Padley David J, Lucas Sebastian B, Saldanha John
Division of Virology, National Institute for Biological Standards and Control, South Mimms, Herts, United Kingdom.
Transplantation. 2003 Jul 27;76(2):432-4. doi: 10.1097/01.TP.0000072780.66347.B1.
Detection of viral nucleic acids in blood samples from cadavers is often difficult because of inhibition of the reverse transcriptase (RT) or polymerase chain reaction (PCR) steps by substances present in the samples. A robust method for the extraction and detection of hepatitis C virus (HCV) RNA from cadaver blood samples by polymerase chain reaction RT-PCR has been developed on the basis of the Qiagen QIAamp DNA mini kit extraction system (Basel, Switzerland). Twenty of 36 samples tested were positive for HCV RNA. Six of the 16 HCV-antibody- and RNA-negative samples contained inhibitors that were successfully removed by pretreatment of samples with the Qiagen AX matrix before extraction.
由于尸体血液样本中存在的物质会抑制逆转录酶(RT)或聚合酶链反应(PCR)步骤,因此从尸体血液样本中检测病毒核酸往往很困难。基于Qiagen QIAamp DNA mini试剂盒提取系统(瑞士巴塞尔),已开发出一种通过聚合酶链反应RT-PCR从尸体血液样本中提取和检测丙型肝炎病毒(HCV)RNA的可靠方法。36份检测样本中有20份HCV RNA呈阳性。16份HCV抗体和RNA均为阴性的样本中有6份含有抑制剂,在提取前用Qiagen AX基质对样本进行预处理可成功去除这些抑制剂。