[高致病性岛型缺失肠聚集性大肠杆菌O42突变株的构建与鉴定]。

Jing Hu, Shou-yi Yu, Biao Kan, Zhi-hua Liu
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引用次数: 0

摘要

目的:构建并鉴定框架内缺失高致病性岛(HPI)的肠聚集性大肠杆菌(EAggEC) O42突变株。方法:将卡那霉素耐药基因(kan)插入irp8和irp5基因序列之间,作为两个同源序列,将重组序列亚克隆到自杀载体pCVD442中,构建重组质粒pCO85。通过同源重组和连接动员,筛选到HPI核心区域缺失约24 kb的EAO85突变体,该突变体横跨irp8至irp5序列。结果:EAggEC O42的Irp8和irp5基因通过pCO85联合动员与蔗糖选择性交换。EAO85突变体的鉴定是由于它们无法产生带有HPI内部区域特异性引物的PCR产物。结论:我们成功构建了一个帧内缺失HPI的EAggEC O42突变体,这可能有助于探索HPI在EAggEC菌株中的作用。
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[Construction and characterization of mutant Enteroaggregative E. coli O42 strain with high-pathogenicity island deletion].

Objective: To construct and characterize a mutant Enteroaggregative E. coli(EAggEC) O42 strain with in-frame deletion of high-pathogenicity island (HPI).

Methods: The kanamycin resistance gene (kan) was inserted between the sequences of irp8 and irp5 genes as the two homologous sequences for construction of the recombinant plasmid pCO85 by subcloning the recombined sequence into the suicide vector pCVD442. By homologous recombination and conjunction mobilization, EAO85 mutant with deletion of the core region of HPI about 24 kb spanning from irp8 to irp5 sequences was screened.

Results: Irp8 and irp5 genes of EAggEC O42 were exchanged by pCO85 by conjunction mobilization with the selection by sucrose. The EAO85 mutant was identified by their failure to yield PCR products with primers specific for the internal regions of HPI.

Conclusion: We have successfully constructed a mutant of EAggEC O42 strain with HPI in-frame deletion, which may facilitate the exploration of the role of HPI in EAggEC strain.

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