Celerá V, Carasová P
Institute of Microbiology and Immunoogy, Veterinary and Pharmaceutical University Bruno, Czech Republic.
J Vet Med B Infect Dis Vet Public Health. 2002 Apr;49(3):155-9. doi: 10.1046/j.1439-0450.2002.00547.x.
Three oligonucleotide primers for semi-nested polymerase chain reaction (PCR) were designed according to already published sequences of porcine circovirus types 1 (PCV-1) and 2 (PCV-2) isolates. These primers were used to detect PCV-2 DNA. A positive amplification reaction was visualized from a DNA suspension containing as few as 10 copies of virus DNA. In total. 77 samples of inguinal lymph nodes and nasal swabs from pigs in the Czech Republic were used to detect the virus. Thirty-seven of them were positive for PCV-2 DNA. In order to confirm specificity of the PCR reaction, seven DNA fragments were sequenced. Czech PCV sequences were found to have a 92-97% homology with other known PCV-2 strains and only 80-83% homology with PCV-1 strains.
根据已发表的猪圆环病毒1型(PCV-1)和2型(PCV-2)分离株序列,设计了3条用于半巢式聚合酶链反应(PCR)的寡核苷酸引物。这些引物用于检测PCV-2 DNA。从含有低至10个病毒DNA拷贝的DNA悬液中可观察到阳性扩增反应。总共使用了来自捷克共和国猪的77份腹股沟淋巴结和鼻拭子样本检测该病毒。其中37份PCV-2 DNA呈阳性。为了确认PCR反应的特异性,对7个DNA片段进行了测序。发现捷克PCV序列与其他已知PCV-2毒株具有92%-97%的同源性,与PCV-1毒株只有80%-83%的同源性。