment and Application of PCR Method for Detection of Porcine Pseudorabies Virus
Sun DeGang,Wu FaXing,Li XiaoCheng,Huang BaoXu,Wang HongBin,Zhang YanXia. Establishment and Application of PCR Method for Detection of Porcine Pseudorabies Virus[J]. China Animal Health Inspection, 2007, 24(2): 29-30
Authors:Sun DeGang  Wu FaXing  Li XiaoCheng  Huang BaoXu  Wang HongBin  Zhang YanXia
Affiliation:1.China Animal Health and Epidemiology Center, Qingdao,266032; 2.Northeast Agricultural University,Harbin
Abstract:According to PRV gD gene sequence in Genebank,a pair of primers were designed to develop a PCR and 25 suspicious samples from a province were detected using the developed method. Of 25,7 samples were positive. The positive rate of PRV approached 30%. It was concluded that the PCR method was of high sensitivity, and it could be applicable to research, clinical diagnosis and epidemiological investigation.
Keywords:PCR  GC buffer
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