摘要
研究比较了核酸斑6杂交技术、多聚酶链反应(PCR)扩增和病毒分离技术在检测MDV中的效果和相关性,试验结果表明:以PCR扩增I型MDV132bp重复序列或以此序列标记的Digoxigenin探针进行Dot-DNA分子杂交检测MDV,均具有较好的效果,灵敏度比常规病毒分离高近万倍,其特异性较强,并能快速鉴别MDVI型毒,使诊断时间缩短了许多。
Sensitvity of detecting March's disease virus (MDV) for the peripherial blood lymphocytes of chickens infected with woodlands No1 and CR/6 strains of MDV were compared among PCR amplification, dot-hybridization and viral isolation. The results showed that PCR amplification of 132 bp repeat sequence of MDV or dot-hybridization were more sensitive than viral isolation. The sensitivity of PCR and dot-hybridization were 103~104 times as high as viral isolation. Both of them demonstrated the high specificity and could be used to distinguish serotype 1 from other two serotypes of MDV. It is suggested that PCR and dot-hybridization were very useful in clinical diagnosis in the future.
出处
《扬州大学学报(自然科学版)》
CAS
CSCD
1998年第1期9-12,共4页
Journal of Yangzhou University:Natural Science Edition
基金
江苏省九五攻关项目
关键词
鸡病
检测
马立克氏病毒
斑点杂交
多聚酶链反应
domestic fowl
viral
separation
detection/Marek's disease virus
dot-hybridization