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Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China
We aimed to clarify the epidemiologic and clinical importance of evolutionary events that occurred in carbapenem-resistant Klebsiella pneumoniae (CRKP). We collected 203 CRKP causing bloodstream infections in a tertiary hospital in China during 2013–2017. We detected a subclonal shift in the dominan...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Centers for Disease Control and Prevention
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986851/ https://www.ncbi.nlm.nih.gov/pubmed/31961299 http://dx.doi.org/10.3201/eid2602.190594 |
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author | Zhou, Kai Xiao, Tingting David, Sophia Wang, Qin Zhou, Yanzi Guo, Lihua Aanensen, David Holt, Kathryn E. Thomson, Nicholas R. Grundmann, Hajo Shen, Ping Xiao, Yonghong |
author_facet | Zhou, Kai Xiao, Tingting David, Sophia Wang, Qin Zhou, Yanzi Guo, Lihua Aanensen, David Holt, Kathryn E. Thomson, Nicholas R. Grundmann, Hajo Shen, Ping Xiao, Yonghong |
author_sort | Zhou, Kai |
collection | PubMed |
description | We aimed to clarify the epidemiologic and clinical importance of evolutionary events that occurred in carbapenem-resistant Klebsiella pneumoniae (CRKP). We collected 203 CRKP causing bloodstream infections in a tertiary hospital in China during 2013–2017. We detected a subclonal shift in the dominant clone sequence type (ST) 11 CRKP in which the previously prevalent capsular loci (KL) 47 had been replaced by KL64 since 2016. Patients infected with ST11-KL64 CRKP had a significantly higher 30-day mortality rate than other CRKP-infected patients. Enhanced virulence was further evidenced by phenotypic tests. Phylogenetic reconstruction demonstrated that ST11-KL64 is derived from an ST11-KL47–like ancestor through recombination. We identified a pLVPK-like virulence plasmid carrying rmpA and peg-344 in ST11-KL64 exclusively from 2016 onward. The pLVPK-like–positive ST11-KL64 isolates exhibited enhanced environmental survival. Retrospective screening of a national collection identified ST11-KL64 in multiple regions. Targeted surveillance of this high-risk CRKP clone is urgently needed. |
format | Online Article Text |
id | pubmed-6986851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-69868512020-02-06 Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China Zhou, Kai Xiao, Tingting David, Sophia Wang, Qin Zhou, Yanzi Guo, Lihua Aanensen, David Holt, Kathryn E. Thomson, Nicholas R. Grundmann, Hajo Shen, Ping Xiao, Yonghong Emerg Infect Dis Research We aimed to clarify the epidemiologic and clinical importance of evolutionary events that occurred in carbapenem-resistant Klebsiella pneumoniae (CRKP). We collected 203 CRKP causing bloodstream infections in a tertiary hospital in China during 2013–2017. We detected a subclonal shift in the dominant clone sequence type (ST) 11 CRKP in which the previously prevalent capsular loci (KL) 47 had been replaced by KL64 since 2016. Patients infected with ST11-KL64 CRKP had a significantly higher 30-day mortality rate than other CRKP-infected patients. Enhanced virulence was further evidenced by phenotypic tests. Phylogenetic reconstruction demonstrated that ST11-KL64 is derived from an ST11-KL47–like ancestor through recombination. We identified a pLVPK-like virulence plasmid carrying rmpA and peg-344 in ST11-KL64 exclusively from 2016 onward. The pLVPK-like–positive ST11-KL64 isolates exhibited enhanced environmental survival. Retrospective screening of a national collection identified ST11-KL64 in multiple regions. Targeted surveillance of this high-risk CRKP clone is urgently needed. Centers for Disease Control and Prevention 2020-02 /pmc/articles/PMC6986851/ /pubmed/31961299 http://dx.doi.org/10.3201/eid2602.190594 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Zhou, Kai Xiao, Tingting David, Sophia Wang, Qin Zhou, Yanzi Guo, Lihua Aanensen, David Holt, Kathryn E. Thomson, Nicholas R. Grundmann, Hajo Shen, Ping Xiao, Yonghong Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title | Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title_full | Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title_fullStr | Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title_full_unstemmed | Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title_short | Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 with Enhanced Virulence and Transmissibility, China |
title_sort | novel subclone of carbapenem-resistant klebsiella pneumoniae sequence type 11 with enhanced virulence and transmissibility, china |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986851/ https://www.ncbi.nlm.nih.gov/pubmed/31961299 http://dx.doi.org/10.3201/eid2602.190594 |
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