Stalking a lethal superbug by whole-genome sequencing and phylogenetics: Influence on unraveling a major hospital outbreak of carbapenem-resistant Klebsiella pneumoniae

被引:20
作者
Kaiser, Thorsten [1 ]
Finstermeier, Knut [1 ]
Haentzsch, Madlen [1 ]
Faucheux, Sarah [2 ]
Kaase, Martin [3 ]
Eckmanns, Tim [4 ]
Bercker, Sven [5 ]
Kaisers, Udo X. [5 ]
Lippmann, Norman [6 ,7 ]
Rodloff, Arne C. [6 ,7 ]
Thiery, Joachim [1 ]
Luebbert, Christoph [7 ,8 ]
机构
[1] Leipzig Univ Hosp, Inst Lab Med Clin Chem & Mol Diagnost, Leipzig, Germany
[2] Leipzig Univ Hosp, Inst Hosp Hyg, Leipzig, Germany
[3] Ruhr Univ Bochum, Natl Reference Ctr Multidrug Resistant Gram Negat, Dept Med Microbiol, Bochum, Germany
[4] Robert Koch Inst, Dept Infect Dis Epidemiol, Berlin, Germany
[5] Leipzig Univ Hosp, Dept Anesthesiol & Intens Care Med, Leipzig, Germany
[6] Leipzig Univ Hosp, Inst Med Microbiol & Epidemiol Infect Dis, Leipzig, Germany
[7] Leipzig Univ Hosp, Interdisciplinary Ctr Infect Dis, Leipzig, Germany
[8] Leipzig Univ Hosp, Div Infect Dis & Trop Med, Dept Gastroenterol & Rheumatol, Liebigstr 20, D-04103 Leipzig, Germany
关键词
Carbapenemase; Enterobacteriaceae; Colonization; Infection; Epidemiologic analysis; Microbiologic screening; Klebsiella pneumoniae; LIVER-TRANSPLANT RECIPIENTS; K-PNEUMONIAE; CLINICAL EPIDEMIOLOGY; EXCESS MORTALITY; INFECTION; BACTERIA; ENTEROBACTERIACEAE; COLONIZATION; TRANSMISSION; GERMANY;
D O I
10.1016/j.ajic.2017.07.022
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: From July 2010-April 2013, Leipzig University Hospital experienced the largest outbreak of a Klebsiella pneumoniae carbapenemase 2 (KPC-2)-producing Klebsiella pneumoniae (KPC-2-Kp) strain observed in Germany to date. After termination of the outbreak, we aimed to reconstruct transmission pathways by phylogenetics based on whole-genome sequencing (WGS). Methods: One hundred seventeen KPC-2-Kp isolates from 89 outbreak patients, 5 environmental KPC-2- Kp isolates, and 24 K pneumoniae strains not linked to the outbreak underwent WGS. Phylogenetic analysis was performed blinded to clinical data and based on the genomic reads. Results: A patient from Greece was confirmed as the source of the outbreak. Transmission pathways for 11 out of 89 patients (12.4%) were plausibly explained by descriptive epidemiology, applying strict definitions. Five of these and an additional 15 (ie, 20 out of 89 patients [22.5%]) were confirmed by phylogenetics. The rate of phylogenetically confirmed transmissions increased significantly from 8 out of 66 (12.1% for the time period before) to 12 out of 23 patients (52.2% for the time period after; P < .001) after implementation of systematic screening for KPC-2-Kp (33,623 screening investigations within 11 months). Using descriptive epidemiology, systematic screening showed no significant effect (7 out of 66 [10.6%] vs 4 out of 23 [17.4%] patients; P = .465). The phylogenetic analysis supported the assumption that a contaminated positioning pillow served as a reservoir for the persistence of KPC-2-Kp. Conclusions: Effective phylogenetic identification of transmissions requires systematic microbiologic screening. Extensive screening and phylogenetic analysis based on WGS should be started as soon as possible in a bacterial outbreak situation. (C) 2018 Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:54 / 59
页数:6
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