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[革兰氏阴性菌的碳青霉烯酶]

[Carbapenemases of gram-negative bacteria].

作者信息

Bedenić Branka, Sardelić Sanda, Vranić-Ladavac Mirna, Barisić Nada, Ladavac Ranko

出版信息

Lijec Vjesn. 2014 Mar-Apr;136(3-4):94-103.

Abstract

Carbapenems are often antibiotics of last resort for the treatment of severe infections. They are stable to most beta-lactamases produced by gram-negative bacteria. However, bacterial enzymes named carbapenemases can efficiently hydrolyze carbapenems. They are produced most frequently by Enterobacteriaceae and non-fermentative bacteria such as Pseudomonas aeruginosa and Acinetobacter baumannnii. They belong to group A (KPC, SME, IMI, NMC), B (VIM, IMP, SPM, GIM, NDM, SIM, DIM, AIM) and D (OXA-23, OXA-24, OXA-48, OXA-58, OXA-143). The accurate and rapid laboratory identification of carbapenem-resistant isolates is important to prevent spread of such multidrug resistant strains and to avoid therapeutic failures. Therapeutic options are often limited because carbapenemases are encoded on mobile genetic elements which often harbour resistance genes to other groups of antibiotics. Thus, colistin is often the only therapeutic option.

摘要

碳青霉烯类药物通常是治疗严重感染的最后一道抗生素防线。它们对革兰氏阴性菌产生的大多数β-内酰胺酶具有稳定性。然而,名为碳青霉烯酶的细菌酶能够有效水解碳青霉烯类药物。这类酶最常见于肠杆菌科细菌以及铜绿假单胞菌和鲍曼不动杆菌等非发酵菌。它们可分为A组(KPC、SME、IMI、NMC)、B组(VIM、IMP、SPM、GIM、NDM、SIM、DIM、AIM)和D组(OXA-23、OXA-24、OXA-48、OXA-58、OXA-143)。准确快速地在实验室鉴定耐碳青霉烯类菌株对于防止此类多重耐药菌株的传播以及避免治疗失败至关重要。由于碳青霉烯酶编码于可移动遗传元件上,而这些元件通常还携带对其他抗生素类别的耐药基因,所以治疗选择往往有限。因此,黏菌素常常是唯一的治疗选择。

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