Urakawa H, Kita-Tsukamoto K, Ohwada K
Ocean Research Institute, University of Tokyo, Japan.
FEMS Microbiol Lett. 1997 Jul 1;152(1):125-32. doi: 10.1111/j.1574-6968.1997.tb10418.x.
The 16S rDNA genotypes among the family Vibrionaceae were determined using PCR/RFLP analysis. Five tetrameric restriction enzymes (HhaI, DdeI, RsaI, Sau3AI and MspI) were used for RFLP analysis and adequate numbers of informative bands were obtained from each enzyme. Twenty-seven genotypes were obtained from 49 type and reference strains including 35 species. Nineteen species could be assigned to specific 16S rDNA genotypes, supporting the application of this analysis for identification. Trees constructed using five endonucleases resolved groups almost identical to those inferred from 16S rRNA gene sequencing. However, the branch lengths and detailed relationships among strains within a group differed from those inferred from sequence comparisons. The results of this study should be useful for genotyping, identification and approximate classification of natural isolates belonging to the family Vibrionaceae.
利用聚合酶链反应/限制性片段长度多态性分析(PCR/RFLP分析)确定了弧菌科中的16S核糖体DNA(rDNA)基因型。使用了五种四聚体限制性内切酶(HhaI、DdeI、RsaI、Sau3AI和MspI)进行RFLP分析,并且从每种酶中都获得了足够数量的信息条带。从49株模式菌株和参考菌株(包括35个物种)中获得了27种基因型。19个物种可以被归为特定的16S rDNA基因型,这支持了该分析在鉴定中的应用。使用五种内切核酸酶构建的树解析出的类群与从16S rRNA基因测序推断出的类群几乎相同。然而,一个类群内菌株之间的分支长度和详细关系与从序列比较推断出的不同。本研究结果应有助于对弧菌科天然分离株进行基因分型、鉴定和近似分类。