Department of Infection Biology, Faculty of Health and Life Sciences, University of Liverpool, Leahurst Campus, Neston, Cheshire, CH64 7TE, UK.
J Virol Methods. 2012 Dec;186(1-2):171-5. doi: 10.1016/j.jviromet.2012.07.013. Epub 2012 Jul 20.
Using reverse genetics, an avian metapneumovirus (AMPV) was modified for use as a positive control for validating all stages of a popular established RT-nested PCR, used in the detection of the two major AMPV subtypes (A and B). Resultant amplicons were of increased size and clearly distinguishable from those arising from unmodified virus, thus allowing false positive bands, due to control virus contamination of test samples, to be identified readily. Absorption of the control virus onto filter paper and subsequent microwave irradiation removed all infectivity while its function as an efficient RT-nested-PCR template was unaffected. Identical amplicons were produced after storage for one year. The modified virus is likely to have application as an internal standard as well as in real time methods. Additions to AMPV of RNA from other RNA viruses, including hazardous examples such HIV and influenza, are likely to yield similar safe RT-PCR controls.
利用反向遗传学,对一种禽偏肺病毒(AMPV)进行了修饰,用作一种阳性对照,以验证一种常用的建立 RT-巢式 PCR 的所有阶段,该 PCR 用于检测两种主要的 AMPV 亚型(A 和 B)。由此产生的扩增产物的大小增加,与未修饰病毒产生的产物明显不同,因此可以很容易地识别出由于对照病毒污染检测样品而导致的假阳性条带。将对照病毒吸附到滤纸上,然后进行微波照射,可消除所有感染性,而其作为高效 RT-巢式 PCR 模板的功能不受影响。储存一年后仍可产生相同的扩增产物。修饰后的病毒可能具有作为内参的应用以及在实时方法中的应用。向 AMPV 添加其他 RNA 病毒(包括 HIV 和流感等危险病毒)的 RNA,可能会产生类似的安全 RT-PCR 对照。