Wang R F, Campbell W L, Cao W W, Colvert R M, Holland M A, Cerniglia C E
National Center for Toxicological Research, FDA, Jefferson, AR 72079, USA.
Mol Cell Probes. 1999 Feb;13(1):29-33. doi: 10.1006/mcpr.1998.0211.
Mouse hepatitis virus (MHV) infection in laboratory mouse populations is a serious problem, because the MHV infections are known to interfere with research results. Confirmation of indirect serological detection methods by viral isolation is difficult. Reverse transcription plus polymerase chain reaction (RT-PCR) was used to test 94 mouse tissue samples from suspected naturally MHV infected mice. Positive results were only obtained from two colon samples and one mixed sample with colon and liver. The low positive rate is probably due to the virus being rapidly cleared by the MHV antibodies produced in the mouse. However, RT-PCR detection of MHV in nude mice placed in the same cages with other non-nude mice or placed in cages with used dirty bedding, showed a very high positive rate: 10 out of 12 colon samples were positive (83%), and 5 out of 10 faecal samples were positive (50%). A single-tube, single step RT-PCR method and two procedures for isolation of the viral RNA for the RT-PCR assay were also included in this article.
实验室小鼠群体中的小鼠肝炎病毒(MHV)感染是一个严重问题,因为已知MHV感染会干扰研究结果。通过病毒分离来确认间接血清学检测方法很困难。采用逆转录加聚合酶链反应(RT-PCR)对94份疑似自然感染MHV的小鼠组织样本进行检测。仅从两份结肠样本和一份结肠与肝脏的混合样本中获得阳性结果。阳性率较低可能是由于病毒被小鼠产生的MHV抗体迅速清除。然而,将裸鼠与其他非裸鼠置于同一笼中或置于铺有使用过的脏垫料的笼中,对其进行RT-PCR检测MHV时,阳性率非常高:12份结肠样本中有10份呈阳性(83%),10份粪便样本中有5份呈阳性(50%)。本文还介绍了一种单管、一步法RT-PCR方法以及两种用于RT-PCR检测的病毒RNA分离程序。