Picard B, Journet-Mancy C, Picard-Pasquier N, Goullet P
Laboratoire de Microbiologie, Faculté de Médecine Xavier Bichat (Université Paris VII), France.
J Gen Microbiol. 1993 Dec;139(12):3079-88. doi: 10.1099/00221287-139-12-3079.
Escherichia coli strains causing human extra-intestinal infections may be divided into two groups, B1 and B2 according to the electrophoretic patterns of carboxylesterase B. This study compares the restriction fragment length polymorphism (RFLP) of ribosomal DNA (rDNA) for 45 B1 strains and 45 B2 strains to examine the genetic structure of B2 strains and to distinguish them from B1 strains. The isolates were chosen for diversity in their allozymes of esterases, B, A, C and I, their production of virulence factors (alpha-haemolysin, mannose resistant haemagglutinin and cytotoxic necrotizing factor) and certain O antigens, and their pathological and geographical origins. DNA was digested with HindIII and BamHI restriction enzymes and analysed by Southern blotting. The resulting rDNA RFLP patterns of B2 strains were distinct from those of the B1 strains. Moreover, the B2 strains appeared to be less heterogeneous than the B1 strains. The B2 strains gave 13 ribotypes (resulting from the combination of the rDNA RFLP patterns obtained with HindIII and BamHI digestions) while the B1 strains gave 32 ribotypes. Correspondence analysis of the data showed that several clusters of strains were identified in the B2 strains by particular ribotypes, certain associations of esterase B and A electrophoretic variants, O serotypes and virulence factor production. In contrast, these parameters appeared to be unrelated in the B1 strains, reflecting their heterogeneity. These findings, which differentiate two levels of genetic heterogeneity within E. coli pathogenic isolates, indicate that the B2 strains constitute a phylogenetically distinct group within the species.
根据羧酸酯酶B的电泳图谱,可将引起人类肠外感染的大肠杆菌菌株分为B1和B2两组。本研究比较了45株B1菌株和45株B2菌株核糖体DNA(rDNA)的限制性片段长度多态性(RFLP),以研究B2菌株的遗传结构,并将它们与B1菌株区分开来。这些分离株因其酯酶B、A、C和I的别构酶、毒力因子(α-溶血素、甘露糖抗性血凝素和细胞毒性坏死因子)的产生、某些O抗原以及它们的病理和地理来源的多样性而被选取。用HindIII和BamHI限制性内切酶消化DNA,并通过Southern印迹法进行分析。B2菌株产生的rDNA RFLP图谱与B1菌株不同。此外,B2菌株的异质性似乎比B1菌株小。B2菌株产生了13种核糖体分型(由HindIII和BamHI消化获得的rDNA RFLP图谱组合而成),而B1菌株产生了32种核糖体分型。对数据的对应分析表明,通过特定的核糖体分型、酯酶B和A电泳变体的某些组合、O血清型和毒力因子产生,在B2菌株中鉴定出了几个菌株簇。相比之下,这些参数在B1菌株中似乎没有关联,这反映了它们的异质性。这些发现区分了大肠杆菌致病分离株内遗传异质性的两个水平,表明B2菌株在该物种内构成了一个系统发育上不同的群体。