Sensitizing carbapenem-resistant Klebsiella pneumoniae using a compact Cascade-Cas3 system

Klebsiella pneumoniae is a ‘superbug’ characterized by high virulence and carbapenem resistance. CRISPR-Cas3 is capable of performing large-scale deletions in bacterial genomes. The purpose of this study is to sensitize Klebsiella pneumoniae A324 to carbapenem antibiotics by eliminating the multidrug resistance plasmid pA324-IMP using a compact Cascade-Cas3 system. Recombinant plasmids were constructed using molecular cloning techniques. Three sgRNAs targeting different positions within the bla IMP−38 gene were designed. Recombinant plasmids were separately transformed into host bacteria carrying bla IMP38 genes. The elimination efficiency of each CRISPR-Cas3 system target was determined by PCR and qPCR. Fluorescence confocal microscopy was used to observe the fluorescence intensity. Bacterial drug susceptibility phenotypes were determined using E-test drug sensitivity strips. In this study, we successfully constructed the high copy number plasmid, the fluorescent plasmid, and the recombinant CRISPR plasmids. PCR and qPCR results demonstrated that the CRISPR-Cas3 system could efficiently eliminate bla IMP−38 genes, with pCas3-T3 showing the highest elimination efficiency. Fluorescence confocal microscopy indicated that the fluorescence intensity of the experimental group significantly decreased compared to the control group. Additionally, drug susceptibility tests revealed that the resistance of Klebsiella pneumoniae to imipenem and meropenem was significantly reduced. Furthermore, CRISPR-Cas3 could enhance the effectiveness of meropenem in killing Klebsiella pneumoniae A324. In conclusion, this work demonstrates that the compact Cascade-Cas3 system can serve as a novel tool to eliminate the resistance gene bla IMP−38 and restore the sensitivity of host bacteria to antibiotics. This strategy shows great potential to combat the spread of the bla IMP−38 gene in Klebsiella pneumoniae and holds significant application value in the field of combating drug-resistant bacteria.

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Publication Details

Journal
International Microbiology
Published
2026-06-29
DOI
https://doi.org/10.1007/s10123-026-00846-9
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.00

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article

Sensitizing carbapenem-resistant Klebsiella pneumoniae using a compact Cascade-Cas3 system

H Liu, P Li, Luyao Huang, Ligui Wang et al.
International Microbiology
CRISPR and Genetic Engineering
article

Sensitizing carbapenem-resistant Klebsiella pneumoniae using a compact Cascade-Cas3 system

H Liu, P Li, Luyao Huang, Ligui Wang, Xinying Du, Shaofu Qiu, Zhengquan Yuan, Jun Huang, Hongbin Song, Jiahui Chen, Chao Wang
article en

Abstract

Klebsiella pneumoniae is a ‘superbug’ characterized by high virulence and carbapenem resistance. CRISPR-Cas3 is capable of performing large-scale deletions in bacterial genomes. The purpose of this study is to sensitize Klebsiella pneumoniae A324 to carbapenem antibiotics by eliminating the multidrug resistance plasmid pA324-IMP using a compact Cascade-Cas3 system. Recombinant plasmids were constructed using molecular cloning techniques. Three sgRNAs targeting different positions within the bla IMP−38 gene were designed. Recombinant plasmids were separately transformed into host bacteria carrying bla IMP38 genes. The elimination efficiency of each CRISPR-Cas3 system target was determined by PCR and qPCR. Fluorescence confocal microscopy was used to observe the fluorescence intensity. Bacterial drug susceptibility phenotypes were determined using E-test drug sensitivity strips. In this study, we successfully constructed the high copy number plasmid, the fluorescent plasmid, and the recombinant CRISPR plasmids. PCR and qPCR results demonstrated that the CRISPR-Cas3 system could efficiently eliminate bla IMP−38 genes, with pCas3-T3 showing the highest elimination efficiency. Fluorescence confocal microscopy indicated that the fluorescence intensity of the experimental group significantly decreased compared to the control group. Additionally, drug susceptibility tests revealed that the resistance of Klebsiella pneumoniae to imipenem and meropenem was significantly reduced. Furthermore, CRISPR-Cas3 could enhance the effectiveness of meropenem in killing Klebsiella pneumoniae A324. In conclusion, this work demonstrates that the compact Cascade-Cas3 system can serve as a novel tool to eliminate the resistance gene bla IMP−38 and restore the sensitivity of host bacteria to antibiotics. This strategy shows great potential to combat the spread of the bla IMP−38 gene in Klebsiella pneumoniae and holds significant application value in the field of combating drug-resistant bacteria.

International Microbiology
Capital Medical University (CN), Chinese Center For Disease Control and Prevention (CN), Chinese PLA General Hospital (CN), Beijing Center for Disease Prevention and Control (CN), China Medical University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 11%
CRISPR and Genetic Engineering
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