Service de Bactériologie-Virologie, Hôpital de Bicêtre, 78 rue du General Leclerc, Le Kremlin Bicêtre 94275, France.
Antimicrob Agents Chemother. 2011 Jun;55(6):2546-51. doi: 10.1128/AAC.00022-11. Epub 2011 Mar 21.
Two bla(OXA-48)-like-positive isolates (Klebsiella pneumoniae and Enterobacter cloacae) were recovered in Argentina in 2008 as part of a large-scale survey focused on multidrug resistance in Enterobacteriaceae. In both cases, sequencing identified β-lactamase OXA-163, differing from OXA-48 by a single amino substitution and a 4-amino-acid deletion. OXA-163 hydrolyzed penicillins, ceftazidime, and cefotaxime, whereas OXA-48 did not. However, OXA-163 had a much lower ability to hydrolyze carbapenems than OXA-48, therefore barely being considered a carbapenemase. In both isolates, the bla(OXA-163) gene was located on plasmids that differed in structure and size. However, a detailed genetic analysis revealed a similar genetic context in those isolates, with the bla(OXA-163) gene being bracketed by novel transposase genes, making this genetic environment different from that reported for the bla(OXA-48) gene. This study identified the first class D β-lactamase compromising both extended-spectrum cephalosporin and carbapenem activities.
2008 年,阿根廷开展了一项大规模调查,旨在研究肠杆菌科的多重耐药性,在此期间发现了两株 bla(OXA-48)-样阳性分离株(肺炎克雷伯菌和阴沟肠杆菌)。测序结果均表明这两种分离株均产生了 bla(OXA-163)β-内酰胺酶,该酶与 OXA-48 仅相差一个氨基酸替换和 4 个氨基酸缺失。OXA-163 可水解青霉素类、头孢他啶和头孢噻肟,但 OXA-48 则不能。然而,OXA-163 对碳青霉烯类的水解能力比 OXA-48 低得多,因此几乎不能被认为是碳青霉烯酶。在这两种分离株中,bla(OXA-163)基因均位于结构和大小不同的质粒上。然而,详细的遗传分析揭示了这些分离株中存在相似的遗传环境,bla(OXA-163)基因被新型转座酶基因包围,这一遗传环境与 bla(OXA-48)基因的报道不同。本研究鉴定出了第一类 D 类β-内酰胺酶,该酶可同时破坏头孢菌素和碳青霉烯的活性。