Aznar R, Ludwig W, Amann R I, Schleifer K H
Lehrstuhl für Mikrobiologie, Technische Universität München, Germany.
Int J Syst Bacteriol. 1994 Apr;44(2):330-7. doi: 10.1099/00207713-44-2-330.
A comparative analysis of seven new 16S rRNA gene sequences of pathogenic Vibrio species with previously published vibrio sequences confirmed that Vibrio vulnificus represents a group that is not closely related to the core organisms of the genus Vibrio. In addition, we found that V. vulnificus, Listonella (Vibrio) anguillarum and Vibrio diazotrophicus branch off separately from the core group. A comparison of the 16S rRNA gene sequences of V. vulnificus strains belonging to biotypes 1 and 2 revealed that the sequences of all but four biotype 1 strains were identical to each other but slightly different (17 bases) from the sequences of the rest of the V. vulnificus strains investigated. In addition, the sequences of variable regions of the 23S rRNA genes of Vibrio fluvialis, Vibrio furnissii, Vibrio harveyi, Vibrio cholerae, and V. vulnificus C7184 and TW1 were determined, aligned, and compared with all available bacterial 23S rRNA sequences in order to search for specific target sites. As a result, four oligonucleotide probes specific for V. vulnificus were synthesized, and the specificities of these probes were evaluated by dot blot hybridization to membrane-bound RNAs from 21 V. vulnificus strains, 13 strains belonging to other Vibrio species, 61 strains belonging to species that are members of the alpha, beta, and gamma subclasses of the Proteobacteria, and 3 eucaryotic microorganisms. Two probes hybridized with all of the V. vulnificus strains tested, and the other two probes distinguished V. vulnificus biotype 1 strains from all other organisms. In situ identification of V. vulnificus by using tetramethylrhodamine- or fluorescein-labelled oligonucleotides is now possible.
对7种致病性弧菌新的16S rRNA基因序列与先前发表的弧菌序列进行的比较分析证实,创伤弧菌代表一个与弧菌属核心生物关系不密切的类群。此外,我们发现创伤弧菌、鳗弧菌(原名鳗利斯顿氏菌,属弧菌属)和固氮弧菌与核心类群分开分支。对生物型1和2的创伤弧菌菌株的16S rRNA基因序列进行比较发现,除4株生物型1菌株外,所有其他生物型1菌株的序列彼此相同,但与所研究的其他创伤弧菌菌株的序列略有不同(相差17个碱基)。此外,还测定了河流弧菌、弗氏弧菌、哈维氏弧菌、霍乱弧菌以及创伤弧菌C7184和TW1的23S rRNA基因可变区的序列,进行了比对,并与所有可用的细菌23S rRNA序列进行比较,以寻找特定的靶位点。结果,合成了4种针对创伤弧菌的寡核苷酸探针,并通过斑点杂交对来自21株创伤弧菌菌株、13株其他弧菌属菌株、61株属于变形菌门α、β和γ亚类的菌株以及3种真核微生物的膜结合RNA进行检测,评估了这些探针的特异性。两种探针与所有测试的创伤弧菌菌株杂交,另外两种探针可将生物型1的创伤弧菌菌株与所有其他生物区分开来。现在可以使用四甲基罗丹明或荧光素标记的寡核苷酸对创伤弧菌进行原位鉴定。