Laboratory of Applied Micro and Nanotechnology, National Veterinary Institute, Technical University of Denmark (DTU-Vet), Hangøvej 2, Dk-8200, Aarhus N, Denmark.
Diagn Microbiol Infect Dis. 2011 Mar;69(3):258-65. doi: 10.1016/j.diagmicrobio.2010.09.022.
Avian influenza virus (AIV) causes great economic losses for the poultry industry worldwide and threatens the human population with a pandemic. The conventional detection method for AIV involves sample preparation of viral RNA extraction and purification from raw sample such as bird droppings. In this study, magnetic beads were applied for immunoseparation and purification of AIV from spiked chicken fecal sample. The beads were conjugated with monoclonal antibodies against the AIV nucleoprotein, which is conserved in all the AIV. The bead-captured virus was detected by reverse transcriptase-polymerase chain reaction (RT-PCR) without RNA extraction because of effective removal of RT-PCR inhibitors. The developed bead-based assay showed a similar detection limit comparable to the RNA extraction and the classic virus isolation method. Using ready-to-use antibody-conjugated bead, the method requires less than 5 h. Furthermore, the method has potential to integrate into a Lab-on-a-chip system for rapid detection and identification of AIV.
禽流感病毒 (AIV) 给全球家禽业造成了巨大的经济损失,并有可能引发人类大流行。AIV 的常规检测方法包括从粪便等原始样本中提取和纯化病毒 RNA。在这项研究中,磁珠被用于从加标鸡粪便样本中分离和纯化 AIV。磁珠与针对 AIV 核蛋白的单克隆抗体偶联,该核蛋白在所有 AIV 中都保守。由于有效地去除了 RT-PCR 抑制剂,因此可以通过逆转录-聚合酶链反应 (RT-PCR) 检测被珠捕获的病毒,而无需提取 RNA。开发的基于磁珠的检测方法显示出与 RNA 提取和经典病毒分离方法相当的检测限。使用即用型抗体偶联珠,该方法耗时不到 5 小时。此外,该方法有可能整合到微流控芯片系统中,用于快速检测和鉴定 AIV。