首页 | 本学科首页   官方微博 | 高级检索  
检索        

聚合酶链反应检测流感嗜血杆菌
引用本文:袁艺,卢竞.聚合酶链反应检测流感嗜血杆菌[J].中华微生物学和免疫学杂志,1997,17(1):25-27.
作者姓名:袁艺  卢竞
作者单位:首都儿科研究所
摘    要:以一对来自编码流感嗜血杆菌(Hi)外膜蛋白P6的基因序列的引物,用聚合酶链反应(PCR)扩增Hi各血清型标准菌株及30株临床分离菌株,均获阳性结果。而7种对照菌扩增结果均为阴性。用PCR反应后琼脂糖凝胶电泳检测的方法,由蒸馏水稀释的菌液及鼻咽深部分泌物模拟标本中分别至少可以检测到3~5个及50个Hi菌体。对40例肺炎患儿鼻咽深部分泌物进行Hi检测,结果20例PCR阳性,其中17例培养也阳性。本文作者还首次用PCR法从6例肺炎患儿尿标本中检测到了Hi。研究表明,PCR可用于Hi的检测,该方法敏感、特异、简便、快速,具有良好的应用前景。

关 键 词:聚合酶链反应  流感嗜血杆菌  细菌外膜蛋白质  基因.细菌  序列分析

Study on detection of Haemophilus influenzae by polymerase chain reaction
Yuan Yi,Lu Jing,Guo Zhanggai. Capital Institute of Pediatrics,Beijing.Study on detection of Haemophilus influenzae by polymerase chain reaction[J].Chinese Journal of Microbiology and Immunology,1997,17(1):25-27.
Authors:Yuan Yi  Lu Jing  Guo Zhanggai Capital Institute of Pediatrics  Beijing
Institution:Yuan Yi,Lu Jing,Guo Zhanggai. Capital Institute of Pediatrics,Beijing 100020
Abstract:By using a primer set selected from the sequence of a gene encoding for Haemophilus influenzae (Hi) outer membrane protein P6,polymerase chain reaction(PCR) were carried out to detect Hi.All the 6 reference strains of serotype a f and 30 field strains examined can be amplified.While all the other 7 genera of bacteria examined gave negative results.In the experiment,PCR DNA amplification was able to detect as few as 3 5 Hi cells from distilled water diluted bacterial liquid and 50 Hi cells from simulated nasalpharynx secretion sample by agarose gel electrophoresis.40 samples of deep nasalpharynx secretion collected from children with pneumonia were investigated by PCR and culture.20 were PCR positive for Hi and 17 of these were also positive in culture.In the study,we had also first detected Hi out of the urine samples of 6 children with pneumonia by PCR. The study shows that PCR is a sensitive and specific technique,and may be used as a rapid and early diagnostic tool for Hi.
Keywords:Heamophilus influenzae      Bacterial outer membrane proteins    Gene  bacterial    Polymerase chain reaction    Sequence analysis  
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号