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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Western blot detection of infectious bursal disease virus infection
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Western blot detection of infectious bursal disease virus infection

机译:免疫印迹法检测法氏囊病病毒感染

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In order to evaluate the use of a Western blot methodology for the diagnosis of infectious bursal disease virus (IBDV) infection, chickens were experimentally infected with IBDV strains and tested for the presence of viral antigens and antibodies by a blocking Western blot test (bWB). The viral proteins obtained from the bursa of Fabricius (BF) were transferred to a nitrocellulose membrane after sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and the chicken sera obtained by heart puncture were used for the detection of these proteins. In order to eliminate nonspecific reactions, we used a rabbit anti-chicken serum (blocking tool). By the use of the bWB test, two distinct viral proteins of 43-kDa (VP2) and 32-kDa (VP3) were detected. We suggest the use of this methodology for the detection of IBDV infection in animals suspected of having IBDV reinfection and a chronic subclinical form of the disease. With the use of the rabbit anti-chicken sera for blocking, this method is practical, sensitive and less time consuming
机译:为了评估使用Western blot方法诊断传染性法氏囊病病毒(IBDV)感染的方法,对鸡进行了IBDV毒株的实验性感染,并通过阻断性Western blot试验(bWB)检测了病毒抗原和抗体的存在。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)后,将从法氏囊(BF)滑囊获得的病毒蛋白转移到硝酸纤维素膜上,并将通过心脏穿刺获得的鸡血清用于检测这些蛋白。为了消除非特异性反应,我们使用了兔抗鸡血清(封闭工具)。通过使用bWB测试,检测到两个截然不同的病毒蛋白,分别为43-kDa(VP2)和32-kDa(VP3)。我们建议使用这种方法来检测怀疑患有IBDV再感染和该疾病的慢性亚临床形式的动物中的IBDV感染。通过使用兔抗鸡血清进行阻断,该方法实用,灵敏且耗时少

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