Defining an extended-spectrum β-lactamase

被引:140
作者
Livermore, D. M. [1 ]
机构
[1] Hlth Protect Agcy Ctr Infect, Antibiot Res Monitoring & Reference Lab, London NW9 5EQ, England
关键词
beta-lactamases; classification; CTX-M; ESBL; extended-spectrum beta-lactamase; review; SHV; TEM;
D O I
10.1111/j.1469-0691.2007.01857.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The term 'extended-spectrum beta-lactamase' (ESBL), initially 'extended-broad-spectrum beta-lactamase', was first coined for derivatives of TEM and SHV enzymes able to hydrolyse oxyimino-cephalosporins. These all belonged to beta-lactamase functional group 2be. Subsequently, the term has been stretched to include: W enzymes with spectra similar to those of TEM and SHV mutants but derived from other sources, e.g., the CTX-M and VEB types; (ii) TEM and SHV mutants with borderline ESBL activity, e.g., TEM-12; and (iii) various beta-lactamases conferring wider resistance than their parent types but not meeting the definition for group 2be, e.g., OXA derivatives and mutant AmpC types with increased activity against cefepime. It seems best-and pragmatic-that the term 'ESBL' retains its broad modern usage, but that should always be accompanied by mention of the enzyme's family as, e.g., in 'TEM ESBL' or 'OXA ESBL', not as a sole moniker.
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页码:3 / 10
页数:8
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