Sato T, Sato M, Matsuyama J, Kalfas S, Sundqvist G, Hoshino E
Department of Oral Microbiology, Niigata University School of Dentistry, Japan.
Oral Microbiol Immunol. 1998 Feb;13(1):23-9. doi: 10.1111/j.1399-302x.1998.tb00746.x.
Restriction fragment-length polymorphism (RFLP) analysis of 16S rDNA amplified by polymerase chain reaction was used to generate restriction profiles of the type strains of oral asaccharolytic Eubacterium species, that is, Eubacterium brachy, Eubacterium exiguum, Eubacterium lentum, Eubacterium minutum, Eubacterium nodatum, Eubacterium saphenum, Eubacterium timidum and 33 asaccharolytic Eubacterium strains isolated from oral sites. The 16S rRNA gene sequences from isolated genomic DNA samples were amplified by polymerase chain reaction (PCR). PCR products were purified and characterized by single digestions with 7 restriction endonucleases. Among the 7 endonucleases, HpaII was found to discriminate the respective reference strains. Twenty-three isolates, out of 33, were assigned to one of the reference species, on the basis of their restriction profiles by digestion with HpaII. The remaining 10 isolates could not be assigned to any of the established species and constituted 4 distinct groups, each of which may be a new species.
采用聚合酶链反应扩增16S rDNA的限制性片段长度多态性(RFLP)分析,对口腔中不产糖的真杆菌属模式菌株,即短真杆菌、微小真杆菌、迟缓真杆菌、极小真杆菌、结节真杆菌、隐匿真杆菌、胆小真杆菌以及从口腔部位分离出的33株不产糖真杆菌菌株进行限制性图谱分析。从分离的基因组DNA样本中,通过聚合酶链反应(PCR)扩增16S rRNA基因序列。PCR产物经纯化后,用7种限制性内切酶进行单酶切鉴定。在这7种内切酶中,发现HpaII能区分各参考菌株。33株分离株中,有23株根据其经HpaII酶切后的限制性图谱被归入某一参考菌种。其余10株分离株无法归入任何已确定的菌种,它们构成了4个不同的组,每组可能代表一个新菌种。