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VEB-1的分子与生化特性,一种由大肠杆菌整合子基因编码的新型A类超广谱β-内酰胺酶

Molecular and biochemical characterization of VEB-1, a novel class A extended-spectrum beta-lactamase encoded by an Escherichia coli integron gene.

作者信息

Poirel L, Naas T, Guibert M, Chaibi E B, Labia R, Nordmann P

机构信息

Service de Bactériologie-Virologie, Hôpital de Bicêtre, Faculté de Médecine Paris-Sud, France.

出版信息

Antimicrob Agents Chemother. 1999 Mar;43(3):573-81. doi: 10.1128/AAC.43.3.573.

Abstract

A clinical isolate, Escherichia coli MG-1, isolated from a 4-month-old Vietnamese orphan child, produced a beta-lactamase conferring resistance to extended-spectrum cephalosporins and aztreonam. In a disk diffusion test, a typical synergistic effect between ceftazidime or aztreonam and clavulanic acid was observed along with an unusual synergy between cefoxitin and cefuroxime. The gene for VEB-1 (Vietnamese extended-spectrum beta-lactamase) was cloned and expressed in E. coli JM109. The recombinant plasmid pRLT1 produced a beta-lactamase with a pI of 5.35 and conferred high-level resistance to extended-spectrum (or oxyimino) cephalosporins and to aztreonam. Vmax values for extended-spectrum cephalosporins were uncommonly high, while the affinity of the enzyme for ceftazidime and aztreonam was relatively low. blaVEB-1 showed significant homology at the DNA level with only blaPER-1 and blaPER-2. Analysis of the deduced protein sequence showed that VEB-1 is a class A penicillinase having very low levels of homology with any other known beta-lactamases. The highest percentage of amino acid identity was 38% with PER-1 or PER-2, two uncommon class A extended-spectrum enzymes. Exploration of the genetic environment of blaVEB-1 revealed the presence of gene cassette features, i.e., (i) a 59-base element associated with blaVEB-1; (ii) a second 59-base element just upstream of blaVEB-1, likely belonging to the aacA1-orfG gene cassette; (iii) two core sites (GTTRRRY) on both sides of blaVEB-1; and (iv) a second antibiotic resistance gene 3' of blaVEB-1, aadB. blaVEB-1 may therefore be the first class A extended-spectrum beta-lactamase that is part of a gene cassette, which itself is likely to be located on a class 1 integron, as sulfamide resistance may indicate. Furthermore, blaVEB-1 is encoded on a large (> 100-kb) transferable plasmid found in a Klebsiella pneumoniae MG-2 isolated at the same time from the same patient, indicating a horizontal gene transfer.

摘要

从一名4个月大的越南孤儿身上分离出的临床分离株大肠杆菌MG-1,产生了一种能赋予对超广谱头孢菌素和氨曲南耐药性的β-内酰胺酶。在纸片扩散试验中,观察到头孢他啶或氨曲南与克拉维酸之间有典型的协同作用,同时头孢西丁和头孢呋辛之间存在不寻常的协同作用。VEB-1(越南超广谱β-内酰胺酶)基因被克隆并在大肠杆菌JM109中表达。重组质粒pRLT1产生了一种pI为5.35的β-内酰胺酶,并赋予对超广谱(或氧亚氨基)头孢菌素和氨曲南的高水平耐药性。超广谱头孢菌素的Vmax值异常高,而该酶对头孢他啶和氨曲南的亲和力相对较低。blaVEB-1在DNA水平上仅与blaPER-1和blaPER-2有显著同源性。对推导的蛋白质序列分析表明,VEB-1是一种A类青霉素酶,与任何其他已知的β-内酰胺酶的同源性都很低。与PER-1或PER-2这两种不常见的A类超广谱酶的氨基酸同一性最高百分比为38%。对blaVEB-1基因环境的探索揭示了基因盒特征的存在,即:(i)与blaVEB-1相关的一个59碱基元件;(ii)在blaVEB-1上游的第二个59碱基元件,可能属于aacA1-orfG基因盒;(iii)blaVEB-1两侧的两个核心位点(GTTRRRY);以及(iv)blaVEB-1 3'端的第二个抗生素耐药基因aadB。因此,blaVEB-1可能是第一个作为基因盒一部分的A类超广谱β-内酰胺酶,该基因盒本身可能位于1类整合子上,如磺胺耐药性可能表明的那样。此外,blaVEB-1编码在一个同时从同一患者分离出的肺炎克雷伯菌MG-2中发现的大(>100 kb)可转移质粒上,表明存在水平基因转移。

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