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Cephalosporin resistance in Klebsiella pneumoniae from Nova Scotia, Canada
被引:11
|作者:
Melano, Roberto G.
Davidson, Ross J.
Musgrave, Heather L.
Forward, Kevin R.
[1
]
机构:
[1] Queen Elizabeth 2 Hlth Sci Ctr, Dept Pathol & Lab Med, Halifax, NS B3H 1V8, Canada
[2] Dalhousie Univ, Dept Pathol, Halifax, NS B3H 1V8, Canada
[3] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 1V8, Canada
[4] Dalhousie Univ, Dept Med, Halifax, NS B3H 1V8, Canada
关键词:
cephalosporin;
Klebsiella pneumoniae;
cephalosporin-resistance;
amp-C;
outer brain protein;
D O I:
10.1016/j.diagmicrobio.2006.04.016
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
From 2116 Klebsiella pneumoniae strains isolated between January 2001 and December 2002 in Nova Scotia, Canada, 25 (1.18%) showed a reduced susceptibility to cefoxitin or extended-spectrum cephalosporins. Narrow-spectrum beta-lactamase genes (bla(SHV-II), bla(SHV-I), bla(SHV-26), b/a(SHV-32), bla(SHV-36), and b/a(SHV-40)) were the most prevalent. Four new variants were identified (bla(LEN-17), bla(OKP-B-13), bla(OKP-B-14), and bla(OKP-A-II)), representing the 1st description of bla(OKP) in the Americas. Among the extended-spectrum beta-lactamase (ESBL) genes, bla(SHV-2), bla(SHV2a), bla(SHV-12), and bla(CTX-M-15) were detected (ESBL prevalence of 0.14%). Nineteen strains were resistant to cefoxitin (MIC, 3 2 to > 256 mu g/mL). Nevertheless, an AmpC-like activity was detected in only I strain, which expressed CMY-2. The combined effects of narrow-spectrum beta-lactamase production and decreased or nonexpression of OmpK35/36 porins did not account for the cefoxitin resistance observed in some of these strains. (c) 2006 Elsevier Inc. All rights reserved.
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页码:197 / 205
页数:9
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