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Heat induced epitope retrieval for rabies virus detection by direct fluorescent antibody test in formalin-fixed dog brain tissues

机译:热诱导表位检索狂犬病固定犬脑组织中直接荧光抗体试验的狂犬病病毒检测

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摘要

There is a great need for a chemical method of tissue preservation that would allow sample storage for extended periods at room temperature. This study aimed at retrieving and detecting rabies virus antigen by direct fluorescent antibody test (DFAT) in formalin-fixed dog brain tissues. Forty fresh dog brain specimens were collected as paired samples from rabies suspected cases that were received for postmortem detection of rabies in the Central Diagnostic Laboratory, National Veterinary Research Institute, Vom. One portion of each paired sample was prepared for fresh fluorescent antibody testing and the other portion was prepared for epitope retrieval and florescent antibody testing following fixation in 10% neutral buffered formalin. DFAT on formalin-fixed tissue exhibited a sensitivity of 100% in comparison to DFAT on fresh-tissue. No false positive result was obtained in formalin-fixed DFAT procedure, demonstrating 100% specificity. There was no apparent difference in the intensity of fluorescence in DFAT on fresh sample and formalin-fixed DFAT following heat induced epitope retrieval (concordance = 98%; 95% C.I. 0.9660 to 0.9903). The strength of agreement between DFAT on formalin-fixed and DFAT on fresh tissue was very good (Cohen’s kappa coefficient value= 1.000; 95% C.I. 1.000-1.000). This study provides new information on the retrieval of rabies antigen by heat induced epitope retrieval for DFAT on formalinized tissues. Formalin could therefore, be used henceforth to fix tissues of rabies suspected cases for routine diagnosis, transportation or archival purposes. The heat induced epitope retrieval can be routinely used to retrieve rabies virus antigen for DFAT in cases where only formalin-fixed tissues are available or when preservation by freezing is difficult.
机译:有一种需要一种组织保存的化学方法,可以在室温下延长延长的时间。该研究旨在通过福尔马林固定犬脑组织中的直接荧光抗体试验(DFAT)检索和检测狂犬病病毒抗原。收集四十鲜力脑标本作为来自狂犬病的配对样品,这些样品是在中央诊断实验室,国家兽医研究所,VOM中获得狂犬病的后期检测。为新鲜流动抗体检测制备每配对样品的一部分,并在10%中性缓冲福尔马林中固定后,为表位检索和荧光抗体检测制备另一部分。与鲜组织上的DFAT相比,Informin-Fi XED组织上的DFAT表现出100%的敏感性。在术语 - FI Xed DFAT程序中没有获得假阳性结果,展示100%的特定城市。在热诱导表位检索后新鲜样品和福尔马林固定DFAT上的DFAT中荧光强度没有明显差异(Concordance = 98%; 95%C.i.0.9660至0.9903)。在福尔马林固定和DFAT上对新鲜组织的DFAT之间的一致性的强度非常好(Cohen的Kappa系数值= 1.000; 95%C.I. 1.000-1.000)。本研究提供了关于在系列组织上的DFAT中热诱导的表位检索狂犬病抗原检索的新信息。因此,福尔马林可以用来用来修复狂犬病的组织疑似案例的常规诊断,运输或档案目的。在仅在福尔马林固定组织可用或通过冷冻保存时,可以常常用于检索DFAT的狂犬病病毒抗原的狂犬病病毒抗原。

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