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

被引:184
作者
Poirel, L
Naas, T
Guibert, M
Chaibi, EB
Labia, R
Nordmann, P
机构
[1] Hop Bicetre, Fac Med Paris Sud, Serv Bacteriol Virol, F-94275 Le Kremlin Bicetre, France
[2] Hop Antoine Beclere, Fac Med Paris Sud, Serv Bacteriol Virol, F-92141 Clamart, France
[3] MNHN, CNRS, UMR 175, F-29000 Quimper, France
关键词
D O I
10.1128/AAC.43.3.573
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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. V-max values for extended-spectrum cephalosporins were uncommonly high, while the affinity of the enzyme for ceftazidime and aztreonam was relatively low. bla(VEB-1) showed significant homology at the DNA level with only bla(PER-1) and bla(PER-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 bla(VEB-1) revealed the presence of gene cassette features, i.e., (i) a 59-base element associated with bla(VEB-1); (ii) a second 59-base element just upstream of bla(VEB-1) likely belonging to the aacA1-orfG gene cassette; (iii) two core sites (GTTRRRY) on both sides of bla(VEB-1); and (iv) a second antibiotic resistance gene 3' of bla(VEB-1), aadB. bla(VEB-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, bla(VEB-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.
引用
收藏
页码:573 / 581
页数:9
相关论文
共 50 条
[2]  
[Anonymous], PAUP VERSION 3 0 PHY
[3]   CHROMOSOMAL BETA-LACTAMASE OF KLEBSIELLA-OXYTOCA, A NEW CLASS-A ENZYME THAT HYDROLYZES BROAD-SPECTRUM BETA-LACTAM ANTIBIOTICS [J].
ARAKAWA, Y ;
OHTA, M ;
KIDO, N ;
MORI, M ;
ITO, H ;
KOMATSU, T ;
FUJII, Y ;
KATO, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (01) :63-70
[4]   A NOVEL INTEGRON-LIKE ELEMENT CARRYING THE METALLO-BETA-LACTAMASE GENE BLA(IMP) [J].
ARAKAWA, Y ;
MURAKAMI, M ;
SUZUKI, K ;
ITO, H ;
WACHAROTAYANKUN, R ;
OHSUKA, S ;
KATO, N ;
OHTA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1612-1615
[5]   BETA-LACTAMASES - DETERMINATION OF THEIR ISOELECTRIC POINTS [J].
BARTHELEMY, M ;
GUIONIE, M ;
LABIA, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1978, 13 (04) :695-698
[6]   CLOSE AMINO-ACID-SEQUENCE RELATIONSHIP BETWEEN THE NEW PLASMID-MEDIATED EXTENDED-SPECTRUM BETA-LACTAMASE-BULLET-MEN-1 AND CHROMOSOMALLY ENCODED ENZYMES OF KLEBSIELLA-OXYTOCA [J].
BARTHELEMY, M ;
PEDUZZI, J ;
BERNARD, H ;
TANCREDE, C ;
LABIA, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1122 (01) :15-22
[7]   Characterization of beta-lactamase gene bla(PER-2,) which encodes an extended-spectrum class A beta-lactamase [J].
Bauernfeind, A ;
Stemplinger, I ;
Jungwirth, R ;
Mangold, P ;
Amann, S ;
Akalin, E ;
Ang, O ;
Bal, C ;
Casellas, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :616-620
[8]   Sequences of p-lactamase genes encoding CTX-M-1 (MEN-1) and CTX-M-2 and relationship of their amino acid sequences with those of other beta-lactamases [J].
Bauernfeind, A ;
Stemplinger, I ;
Jungwirth, R ;
Ernst, S ;
Casellas, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (02) :509-513
[9]  
BOISSINOT M, 1990, J BIOL CHEM, V265, P1225
[10]   Role of residues 104, 164, 166, 238 and 240 in the substrate profile of PER-1 β-lactamase hydrolysing third-generation cephalosporins [J].
Bouthors, AT ;
Dagoneau-Blanchard, N ;
Naas, T ;
Nordmann, P ;
Jarlier, V ;
Sougakoff, W .
BIOCHEMICAL JOURNAL, 1998, 330 :1443-1449