Epidemiological characteristics and molecular evolution mechanisms of carbapenem-resistant hypervirulent Klebsiella pneumoniae
Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP), a type of Klebsiella pneumoniae (KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global pu...
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| Published in: | Frontiers in microbiology Vol. 13; p. 1003783 |
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| Main Authors: | , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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12.09.2022
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| ISSN: | 1664-302X, 1664-302X |
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| Abstract | Carbapenem-resistant hypervirulent
Klebsiella pneumoniae
(CR-hvKP), a type of
Klebsiella pneumoniae
(KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global public health and is associated with significant morbidity and mortality. There are many mechanisms responsible for the evolution of the hypervirulence and carbapenem resistance phenotypes, such as the horizontal transfer of the plasmid carrying the carbapenem resistance gene to hypervirulent
Klebsiella pneumoniae
(hvKP) or carbapenemase-producing
Klebsiella pneumoniae
(CRKP) acquiring a hypervirulence plasmid carrying a virulence-encoding gene. Notably, KP can evolve into CR-hvKP by acquiring a hybrid plasmid carrying both the carbapenem resistance and hypervirulence genes. In this review, we summarize the evolutionary mechanisms of resistance and plasmid-borne virulence as well as the prevalence of CR-hvKP. |
|---|---|
| AbstractList | Carbapenem-resistant hypervirulent
Klebsiella pneumoniae
(CR-hvKP), a type of
Klebsiella pneumoniae
(KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global public health and is associated with significant morbidity and mortality. There are many mechanisms responsible for the evolution of the hypervirulence and carbapenem resistance phenotypes, such as the horizontal transfer of the plasmid carrying the carbapenem resistance gene to hypervirulent
Klebsiella pneumoniae
(hvKP) or carbapenemase-producing
Klebsiella pneumoniae
(CRKP) acquiring a hypervirulence plasmid carrying a virulence-encoding gene. Notably, KP can evolve into CR-hvKP by acquiring a hybrid plasmid carrying both the carbapenem resistance and hypervirulence genes. In this review, we summarize the evolutionary mechanisms of resistance and plasmid-borne virulence as well as the prevalence of CR-hvKP. Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP), a type of Klebsiella pneumoniae (KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global public health and is associated with significant morbidity and mortality. There are many mechanisms responsible for the evolution of the hypervirulence and carbapenem resistance phenotypes, such as the horizontal transfer of the plasmid carrying the carbapenem resistance gene to hypervirulent Klebsiella pneumoniae (hvKP) or carbapenemase-producing Klebsiella pneumoniae (CRKP) acquiring a hypervirulence plasmid carrying a virulence-encoding gene. Notably, KP can evolve into CR-hvKP by acquiring a hybrid plasmid carrying both the carbapenem resistance and hypervirulence genes. In this review, we summarize the evolutionary mechanisms of resistance and plasmid-borne virulence as well as the prevalence of CR-hvKP. Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP), a type of Klebsiella pneumoniae (KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global public health and is associated with significant morbidity and mortality. There are many mechanisms responsible for the evolution of the hypervirulence and carbapenem resistance phenotypes, such as the horizontal transfer of the plasmid carrying the carbapenem resistance gene to hypervirulent Klebsiella pneumoniae (hvKP) or carbapenemase-producing Klebsiella pneumoniae (CRKP) acquiring a hypervirulence plasmid carrying a virulence-encoding gene. Notably, KP can evolve into CR-hvKP by acquiring a hybrid plasmid carrying both the carbapenem resistance and hypervirulence genes. In this review, we summarize the evolutionary mechanisms of resistance and plasmid-borne virulence as well as the prevalence of CR-hvKP.Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP), a type of Klebsiella pneumoniae (KP) that exhibits hypervirulence and carbapenem resistance phenotypes, can cause severe infections, both hospital- and community-acquired infections. CR-hvKP has brought great challenges to global public health and is associated with significant morbidity and mortality. There are many mechanisms responsible for the evolution of the hypervirulence and carbapenem resistance phenotypes, such as the horizontal transfer of the plasmid carrying the carbapenem resistance gene to hypervirulent Klebsiella pneumoniae (hvKP) or carbapenemase-producing Klebsiella pneumoniae (CRKP) acquiring a hypervirulence plasmid carrying a virulence-encoding gene. Notably, KP can evolve into CR-hvKP by acquiring a hybrid plasmid carrying both the carbapenem resistance and hypervirulence genes. In this review, we summarize the evolutionary mechanisms of resistance and plasmid-borne virulence as well as the prevalence of CR-hvKP. |
| Author | Cao, Xi-Shan Hu, Zhi-De Wen, Xu-Hui Zheng, Wen-Qi Wen, Jian-Xun Han, Yu-Ling Zhao, Wen Wang, Jun-Rui |
| AuthorAffiliation | 1 Department of Laboratory Medicine, The Affiliated Hospital of Inner Mongolia Medical University , Hohhot , China 2 Department of Parasitology, The Basic Medical College of Inner Mongolia Medical University , Hohhot , China 3 Department of Medical Experiment Center, The Basic Medical Sciences College of Inner Mongolia Medical University , Hohhot , China |
| AuthorAffiliation_xml | – name: 1 Department of Laboratory Medicine, The Affiliated Hospital of Inner Mongolia Medical University , Hohhot , China – name: 2 Department of Parasitology, The Basic Medical College of Inner Mongolia Medical University , Hohhot , China – name: 3 Department of Medical Experiment Center, The Basic Medical Sciences College of Inner Mongolia Medical University , Hohhot , China |
| Author_xml | – sequence: 1 givenname: Yu-Ling surname: Han fullname: Han, Yu-Ling – sequence: 2 givenname: Xu-Hui surname: Wen fullname: Wen, Xu-Hui – sequence: 3 givenname: Wen surname: Zhao fullname: Zhao, Wen – sequence: 4 givenname: Xi-Shan surname: Cao fullname: Cao, Xi-Shan – sequence: 5 givenname: Jian-Xun surname: Wen fullname: Wen, Jian-Xun – sequence: 6 givenname: Jun-Rui surname: Wang fullname: Wang, Jun-Rui – sequence: 7 givenname: Zhi-De surname: Hu fullname: Hu, Zhi-De – sequence: 8 givenname: Wen-Qi surname: Zheng fullname: Zheng, Wen-Qi |
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| ContentType | Journal Article |
| Copyright | Copyright © 2022 Han, Wen, Zhao, Cao, Wen, Wang, Hu and Zheng. Copyright © 2022 Han, Wen, Zhao, Cao, Wen, Wang, Hu and Zheng. 2022 Han, Wen, Zhao, Cao, Wen, Wang, Hu and Zheng |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Edited by: Ernesto Perez-Rueda, Universidad Nacional Autónoma de México, Mexico This article was submitted to Evolutionary and Genomic Microbiology, a section of the journal Frontiers in Microbiology Reviewed by: Carlos Henrique Camargo, Adolfo Lutz Institute, Brazil; Hamid Solgi, Isfahan University of Medical Sciences, Iran |
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