Yue Fengxiong, Cui Shangjin, Zhang Chaofan, Yoon Kyoung-Jin
Swine Infectious Disease Division, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Heilongjiang, People's Republic of China.
Virus Genes. 2009 Jun;38(3):392-7. doi: 10.1007/s11262-009-0333-6. Epub 2009 Feb 12.
A multiplex PCR (mPCR) assay was developed and evaluated for its ability to simultaneously detect multiple viral infections of swine. Specific primers were designed for each of the following four DNA or RNA viruses: porcine circovirus type 2 (PCV2), porcine parvovirus (PPV), pseudorabies virus (PRV), and porcine reproductive and respiratory syndrome virus (PRRSV). Each target produced a specific amplicon with a size of 353 bp (PCV2), 271 bp (PPV), 194 bp (PRV), or 434 bp (PRRSV). The assay was sensitive and specific in detecting each target agent in composite cell cultures and clinical specimens. Results from mPCR were confirmed by PCR for individual viruses and by virus isolation. In conclusion, the mPCR has the potential to be useful for routine molecular diagnosis and epidemiology.
开发并评估了一种多重聚合酶链反应(mPCR)检测方法,以检测其同时检测猪多种病毒感染的能力。针对以下四种DNA或RNA病毒分别设计了特异性引物:猪圆环病毒2型(PCV2)、猪细小病毒(PPV)、伪狂犬病病毒(PRV)和猪繁殖与呼吸综合征病毒(PRRSV)。每个靶标产生一个大小为353 bp(PCV2)、271 bp(PPV)、194 bp(PRV)或434 bp(PRRSV)的特异性扩增子。该检测方法在复合细胞培养物和临床标本中检测每种靶标病原体时具有敏感性和特异性。mPCR的结果通过针对单个病毒的PCR和病毒分离进行了确认。总之,mPCR有潜力用于常规分子诊断和流行病学研究。