Naas T, Poirel L, Nordmann P
Service de Bactériologie-Virologie, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris-Sud, Université Paris XI, 94275 K.-Bicêtre, France.
Clin Microbiol Infect. 2008 Jan;14 Suppl 1:42-52. doi: 10.1111/j.1469-0691.2007.01861.x.
Extended-spectrum beta-lactamases (ESBLs) are usually plasmid-mediated enzymes that confer resistance to a broad range of beta-lactams. Initially, resistance to third-generation cephalosporins in Gram-negative rods was mainly due to the dissemination of TEM- and SHV-type ESBLs, which are point mutants of the classic TEM and SHV enzymes with extended substrate specificity. During the last ten years, CTX-M-type ESBLs have become increasingly predominant, but less frequent class A beta-lactamases have also been described, including SFO, BES, BEL, TLA, GES, PER and VEB types. While several of these latter are rarely identified, or are very localised, others are becoming locally prevalent, or are increasingly isolated worldwide. In addition, mutations can extend the spectrum of some OXA-type beta-lactamases to include expanded-spectrum cephalosporins, and several of these enzymes are considered to be ESBLs.
超广谱β-内酰胺酶(ESBLs)通常是由质粒介导的酶,可赋予对多种β-内酰胺类抗生素的耐药性。最初,革兰氏阴性杆菌对第三代头孢菌素的耐药性主要归因于TEM型和SHV型ESBLs的传播,它们是经典TEM和SHV酶的点突变体,具有扩展的底物特异性。在过去十年中,CTX-M型ESBLs变得越来越占主导地位,但也有较少见的A类β-内酰胺酶被描述,包括SFO、BES、BEL、TLA、GES、PER和VEB型。虽然其中一些后者很少被鉴定出来,或者非常局限,但其他一些正在局部流行,或者在全球范围内越来越多地被分离出来。此外,突变可使某些OXA型β-内酰胺酶的谱扩展至包括超广谱头孢菌素,其中几种酶被认为是ESBLs。