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OXA-48 样碳青霉烯酶:无形的威胁。

OXA-48-like carbapenemases: the phantom menace.

作者信息

Poirel Laurent, Potron Anaïs, Nordmann Patrice

机构信息

Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Faculté de Médecine et Université Paris-Sud, 94275 K.-Bicêtre, France.

出版信息

J Antimicrob Chemother. 2012 Jul;67(7):1597-606. doi: 10.1093/jac/dks121. Epub 2012 Apr 11.

Abstract

OXA-48-type carbapenem-hydrolysing class D β-lactamases are increasingly reported in enterobacterial species. To date, six OXA-48-like variants have been identified, with OXA-48 being the most widespread. They differ by a few amino acid substitutions or deletions (one to five amino acids). The enzymes hydrolyse penicillins at a high level and carbapenems at a low level, sparing broad-spectrum cephalosporins, and are not susceptible to β-lactamase inhibitors. When combining permeability defects, OXA-48-like producers may exhibit a high level of resistance to carbapenems. OXA-163 is an exception, hydrolysing broad-spectrum cephalosporins but carbapenems at a very low level, and being susceptible to β-lactamase inhibitors. The bla(OXA-48)-type genes are always plasmid-borne and have been identified in association with insertion sequences involved in their acquisition and expression. The current spread of the bla(OXA-48) gene is mostly linked to the dissemination of a single IncL/M-type self-transferable plasmid of 62 kb that does not carry any additional resistance gene. OXA-48-type carbapenemases have been identified mainly from North African countries, the Middle East, Turkey and India, those areas constituting the most important reservoirs; however, occurrence of OXA-48 producers in European countries is now well documented, with some reported hospital outbreaks. Since many OXA-48-like producers do not exhibit resistance to broad-spectrum cephalosporins, or only decreased susceptibility to carbapenems, their recognition and detection can be challenging. Adequate screening and detection methods are therefore required to prevent and control their dissemination.

摘要

肠杆菌科细菌中越来越多地报道了OXA-48型碳青霉烯水解D类β-内酰胺酶。迄今为止,已鉴定出六种OXA-48样变体,其中OXA-48最为广泛。它们之间的差异在于几个氨基酸的替换或缺失(一到五个氨基酸)。这些酶能高效水解青霉素,低效水解碳青霉烯,对广谱头孢菌素无影响,且对β-内酰胺酶抑制剂不敏感。当合并通透性缺陷时,OXA-48样产生菌可能对碳青霉烯表现出高度耐药性。OXA-163是个例外,它能水解广谱头孢菌素,但对碳青霉烯的水解水平极低,且对β-内酰胺酶抑制剂敏感。bla(OXA-48)型基因总是由质粒携带,并且已被鉴定与参与其获得和表达的插入序列有关。bla(OXA-48)基因目前的传播主要与一个62 kb的单一IncL/M型自我转移质粒的传播有关,该质粒不携带任何其他耐药基因。OXA-48型碳青霉烯酶主要在北非国家、中东、土耳其和印度被发现,这些地区是最重要的储存库;然而,欧洲国家现在也有OXA-48产生菌出现的充分记录,并有一些医院暴发的报道。由于许多OXA-48样产生菌对广谱头孢菌素不表现耐药性,或仅对碳青霉烯的敏感性降低,它们的识别和检测可能具有挑战性。因此,需要适当的筛查和检测方法来预防和控制它们的传播。

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