Xie Z, Fadl A A, Girshick T, Khan M I
Department of Pathobiology, College of Agriculture and Natural Resources, University of Connecticut, Storrs 06269-3089, USA.
Avian Dis. 1999 Jan-Mar;43(1):98-105.
An avian adenovirus-specific polymerase chain reaction was developed. The origin of primers was from the DNA sequence data of the chicken embryo lethal orphan avian adenovirus virus genome. An avian adenovirus-specific 421-bp DNA product was amplified by these primers from group I of adenovirus containing 12 serotypes and serotypes of adenovirus from group II and group III. The adenovirus-specific DNA product was also amplified from the 19 field isolates of avian adenoviruses but not from the mammalian adenovirus and other avian pathogenic viruses and bacteria. As little as 1 fg of avian adenovirus DNA was detected by gel electrophoresis and Southern blot analysis.
开发了一种禽腺病毒特异性聚合酶链反应。引物来源于鸡胚致死孤儿禽腺病毒病毒基因组的DNA序列数据。通过这些引物从含有12种血清型的腺病毒I组以及腺病毒II组和III组的血清型中扩增出一条421bp的禽腺病毒特异性DNA产物。该腺病毒特异性DNA产物也从19株禽腺病毒野外分离株中扩增得到,但未从哺乳动物腺病毒以及其他禽致病病毒和细菌中扩增得到。通过凝胶电泳和Southern印迹分析,可检测到低至1fg的禽腺病毒DNA。