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革兰氏阴性需氧菌中新型碳青霉烯酶的出现。

Emerging carbapenemases in Gram-negative aerobes.

作者信息

Nordmann P, Poirel L

机构信息

Service de Bactériologie-Virologie, Hôpital de Bicêtre, Assistance Publique-Hôpitaux de Paris and Faculté de Médecine Paris-Sud, Université Paris XI, Paris, France.

出版信息

Clin Microbiol Infect. 2002 Jun;8(6):321-31. doi: 10.1046/j.1469-0691.2002.00401.x.

Abstract

Carbapenemases may be defined as beta-lactamases that significantly hydrolyze at least imipenem or/and meropenem. Carbapenemases involved in acquired resistance are of Ambler molecular classes A, B, and D. Class A, clavulanic acid-inhibited carbapenemases are rare. They are either chromosomally encoded (NMC-A, Sme-1 to Sme-3, IMI-1) in Enterobacter cloacae and Serratia marcescens, or plasmid encoded, such as KPC-1 in Klebsiella pneumoniae and GES-2 in Pseudomonas aeruginosa, the latter being a point-mutant of the clavulanic acid-inhibited extended-spectrum beta-lactamase GES-1. The class B enzymes are the most clinically significant carbapenemases. They are metalloenzymes of the IMP or VIM series. They have been reported worldwide but mostly from South East Asia and Europe. Metalloenzymes, whose genes are plasmid and integron located, hydrolyze virtually all beta-lactams except aztreonam. Finally, the class D carbapenemases are increasingly reported in Acinetobacter baumannii but compromise imipenem and meropenem susceptibility only marginally. The sources of the acquired carbapenemase genes remain unknown, as does the relative importance of the spread of epidemic strains as opposed to the spread of plasmid- or integron-borne genes. Because most of these carbapenemases confer only reduced susceptibility to carbapenems in Enterobacteriaceae, they may remain underestimated as a consequence of the lack of their detection.

摘要

碳青霉烯酶可定义为能显著水解至少亚胺培南或/和美罗培南的β-内酰胺酶。参与获得性耐药的碳青霉烯酶属于安布勒分子分类A、B和D类。A类,克拉维酸抑制的碳青霉烯酶较为罕见。它们要么在阴沟肠杆菌和粘质沙雷氏菌中由染色体编码(NMC-A、Sme-1至Sme-3、IMI-1),要么由质粒编码,如肺炎克雷伯菌中的KPC-1和铜绿假单胞菌中的GES-2,后者是克拉维酸抑制的超广谱β-内酰胺酶GES-1的点突变体。B类酶是临床上最重要的碳青霉烯酶。它们是IMP或VIM系列的金属酶。已在全球范围内报道,但大多来自东南亚和欧洲。其基因位于质粒和整合子上的金属酶几乎能水解除氨曲南以外的所有β-内酰胺类抗生素。最后,D类碳青霉烯酶在鲍曼不动杆菌中报道越来越多,但仅轻微影响亚胺培南和美罗培南的敏感性。获得性碳青霉烯酶基因的来源仍然未知,与质粒或整合子携带基因的传播相比,流行菌株传播的相对重要性也未知。由于这些碳青霉烯酶大多数仅使肠杆菌科细菌对碳青霉烯类抗生素的敏感性降低,因此由于缺乏检测,它们可能仍然被低估。

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