Rong-Fu W, Beasley J N, Cao W W, Slavik M F, Johnson M G
Department of Food Science, University of Arkansas, Fayetteville, 72701.
Mol Cell Probes. 1993 Apr;7(2):127-31. doi: 10.1006/mcpr.1993.1017.
A rapid polymerase chain reaction (PCR) assay specific for Marek's Disease Virus (MDV) was developed. This assay was able to detect MDV in inoculated chick kidney cells at dilutions of 10(-5). Negative PCR results were obtained using uninoculated chick cells, Marek's Disease Vaccine (SB), Herpesvirus of Turkeys (HVT) and Fowl Laryngotracheitis Vaccine (LT). Bursae, feathers and kidneys from MDV infected chickens were positive in the PCR assay. The same tissues from normal chickens were negative. This method required only 0.5 h for sample preparatory, 3 h for PCR application and 1 h for electrophoresis. Internal probe hybridization confirmed that the PCR products are from MDV, but this hybridization will not be necessary for future MDV detection.
开发了一种针对马立克氏病病毒(MDV)的快速聚合酶链反应(PCR)检测方法。该检测方法能够在接种的鸡肾细胞中检测到稀释度为10^(-5) 的MDV。使用未接种的鸡细胞、马立克氏病疫苗(SB)、火鸡疱疹病毒(HVT)和鸡喉气管炎疫苗(LT)获得了PCR阴性结果。MDV感染鸡的法氏囊、羽毛和肾脏在PCR检测中呈阳性。正常鸡的相同组织呈阴性。该方法样品制备仅需0.5小时,PCR扩增需3小时,电泳需1小时。内部探针杂交证实PCR产物来自MDV,但未来MDV检测无需这种杂交。