Boyle J, Blackwell J
Department of Biochemistry and Molecular Biology, Mississippi State University 39762.
Am J Vet Res. 1991 Dec;52(12):1965-8.
Polymerase chain reaction was used to detect an economically important herpesvirus, channel catfish virus (CCV). A segment of the viral DNA was sequenced and oligonucleotide primers were produced from that sequence. After the primers were tested for the possibility of hybridization to catfish DNA, they were used to prime the polymerase chain reaction, using pure CCV DNA, CCV DNA added to catfish DNA, and DNA from catfish infected and not infected with CCV. In all cases, the method proved to be simple and sensitive in its detection by CCV DNA. When catfish DNA was present, less than 0.1 pg of CCV DNA was detectable. Channel catfish virus DNA in a latent carrier of CCV was readily detectable.
聚合酶链反应被用于检测一种具有重要经济意义的疱疹病毒——斑点叉尾鮰病毒(CCV)。对一段病毒DNA进行了测序,并根据该序列制备了寡核苷酸引物。在测试引物与鮰鱼DNA杂交的可能性之后,将其用于引发聚合酶链反应,使用的模板分别是纯CCV DNA、添加到鮰鱼DNA中的CCV DNA以及来自感染和未感染CCV的鮰鱼的DNA。在所有情况下,该方法在检测CCV DNA时都被证明是简单且灵敏的。当存在鮰鱼DNA时,可检测到的CCV DNA量少于0.1皮克。CCV潜伏携带者中的斑点叉尾鮰病毒DNA很容易被检测到。