中国感染控制杂志2016，Vol.15Issue(4)：222-226,5.DOI:10.3969/j.issn.1671-9638.2016.04.002
基于细菌16S rRNA基因扩增临床不常见病原菌的价值
Value of 16S rRNA gene amplification for identification of clinical rare pathogens
摘要
Abstract
Objective To evaluate the value of amplification and sequencing of 16S rRNA gene in the identification of clinical rare pathogenic bacteria,and guide the diagnosis and treatment for related clinical infection.Methods 12 bacterial isolates that were difficult,or unable to be identified with conventional laboratory methods,or with special phenotypes were collected. The 16S rRNA gene was amplified by polymerase chain reaction (PCR),then sequenced for identifying bacterial species through BLAST comparison,clinical characteristics of related infection were ana-lyzed.Results 12 clinical isolates were all positive for PCR amplification (about 1500 bp),species were all identi-fied (similarity≥99% ),the identified strains were Listeriamonocytogenes(n= 2),Brucellamelitensis(n= 2),Fu-sobacteriummortiferum(n= 1),Rothiaaeria(n= 1),Nocardiafarcinica(n= 1),Staphylococcussaccharolyticus (n= 1 ),Rhizobiumradiobacter(n= 1 ),Prevotellabivia(n= 1 ),Ralstoniamannitolilytica(n= 1 ),and Atopobium vaginae(n= 1 ). The sensitivity of 16S rRNA gene amplification was high,and the minimum detection limit of Escherichiacoli ATCC 25922 was 1.5×101 CFU/mL. Clinical data of 12 patients revealed that these strains can cause multi-sites and multi-types of infection,after patients received targeted antimicrobial therapy,11 improved, and 1 died.Conclusion Sequencing for 16S rRNA gene can rapidly and accurately identify rare,anaerobic,and difficult cultured bacteria,provide laboratory evidence for etiological diagnosis and treatment of different types of infection.关键词
16SrRNA/病原菌/鉴定/感染/分子生物方法/聚合酶链反应Key words
16S rRNA/pathogen/identification/infection/molecular biological method/polymerase chain reaction分类
医药卫生引用本文复制引用
曹敬荣,高世超,陈典典,陈静,闵嵘,王培昌..基于细菌16S rRNA基因扩增临床不常见病原菌的价值[J].中国感染控制杂志,2016,15(4):222-226,5.基金项目
首都临床特色应用研究重点专项课题(Z141107002514012) （Z141107002514012）
