UR 12 SP 37, Emerging Bacterial Resistance and Safety of Care, Department of Clinical Microbiology, University Hospital of Sahloul, Sousse, Tunisia; Clinical Microbiology Laboratory, University Hospital of Sahloul, Sousse, Tunisia; EA7361, Université Paris-Sud, Université Paris-Saclay, LabEx Lermit, Bacteriology-Hygiene Unit, APHP, Hôpital Bicêtre, Le Kremlin-Bicêtre, France; Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
EA7361, Université Paris-Sud, Université Paris-Saclay, LabEx Lermit, Bacteriology-Hygiene Unit, APHP, Hôpital Bicêtre, Le Kremlin-Bicêtre, France; EERA 'Evolution and Ecology of Resistance to Antibiotics' Unit, Institut Pasteur-APHP-Université Paris Sud, Paris, France; Associated French National Reference Centre for Antibiotic Resistance 'Carbapenemase-producing Enterobacteriaceae', Le Kremlin-Bicêtre, France.
Int J Antimicrob Agents. 2018 Dec;52(6):916-921. doi: 10.1016/j.ijantimicag.2018.05.017. Epub 2018 May 30.
New Delhi metallo-β-lactamase (NDM)-producing Acinetobacter baumannii have been described in several countries worldwide, and studies have suggested that Acinetobacter spp. could play the role of intermediate progenitor of the bla gene between environmental progenitor and Enterobacteriaceae.
In total, 246 carbapenem-resistant A. baumannii isolates from a teaching hospital in Sousse, Tunisia were investigated between 1 June 2013 and 31 December 2015 to detect metallo-ß-lactamase (MBL) production. Polymerase chain reaction (PCR), antibiotic susceptibility testing, and genetic and whole-genome sequencing tools were used to study the underlying carbapenem resistance mechanisms.
PCR screening of the 246 carbapenem-resistant A. baumannii isolates revealed that 242 of 246 isolates harboured carbapenemase genes (seven of 246 positive for bla, four of 246 positive for bla and bla, 231 positive for bla). Conjugation and electroporation experiments suggested that the bla gene is likely to be chromosomally located. All the NDM-1-producing A. baumannii isolates were clonally related, and belonged to ST85 according to the Pasteur Institute's multi-locus sequence typing scheme. Analysis of the immediate genetic environment of the bla gene revealed that the gene was located within a truncated isoform of Tn125 transposon (ΔTn125). The bla gene was located within transposon Tn2008.
This study showed the dissemination of a single clone of NDM-1-producing A. baumannii in a Tunisian hospital. Countries in north Africa may constitute a significant reservoir for NDM-1-producing A. baumannii. The spread of the bla gene in A. baumannii was linked to clonal spread in this study.
新德里金属β-内酰胺酶(NDM)产生的鲍曼不动杆菌已在世界上多个国家/地区被描述,研究表明,不动杆菌属。可能在 bla 基因的环境前体和肠杆菌科之间发挥金属-β-内酰胺酶(MBL)产生的中间祖细胞的作用。
2013 年 6 月 1 日至 2015 年 12 月 31 日,我们对突尼斯苏塞的一家教学医院的 246 株碳青霉烯类耐药鲍曼不动杆菌进行了调查,以检测金属-β-内酰胺酶(MBL)的产生。聚合酶链反应(PCR)、抗生素敏感性测试、遗传和全基因组测序工具用于研究潜在的碳青霉烯类耐药机制。
对 246 株碳青霉烯类耐药鲍曼不动杆菌的 PCR 筛查显示,242 株(246 株中有 7 株阳性,246 株中有 4 株阳性,231 株阳性)携带碳青霉烯酶基因。接合和电穿孔实验表明,bla 基因可能位于染色体上。所有 NDM-1 产生的鲍曼不动杆菌分离株具有克隆相关性,根据巴斯德研究所的多位点序列分型方案,属于 ST85。对 bla 基因的直接遗传环境进行分析表明,该基因位于截断的 Tn125 转座子(ΔTn125)的同种型内。bla 基因位于转座子 Tn2008 内。
本研究表明,在突尼斯一家医院中,NDM-1 产生的鲍曼不动杆菌单一克隆的传播。北非国家可能是 NDM-1 产生的鲍曼不动杆菌的重要储存库。在本研究中,bla 基因在鲍曼不动杆菌中的传播与克隆传播有关。