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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Overexpression of vmeTUV encoding a multidrug efflux transporter of Vibrio parahaemolyticus causes bile acid resistance
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Overexpression of vmeTUV encoding a multidrug efflux transporter of Vibrio parahaemolyticus causes bile acid resistance

机译:vmetuv的过度表达编码vibrio parahaemolyticus的vibrio vibrio的流出转运蛋白导致胆汁酸性抗性

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摘要

We isolated deoxycholate-resistant mutants from Vibrio parahaemolyticus RTM34, which lacks four multidrug efflux transporters belonging to the resistance nodulation cell division (RND) family. RTM34 showed sensitivity to many antimicrobial agents such as cholate and deoxycholate. Deoxycholate-resistant mutants from RTM34 have elevated resistance to not only deoxycholate, but also antibiotics, disinfectants, and dyes. RT-PCR analysis revealed that the expression of vmeV, which encodes an RND-type multidrug efflux transporter, was higher in deoxycholate-resistant mutants than in parental strain RTM34. VPA0806, designated as vdeR, was located upstream of the vmeTUV operon, was oriented in the opposite direction of this operon, and encoded a putative TetR family transcriptional regulator. We determined the nucleotide sequences of vdeR and the vmeT promoter region in the genomes of deoxycholate-resistant mutants. A point mutation was identified in vdeR of seven deoxycholate-resistant mutants and a deletion mutation was identified in vdeR of one deoxycholate-resistant mutant. Since most mutations cause a frame shift mutation and premature stop codon, the function of VdeR is thought to be lost in these mutants. Taken together, the results of the present study indicate that deoxycholate resistance in these mutants was due to the overexpression of vmeTUV caused by a loss in the repression by VdeR.
机译:我们从Vibrio Parahaemolyticus RTM34中分离脱氧抗官果突变体,其缺乏属于抗性染色细胞分裂(RND)家族的四种多药中流出转运蛋白。 RTM34对许多抗微生物剂如胆酸盐和脱氧胆酸盐表现出敏感性。来自RTM34的脱氧胆酸盐突变体具有耐高采烈的耐氧合含量,也具有抗生素,消毒剂和染料。 RT-PCR分析表明,在脱氧溶解突变体中,耐氧合型多药中输送器的VMEV的表达高于治疗菌株RTM34。指定为vder的VPA0806位于VMETUV操纵子的上游,沿该操纵子的相反方向定向,并编码推定的十六族转录调节器。我们确定了脱氧胆酸盐突变体的基因组中的vder和v met启动子区域的核苷酸序列。在氧氧化含氧晶型突变体的vder中鉴定了一种点突变,并且在一种脱氧氧酸盐抗突变体的vder中鉴定了缺失突变。由于大多数突变导致框架移位突变和过早的止转密码子,因此被认为在这些突变体中丢失了vder的功能。在一起,本研究结果表明,这些突变体中的脱氧胆酸酯抗性是由于vets抑制损失引起的vmetuv的过表达。

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