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对铜绿假单胞菌的质粒pAMBL1和pAMBL2进行测序,发现blaVIM-1扩增导致高水平碳青霉烯耐药性。

Sequencing of plasmids pAMBL1 and pAMBL2 from Pseudomonas aeruginosa reveals a blaVIM-1 amplification causing high-level carbapenem resistance.

作者信息

San Millan Alvaro, Toll-Riera Macarena, Escudero Jose Antonio, Cantón Rafael, Coque Teresa M, MacLean R Craig

机构信息

Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK

Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK.

出版信息

J Antimicrob Chemother. 2015 Nov;70(11):3000-3. doi: 10.1093/jac/dkv222. Epub 2015 Jul 24.

Abstract

BACKGROUND

Carbapenemases are a major concern for the treatment of infectious diseases caused by Gram-negative bacteria. Although plasmids are responsible for the spread of resistance genes among these pathogens, there is limited information on the nature of the mobile genetic elements carrying carbapenemases in Pseudomonas aeruginosa.

METHODS

We combined data from two different next-generation sequencing platforms, Illumina HiSeq2000 and PacBio RSII, to obtain the complete nucleotide sequences of two blaVIM-1-carrying plasmids (pAMBL1 and pAMBL2) isolated from P. aeruginosa clinical isolates.

RESULTS

Plasmid pAMBL1 has 26 440 bp and carries a RepA_C family replication protein. pAMBL1 is similar to plasmids pNOR-2000 and pKLC102 from P. aeruginosa and pAX22 from Achromobacter xylosoxidans, which also carry VIM-type carbapenemases. pAMBL2 is a 24 133 bp plasmid with a replication protein that belongs to the Rep_3 family. It shows a high degree of homology with a fragment of the blaVIM-1-bearing plasmid pPC9 from Pseudomonas putida. Plasmid pAMBL2 carries three copies of the blaVIM-1 cassette in an In70 class 1 integron conferring, unlike pAMBL1, high-level resistance to carbapenems.

CONCLUSIONS

We present two new plasmids coding for VIM-1 carbapenemase from P. aeruginosa and report that the presence of three copies of blaVIM-1 in pAMBL2 produces high-level resistance to carbapenems.

摘要

背景

碳青霉烯酶是治疗革兰氏阴性菌引起的传染病的主要关注点。虽然质粒负责这些病原体中耐药基因的传播,但关于铜绿假单胞菌中携带碳青霉烯酶的移动遗传元件的性质的信息有限。

方法

我们结合了来自两个不同的下一代测序平台Illumina HiSeq2000和PacBio RSII的数据,以获得从铜绿假单胞菌临床分离株中分离出的两个携带blaVIM-1的质粒(pAMBL1和pAMBL2)的完整核苷酸序列。

结果

质粒pAMBL1有26440 bp,携带一个RepA_C家族复制蛋白。pAMBL1与来自铜绿假单胞菌的质粒pNOR-2000和pKLC102以及来自木糖氧化无色杆菌的pAX22相似,它们也携带VIM型碳青霉烯酶。pAMBL2是一个24133 bp的质粒,其复制蛋白属于Rep_3家族。它与来自恶臭假单胞菌的携带blaVIM-1的质粒pPC9的一个片段显示出高度同源性。与pAMBL1不同,质粒pAMBL2在一个In70 1类整合子中携带三个blaVIM-1盒式结构,赋予对碳青霉烯类的高水平耐药性。

结论

我们展示了两个来自铜绿假单胞菌的编码VIM-1碳青霉烯酶的新质粒,并报告pAMBL2中三个blaVIM-1拷贝的存在产生了对碳青霉烯类的高水平耐药性。

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