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Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector.

机译:通过使用正选择自杀载体构建肠致病性大肠杆菌的eae缺失突变体。

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摘要

The ability to attach to epithelial cells, efface the microvillus surface, and disrupt the underlying cytoskeleton is characteristic of enteropathogenic Escherichia coli (EPEC). Recently, eae, a gene necessary for this phenomenon, was described (A. E. Jerse, J. Yu, B. D. Tall, and J. B. Kaper, Proc. Natl. Acad. Sci. USA 87:7839-7843, 1990). We report the use of a novel suicide vector containing the pir-dependent R6K replicon and the sacB gene of Bacillus subtilis to construct an eae deletion mutant of EPEC. This system enables positive selection for the loss of vector sequences. The resulting mutant, CVD206, is indistinguishable from the wild-type strain except for the loss of a 94-kDa outer membrane protein and attaching and effacing ability. Both the 94-kDa outer membrane protein and attaching and effacing ability are restored upon reintroduction of the eae gene on a plasmid. These results confirm the role of the eae gene in the attaching and effacing activity of EPEC and establish the utility of a new system for the construction of deletion mutations.
机译:附着于上皮细胞,抹去微绒毛表面并破坏潜在的细胞骨架的能力是肠致病性大肠杆菌(EPEC)的特征。最近,描述了eae,该基因是该现象所必需的基因(A.E.Jerse,J.Yu,B.D.Tall和J.B.Kaper,美国国家科学院院刊87:7839-7843,1990)。我们报告了使用新型的自杀载体,该载体包含依赖于pir的R6K复制子和枯草芽孢杆菌的sacB基因,以构建EPEC的eae缺失突变体。该系统使得能够正确选择载体序列的丢失。产生的突变体CVD206与野生型菌株没有区别,除了94 kDa外膜蛋白的损失以及附着和消失能力。在质粒上重新导入eae基因后,94-kDa的外膜蛋白以及附着和消失能力都得以恢复。这些结果证实了eae基因在EPEC的附着和消失活性中的作用,并建立了用于构建缺失突变的新系统的实用性。

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