Molecular Epidemiology of Multidrug-Resistant Klebsiella pneumoniae Isolates in a Brazilian Tertiary Hospital

被引:23
|
作者
Palmeiro, Jussara Kasuko [1 ,2 ,3 ]
de Souza, Robson Francisco [4 ]
Schorner, Marcos Andre [5 ]
Passarelli-Araujo, Hemanoel [6 ,7 ]
Grazziotin, Ana Laura [6 ]
Vidal, Newton Medeiros [6 ,8 ]
Venancio, Thiago Motta [6 ]
Dalla-Costa, Libera Maria [2 ]
机构
[1] Univ Fed Parana, Lab Bacteriol & Bol Mol, Unidade Lab Anal Clin, Complexo Hosp Clin, Curitiba, Parana, Brazil
[2] Inst Pesquisa Pele Pequeno Principe, Fac Pequeno Principe, Curitiba, Parana, Brazil
[3] Univ Fed Santa Catarina, Ctr Ciencias Saude, Dept Anal Clin, Florianopolis, SC, Brazil
[4] Univ Sao Paulo, Inst Ciencias Biomed 2, Lab Estrutura & Evolucao Prot, Sao Paulo, Brazil
[5] Univ Fed Santa Catarina, Hosp Univ, Florianopolis, SC, Brazil
[6] Univ Estadual Norte Fluminense, Lab Quim & Funcao Prot & Peptideos, Ctr Biociencias & Biotecnol, Campos Dos Goytacazes, Brazil
[7] Univ Fed Minas Gerais, Dept Bioquim & Imunol, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
[8] NLM, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
来源
FRONTIERS IN MICROBIOLOGY | 2019年 / 10卷
基金
美国国家卫生研究院;
关键词
Brazil; hospital outbreak; MLST; antimicrobial resistance; clonal group 258; whole-genome sequencing; CARBAPENEM RESISTANCE; PLASMIDS; SPREAD; PORIN; EXPANSION; INSIGHTS; OMPK35;
D O I
10.3389/fmicb.2019.01669
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Multidrug-resistant (MDR) Klebsiella pneumoniae (Kp) is a major bacterial pathogen responsible for hospital outbreaks worldwide, mainly via the spread of high-risk clones and epidemic resistance plasmids. In this study, we evaluated the molecular epidemiology and beta-lactam resistance mechanisms of MDR-Kp strains isolated in a Brazilian academic care hospital. We used whole-genome sequencing to study drug resistance mechanisms and their relationships with a K. pneumoniae carbapenemase-producing (KPC) Kp outbreak. Forty-three Kp strains were collected between 2003 and 2012. Antimicrobial susceptibility testing was performed for 15 antimicrobial agents, and polymerase chain reaction (PCR) was used to detect 32 resistance genes. Mutations in ompk35, ompk36, and ompk37 were evaluated by PCR and DNA sequencing. Pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) were carried out to differentiate the strains. Based on distinct epidemiological periods, six Kp strains were subjected to whole-genome sequencing. beta-lactamase coding genes were widely distributed among isolates. Almost all isolates had mutations in porin genes, particularly ompk35. The presence of bla(KPC) promoted a very high increase in carbapenem minimum inhibitory concentration only when ompk35 and ompk36 were interrupted by insertion sequences. A major cluster was identified by PFGE analysis and all isolates from this cluster belonged to clonal group (CG) 258. We have also identified a large repertoire of resistance genes in the sequenced isolates. A bla(KPC-2)-bearing plasmid (pUFPRA2) was also identified, which was very similar to a plasmid previously described in the first Brazilian KPC-Kp (2005). We found high-risk clones (CG258) and an epidemic resistance plasmid throughout the duration of the study (2003 to 2012), emphasizing a persistent presence of MDR-Kp strains in the hospital setting. Finally, we found that horizontal transfer of resistance genes between clones may have played a key role in the evolution of the outbreak.
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页数:11
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