Watzinger F, Suda M, Preuner S, Baumgartinger R, Ebner K, Baskova L, Niesters H G M, Lawitschka A, Lion T
Division of Molecular Microbiology and Development of Genetic Diagnostics, Children's Cancer Research Institute, Vienna, Austria.
J Clin Microbiol. 2004 Nov;42(11):5189-98. doi: 10.1128/JCM.42.11.5189-5198.2004.
A panel of 23 real-time PCR assays based on TaqMan technology has been developed for the detection and monitoring of 16 different viruses and virus families including human polyomaviruses BK virus and JC virus, human herpesviruses 6, 7, and 8, human adenoviruses, herpes simplex viruses 1 and 2, varicella-zoster virus, cytomegalovirus, Epstein-Barr virus, parvovirus B19, influenza A and B viruses, parainfluenza viruses 1 to 3, enteroviruses, and respiratory syncytial virus. The test systems presented have a broad dynamic range and display high sensitivity, reproducibility, and specificity. Moreover, the assays allow precise quantification of viral load in a variety of clinical specimens. The ability to use uniform PCR conditions for all assays permits simultaneous processing and detection of many different viruses, thus economizing the diagnostic work. Our observations based on more than 50,000 assays reveal the potential of the real-time PCR tests to facilitate early diagnosis of infection and to monitor the kinetics of viral proliferation and the response to treatment. We demonstrate that, in immunosuppressed patients with invasive virus infections, surveillance by the assays described may permit detection of increasing viral load several days to weeks prior to the onset of clinical symptoms. In virus infections for which specific treatment is available, the quantitative PCR assays presented provide reliable diagnostic tools for timely initiation of appropriate therapy and for rapid assessment of the efficacy of antiviral treatment strategies.
已开发出一组基于TaqMan技术的23种实时PCR检测方法,用于检测和监测16种不同的病毒及病毒科,包括人多瘤病毒BK病毒和JC病毒、人疱疹病毒6型、7型和8型、人腺病毒、单纯疱疹病毒1型和2型、水痘-带状疱疹病毒、巨细胞病毒、爱泼斯坦-巴尔病毒、细小病毒B19、甲型和乙型流感病毒、副流感病毒1至3型、肠道病毒和呼吸道合胞病毒。所展示的检测系统具有广泛的动态范围,且表现出高灵敏度、可重复性和特异性。此外,这些检测方法能够对多种临床标本中的病毒载量进行精确量化。对所有检测方法使用统一PCR条件的能力允许同时处理和检测多种不同病毒,从而节省诊断工作。我们基于超过50000次检测的观察结果揭示了实时PCR检测在促进感染早期诊断以及监测病毒增殖动力学和治疗反应方面的潜力。我们证明,在患有侵袭性病毒感染的免疫抑制患者中,通过所述检测方法进行监测可能会在临床症状出现前数天至数周检测到病毒载量的增加。对于有特定治疗方法的病毒感染,所展示的定量PCR检测方法为及时开始适当治疗以及快速评估抗病毒治疗策略的疗效提供了可靠的诊断工具。