Dewhirst F E, Paster B J, Tzellas N, Coleman B, Downes J, Spratt D A, Wade W G
Int J Syst Evol Microbiol. 2001 Sep;51(Pt 5):1797-1804. doi: 10.1099/00207713-51-5-1797.
The diversity of organisms present in the subgingival pockets of patients with periodontitis and acute necrotizing ulcerative gingivitis (ANUG) were examined previously. The 16S rRNA genes of subgingival plaque bacteria were amplified using PCR with a universal forward primer and a spirochaete-selective reverse primer. The amplified DNA was cloned into Escherichia coli. In one subject with ANUG, 70 clones were sequenced. Seventy-five per cent of the clones were spirochaetal, as expected. Twelve of the remaining clones fell into two clusters that represent novel phylotypes in the family Coriobacteriaceae. The first novel phylotype was most closely related to Atopobium rimae (98% similarity). The phylotype probably represents a novel Atopobium species, but will not be named until cultivable strains are obtained. The second novel phylotype was only 91% similar to described Atopobium species and 84% similar to Coriobacterium glomerans. The 16S rRNA sequences of the type strain of Lactobacillus uli and a strain representing the Moores' Eubacterium group D52 were determined as part of on ongoing sequence analysis of oral bacteria. The sequence for L. uli was more than 99.8% similar to sequences for the second clone phylotype. It therefore appears that the second clone phylotype and L. uli represent the same species. The sequence for the Eubacterium D52 strain was 95.6% similar to that of L. uli. The G+C content of the DNA of L. uli and Eubacterium D52 is 63-64 mol %. These organisms are thus distinct from the neighbouring genus Atopobium, which has a DNA G+C content of 35-46 mol%. A new genus, Olsenella gen. nov., is proposed for these two species on the basis of phenotypic characteristics and 16S rRNA sequence analysis to include Olsenella uli comb. nov. and Olsenella profusa sp. nov.
先前已对牙周炎和急性坏死性溃疡性龈炎(ANUG)患者龈下袋中的微生物多样性进行了检测。使用通用正向引物和螺旋体选择性反向引物通过PCR扩增龈下菌斑细菌的16S rRNA基因。将扩增的DNA克隆到大肠杆菌中。在一名患有ANUG的受试者中,对70个克隆进行了测序。正如预期的那样,75%的克隆是螺旋体。其余克隆中有12个分为两个簇,代表了丙酸杆菌科中的新系统发育型。第一个新系统发育型与纤细阿托波菌关系最为密切(相似度为98%)。该系统发育型可能代表一个新的阿托波菌物种,但在获得可培养菌株之前不会命名。第二个新系统发育型与已描述的阿托波菌物种相似度仅为91%,与球形丙酸杆菌相似度为84%。作为正在进行的口腔细菌序列分析的一部分,测定了尤氏乳杆菌模式菌株和代表穆尔斯真杆菌D52组的一个菌株的16S rRNA序列。尤氏乳杆菌的序列与第二个克隆系统发育型的序列相似度超过99.8%。因此,第二个克隆系统发育型和尤氏乳杆菌似乎代表同一物种。真杆菌D52菌株的序列与尤氏乳杆菌的序列相似度为95.6%。尤氏乳杆菌和真杆菌D52的DNA的G+C含量为63 - 64 mol%。因此,这些微生物与邻近的阿托波菌属不同,后者的DNA G+C含量为35 - 46 mol%。基于表型特征和16S rRNA序列分析,为这两个物种提出了一个新属,即奥尔森菌属(Olsenella gen. nov.),包括新组合的尤氏奥尔森菌(Olsenella uli comb. nov.)和新种丰富奥尔森菌(Olsenella profusa sp. nov.)。