Kim J, Chae C
Department of Veterinary Pathology, College of Veterinary Medicine and School of Agricultural Biotechnology, Seoul National University, Suwon 441-744, Kyounggi-Do, South Korea.
J Virol Methods. 2001 Apr;92(2):105-11. doi: 10.1016/s0166-0934(00)00255-x.
Optimized DNA extraction method and nested polymerase chain reaction (PCR) were developed for the detection of porcine circovirus 2 (PCV2) from formalin-fixed, paraffin-embedded tissues. Conventional PCR, nested PCR, and in situ hybridization methods were also compared for the detection of PCV2 in archival tissues. A method based on xylene deparaffinization followed by proteinase K digestion yielded DNA of sufficient quality for PCR analyses reliably and consistently. Twenty-six (70%) of the 37 tissues examined gave positive results with conventional PCR, whereas all the 37 tissues gave positive results using the nested PCR. A distinct positive signal for PCV2 was detected in spleen and lymph node from all the 37 pigs by in situ hybridization. The nested PCR and in situ hybridization could be applied successfully to archival tissues for the detection of porcine circovirus 2 DNA.
开发了优化的DNA提取方法和巢式聚合酶链反应(PCR),用于从福尔马林固定、石蜡包埋组织中检测猪圆环病毒2型(PCV2)。还比较了常规PCR、巢式PCR和原位杂交方法用于检测存档组织中的PCV2。一种基于二甲苯脱蜡然后蛋白酶K消化的方法能够可靠且一致地产生质量足以进行PCR分析的DNA。在接受检测的37个组织中,26个(70%)通过常规PCR得出阳性结果,而使用巢式PCR时所有37个组织均呈阳性结果。通过原位杂交在所有37头猪的脾脏和淋巴结中检测到PCV2的明显阳性信号。巢式PCR和原位杂交可成功应用于存档组织以检测猪圆环病毒2型DNA。