Shin Yeun-Kyung, Yoon Soon-Seek, Song Jae-Young, Kim Joon-Bae, Hang Do Thi Thu, Park Jin-Woo, Kim Min-Young, Kim Seong-Hee, Park Choi-Kyu, Li O-Soo
Virology Division, National Veterinary Research and Quarantine Service, Ministry for Food, Agriculture, Forestry and Fisheries, Gyeonggi-do, Republic of Korea.
J Vet Med Sci. 2011 Jan;73(1):55-63. doi: 10.1292/jvms.10-0218. Epub 2010 Aug 24.
Pandemic (H1N1) 2009 influenza has spread throughout the world since April 2009 and has caused many human deaths since its first report in humans. Pandemic (H1N1) 2009 influenza virus was first identified in a Canadian pig herd in April 2009 and has been reported in more than ten countries, including Korea. We developed a one-step multiplex reverse transcriptase polymerase chain reaction (RT-PCR) assay based on the matrix gene that discriminates pandemic (H1N1) 2009 influenza virus from endemic swine influenza viruses. The sensitivity of this assay was 100 copies of in vitro-transcribed target RNA and 0.01 tissue culture infective dose (TCID(50)/ml) of virus and was as high as those of conventional influenza A virus common matrix reverse transcriptase PCR assays and real-time reverse transcriptase PCR assays (1 to 200 copies) developed for detecting pandemic (H1N1) 2009 influenza viruses from human and pig samples. This one-step multiplex RT-PCR assay would be a good tool in monitoring pandemic (H1N1) 2009 influenza virus among pig herds on a regular basis.
2009年甲型H1N1流感自2009年4月以来已在全球蔓延,自首次报告人类感染病例以来已导致许多人死亡。2009年甲型H1N1流感病毒于2009年4月在加拿大猪群中首次发现,包括韩国在内的十多个国家均有报告。我们基于基质基因开发了一种一步多重逆转录聚合酶链反应(RT-PCR)检测方法,可将2009年甲型H1N1流感病毒与地方性猪流感病毒区分开来。该检测方法的灵敏度为体外转录靶RNA的100个拷贝以及病毒的0.01组织培养感染剂量(TCID(50)/ml),与用于从人和猪样本中检测2009年甲型H1N1流感病毒的传统甲型流感病毒通用基质逆转录PCR检测方法和实时逆转录PCR检测方法(1至200个拷贝)的灵敏度一样高。这种一步多重RT-PCR检测方法将是定期监测猪群中2009年甲型H1N1流感病毒的良好工具。