Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Clin Infect Dis. 2020 Sep 12;71(6):1524-1531. doi: 10.1093/cid/ciz973.
Antimicrobial resistance (AMR) is a major challenge in the treatment of infections caused by Pseudomonas aeruginosa. Highly drug-resistant infections are disproportionally caused by a small subset of globally distributed P. aeruginosa sequence types (STs), termed "high-risk clones." We noted that clonal complex (CC) 446 (which includes STs 298 and 446) isolates were repeatedly cultured at 1 medical center and asked whether this lineage might constitute an emerging high-risk clone.
We searched P. aeruginosa genomes from collections available from several institutions and from a public database for the presence of CC446 isolates. We determined antibacterial susceptibility using microbroth dilution and examined genome sequences to characterize the population structure of CC446 and investigate the genetic basis of AMR.
CC446 was globally distributed over 5 continents. CC446 isolates demonstrated high rates of AMR, with 51.9% (28/54) being multidrug-resistant (MDR) and 53.6% of these (15/28) being extensively drug-resistant (XDR). Phylogenetic analysis revealed that most MDR/XDR isolates belonged to a subclade of ST298 (designated ST298*) of which 100% (21/21) were MDR and 61.9% (13/21) were XDR. XDR ST298* was identified repeatedly and consistently at a single academic medical center from 2001 through 2017. These isolates harbored a large plasmid that carries a novel antibiotic resistance integron.
CC446 isolates are globally distributed with multiple occurrences of high AMR. The subclade ST298* is responsible for a prolonged epidemic (≥16 years) of XDR infections at an academic medical center. These findings indicate that CC446 is an emerging high-risk clone deserving further surveillance.
抗微生物药物耐药性(AMR)是治疗铜绿假单胞菌引起的感染的主要挑战。高度耐药感染主要由一小部分在全球分布的铜绿假单胞菌序列型(ST)引起,这些 ST 被称为“高风险克隆”。我们注意到克隆复合体(CC)446(包括 ST298 和 446)分离株在 1 家医疗中心反复培养,并询问该谱系是否可能构成新兴的高风险克隆。
我们在多个机构的收藏和公共数据库中搜索铜绿假单胞菌基因组,以确定 CC446 分离株的存在。我们使用微量肉汤稀释法测定抗菌药物敏感性,并检查基因组序列以表征 CC446 的种群结构,并研究 AMR 的遗传基础。
CC446 在全球 5 大洲分布。CC446 分离株表现出高耐药率,51.9%(28/54)为多药耐药(MDR),其中 53.6%(15/28)为广泛耐药(XDR)。系统发育分析显示,大多数 MDR/XDR 分离株属于 ST298 的一个亚克隆(称为 ST298*),其中 100%(21/21)为 MDR,61.9%(13/21)为 XDR。XDR ST298* 于 2001 年至 2017 年在一家学术医疗中心反复且一致地被鉴定出来。这些分离株携带一种新型抗生素耐药整合子的大型质粒。
CC446 分离株在全球分布,具有多种高 AMR 发生。亚克隆 ST298* 负责学术医疗中心 XDR 感染的长期流行(≥16 年)。这些发现表明 CC446 是一个新兴的高风险克隆,值得进一步监测。