A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression

Abstract The emergence and prevalence of hypervirulent Klebsiella pneumoniae (hvKP) have proposed a great challenge to control this infection. Therefore, exploring some new drugs or strategies for treating hvKP infection is an urgent issue for scientific researchers. In the present study, the clpV g...

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Main Authors: Wenke Liu, Dan Wang, Qiangxing He, Shiwen Cao, Jiaxin Cao, Huajie Zhao, Junwei Cui, Fan Yang
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Microbiology
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Online Access:https://doi.org/10.1186/s12866-025-03748-4
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author Wenke Liu
Dan Wang
Qiangxing He
Shiwen Cao
Jiaxin Cao
Huajie Zhao
Junwei Cui
Fan Yang
author_facet Wenke Liu
Dan Wang
Qiangxing He
Shiwen Cao
Jiaxin Cao
Huajie Zhao
Junwei Cui
Fan Yang
author_sort Wenke Liu
collection DOAJ
description Abstract The emergence and prevalence of hypervirulent Klebsiella pneumoniae (hvKP) have proposed a great challenge to control this infection. Therefore, exploring some new drugs or strategies for treating hvKP infection is an urgent issue for scientific researchers. In the present study, the clpV gene deletion strain of hvKP (ΔclpV-hvKP) was constructed using CRISPR-Cas9 technology, and the biological characteristics of ΔclpV-hvKP were investigated to explore the new targets for controlling this pathogen. The results showed that clpV gene deletion did not affect the growth ability of hvKP. However, knocking out the clpV gene markedly decreased the mucoid phenotype and the biofilm formation ability of hvKP. It reduced the interspecific competition of hvKP with Escherichia coli, Salmonella, Pseudomonas aeruginosa, and Staphylococcus aureus. The clpV deletion significantly changed the transcriptome profile of hvKP, inhibited the expression of virulence factors, and decreased the lethality of hvKP against Galleria mellonella larvae. In vitro experiments showed that lithocholic acid could inhibit the expression of the clpV gene and reduce the virulence of hvKP. Our data suggested that the clpV gene may be a potential target for decreasing hvKP infection risk.
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institution Kabale University
issn 1471-2180
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publisher BMC
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series BMC Microbiology
spelling doaj-art-3eca0ac757294e87b053ea35e59035082025-01-19T12:12:25ZengBMCBMC Microbiology1471-21802025-01-0125111210.1186/s12866-025-03748-4A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expressionWenke Liu0Dan Wang1Qiangxing He2Shiwen Cao3Jiaxin Cao4Huajie Zhao5Junwei Cui6Fan Yang7The First Affiliated Hospital of Xinxiang Medical UniversityDepartment of Pathogenic Biology, School of Basic Medical Science, Xinxiang Medical UniversityThe First Affiliated Hospital of Xinxiang Medical UniversityDepartment of Pathogenic Biology, School of Basic Medical Science, Xinxiang Medical UniversityDepartment of Pathogenic Biology, School of Basic Medical Science, Xinxiang Medical UniversityDepartment of Pathogenic Biology, School of Basic Medical Science, Xinxiang Medical UniversityThe First Affiliated Hospital of Xinxiang Medical UniversityThe First Affiliated Hospital of Xinxiang Medical UniversityAbstract The emergence and prevalence of hypervirulent Klebsiella pneumoniae (hvKP) have proposed a great challenge to control this infection. Therefore, exploring some new drugs or strategies for treating hvKP infection is an urgent issue for scientific researchers. In the present study, the clpV gene deletion strain of hvKP (ΔclpV-hvKP) was constructed using CRISPR-Cas9 technology, and the biological characteristics of ΔclpV-hvKP were investigated to explore the new targets for controlling this pathogen. The results showed that clpV gene deletion did not affect the growth ability of hvKP. However, knocking out the clpV gene markedly decreased the mucoid phenotype and the biofilm formation ability of hvKP. It reduced the interspecific competition of hvKP with Escherichia coli, Salmonella, Pseudomonas aeruginosa, and Staphylococcus aureus. The clpV deletion significantly changed the transcriptome profile of hvKP, inhibited the expression of virulence factors, and decreased the lethality of hvKP against Galleria mellonella larvae. In vitro experiments showed that lithocholic acid could inhibit the expression of the clpV gene and reduce the virulence of hvKP. Our data suggested that the clpV gene may be a potential target for decreasing hvKP infection risk.https://doi.org/10.1186/s12866-025-03748-4Hypervirulent Klebsiella pneumoniaeclpV geneVirulenceLithocholic acid
spellingShingle Wenke Liu
Dan Wang
Qiangxing He
Shiwen Cao
Jiaxin Cao
Huajie Zhao
Junwei Cui
Fan Yang
A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
BMC Microbiology
Hypervirulent Klebsiella pneumoniae
clpV gene
Virulence
Lithocholic acid
title A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
title_full A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
title_fullStr A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
title_full_unstemmed A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
title_short A strategy for controlling Hypervirulent Klebsiella pneumoniae: inhibition of ClpV expression
title_sort strategy for controlling hypervirulent klebsiella pneumoniae inhibition of clpv expression
topic Hypervirulent Klebsiella pneumoniae
clpV gene
Virulence
Lithocholic acid
url https://doi.org/10.1186/s12866-025-03748-4
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