Vaneechoutte M, Riegel P, de Briel D, Monteil H, Verschraegen G, De Rouck A, Claeys G
Department of Clinical Chemistry, Microbiology and Immunology, University Hospital, State University Ghent, Belgium.
Res Microbiol. 1995 Oct;146(8):633-41. doi: 10.1016/0923-2508(96)81061-8.
The 16S rRNA genes (rDNA) of 50 strains belonging to 26 different coryneform bacterial species and genomospecies and of the type strain of Rhodococcus equi were enzymatically amplified. Amplified rDNA restriction analysis (ARDRA) with the enzymes AluI, CfoI and RsaI was carried out. The combination of the ARDRA patterns obtained after restriction with these three different enzymes enabled the differentiation between the following species: Corynebacterium accolens (number of strains = 2), C. afermentans subsp. afermentans (2), C. afermentans subsp. lipophilum (2), C. amycolatum (3), CDC coryneform group ANF-1-like (1), CDC coryneform group ANF-3-like (1), C. cystitidis (1), C. diphtheriae (4), C. jeikeium (3), C. macginleyi (2), C. minutissimum (1), C. pilosum (1), C. pseudotuberculosis (2), C. renale (2), C. striatum (2), C. urealyticum (3), C. xerosis (1), CDC coryneform groups B-1 (2), B-3 (2), F-1, genomospecies 1 and 2 (6), G, genomospecies 1 (1) and G, genomospecies 2 (2). The following strains or species could not be differentiated from each other: C. pseudodiphtheriticum (2) from C. propinquum (former CDC coryneform group ANF-3) (2), CDC coryneform group F-1, genomospecies 1 (4) from genomospecies 2 (2) and C. jeikeium genomospecies A (1) from genomospecies C (2). ARDRA may represent a possible alternative for identification of coryneforms, since this technique enabled the identification of most coryneforms tested and since DNA extraction (i.e. cell lysis by boiling), amplification, restriction and electrophoresis can be carried out within 8 hours. This might allow quick identification of C. diphtheriae and other possible pathogens of the genus Corynebacterium.
对属于26个不同棒状细菌物种和基因组种的50株菌株以及马红球菌模式菌株的16S rRNA基因(rDNA)进行了酶促扩增。使用AluI、CfoI和RsaI酶进行扩增rDNA限制性分析(ARDRA)。用这三种不同酶进行限制性酶切后获得的ARDRA图谱组合能够区分以下物种:粘附棒状杆菌(菌株数 = 2)、发酵棒状杆菌发酵亚种(2)、发酵棒状杆菌嗜脂亚种(2)、无枝菌酸棒状杆菌(3)、疾病控制和预防中心(CDC)棒状菌群ANF-1样(1)、CDC棒状菌群ANF-3样(1)、膀胱棒状杆菌(1)、白喉棒状杆菌(4)、杰氏棒状杆菌(3)、麦氏棒状杆菌(2)、极小棒状杆菌(1)、毛状棒状杆菌(1)、假结核棒状杆菌(2)、肾棒状杆菌(2)、纹带棒状杆菌(2)、解脲棒状杆菌(3)、干燥棒状杆菌(1)、CDC棒状菌群B-1(2)、B-3(2)、F-1、基因组种1和2(6)、G、基因组种1(1)和G、基因组种2(2)。以下菌株或物种彼此无法区分:假白喉棒状杆菌(2)与近似棒状杆菌(原CDC棒状菌群ANF-3)(2)、CDC棒状菌群F-1、基因组种1(4)与基因组种2(2)以及杰氏棒状杆菌基因组种A(1)与基因组种C(2)。ARDRA可能是鉴定棒状杆菌的一种可行替代方法,因为该技术能够鉴定大多数测试的棒状杆菌,并且DNA提取(即通过煮沸进行细胞裂解)、扩增、限制性酶切和电泳可在8小时内完成。这可能有助于快速鉴定白喉棒状杆菌和棒状杆菌属的其他可能病原体。