摘要
根据羊口疮病毒(ORFV)H2L基因序列,设计合成1对引物,通过确定最佳的PCR反应条件,建立了检测羊口疮病毒DNA的PCR检测方法。结果显示,用这1对引物均能扩增出羊口疮病毒507 bp的特异性片段,同时检测口蹄疫病毒和山羊痘病毒,结果均为阴性,最小检出量为5 pg。该方法具有良好的特异性和敏感性,可对临床组织病料中的ORFV进行快速检测。
A pair of specific primers were designed and synthesized according to H2L gene sequence of orf virus(ORFV) and the PCR method for detecting DNA of ORFV was established by determining the optimum reaction condition of PCR.The results showed that the specificity fragment of ORFV 507bp could be amplified by a pair of specific primers.The established PCR method could detect viruses of goat poxvirus or foot-and-mouth disease at the same time and the minimum detectable amount was 5pg.The established PCR method with good specificity and sensitivity can be applied in quick detection of ORFV.
出处
《贵州农业科学》
CAS
北大核心
2010年第7期145-147,共3页
Guizhou Agricultural Sciences
基金
贵州省科学技术基金项目"贵州省羊口疮的病原学与检测技术研究"[黔科合J字(2010)2260]
贵州大学引进人才科研项目"贵州省羊口疮的诊断与防控技术研究"[贵大人基合字(2009)024]
国家自然科学基金项目"基于山羊痘病毒P32基因的山羊粘膜免疫研究"(No.30940054)