两株创伤弧菌16S-23S rDNA基因间隔片段的克隆、测序及分析

DENG Xian-Yu , CHEN Xiao-Yan , WANG Zhi-Xue , OU Pu , HE Jian-Guo
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引用次数: 4

摘要

根据16S 3′端和23S 5′端rDNA的保守序列设计PCR引物,通过PCR扩增出两株创伤弧菌的16S-23S rDNA基因间间隔(IGSs),并将其克隆到pGEM-T载体上。选择不同的克隆进行测序,用BLAST和DNAstar软件对序列进行分析。IGS序列分析表明,菌株ZSU006含有5种多态性16S-23S rDNA基因间间隔物,分别为IGSGLAV、IGSGLV、IGSlA、IGSG和IGSA;而菌株CG021除了缺乏IGSA外,具有相同类型的IGSs。在这5种IGS类型中,IGSGLAV是最大的类型,包括tRNAGlu - tRNALys - tRNAAla - tRNAVal基因簇;IGSGLV包括tRNAGlu-tRNALys-tRNAVal;IGSAG tRNAAla-tRNAGlu;IGSIA tRNAIle-tRNAAla;IGSG, tRNAGlu和IGSA, tRNAAla。将这两种菌株的所有IGS序列与GenBank上的创伤弧菌ATCC27562序列进行种内多重比对,发现所有菌株tRNA基因侧翼的非编码区都有几个高度保守的序列块,最显著的是前40和后200个核苷酸,可用于设计种特异性PCR引物或检测探针。16S-23S rDNA基因间间隔段的结构变异为创伤弧菌诊断方法的建立奠定了基础。
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Cloning, Sequencing and Analysis of the 16S-23S rDNA Intergenic Spacers (IGSs) of Two Strains of Vibrio vulnificus

According to the conserved sequences flanking the 3′ end of the 16S and the 5′ end of the 23S rDNAs, PCR primers were designed, and the 16S-23S rDNA intergenic spacers (IGSs) of two strains of Vibrio vulnificus were amplified by PCR and cloned into pGEM-T vector. Different clones were selected to be sequenced and the sequences were analyzed with BLAST and the software DNAstar. Analyses of the IGS sequences suggested that the strain ZSU006 contains five types of polymorphic 16S-23S rDNA intergenic spacers, namely, IGSGLAV, IGSGLV, IGSlA, IGSG and IGSA; while the strain CG021 has the same types of IGSs except lacking IGSA. Among these five IGS types, IGSGLAV is the biggest type, including the gene cluster of tRNAGlu - tRNALys - tRNAAla - tRNAVal; IGSGLV includes that of tRNAGlu-tRNALys-tRNAVal; IGSAG, tRNAAla-tRNAGlu; IGSIA, tRNAIle-tRNAAla; IGSG, tRNAGlu and IGSA, tRNAAla. Intraspecies multiple alignment of all the IGS sequences of these two strains with those of V. vulnificus ATCC27562 available at GenBank revealed several highly conserved sequence blocks in the non-coding regions flanking the tRNA genes within all of strains, most notably the first 40 and last 200 nucleotides, which can be targeted to design species-specific PCR primers or detection probes. The structural variations of the 16S-23S rDNA intergenic spacers lay a foundation for developing diagnostic methods for V. vulnificus.

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