Murata Shiro, Chang Kyung-Soo, Lee Sung-Il, Konnai Satoru, Onuma Misao, Ohashi Kazuhiko
Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.
J Vet Diagn Invest. 2007 Sep;19(5):471-8. doi: 10.1177/104063870701900503.
For the easy survey of Marek's disease virus (MDV), feather tip-derived DNA from MDV-infected chickens can be used because feather tips are easy to collect and feather follicle epithelium is known to be the only site of productive replication of cell-free MDV. To develop a diagnostic method to differentiate highly virulent strains of MDV from the attenuated MDV vaccine strain, CVI988, which is widely used, nested polymerase chain reaction (PCR) was performed to detect a segment of the meq gene in feather tip samples of chickens experimentally infected with MDV. In chickens infected with Md5, a strain of oncogenic MDV, the meq gene was consistently detected, whereas the L-meq gene, in which a 180-base pair (180-bp) sequence is inserted into the meq gene, was detected in CVI988-infected chickens. Moreover, the meq gene was mainly detected even in chickens co-infected with both Md5 and CVI988. These results suggest that this method is appropriate for the surveillance of the highly virulent MDV infection in the field.
为便于对马立克氏病病毒(MDV)进行检测,可使用来自感染MDV的鸡的羽尖DNA,因为羽尖易于采集,且已知毛囊上皮是无细胞MDV进行有效复制的唯一部位。为开发一种诊断方法,以区分MDV的高毒株和广泛使用的减毒MDV疫苗株CVI988,采用巢式聚合酶链反应(PCR)检测经MDV实验感染的鸡羽尖样本中的meq基因片段。在感染致癌性MDV毒株Md5的鸡中,可始终检测到meq基因,而在感染CVI988的鸡中,检测到L-meq基因,该基因在meq基因中插入了一段180个碱基对(180-bp)的序列。此外,即使在同时感染Md5和CVI988的鸡中,也主要检测到meq基因。这些结果表明,该方法适用于现场高致病性MDV感染的监测。