Jamil S, Wilson S M, Hacket M, Hussain R, Stoker N G
Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, U.K.
Int J Lepr Other Mycobact Dis. 1994 Dec;62(4):512-20.
A one-tube nested polymerase chain reaction (PCR) method for the diagnosis of paucibacillary leprosy was developed using the repetitive RLEP sequence as a target. Detection of the PCR products was simplified by the adaptation of a colorimetric method. The test was specific for Mycobacterium leprae, and the sensitivity of the assay was 1 fg of purified genomic M. leprae DNA (less than one genome). Complete concordance was seen between the development of color and resolution on agarose gels. The results of frozen skin sections from untreated patients showed that the assay could detect 100% of multibacillary samples [bacterial index (BI) of 2 or more] and 69% and 70% of the samples with BIs of 1 and 0, respectively. The use of one-tube nested PCR in assessing the effectiveness of multidrug therapy (MDT) in leprosy also was determined. The simplified colorimetric assay was found to be sensitive, rapid and specific, and is suitable for use in routing diagnostic laboratories.
开发了一种以重复性RLEP序列为靶标的单管巢式聚合酶链反应(PCR)方法用于诊断少菌型麻风。通过采用比色法简化了PCR产物的检测。该检测对麻风分枝杆菌具有特异性,检测灵敏度为1 fg纯化的麻风分枝杆菌基因组DNA(少于一个基因组)。比色显色与琼脂糖凝胶上的条带分辨率完全一致。未经治疗患者的冷冻皮肤切片结果显示,该检测可分别检测出100%的多菌型样本[细菌指数(BI)为2或更高]以及69%和70%的BI为1和0的样本。还确定了使用单管巢式PCR评估麻风多药联合化疗(MDT)的有效性。发现这种简化的比色检测灵敏、快速且特异,适用于常规诊断实验室。