首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Transposition and homologous recombination drive evolution of pUO-StVR2, a multidrug resistance derivative of pSLT, the virulence plasmid specific of Salmonella enterica serovar Typhimurium
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Transposition and homologous recombination drive evolution of pUO-StVR2, a multidrug resistance derivative of pSLT, the virulence plasmid specific of Salmonella enterica serovar Typhimurium

机译:转座和同源重组驱动pSLT的多药抗性衍生物pUO-StVR2的进化,pSLT是肠炎沙门氏菌血清鼠伤寒沙门氏菌特异的毒力质粒

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摘要

Five variants of a resistant derivative of pSLT (termed pUO-StVR2) were detected in clinical isolates of Salmonella enterica serovar Typhimurium recovered in Spain. The structure of these variants revealed the involvement of IS1, IS26 and Tn21-like transposition, as Well as homologous recombination in the generation of deletions, inversions and insertions which, depending on the variant, affected an orf of unknown function, genes encoding a possible iron acquisition system, and/or resistance properties. These variants, which appeared at a relatively low frequency, can be used as a model to understand the co-selection mechanisms that are helping to maintain multidrug resistance in bacterial pathogens, despite the structural instability of the responsible DNA. (C) 2014 Elsevier B.V. All rights reserved.
机译:在西班牙回收的肠炎沙门氏菌血清型鼠伤寒沙门氏菌临床分离物中检测到pSLT抗性衍生物的五个变体(称为pUO-StVR2)。这些变体的结构揭示了IS1,IS26和Tn21样转座的参与以及在缺失,转化和插入中的同源重组,这取决于变体,影响未知功能的orf,编码可能的基因铁采集系统和/或电阻特性。这些变异以相对较低的频率出现,可以用作模型来理解共同选择机制,尽管负责DNA的结构不稳定,但这些共同选择机制有助于在细菌病原体中维持多药耐药性。 (C)2014 Elsevier B.V.保留所有权利。

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