Genetic structures of the B2 and B1 Escherichia coli strains responsible for extra-intestinal infections.

B Picard, C Journet-Mancy, N Picard-Pasquier, P Goullet
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引用次数: 26

Abstract

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.

引起肠外感染的大肠杆菌B2和B1菌株的遗传结构。
根据羧酸酯酶b的电泳模式,可将引起人类肠道外感染的大肠杆菌菌株分为B1和B2两类。本研究比较了45株B1菌株和45株B2菌株的核糖体DNA (rDNA)限制性内切片段长度多态性(RFLP),以研究B2菌株的遗传结构,并将其与B1菌株区分。选择这些分离株的原因在于它们的酯酶B、A、C和I的同工酶的多样性,它们产生的毒力因子(α -溶血素、甘露糖抗性血凝素和细胞毒性坏死因子)和某些O抗原的多样性,以及它们的病理和地理来源。DNA用HindIII和BamHI酶切,用Southern blotting分析。结果表明,B2菌株的rDNA RFLP模式与B1菌株的rDNA RFLP模式不同。此外,B2菌株的异质性明显低于B1菌株。B2菌株有13种核型(由HindIII和BamHI消化得到的rDNA RFLP模式组合而成),而B1菌株有32种核型。数据的对应分析表明,根据特定的核糖型、酯酶B和A的电泳变异、O血清型和毒力因子的产生,在B2菌株中鉴定出了几个菌株群。相比之下,这些参数在B1株中似乎无关,反映了它们的异质性。这些发现区分了大肠杆菌致病性分离株中两个水平的遗传异质性,表明B2菌株在该物种中构成了一个系统发育上不同的群体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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