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首页> 外文期刊>Bulletin of the Veterinary Institute in Pulawy >DETECTION OF BLUETONGUE VIRUS IN BLOOD SAMPLES OF INFECTED RUMINANTS BY RT-PCR FOR GENOME SEGMENT 7
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DETECTION OF BLUETONGUE VIRUS IN BLOOD SAMPLES OF INFECTED RUMINANTS BY RT-PCR FOR GENOME SEGMENT 7

机译:RT-PCR检测基因组7段反刍动物血样中的乙型肝炎病毒

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摘要

RT-PCR for the detection of bluetongue virus (BTV) in blood samples, collected from infected animals, were described . Two primer sets targeting genome segment 7 of BTV were selected. The full-length S7 cDNA (1156 bp) was amplified in all samples of EDTA blood taken from BTV infected animals. No viral RNA was detected in samples from uninfected animals and seropositive cattle of Dutch origin, imported from Belgium on 7 August 2006. The method proved to be specific, as no positive reaction for foot and mouth disease virus, serotypes O and A, was observed. The applied RT-PCR is an accurate and reliable technique for the detection of BTV in EDTA blood samples. This assay is easy and quick to perform and the results are available within 10 h.
机译:描述了从感染动物采集的血液样本中检测蓝舌病毒(BTV)的RT-PCR。选择了靶向BTV基因组区段7的两个引物组。在从感染BTV的动物身上提取的所有EDTA血液样本中,扩增了全长S7 cDNA(1156 bp)。在2006年8月7日从比利时进口的未感染动物和荷兰阳性血清阳性牛的样品中未检测到病毒RNA。该方法被证明具有特异性,因为未观察到O型和A型口蹄疫病毒的阳性反应。所应用的RT-PCR是检测EDTA血样中BTV的准确可靠的技术。该测定法简便快捷,结果可在10小时内获得。

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