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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Evolutionary mapping of the SHV beta-lactamase and evidence for two separate IS26-dependent blaSHV mobilization events from the Klebsiella pneumoniae chromosome.
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Evolutionary mapping of the SHV beta-lactamase and evidence for two separate IS26-dependent blaSHV mobilization events from the Klebsiella pneumoniae chromosome.

机译:SHVβ-内酰胺酶的进化作图和肺炎克雷伯菌的两个独立的IS26依赖性blaSHV动员事件的证据。

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摘要

OBJECTIVES: To determine the most likely evolutionary pathway that has led to the development of extended-spectrum SHV derivatives, and to the mobilization of blaSHV. MATERIALS AND METHODS: Evolutionary mapping used a shortest-path analysis of aligned blaSHV variants, and other basic bioinformatic approaches, such as CLUSTAL W and Blast were employed. RESULTS: Two main branches of the blaSHV evolutionary tree were located; both are derived from variant blaSHV-1 alleles. Identical mutations, responsible for extended-spectrum SHV substrate profiles, have been selected independently in each branch. There is evidence for a pool of non-mobile blaSHV framework sequences. Analysis of the genome sequence of Klebsiella pneumoniae confirms the chromosomal origin of blaSHV, whose mobilization has occurred at least twice, once for each of the main evolutionary branches. Both these mobilization events have been catalysed by IS26. Evolution of blaSHV to give common extended-spectrum variants is most likely to have occurred following mobilization. CONCLUSIONS: These data shed new light on the evolution and mobilization of blaSHV, and these observations may be useful in predicting what might happen in future, both for blaSHV, and for other beta-lactamase genes.
机译:目的:确定最可能的进化途径,导致发展广谱SHV衍生物,并动员blaSHV。材料与方法:进化图谱使用最短路径分析的对齐的blaSHV变异,并采用了其他基本的生物信息学方法,例如CLUSTAL W和Blast。结果:blaSHV进化树的两个主要分支被定位;两者均源自变体blaSHV-1等位基因。在每个分支中都独立选择了导致大范围SHV底物分布的相同突变。有证据表明存在非移动的blaSHV框架序列。对肺炎克雷伯菌的基因组序列的分析证实了blaSHV的染色体起源,其动员至少发生了两次,每个主要进化分支发生一次。这两个动员事件都被IS26催化。 blaSHV进化为常见的广谱变体最有可能发生在动员之后。结论:这些数据为blaSHV的进化和动员提供了新的思路,这些观察结果可能对预测blaSHV和其他β-内酰胺酶基因的未来可能有用。

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