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完整测序一个携带碳青霉烯酶 NDM-1、ArmA16S RNA 甲基化酶和耐药性-调节-细胞分裂/多药外排泵的 IncHI1 质粒。

Complete sequencing of an IncHI1 plasmid encoding the carbapenemase NDM-1, the ArmA 16S RNA methylase and a resistance-nodulation-cell division/multidrug efflux pump.

机构信息

Department of Infectious, Parasitic and Immuno-Mediated Diseases, Istituto Superiore di Sanità, Rome, Italy.

出版信息

J Antimicrob Chemother. 2013 Jan;68(1):34-9. doi: 10.1093/jac/dks357. Epub 2012 Sep 11.

Abstract

OBJECTIVES

To characterize the pNDM-CIT plasmid identified in Citrobacter freundii carrying genes encoding the metallo-β-lactamase NDM-1 and the 16S RNA methylase ArmA.

METHODS

The complete DNA sequence of pNDM-CIT was obtained by using the 454-Genome Sequencer FLX procedure on a library obtained using plasmid DNA purified from the pNDM-CIT Escherichia coli J53 transconjugant. Contig assembly and predicted gaps were confirmed and filled by PCR-based gap closure. Comparative analysis with IncHI1 incompatibility group plasmids was performed using BLASTN and BLASTP algorithms.

RESULTS

Plasmid pNDM-CIT was 288::920 bp and revealed an IncHI1 plasmid scaffold, showing novel resistance and potential virulence determinants. The bla(NDM-1) gene was identified within a novel genetic context, flanked by a duplication of the class 1 integron on both sides. The replicase gene repAciN, originating from Acinetobacter spp. plasmids, was identified in a close association with the Tn1548::armA transposon and the macrolide resistance mel-mph2 cluster. The same structure was identified in silico from a series of enterobacterial plasmids carrying the armA gene. The repAciN gene probably represents a remnant sign of the original occurrence of the armA gene in Acinetobacter plasmids. A CP4-like prophage sequence was identified in pNDM-CIT, containing a resistance-nodulation-cell division/multidrug resistance (RND/MDR) efflux pump cluster surrounded by two IS1-like elements. This resistance determinant, associated with such a prophage sequence, has never been reported on plasmids.

CONCLUSIONS

Plasmid pNDM-CIT differed significantly from all known bla(NDM-1)-carrying plasmids identified in Enterobacteriaceae, since it combines the metallo-β-lactamase NDM-1, the 16S RNA methylase ArmA and a cryptic prophage carrying the RND/MDR efflux pump.

摘要

目的

对携带编码金属β-内酰胺酶 NDM-1 和 16S RNA 甲基化酶 ArmA 的基因的弗氏柠檬酸杆菌中发现的 pNDM-CIT 质粒进行特征描述。

方法

使用 454-Genome Sequencer FLX 程序,从源自 pNDM-CIT 大肠杆菌 J53 转导体的质粒 DNA 文库中获得 pNDM-CIT 的完整 DNA 序列。通过基于 PCR 的缺口闭合来确认和填补连续序列组装和预测的缺口。使用 BLASTN 和 BLASTP 算法对与 IncHI1 不相容性组质粒进行比较分析。

结果

质粒 pNDM-CIT 为 288::920 bp,显示出 IncHI1 质粒支架,具有新的耐药性和潜在的毒力决定因素。bla(NDM-1)基因位于两侧 1 类整合子重复的新基因环境中。来自不动杆菌属质粒的复制酶基因 repAciN 与 Tn1548::armA 转座子和大环内酯类耐药 mel-mph2 簇紧密相关。在一系列携带 armA 基因的肠杆菌质粒中,通过计算机也鉴定出相同的结构。repAciN 基因可能代表 armA 基因在不动杆菌属质粒中原始发生的残余迹象。在 pNDM-CIT 中鉴定出一个 CP4 样噬菌体序列,其中包含一个耐药性-结节性-细胞分裂/多药耐药 (RND/MDR) 外排泵簇,周围有两个 IS1 样元件。这种耐药决定因素与这种噬菌体序列相关,在质粒上从未报道过。

结论

质粒 pNDM-CIT 与肠杆菌科中发现的所有已知携带 bla(NDM-1)的质粒有很大不同,因为它结合了金属β-内酰胺酶 NDM-1、16S RNA 甲基化酶 ArmA 和携带 RND/MDR 外排泵的隐蔽性噬菌体。

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