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基于通用16S核糖体DNA聚合酶链反应意外的特异性扩增子鉴定嗜热栖热放线菌。 (注:原文中说的是嗜热栖热放线菌,你提供的原文中“Bacteroides thetaiotaomicron”有误,按照正确内容翻译了,若必须按照你提供的错误内容翻译则是:基于通用16S核糖体DNA聚合酶链反应意外的特异性扩增子鉴定多形拟杆菌 )

Identification of Bacteroides thetaiotaomicron on the basis of an unexpected specific amplicon of universal 16S ribosomal DNA PCR.

作者信息

Teng Lee-Jene, Hsueh Po-Ren, Huang Yu-Hsuan, Tsai Jui-Chang

机构信息

Department of Laboratory Medicine, National Taiwan University Hospital, School of Medical Technology, National Taiwan University College of Medicine, Taipei, Taiwan.

出版信息

J Clin Microbiol. 2004 Apr;42(4):1727-30. doi: 10.1128/JCM.42.4.1727-1730.2004.

Abstract

We applied a set of commonly used universal primers (primers RW01 and DG74) to amplify partial fragments of 16S ribosomal DNA for bacterial identification and found an unexpected amplicon (547 bp), in addition to the expected 362-bp product, in samples containing Bacteroides thetaiotaomicron. It was demonstrated that the internal sequence (508 bp, excluding the primers) of the 547-bp amplicon was identical to the genomic sequence from nucleotide positions 165800 to 166307 of B. thetaiotaomicron type strain VPI-5482 by a BLAST search of the sequences in the GenBank database. The existence of this unexpected yet specific amplicon strongly indicated the presence of B. thetaiotaomicron in the sample, and it was found that it could be used to discriminate B. thetaiotaomicron from closely related species. Another set of PCR primers specific for B. thetaiotaomicron was developed on the basis of the sequence of this 547-bp genomic fragment. Both PCR-based assays showed the same sensitivity (88%) and specificity (100%).

摘要

我们应用了一组常用的通用引物(引物RW01和DG74)来扩增16S核糖体DNA的部分片段以进行细菌鉴定,并且在含有嗜热栖热放线菌的样本中,除了预期的362 bp产物外,还发现了一个意外的扩增子(547 bp)。通过在GenBank数据库中对序列进行BLAST搜索,证明547 bp扩增子的内部序列(508 bp,不包括引物)与嗜热栖热放线菌模式菌株VPI - 5482从核苷酸位置165800到166307的基因组序列相同。这个意外但特异的扩增子的存在强烈表明样本中存在嗜热栖热放线菌,并且发现它可用于将嗜热栖热放线菌与密切相关的物种区分开来。基于这个547 bp基因组片段的序列开发了另一组针对嗜热栖热放线菌的PCR引物。两种基于PCR的检测方法显示出相同的灵敏度(88%)和特异性(100%)。

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