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肺炎克雷伯菌多重耐药质粒pJHCMW1的全核苷酸序列

Complete nucleotide sequence of Klebsiella pneumoniae multiresistance plasmid pJHCMW1.

作者信息

Sarno Renee, McGillivary Glen, Sherratt David J, Actis Luis A, Tolmasky Marcelo E

机构信息

Department of Biological Science, Institute of Molecular Biology and Nutrition, College of Natural Science and Mathematics, California State University Fullerton, Fullerton, California 92834-6850, USA.

出版信息

Antimicrob Agents Chemother. 2002 Nov;46(11):3422-7. doi: 10.1128/AAC.46.11.3422-3427.2002.

Abstract

The multiresistance plasmid pJHCMW1, harbored by a clinical Klebsiella pneumoniae strain isolated from a neonate with meningitis, was sequenced. A circular sequence of 11,354 bp was generated, of which 7,993 bp make up Tn1331, a transposon including the antibiotic resistance genes aac(6')-Ib, aadA1, bla(OXA-9), and bla(TEM-1). The gene aac(6')-Ib is included in a gene cassette, and both aadA1 and bla(OXA-9) are included in a single-gene cassette that may have arisen as a consequence of a recombination event involving two integrons. The pJHCMW1 plasmid replicates through a ColE1-like RNA-regulated mechanism, includes a functional oriT, and two loci with similarity to XerCD site-specific recombination target sites involved in plasmid stabilization by the resolution of multimers. One of these two loci, mwr, is active and has been the subject of previous studies, and the other, dxs, is not functional but binds the recombinase XerD with low affinity. Two additional open reading frames were identified, one with low similarity to two hypothetical membrane proteins from Mycobacterium tuberculosis and Mycobacterium leprae and the other with low similarity to psiB, a gene encoding a function that facilitates the establishment of the transferring plasmid in the recipient bacterial cell during the process of conjugation.

摘要

对从一名患脑膜炎的新生儿分离出的临床肺炎克雷伯菌菌株携带的多重耐药质粒pJHCMW1进行了测序。生成了一个11354 bp的环状序列,其中7993 bp构成转座子Tn1331,该转座子包含抗生素抗性基因aac(6')-Ib、aadA1、bla(OXA-9)和bla(TEM-1)。基因aac(6')-Ib包含在一个基因盒中,而aadA1和bla(OXA-9)都包含在一个单基因盒中,该单基因盒可能是由于涉及两个整合子的重组事件而产生的。pJHCMW1质粒通过一种类似ColE1的RNA调控机制进行复制,包含一个功能性oriT,以及两个与XerCD位点特异性重组靶位点相似的位点,这些位点通过多聚体的分解参与质粒的稳定。这两个位点之一,即mwr,是活跃的,并且是先前研究的对象,另一个位点dxs没有功能,但以低亲和力结合重组酶XerD。还鉴定出另外两个开放阅读框,一个与来自结核分枝杆菌和麻风分枝杆菌的两个假定膜蛋白具有低相似性,另一个与psiB具有低相似性,psiB是一个编码在接合过程中促进转移质粒在受体细菌细胞中建立功能的基因。

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