Wolska-Goszka L, Nowak A, Galiński J, Słomiński J M
Katedry i Kliniki Chorób Płuc i Gruźlicy Kierownik, Akademii Medycznej, Gdańsku.
Pneumonol Alergol Pol. 1998;66(1-2):31-7.
The polymerase chain reaction (PCR) and direct culture were applied for detection of Mycobacterium tuberculosis complex in samples obtained from patients with suspicion of pulmonary and extra-pulmonary tuberculosis. In the reaction of amplification IS6110 was applied as a target region, and PCR reaction products were of the size of 123 bp and 317 bp. A total of 278 samples (158 sputum, 36 urine, 25 pleural effusion, 23 bronchial washings, 8 blood, 4 stomach washings, 3 cerebrospinal fluid, 2 fragments of skin, 2 pleural effusion, and 17 others samples) from 181 patients were tested. Mycobacterium tuberculosis complex was detected by PCR in 144 out of 278 samples and by culture in 68 of 278 samples. The PCR test enabled a rapid and sensitive diagnosis particularly in a number of samples which were negative on culture.
采用聚合酶链反应(PCR)和直接培养法检测疑似肺结核和肺外结核患者样本中的结核分枝杆菌复合群。在扩增反应中,将IS6110作为靶区域,PCR反应产物大小为123 bp和317 bp。共检测了181例患者的278份样本(158份痰液、36份尿液、25份胸腔积液、23份支气管灌洗液、8份血液、4份洗胃样本、3份脑脊液、2份皮肤组织、2份胸腔积液以及17份其他样本)。278份样本中,144份通过PCR检测出结核分枝杆菌复合群,68份通过培养检测出。PCR检测能够实现快速、灵敏的诊断,尤其是对于一些培养结果为阴性的样本。