Antimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan
Antimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Antimicrob Agents Chemother. 2018 Jan 25;62(2). doi: 10.1128/AAC.02190-17. Print 2018 Feb.
Multidrug-resistant (MDR) spp. have been globally disseminated in association with the successful clonal lineage international clone II (IC II). Because the prevalence of MDR spp. in Japan remains very low, we characterized all spp. ( = 866) from 76 hospitals between October 2012 and March 2013 to describe the entire molecular epidemiology of spp. The most prevalent species was ( = 645; 74.5%), with IC II ( = 245) accounting for 28.3% of the total. Meropenem-resistant isolates accounted for 2.0% ( = 17) and carried IS ( = 10), ( = 4), or IS ( = 3). Multilocus sequence typing of 110 representative isolates revealed the considerable prevalence of domestic sequence types (STs). IC II isolates were divided into the domestic sequence type 469 (ST469) ( = 18) and the globally disseminated STs ST208 ( = 14) and ST219 ( = 4). ST469 isolates were susceptible to more antimicrobial agents, while ST208 and ST219 overproduced the intrinsic AmpC β-lactamase. IC II and some non-IC II STs (e.g., ST149 and ST246) were associated with fluoroquinolone resistance. This study revealed that carbapenem-susceptible IC II was moderately disseminated in Japan. The low prevalence of acquired carbapenemase genes and presence of domestic STs could contribute to the low prevalence of MDR A similar epidemiology might have appeared before the global dissemination of MDR epidemic lineages. In addition, fluoroquinolone resistance associated with IC II may provide insight into the significance of epidemic clones.
耐多药(MDR) spp. 已在全球范围内传播,与成功的克隆谱系国际克隆 II(IC II)有关。由于日本 MDR spp. 的流行率仍然非常低,我们对 2012 年 10 月至 2013 年 3 月期间 76 家医院的所有 spp.(=866)进行了特征描述,以描述 spp. 的整个分子流行病学。最常见的物种是 (=645;74.5%),其中 IC II(=245)占总数的 28.3%。耐美罗培南分离株占 2.0%(=17),携带 IS(=10)、(=4)或 IS(=3)。110 株代表性 株的多位点序列分型显示出相当数量的国内序列型(STs)。IC II 分离株分为国内序列型 469(ST469)(=18)和全球传播的 ST208(=14)和 ST219(=4)。ST469 分离株对更多抗菌药物敏感,而 ST208 和 ST219 过度产生固有 AmpC β-内酰胺酶。IC II 和一些非 IC II STs(如 ST149 和 ST246)与氟喹诺酮耐药有关。本研究表明,耐碳青霉烯的 IC II 在日本中度传播。获得性碳青霉烯酶基因的低流行率和国内 STs 的存在可能导致 MDR 的低流行率。这种类似的流行病学可能在 MDR 流行谱系的全球传播之前就已经出现。此外,与 IC II 相关的氟喹诺酮耐药可能提供了对流行克隆重要性的深入了解。