Fernández F, Gutiérrez J, Sorlózano A, Romero J M, Soto M J, Ruiz-Cabello F
Department of Microbiology, Service of Immunology, University of Granada, Virgen de las Nieves University Hospital, Granada, Spain.
Microbiol Res. 2006;161(2):158-63. doi: 10.1016/j.micres.2005.07.007. Epub 2005 Aug 30.
A comparative study was conducted of a novel real-time quantitative PCR test (LightCycler System) with FastStart DNA Master(PLUS) SYBR Green I dye to detect DNA of human herpes virus 6 (HHV-6). Results were compared with those of a real-time quantitative PCR with hybridization probe (HP) formats using the fluorescence resonance energy transfer method, and with those of a single qualitative PCR test. The detection limit of the test with SYBR Green I dye was 20 copies of the virus, similar to that of the other two tests. The reproducibility was satisfactory. The new test has the same advantages as real-time PCR with HP formats and offers a greater versatility at lower cost.
进行了一项比较研究,采用新型实时定量聚合酶链反应检测(LightCycler系统)和FastStart DNA Master(PLUS)SYBR Green I染料来检测人疱疹病毒6型(HHV-6)的DNA。将结果与使用荧光共振能量转移方法的带有杂交探针(HP)形式的实时定量聚合酶链反应以及单一的定性聚合酶链反应检测结果进行比较。使用SYBR Green I染料的检测限为20个病毒拷贝,与其他两项检测相似。重复性令人满意。新检测方法具有与带有HP形式的实时聚合酶链反应相同的优点,并且以更低的成本提供了更大的通用性。