Dorman M A, Blair C D, Collins J K, Beaty B J
J Clin Microbiol. 1985 Dec;22(6):990-5. doi: 10.1128/jcm.22.6.990-995.1985.
A molecular hybridization technique using biotinylated DNA probes was used to detect bovine herpesvirus 1 (BHV-1) nucleic acid species immobilized on nitrocellulose. Seventeen recombinant plasmids containing HindIII restriction fragments of the BHV-1 genome were compared for their ability to detect immobilized BHV-1 DNA from purified virus and infected cells. One probe, pCB2, labeled by nick translation with either 3H or biotin, detected as little as 10 pg of viral DNA. In time course experiments, BHV-1 DNA could be detected by 2 h postinfection in 10(6) infected cells. BHV-1 DNA was detected in nasal swabs and exudate from experimentally infected cattle, even when specimens had been stored for over a year. In a retrospective study of a respiratory disease outbreak in a feedlot, hybridization was compared with virus isolation for diagnosis of BHV-1 infections. The sensitivity rate was 0.68 with virus isolation as the referent standard. Blot hybridization provides a novel approach with unique applications for the diagnosis of bovine herpesvirus infections.
一种使用生物素化DNA探针的分子杂交技术被用于检测固定在硝酸纤维素膜上的牛疱疹病毒1型(BHV - 1)核酸种类。对17个含有BHV - 1基因组HindIII限制性片段的重组质粒检测固定化的来自纯化病毒和感染细胞的BHV - 1 DNA的能力进行了比较。一个探针pCB2,通过用³H或生物素进行缺口平移标记,能检测低至10 pg的病毒DNA。在时间进程实验中,感染后2小时就能在10⁶个感染细胞中检测到BHV - 1 DNA。在实验感染牛的鼻拭子和渗出物中检测到了BHV - 1 DNA,即使样本已储存超过一年。在一项对饲养场呼吸道疾病爆发的回顾性研究中,将杂交与病毒分离用于诊断BHV - 1感染进行了比较。以病毒分离作为参照标准,灵敏度为0.68。印迹杂交为牛疱疹病毒感染的诊断提供了一种具有独特应用的新方法。