Spackman Erica, Senne Dennis A, Myers T J, Bulaga Leslie L, Garber Lindsey P, Perdue Michael L, Lohman Kenton, Daum Luke T, Suarez David L
Southeast Poultry Research Laboratory, USDA Agricultural Research Service, Athens, Georgia 30605, USA.
J Clin Microbiol. 2002 Sep;40(9):3256-60. doi: 10.1128/JCM.40.9.3256-3260.2002.
A real-time reverse transcriptase PCR (RRT-PCR) assay based on the avian influenza virus matrix gene was developed for the rapid detection of type A influenza virus. Additionally, H5 and H7 hemagglutinin subtype-specific probe sets were developed based on North American avian influenza virus sequences. The RRT-PCR assay utilizes a one-step RT-PCR protocol and fluorogenic hydrolysis type probes. The matrix gene RRT-PCR assay has a detection limit of 10 fg or approximately 1,000 copies of target RNA and can detect 0.1 50% egg infective dose of virus. The H5- and H7-specific probe sets each have a detection limit of 100 fg of target RNA or approximately 10(3) to 10(4) gene copies. The sensitivity and specificity of the real-time PCR assay were directly compared with those of the current standard for detection of influenza virus: virus isolation (VI) in embryonated chicken eggs and hemagglutinin subtyping by hemagglutination inhibition (HI) assay. The comparison was performed with 1,550 tracheal and cloacal swabs from various avian species and environmental swabs obtained from live-bird markets in New York and New Jersey. Influenza virus-specific RRT-PCR results correlated with VI results for 89% of the samples. The remaining samples were positive with only one detection method. Overall the sensitivity and specificity of the H7- and H5-specific RRT-PCR were similar to those of VI and HI.
开发了一种基于禽流感病毒基质基因的实时逆转录酶PCR(RRT-PCR)检测方法,用于快速检测甲型流感病毒。此外,还基于北美禽流感病毒序列开发了H5和H7血凝素亚型特异性探针组。该RRT-PCR检测方法采用一步法RT-PCR方案和荧光水解型探针。基质基因RRT-PCR检测方法的检测限为10 fg或约1000个目标RNA拷贝,能够检测0.1 50%鸡胚感染剂量的病毒。H5和H7特异性探针组的检测限均为100 fg目标RNA或约10³至10⁴个基因拷贝。将实时PCR检测方法的敏感性和特异性与当前流感病毒检测标准直接进行比较:鸡胚病毒分离(VI)和血凝抑制(HI)试验进行血凝素亚型分型。使用从纽约和新泽西州活禽市场采集的1550份来自各种禽类的气管和泄殖腔拭子以及环境拭子进行比较。89%的样本中,流感病毒特异性RRT-PCR结果与VI结果相关。其余样本仅在一种检测方法中呈阳性。总体而言,H7和H5特异性RRT-PCR的敏感性和特异性与VI和HI相似。