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作 者:邓先余[1] 陈晓艳[2] 王智学[3] 欧普[1] 何建国[3]
机构地区:[1]湖南科技大学生命科学学院,湘潭411201 [2]暨南大学生物工程系,广州510352 [3]中山大学生命科学学院,广州510275
出 处:《Acta Genetica Sinica》2006年第4期365-372,共8页
基 金:This work was supported by Chinese National Programs for High Technology and Development (863 Program)(No. 2001AA622020),a Special Research Grant from the Sciences and Technology Bureau of Guangdong Province (No.2KB05301N) and a PH. D Grant from Hunan University of Science and Technology (No. E50437).
摘 要:根据细菌的16S rDNA 3′端和23S rDNA 5′端的高度保守区设计引物,PCR扩增了2株创伤弧菌(Vibrio vulnificus)的16S-23S rDNA 间区(Intergenic spacer,IGS),克隆到pGEM-T载体上,测序。用BLAST和 DNAstar软件对16S-23S rDNA 间区序列及其内的 tRNA 基因进行比较分析。结果表明,2 株创伤弧菌共测出 9 条 16S-23S rDNA 间区序列, 其中ZSU006 测出 5 条, 间区类型分别为:IGSGLAV、IGSGLV、IGSIA 、IGSA和 IGSG。其中 IGSGLAV最大,包含 tRNAGlu、tRNALys、tRNAAla 和 tRNAVal基因;IGSGLV包含 tRNAGlu、tRNALys和 tRNAVal基因; IGSIA,则包含 tRNAIle和 tRNAAla基因;IGSG仅包含tRNAGlu基因;而IGSA仅包含tRNA Ala基因。菌株CG021测出的16S-23S rDNA IGS序列有4条,除缺少IGSA外,其余的IGS类型均与ZSU006的相同。与GenBank内的创伤弧菌ATCC27562 的IGS序列比较,发现创伤弧菌所有类型的IGS的tRNA基因两端的非编码区具有较高的种内同源性。16S-23S rDNA 间区结构的差异为建立一种新的创伤弧菌检测方法奠定了基础。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, IGS^GLAv, IGS^GLV, IGS^IA, IGS^G and IGS^A; while the strain CG021 has the same types of IGSs except lacking IGS^A. Among these five IGS types, IGS^GLAV is the biggest type, including the gene cluster of tRNA^Glu - tRNA^Lys- tRNA^Ala - tRNA^Val ; IGS^GLV includes that of tRNA^Glu-tRNA^Lys-tRNA^Val ; IGS^AG, tRNA^Ala -tRNA^Glu; IGS^IA, tRNA^Ile -tRNA^Ala; IGS^G, tRNA^GlU and IGS^A, tRNA^Ala. 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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