Diversity of chromosomal AmpC β-lactamases from Enterobacter cloacae isolates in a Portuguese hospital

被引:12
作者
Conceiçào, T
Faria, N
Lito, L
Cristino, JM
Salgado, MJ
Duarte, A
机构
[1] Fac Pharm, P-1619049 Lisbon, Portugal
[2] Hosp Santa Maria, Fac Med, Lisbon, Portugal
关键词
Enterobacter cloacae; beta-lactamase; AmpC;
D O I
10.1016/S0378-1097(03)00891-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Six clinical isolates of Enterobacter cloacae isolated in a Portuguese hospital, between April 1999 and November 2000, demonstrated resistance to almost all broad-spectrum cephalosporins, except to cefepime. These isolates were susceptible to quinolones and to aminoglycosides. lsoelectric focusing demonstrated production of beta-lactamases with pIs > 8.0 and by all six isolates, exhibiting a cephalosporinase phenotype. The results of pulsed field gel electrophoresis revealed that these isolates were genetically unrelated. The amino acid sequence of six AmpC beta-lactamases (EclolFF, Eclo6FF, Eclo9FF, Eclo1OFF, Eclo11FF and Eclol5FF) shared 97-99% homology with the chromosomal AmpC beta-lactamase from E. cloacae P99 and 86-87% homology with those of two plasmid-mediated AmpC beta-lactamases, MIR-1 and ACT-1. This is the first report of chromosomal AmpC beta-lactamase production by E cloacae isolates in a Portuguese hospital. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:197 / 202
页数:6
相关论文
共 25 条
[1]   A STANDARD NUMBERING SCHEME FOR THE CLASS-A BETA-LACTAMASES [J].
AMBLER, RP ;
COULSON, AFW ;
FRERE, JM ;
GHUYSEN, JM ;
JORIS, B ;
FORSMAN, M ;
LEVESQUE, RC ;
TIRABY, G ;
WALEY, SG .
BIOCHEMICAL JOURNAL, 1991, 276 :269-270
[2]  
[Anonymous], 2000, M7A5 NAT COMM CLIN L, pM7
[3]  
Barnaud G, 2001, FEMS MICROBIOL LETT, V195, P185, DOI 10.1111/j.1574-6968.2001.tb10519.x
[4]   Three bovine α2-fucosyltransferase genes encode enzymes that preferentially transfer fucose on Galβ1-3GalNAc acceptor substrates [J].
Barreaud, JP ;
Saunier, K ;
Souchaire, J ;
Delourme, D ;
Oulmouden, A ;
Oriol, R ;
Levéziel, H ;
Julien, R ;
Petit, JM .
GLYCOBIOLOGY, 2000, 10 (06) :611-621
[5]   Imipenem resistance in Klebsiella pneumoniae is associated with the combination of ACT-1, a plasmid-mediated AmpC beta-lactamase, and the loss of an outer membrane protein [J].
Bradford, PA ;
Urban, C ;
Mariano, N ;
Projan, SJ ;
Rahal, JJ ;
Bush, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :563-569
[6]   SEQUENCE AND COMPARATIVE-ANALYSIS OF 3 ENTEROBACTER-CLOACAE-AMPC BETA-LACTAMASE GENES AND THEIR PRODUCTS [J].
GALLENI, M ;
LINDBERG, F ;
NORMARK, S ;
COLE, S ;
HONORE, N ;
JORIS, B ;
FRERE, JM .
BIOCHEMICAL JOURNAL, 1988, 250 (03) :753-760
[7]   Biochemical-genetic characterization and regulation of expression of an ACC-1-like chromosome-borne cephalosporinase from Hafnia alvei [J].
Girlich, D ;
Naas, T ;
Bellais, S ;
Poirel, L ;
Karim, A ;
Nordmann, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) :1470-1478
[8]   Characterization, cloning and sequence analysis of the inducible Ochrobactrum anthropi AmpC β-lactamase [J].
Higgins, CS ;
Avison, MB ;
Jamieson, L ;
Simm, AM ;
Bennett, PM ;
Walsh, TR .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 47 (06) :745-754
[9]   Sequence of the MIR-1 β-lactamase gene [J].
Jacoby, GA ;
Tran, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (07) :1759-1760
[10]   ampR gene mutations that greatly increase class C β-lactamase activity in Enterobacter cloacae [J].
Kuga, A ;
Okamoto, R ;
Inoue, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) :561-567