Genetic and biochemical characterization of GES-5, an extended-spectrum class A β-lactamase from Klebsiella pneumoniae

被引:45
作者
Bae, Il Kwon
Lee, You-Nae
Jeong, Seok Hoon
Hong, Seong Geun
Lee, Jung Hun
Lee, Sang Hee
Kim, Hyoung Jin
Youn, Hasik
机构
[1] Kosin Univ, Coll Med, Res Inst Antimicrobial Resistance, Pusan 602030, South Korea
[2] Kosin Univ, Coll Med, Dept Lab Med, Pusan 602030, South Korea
[3] Pochon CHA Univ, Coll Med, Dept Lab Med, Songnam 463712, South Korea
[4] Myongji Univ, Sch Biotechnol & Environm Engn, Dept Biol Sci, Yongin 449728, Gyeonggido, South Korea
[5] LG Life Sci, R&D Pk, Taejon 305380, South Korea
关键词
integron; OXA-17; AAC(6')-IIa; imipenem;
D O I
10.1016/j.diagmicrobio.2007.02.013
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The present study was conducted to characterize a new class I integron containing the bla(GES-5) gene cassette in Klebsiella pneumoniae clinical isolate CHAK36 and measure the kinetic parameters of GES-5 beta-lactamase. Long-range polymerase chain reactions (PCRs) and sequence analysis were performed to identify and analyze the bla(GES-5) gene cassette-containing integrons. Kinetic parameters were determined from purified GES-5. Sequencing of the 6190-bp PCR amplicon from K pneumoniae CHAK36 isolate revealed the new structure of class 1 integron. The integron has 3 unique gene cassettes (bla(GEs-5)-aac(6')-IIa-bla(OXA-17)/orf4), but the 59-base element of the bla(OXA-17) gene cassette was interrupted by a putative transposase gene, orf4. The kinetic parameters of GES-5 showed its broad-spectrum activity against most beta-lactams, including benzylpenicillin, cefaloridine, cefotaxime, and imipenem. This work shows that the bla(GES-5) gene was located on a new class I integron as a gene cassette. Our kinetic characterizations show that GES-5 was more active against impenem than GES-2 and GES-4. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:465 / 468
页数:4
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