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[应用聚合酶链反应(PCR)检测嗜肺军团菌的研究]

[Studies on the detection of Legionella pneumophila by the application of polymerase chain reaction (PCR)].

作者信息

Yu C, Wan C, Deng C

机构信息

Institute of Epidemiology and Microbiology, Chinese Academy of Preventive Medicine, Beijing.

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 1994 Apr;15(2):117-20.

PMID:7923334
Abstract

DNA fragment of Legionella pneumophila, the PCR was performed with a pair of artificial synthesized primer. Results of agarose electrophoresis and EB staining showed that there was a 870 bp band shared by serogroups 1-14 of L.pneumophila. The sensitivity of PCR in detecting Legionella from water was 350cfu/ml, however, the specific DNA probe labeled with 32P was .43cfu/ml by blot hybridization. The positive rate of tissue specimens from infected guinea-pigs with Legionella pneumophila was 83.3% by PCR detection, and only 26.6% by bacteriological culture method. An outbeak caused by Lp10 was verified by PCR. The result showed that the PCR could detect the infection of Legionella rapidly, specifically and sensitively.

摘要

嗜肺军团菌的DNA片段,用一对人工合成引物进行聚合酶链反应(PCR)。琼脂糖电泳和溴化乙锭染色结果显示,嗜肺军团菌血清群1 - 14有一条870 bp的条带。PCR检测水中军团菌的灵敏度为350 cfu/ml,然而,用32P标记的特异性DNA探针通过印迹杂交检测为0.43 cfu/ml。通过PCR检测,感染嗜肺军团菌的豚鼠组织标本阳性率为83.3%,而细菌培养法仅为26.6%。通过PCR证实了由Lp10引起的一次暴发。结果表明,PCR能快速、特异性和灵敏地检测军团菌感染。

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