Lisby G
Klinisk mikrobiologisk afdeling, Københavns Amts Sygehus i Herlev.
Ugeskr Laeger. 1993 May 31;155(22):1708-12.
The discovery of the polymerase chain reaction (PCR) enables the detection of just a few target gene copies present in almost every kind of tissue. The PCR technique uses two separated specific DNA-sequences for identification of a desired genetic sequence. This identification is followed by an almost unlimited production of the specific target gene sequence by a heat stable DNA-polymerase. The PCR technique will revolutionize several diagnostic areas, and especially the identification of virus, fungi and slowly growing bacteria will benefit from this new genetic technology. The impressive sensitivity is, however, the greatest pitfall of the technique, as just a few contaminating DNA fragments can initiate a false positive result. Great care is therefore needed when designing a PCR laboratory, as well as high demands upon the motivation and technical skills of the personnel involved. PCR is so far limited to research, but is expected to be released for routine diagnostic purposes in 1993.
聚合酶链反应(PCR)的发现使得几乎能在各类组织中检测出仅有的几个目标基因拷贝。PCR技术利用两个分离的特定DNA序列来鉴定所需的基因序列。在这一鉴定之后,通过热稳定DNA聚合酶几乎能无限量地产生特定的目标基因序列。PCR技术将给多个诊断领域带来变革,尤其是病毒、真菌及生长缓慢细菌的鉴定将受益于这项新的基因技术。然而,该技术令人瞩目的灵敏度却是其最大的缺陷,因为仅有几个污染性DNA片段就能引发假阳性结果。因此,在设计PCR实验室时需格外谨慎,对相关人员的积极性和技术技能也有很高要求。到目前为止,PCR仅限于研究领域,但预计在1993年将用于常规诊断目的。