Pereira Polyana Silva, Borghi Mirla, de Araújo Carlos Felipe Machado, Aires Caio Augusto Martins, Oliveira Jane Cleide Ribeiro, Asensi Marise Dutra, Carvalho-Assef Ana Paula D'Alincourt
Laboratório de Pesquisa em Infecção Hospitalar, Instituto Oswaldo Cruz-Fiocruz, Rio de Janeiro, Brazil.
Laboratório Central de Saúde Pública do Rio de Janeiro Noel Nutels, Rio de Janeiro, Brazil.
Antimicrob Agents Chemother. 2015 Aug;59(8):4453-6. doi: 10.1128/AAC.04243-14. Epub 2015 May 18.
Enzymes of the OXA-48 family have become some of the most important beta-lactamases in the world. A new OXA-48 variant (OXA-370) was first described for an Enterobacter hormaechei strain isolated in Rio Grande do Sul (southern region of Brazil) in 2013. Here we report detection of the blaOXA-370 gene in 24 isolates belonging to three Enterobacteriaceae species (22 Klebsiella pneumoniae isolates, 1 Enterobacter cloacae isolate, and 1 Enterobacter aerogenes isolate) collected from five hospitals in Rio de Janeiro, Brazil, in 2013 and 2014. The isolates showed a multidrug resistance profile, and 12.5% were resistant to polymyxin B. Besides blaOXA-370, no other carbapenemase genes were observed by PCR, whereas blaOXA-1 was found in all isolates and 22 isolates (91.6%) possessed blaCTX-M-15. Molecular typing of the K. pneumoniae isolates by pulsed-field gel electrophoresis (PFGE) showed the presence of two clonal groups, i.e., KpA (21 isolates) and KpB (1 isolate). KpA was characterized as sequence type 16 (ST16) and KpB as ST1041 by multilocus sequence typing (MLST). ST16 has been observed for KPC-producing K. pneumoniae in Rio de Janeiro. Plasmid analysis performed with six representative OXA-370-producing isolates showed plasmids harboring the blaOXA-370 gene in all strains, ranging from 25 kb to 150 kb. This study suggests that there is an urgent need to investigate the presence of OXA-370 and dissemination of the K. pneumoniae ST16 clone carrying this gene in Brazil.
OXA-48家族的酶已成为世界上一些最重要的β-内酰胺酶。2013年,在巴西南部南里奥格兰德州分离出的一株霍氏肠杆菌中首次描述了一种新的OXA-48变体(OXA-370)。在此,我们报告在2013年和2014年从巴西里约热内卢五家医院收集的属于三个肠杆菌科物种的24株分离株(22株肺炎克雷伯菌分离株、1株阴沟肠杆菌分离株和1株产气肠杆菌分离株)中检测到blaOXA-370基因。这些分离株呈现多药耐药谱,12.5%对多粘菌素B耐药。除blaOXA-370外,PCR未检测到其他碳青霉烯酶基因,而所有分离株中均发现blaOXA-1,22株(91.6%)拥有blaCTX-M-15。通过脉冲场凝胶电泳(PFGE)对肺炎克雷伯菌分离株进行分子分型显示存在两个克隆群,即KpA(21株)和KpB(1株)。通过多位点序列分型(MLST),KpA被鉴定为序列型16(ST16),KpB为ST1041。在里约热内卢,产KPC的肺炎克雷伯菌中已观察到ST16。对六株代表性产OXA-370分离株进行的质粒分析显示,所有菌株中携带blaOXA-370基因的质粒大小从25 kb到150 kb不等。本研究表明,迫切需要调查巴西OXA-370的存在情况以及携带该基因的肺炎克雷伯菌ST16克隆的传播情况。