Druce Julian, Catton Mike, Chibo Doris, Minerds Kirsty, Tyssen David, Kostecki Renata, Maskill Bill, Leong-Shaw Wendy, Gerrard Marie, Birch Chris
Victorian Infectious Diseases Reference Laboratory (VIDRL), 10 Wreckyn Street, North Melbourne 3051, Victoria, Australia.
J Clin Microbiol. 2002 May;40(5):1728-32. doi: 10.1128/JCM.40.5.1728-1732.2002.
A multiplex PCR was designed to amplify herpes simplex virus types 1 and 2, cytomegalovirus, and varicella-zoster virus DNA present in a diverse range of clinical material. The susceptibility of these viruses to in vivo inhibition by at least one antiviral drug was an important consideration in their inclusion in the multiplex detection system. An aliquot of equine herpesvirus was introduced into each specimen prior to extraction and served as an indicator of potential inhibitors of the PCR and a detector of suboptimal PCR conditions. Compared to virus isolation and immunofluorescence-based antigen detection, the multiplex assay yielded higher detection rates for all viruses represented in the assay. The turnaround time for performance of the assay was markedly reduced compared to those for the other techniques used to identify these viruses. More than 21,000 tests have been performed using the assay. Overall, the multiplex PCR enabled the detection of substantially increased numbers of herpesviruses, in some cases in specimens or anatomical sites where previously they were rarely if ever identified using traditional detection methods.
设计了一种多重PCR,用于扩增存在于多种临床材料中的1型和2型单纯疱疹病毒、巨细胞病毒以及水痘-带状疱疹病毒的DNA。这些病毒对至少一种抗病毒药物的体内抑制敏感性是将它们纳入多重检测系统的一个重要考虑因素。在提取之前,将一份马疱疹病毒引入每个样本中,作为PCR潜在抑制剂的指标和次优PCR条件的检测器。与病毒分离和基于免疫荧光的抗原检测相比,多重检测法对检测中所涵盖的所有病毒都有更高的检出率。与用于鉴定这些病毒的其他技术相比,该检测法的周转时间明显缩短。使用该检测法已进行了超过21000次检测。总体而言,多重PCR能够检测到数量大幅增加的疱疹病毒,在某些情况下,在以前使用传统检测方法很少甚至从未鉴定出疱疹病毒的样本或解剖部位也能检测到。