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作 者:陈坚[1,2] 刘业兵[1] 张磊[1] 罗俊[1] 宁宜宝[1]
机构地区:[1]中国兽医药品监察所,北京100081 [2]广东永顺生物制药有限公司,广州511356
出 处:《中国兽药杂志》2009年第11期17-20,共4页Chinese Journal of Veterinary Drug
基 金:十一五国家科技支撑计划(2007BAD86B04-4)
摘 要:根据GenBank上发表的多株猪流感病毒(SIV)序列,在保守区域设计1对引物,并对RT-PCR反应条件进行优化,建立了可检测出多种亚型猪源流感病毒的RT-PCR方法。通过对反应产物测序分析,与预期结果相符,证明该方法具有很强的特异性;该方法可以检测出约1个TCID50的猪流感病毒,显示较高的敏感性。通过对12份临床样品进行检测,结果发现:该方法和其他两种方法分离病毒符合率相当。本研究建立的猪流感RT-PCR诊断方法具有高特异性和敏感性,适用于SIV的诊断应用和推广。A pair of primers were designed from Conserved regions according to the published swine influenza virus (SIV) sequences in GenBank. The RT - PCR diagnostic method for swine influenza virus was established base on the optimization of RT - PCR reaction conditions. This method can specific detect a wide range of subtypes of swine influenza viruses. Sequence analysis of PCR products was in line with the expected results. This method has a sensitivity of detecting at least approximately one TCID50 swine influenza virus. Through 12 clinical samples showed that the method was in line with the rate of using other two methods to separate virus, In this study, the establishment of the swine influenza diagnostic RT - PCR method has high specificity and sensitivity for the SIV diagnostic application and promotion.
分 类 号:S858.286.3[农业科学—临床兽医学]
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