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作 者:郭醒华 李月久[1,2,3] 郭军巧 金抗[1,2,3]
机构地区:[1]辽宁省卫生防疫站 [2]中国医科大学公共卫生学院 [3]中国医科大学附属第一医院
出 处:《中国公共卫生》1998年第8期490-491,共2页Chinese Journal of Public Health
基 金:辽宁省自然科学基金
摘 要:应用套式聚合酶链反应(nested-PCR)技术,建立了扩增嗜肺军团菌巨噬细胞感染增强因子(mip)基因序列的方法。对14株标准军团菌和5株标准大肠埃希氏菌等进行检测。结果仅嗜肺军团菌扩增出649bp特异性片段,扩增灵敏度为100CFU/ml。对17份人血标本进行检测。The nested polymerase Chan reactiion (nestedPCR)has been adopted to amplily the specific sequences of the macrophage infectivity potentiator(mip)gene of Legionella pneumophila(Lp).14 strains of Lp and 5 strains of non Legionella were tested.The results shown that only Lp amplified products had 649 bp specific DNA fragment.The sensitivity of amplification was about 100CFU/ml DAN of Lp.It was used to detect Legionella DNA in 17 blood specimens (including 6 specimens collected from patients with Legionnaires′ disease).It was shown that the sensitivity of nestedPCK was significantly higher than that of serological and bacteriological culture method.The specificity were 100%,too.The above results suggest that nestedPCR may be a specific,sensititive and rapid technique for the diagnosis of Legionnaires disease
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