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Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns

K1/K2 hvKP strains acquire carbapenem-resistance plasmids, known as CR-hvKp, and carbapenem-resistant Klebsiella pneumoniae (CRKP) strains obtain virulence plasmids, recognized as hv-CRKP. The two different evolution patterns of hypervirulent combined carbapenem-resistant Klebsiella pneumoniae may l...

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Autores principales: Tian, Dongxing, Liu, Xiao, Chen, Wenjie, Zhou, Ying, Hu, Dakang, Wang, Weiwen, Wu, Jinzuan, Mu, Qing, Jiang, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359173/
https://www.ncbi.nlm.nih.gov/pubmed/35844192
http://dx.doi.org/10.1080/22221751.2022.2103454
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author Tian, Dongxing
Liu, Xiao
Chen, Wenjie
Zhou, Ying
Hu, Dakang
Wang, Weiwen
Wu, Jinzuan
Mu, Qing
Jiang, Xiaofei
author_facet Tian, Dongxing
Liu, Xiao
Chen, Wenjie
Zhou, Ying
Hu, Dakang
Wang, Weiwen
Wu, Jinzuan
Mu, Qing
Jiang, Xiaofei
author_sort Tian, Dongxing
collection PubMed
description K1/K2 hvKP strains acquire carbapenem-resistance plasmids, known as CR-hvKp, and carbapenem-resistant Klebsiella pneumoniae (CRKP) strains obtain virulence plasmids, recognized as hv-CRKP. The two different evolution patterns of hypervirulent combined carbapenem-resistant Klebsiella pneumoniae may lead to their different prevalence in hospitals. Our study aimed to investigate the prevalence of hv-CRKP and CR-hvKp strains and to analyze factors influencing their evolution and prevalence. We collected 890 K. pneumoniae genomes from GenBank and 530 clinical K. pneumoniae isolates from nine hospitals. Our study found that hv-CRKP strains were more prevalent than CR-hvKp strains and both were dominated by bla(KPC-2) gene. The bla(KPC-2)-carrying plasmids could mobilize non-conjugative virulence plasmids from hvKp strains to CRKP strains. The conserved oriT of virulence plasmids and the widespread of conjugative helper plasmids were potential factors for the mobilization of non-conjugative virulence plasmids. HvKp strains with KPC plasmid could hardly simultaneously exhibit hypervirulence and carbapenem resistance as CRKP strains with virulence plasmid, and we found that rfaH mutation reduced capsular synthesis and increased carbapenem resistance of the CR-hvKp strain. In summary, this study revealed that hv-CRKP strains were more suitable for survival in hospital settings than CR-hvKp strains and the widespread conjugative KPC-producing plasmids contributed to the emergence and prevalence of hv-CRKP strains.
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spelling pubmed-93591732022-08-10 Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns Tian, Dongxing Liu, Xiao Chen, Wenjie Zhou, Ying Hu, Dakang Wang, Weiwen Wu, Jinzuan Mu, Qing Jiang, Xiaofei Emerg Microbes Infect Antimicrobial Agents K1/K2 hvKP strains acquire carbapenem-resistance plasmids, known as CR-hvKp, and carbapenem-resistant Klebsiella pneumoniae (CRKP) strains obtain virulence plasmids, recognized as hv-CRKP. The two different evolution patterns of hypervirulent combined carbapenem-resistant Klebsiella pneumoniae may lead to their different prevalence in hospitals. Our study aimed to investigate the prevalence of hv-CRKP and CR-hvKp strains and to analyze factors influencing their evolution and prevalence. We collected 890 K. pneumoniae genomes from GenBank and 530 clinical K. pneumoniae isolates from nine hospitals. Our study found that hv-CRKP strains were more prevalent than CR-hvKp strains and both were dominated by bla(KPC-2) gene. The bla(KPC-2)-carrying plasmids could mobilize non-conjugative virulence plasmids from hvKp strains to CRKP strains. The conserved oriT of virulence plasmids and the widespread of conjugative helper plasmids were potential factors for the mobilization of non-conjugative virulence plasmids. HvKp strains with KPC plasmid could hardly simultaneously exhibit hypervirulence and carbapenem resistance as CRKP strains with virulence plasmid, and we found that rfaH mutation reduced capsular synthesis and increased carbapenem resistance of the CR-hvKp strain. In summary, this study revealed that hv-CRKP strains were more suitable for survival in hospital settings than CR-hvKp strains and the widespread conjugative KPC-producing plasmids contributed to the emergence and prevalence of hv-CRKP strains. Taylor & Francis 2022-08-05 /pmc/articles/PMC9359173/ /pubmed/35844192 http://dx.doi.org/10.1080/22221751.2022.2103454 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Antimicrobial Agents
Tian, Dongxing
Liu, Xiao
Chen, Wenjie
Zhou, Ying
Hu, Dakang
Wang, Weiwen
Wu, Jinzuan
Mu, Qing
Jiang, Xiaofei
Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title_full Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title_fullStr Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title_full_unstemmed Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title_short Prevalence of hypervirulent and carbapenem-resistant Klebsiella pneumoniae under divergent evolutionary patterns
title_sort prevalence of hypervirulent and carbapenem-resistant klebsiella pneumoniae under divergent evolutionary patterns
topic Antimicrobial Agents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359173/
https://www.ncbi.nlm.nih.gov/pubmed/35844192
http://dx.doi.org/10.1080/22221751.2022.2103454
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