Darwish Ahmed M, Ismaiel Adnan A
Agricultural Research Service, United States Department of Agriculture, Harry K. Dupree Stuttgart National Aquaculture Research Center, P.O. Box 1050, Stuttgart, AR 72160, USA.
Mol Cell Probes. 2005 Aug;19(4):267-74. doi: 10.1016/j.mcp.2005.04.003.
Genetic variability among strains of Flavobacterium columnare, isolated in the United States, was characterized by restriction fragment length polymorphism (RFLP) and phylogenetic analysis based on the sequence of the 16S rRNA gene. Twenty-seven isolates of F. columnare were differentiated into three genotypes. The isolates within the genotypes were further grouped based on RFLP of the 16S-23S rDNA spacer. The first genotype had five strains that were further divided into group A (4 strains) and B (1 strain) while the second genotype had 10 strains that were also further divided into group A (4 strains) and B (6 stains). The third genotype had 12 isolates with no differences in the RFLP patterns of the 16S-23S rDNA spacers. The 16S rRNA gene sequences representing the three identified genotypes were compared to the different published sequences by phylogenetic analysis and the results showed the American genotypes 1, 2 and 3 corresponding to genomovar 1, 2, and 3, respectively, reported by Triyanto and Wakabayashi [Triyanto, Wakabayashi H. Genotyping of strains of Flavobacterium columnare from diseased fishes. Fish Pathol 1999; 34: 65-71]. The study demonstrates a method for RFLP and sequencing of the 16S rRNA gene and the 16-23S rDNA spacer as a useful tool in epidemiological studies of F. columnare.
对从美国分离出的柱状黄杆菌菌株的遗传变异性进行了特征分析,采用限制性片段长度多态性(RFLP)以及基于16S rRNA基因序列的系统发育分析。27株柱状黄杆菌分离株被分为三种基因型。基于16S - 23S rDNA间隔区的RFLP,各基因型内的分离株进一步分组。第一种基因型有5个菌株,进一步分为A组(4个菌株)和B组(1个菌株);而第二种基因型有10个菌株,也进一步分为A组(4个菌株)和B组(6个菌株)。第三种基因型有12个分离株,其16S - 23S rDNA间隔区的RFLP模式没有差异。通过系统发育分析,将代表三种已鉴定基因型的16S rRNA基因序列与不同的已发表序列进行比较,结果表明美国的基因型1、2和3分别对应于Triyanto和Wakabayashi报道的基因变种1、2和3 [Triyanto, Wakabayashi H. Genotyping of strains of Flavobacterium columnare from diseased fishes. Fish Pathol 1999; 34: 65 - 71]。该研究证明了一种对16S rRNA基因和16 - 23S rDNA间隔区进行RFLP分析和测序的方法,可作为柱状黄杆菌流行病学研究的有用工具。