Babiker Ahmed, Evans Daniel R, Griffith Marissa P, McElheny Christi L, Hassan Mohamed, Clarke Lloyd G, Mettus Roberta T, Harrison Lee H, Doi Yohei, Shields Ryan K, Van Tyne Daria
Division of Infectious Diseases, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Microbial Genomic Epidemiology Laboratory, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Clin Microbiol. 2020 Aug 24;58(9). doi: 10.1128/JCM.00275-20.
Carbapenem-nonsusceptible spp. (CNSC) are increasingly recognized as health care-associated pathogens. Information regarding their clinical epidemiology, genetic diversity, and mechanisms of carbapenem resistance is lacking. We examined microbiology records of adult patients at the University of Pittsburgh Medical Center (UMPC) Presbyterian Hospital (PUH) from 2000 to 2018 for CNSC, as defined by ertapenem nonsusceptibility. Over this time frame, the proportion of CNSC increased from 4% to 10% (0.03), as did daily defined carbapenem doses/1,000 patient days (6.52 to 34.5; = 0.831; 0.001), which correlated with the observed increase in CNSC (lag = 0 years; = 0.660). Twenty CNSC isolates from 19 patients at PUH and other UPMC hospitals were available for further analysis, including whole-genome short-read sequencing and additional antimicrobial susceptibility testing. Of the 19 patients, nearly all acquired CNSC in the health care setting and over half had polymicrobial cultures containing at least one other organism. Among the 20 CNSC isolates, was the predominant species identified (60%). CNSC genomes were compared with genomes of carbapenem-susceptible spp. from UPMC and with other publicly available CNSC genomes. Isolates carrying genes encoding carbapenemases (, and ) were also long-read sequenced, and their carbapenemase-encoding plasmid sequences were compared with one another and with publicly available sequences. Phylogenetic analysis of 102 UPMC genomes showed that CNSC from our setting did not cluster together. Similarly, a global phylogeny of 64 CNSC genomes showed a diverse population structure. Our findings suggest that both local and global CNSC populations are genetically diverse and that CNSC harbor carbapenemase-encoding plasmids found in other .
碳青霉烯不敏感菌(CNSC)越来越被认为是与医疗保健相关的病原体。目前缺乏关于其临床流行病学、遗传多样性和碳青霉烯耐药机制的信息。我们检查了匹兹堡大学医学中心(UMPC)长老会医院(PUH)2000年至2018年成年患者的微生物学记录,以查找由厄他培南不敏感定义的CNSC。在此时间范围内,CNSC的比例从4%增加到10%(0.03),每日定义的碳青霉烯剂量/1000患者日也增加了(从6.52增加到34.5; = 0.831;0.001),这与观察到的CNSC增加相关(滞后 = 0年; = 0.660)。从PUH和其他UMPC医院的19名患者中获得了20株CNSC分离株用于进一步分析,包括全基因组短读测序和额外的抗菌药物敏感性测试。在这19名患者中,几乎所有人都是在医疗保健环境中获得CNSC的,超过一半的患者有多微生物培养物,其中至少含有一种其他生物体。在这20株CNSC分离株中, 是鉴定出的主要菌种(60%)。将CNSC基因组与来自UMPC的碳青霉烯敏感菌基因组以及其他公开可用的CNSC基因组进行了比较。携带编码碳青霉烯酶( 、 和 )基因的分离株也进行了长读测序,并将其编码碳青霉烯酶的质粒序列相互比较以及与公开可用序列进行比较。对102株UMPC菌基因组的系统发育分析表明,我们环境中的CNSC没有聚集在一起。同样,对64个CNSC基因组的全球系统发育分析显示出多样化的种群结构。我们的研究结果表明,本地和全球的CNSC种群在遗传上都是多样化的,并且CNSC携带在其他菌中发现的编码碳青霉烯酶的质粒。