Pearce M A, Dixon R A, Gharbia S E, Shah H N, Devine D A
Department of Biomedical Sciences, University of Bradford, United Kingdom.
Oral Microbiol Immunol. 1996 Jun;11(3):135-41. doi: 10.1111/j.1399-302x.1996.tb00348.x.
Restriction endonuclease analysis, rRNA gene restriction analysis (ribotyping), multilocus enzyme electrophoresis and lipase production were investigated for their potential to differentiate isolates belonging to the closely-related species Prevotella intermedia and Prevotella nigrescens. Of 122 strains identified originally as P. intermedia, 52 were assigned to P. intermedia and 68 to P. nigrescens using multilocus enzyme electrophoresis. All 39 P. intermedia and 52 out of 53 P. nigrescens tested produced lipase. Restriction endonuclease analysis identified clonal variants, but did not facilitate the differentiation of strains into species. Taq I ribotyping of 99 strains revealed that all P. intermedia demonstrated a species-specific fragment of 0.40 kbp, which was always associated with a second fragment of 0.57 kbp, and all P. nigrescens tested shared a species-specific fragment of 2.21 kbp. Two strains atypical by multilocus enzyme electrophoresis had none of the above species-specific fragments. Thus, lipase production and restriction endonuclease analysis did not distinguish between P. intermedia and P. nigrescens, but Taq I ribotyping did and also allowed the characterization of individual strains.
研究了限制性内切酶分析、rRNA基因限制性分析(核糖分型)、多位点酶电泳和脂肪酶产生情况,以评估其区分密切相关的中间普氏菌和变黑普氏菌菌株的潜力。在最初鉴定为中间普氏菌的122株菌株中,使用多位点酶电泳将52株归为中间普氏菌,68株归为变黑普氏菌。测试的所有39株中间普氏菌和53株变黑普氏菌中的52株都产生脂肪酶。限制性内切酶分析鉴定出了克隆变体,但未有助于将菌株区分为不同物种。对99株菌株进行的Taq I核糖分型显示,所有中间普氏菌都有一个0.40 kbp的物种特异性片段,该片段总是与一个0.57 kbp的第二个片段相关联,并且所有测试的变黑普氏菌都有一个2.21 kbp的物种特异性片段。通过多位点酶电泳鉴定为非典型的两株菌株没有上述任何物种特异性片段。因此,脂肪酶产生和限制性内切酶分析不能区分中间普氏菌和变黑普氏菌,但Taq I核糖分型可以区分,并且还能对单个菌株进行特征描述。