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编码霍乱弧菌O1型甘露糖-岩藻糖抗性血凝素的核苷酸序列及突变体的构建

Nucleotide sequence encoding the mannose-fucose-resistant hemagglutinin of Vibrio cholerae O1 and construction of a mutant.

作者信息

Franzon V L, Barker A, Manning P A

机构信息

Department of Microbiology and Immunology, University of Adelaide, Australia.

出版信息

Infect Immun. 1993 Jul;61(7):3032-7. doi: 10.1128/iai.61.7.3032-3037.1993.

Abstract

The region of DNA encoding the mannose-fucose-resistant hemagglutinin (MFRHA) of Vibrio cholerae O1 has been localized, and the nucleotide sequence has been determined. The region contains a single open reading frame encoding 230 amino acids, corresponding to a protein of 26.9 kDa. The N terminus of this protein is atypical for a protein localized in the outer membrane. A mutant lacking MFRHA activity has been constructed by allelic exchange after inactivation via the insertion of a kanamycin resistance gene cartridge. The MFRHA-negative mutant has been assessed for virulence in the infant mouse cholera model. This mutant shows a marked defect in its ability to persist in the infant mouse gut and is incapable of competing with the wild-type organism, even when given in 25-fold excess. This defect also leads to a > 100-fold increase in the 50% lethal dose. These data suggest that the MFRHA is an important colonization factor in the infant mouse model.

摘要

霍乱弧菌O1型编码甘露糖-岩藻糖抗性血凝素(MFRHA)的DNA区域已被定位,并确定了核苷酸序列。该区域包含一个单一的开放阅读框,编码230个氨基酸,对应于一个26.9 kDa的蛋白质。该蛋白质的N末端对于定位在外膜的蛋白质来说是非典型的。通过插入卡那霉素抗性基因盒使其失活后,经等位基因交换构建了一个缺乏MFRHA活性的突变体。已在幼鼠霍乱模型中评估了MFRHA阴性突变体的毒力。该突变体在幼鼠肠道中持续存在的能力存在明显缺陷,即使给予25倍过量也无法与野生型菌株竞争。这种缺陷还导致50%致死剂量增加了100倍以上。这些数据表明,MFRHA是幼鼠模型中的一个重要定植因子。

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