Bactériologie-Hygiène Unit, Bicêtre Hospital, APHP, Le Kremlin-Bicêtre, France.
EA7361 'Structure, Dynamic, Function and Expression of Broad Spectrum β-Lactamases' Paris-Sud University, LabEx LERMIT, Le Kremlin-Bicêtre, France.
J Antimicrob Chemother. 2019 Jan 1;74(1):42-47. doi: 10.1093/jac/dky372.
Available commercial tools (molecular methods or immunochromatographic assays) usually allow the detection of the five most prevalent carbapenemases (KPC, NDM, VIM, IMP and OXA-48-like), but miss minor carbapenemases. Here, we characterize two enterobacterial isolates with reduced susceptibility to carbapenems and negative for the most commonly encountered carbapenemase genes.
Enterobacter hormaechei and Citrobacter freundii isolates were recovered from a bile sample and rectal screening, respectively. Both isolates were investigated by WGS. Resistance genes were detected using ResFinder. The blaTMB-1-harbouring plasmid was reconstructed using CLC genomic workbench 10.0 and was annotated using the RAST tool. Transfer frequency was determined by conjugation experiments using the laboratory strain Escherichia coli J53.
The two isolates were resistant to broad-spectrum cephalosporins and carbapenems. WGS revealed the presence of blaTMB-1, which has previously only been described in non-fermenters. blaTMB-1 was located within an ISKpn19-based composite class 1 transposon. Comparative genomics revealed that this structure was carried on a conjugative IncN-type plasmid within an integration hotspot. Conjugation experiments revealed high transfer frequencies of ∼1 × 10-3.
To the best of our knowledge, this study corresponds to the first report of Tripoli MBL 1-producing Enterobacteriaceae. Despite always being described as likely to be chromosomally located in non-fermenters, the blaTMB-1 gene is now found to be carried by a conjugative plasmid among Enterobacteriaceae, raising concern about the possible dissemination of this carbapenemase. The blaTMB-1 gene should now be suspected when PCRs targeting the main carbapenemases remain negative.
市售的商业工具(分子方法或免疫层析测定法)通常可检测到五种最常见的碳青霉烯酶(KPC、NDM、VIM、IMP 和 OXA-48 样),但会遗漏次要的碳青霉烯酶。在此,我们对两株对碳青霉烯类药物敏感性降低且未检出最常见碳青霉烯酶基因的肠杆菌进行了特征描述。
Enterobacter hormaechei 和 Citrobacter freundii 分离株分别从胆汁样本和直肠筛查中回收。均采用 WGS 进行研究。使用 ResFinder 检测耐药基因。使用 CLC genomic workbench 10.0 构建携带 blaTMB-1 的质粒,并使用 RAST 工具进行注释。通过使用实验室菌株 Escherichia coli J53 进行的接合实验确定转移频率。
两株分离株对广谱头孢菌素类和碳青霉烯类药物均具有耐药性。WGS 显示存在 blaTMB-1,该基因以前仅在非发酵菌中描述过。blaTMB-1 位于基于 ISKpn19 的复合 1 类转座子内。比较基因组学显示,该结构位于整合热点内的可接合 IncN 型质粒上。接合实验显示出较高的转移频率,约为 1 × 10-3。
据我们所知,本研究是首次报道产生 Tripoli MBL 1 的肠杆菌科。尽管 blaTMB-1 基因一直被认为可能位于非发酵菌的染色体上,但现在发现该基因存在于肠杆菌科的可接合质粒上,这引起了对该碳青霉烯酶可能传播的关注。当针对主要碳青霉烯酶的 PCR 仍为阴性时,应怀疑存在 blaTMB-1 基因。