Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient

Background: The carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a serious threat to antibiotic applicability and public health. During treatment, K. pneumoniae (KP) frequently exhibits shifts in drug-resistant phenotypes, complicating clinical treatment as it transitions from sensitivity to...

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Main Authors: Yongjin Hu, Rong Tang, Shanshan Jin, Jiahao Guan, Xiaoxiao Meng, Zengpeijie Dan, Ruilan Wang, Hong-Yu Ou, Jian Lu
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Journal of Global Antimicrobial Resistance
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Online Access:http://www.sciencedirect.com/science/article/pii/S2213716524004442
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author Yongjin Hu
Rong Tang
Shanshan Jin
Jiahao Guan
Xiaoxiao Meng
Zengpeijie Dan
Ruilan Wang
Hong-Yu Ou
Jian Lu
author_facet Yongjin Hu
Rong Tang
Shanshan Jin
Jiahao Guan
Xiaoxiao Meng
Zengpeijie Dan
Ruilan Wang
Hong-Yu Ou
Jian Lu
author_sort Yongjin Hu
collection DOAJ
description Background: The carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a serious threat to antibiotic applicability and public health. During treatment, K. pneumoniae (KP) frequently exhibits shifts in drug-resistant phenotypes, complicating clinical treatment as it transitions from sensitivity to resistance. In this study, we analysed the clinical and molecular characteristics of drug resistance changes in KP strains isolated from a single patient, and the potential mechanisms underlying these resistance changes. Methods: Antimicrobial susceptibility test and string test were conducted to evaluate the resistant and virulent characterization of the strains. Pulsed-field gel electrophoresis (PFGE) was used to investigate the homology relationship between the strains. The whole genome sequencing and phylogenetic analysis of 9 representative isolates was also performed. The transfer ability of the drug-resistant plasmid was studied by plasmid conjugation experiment. The transconjugants were verified by polymerase chain reaction amplification of specific genes, antimicrobial susceptibility test and PFGE. Results: Our results revealed that 9 KP strains, isolated from the same patient, exhibited ‘resistance-sensitivity-resistance-sensitivity’ alternately to carbapenems. The differences in DNA fingerprint bands among the nine KP isolates were ≤3, which can be classified as the same PFGE type. Phylogenetic analysis showed that these 9 strains constituted a distinct branch within the phylogenetic tree. All nine KP strains belonged to the ST15-KL19 clone. Six of the strains were classified as CRKP, all of which carried 11 drug resistance genes: oqxB, oqxA, fosA6, aac(3)-lld, blaSHV-28, blaKPC-2, blaOXA-1, mph(A), tet(A), catB3 and aac(6′)-lb-cr, mediating drug resistance to quinolones, fosfomycin, aminoglycosides, β-lactam, carbapenems, macrolides and chloramphenicol, belonging to multi-drug resistant bacteria. The carbapenem-resistant plasmid p2-KP3762–1 was found to transfer within species, from CRKP to hypervirulent KPRJF293HA, carbapenem-sensitive KP KP3657 and Escherichia coli C600 at a frequency of (1.19 ± 1.58) ×10−6, (1.09 ± 1.38) ×10−7 and (10.9 ± 9.53) ×10−6 respectively, resulting in the dissemination of carbapenem resistance genes. Conclusions: In this study, KP strains isolated from a single patient exhibited an alternating phenotype of resistant-sensitive-resistant-sensitive to carbapenems. The 9 KP isolates share a high degree of genetic similarity. The plasmid p2-KP3762–1, harbouring the carbapenem resistance gene blaKPC-2, may undergo inter-strain and inter-clone transfer via conjugation in the patient during treatment. Furthermore, our findings suggest that the pathogens in this patient are likely to have a common ancestral origin.
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spelling doaj-art-2aca003d23584983981ac99a933f1c5a2025-02-08T05:00:24ZengElsevierJournal of Global Antimicrobial Resistance2213-71652025-01-01407280Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patientYongjin Hu0Rong Tang1Shanshan Jin2Jiahao Guan3Xiaoxiao Meng4Zengpeijie Dan5Ruilan Wang6Hong-Yu Ou7Jian Lu8Department of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Clinical Laboratory, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaSchool of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaSchool of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Corresponding author. Mailing address: Department of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No. 100 Haining Road, Hongkou District, Shanghai 200080, China.Background: The carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a serious threat to antibiotic applicability and public health. During treatment, K. pneumoniae (KP) frequently exhibits shifts in drug-resistant phenotypes, complicating clinical treatment as it transitions from sensitivity to resistance. In this study, we analysed the clinical and molecular characteristics of drug resistance changes in KP strains isolated from a single patient, and the potential mechanisms underlying these resistance changes. Methods: Antimicrobial susceptibility test and string test were conducted to evaluate the resistant and virulent characterization of the strains. Pulsed-field gel electrophoresis (PFGE) was used to investigate the homology relationship between the strains. The whole genome sequencing and phylogenetic analysis of 9 representative isolates was also performed. The transfer ability of the drug-resistant plasmid was studied by plasmid conjugation experiment. The transconjugants were verified by polymerase chain reaction amplification of specific genes, antimicrobial susceptibility test and PFGE. Results: Our results revealed that 9 KP strains, isolated from the same patient, exhibited ‘resistance-sensitivity-resistance-sensitivity’ alternately to carbapenems. The differences in DNA fingerprint bands among the nine KP isolates were ≤3, which can be classified as the same PFGE type. Phylogenetic analysis showed that these 9 strains constituted a distinct branch within the phylogenetic tree. All nine KP strains belonged to the ST15-KL19 clone. Six of the strains were classified as CRKP, all of which carried 11 drug resistance genes: oqxB, oqxA, fosA6, aac(3)-lld, blaSHV-28, blaKPC-2, blaOXA-1, mph(A), tet(A), catB3 and aac(6′)-lb-cr, mediating drug resistance to quinolones, fosfomycin, aminoglycosides, β-lactam, carbapenems, macrolides and chloramphenicol, belonging to multi-drug resistant bacteria. The carbapenem-resistant plasmid p2-KP3762–1 was found to transfer within species, from CRKP to hypervirulent KPRJF293HA, carbapenem-sensitive KP KP3657 and Escherichia coli C600 at a frequency of (1.19 ± 1.58) ×10−6, (1.09 ± 1.38) ×10−7 and (10.9 ± 9.53) ×10−6 respectively, resulting in the dissemination of carbapenem resistance genes. Conclusions: In this study, KP strains isolated from a single patient exhibited an alternating phenotype of resistant-sensitive-resistant-sensitive to carbapenems. The 9 KP isolates share a high degree of genetic similarity. The plasmid p2-KP3762–1, harbouring the carbapenem resistance gene blaKPC-2, may undergo inter-strain and inter-clone transfer via conjugation in the patient during treatment. Furthermore, our findings suggest that the pathogens in this patient are likely to have a common ancestral origin.http://www.sciencedirect.com/science/article/pii/S2213716524004442Carbapenem resistanceST15Klebsiella pneumoniaePlasmid transferConjugative plasmidAntibiotic resistance
spellingShingle Yongjin Hu
Rong Tang
Shanshan Jin
Jiahao Guan
Xiaoxiao Meng
Zengpeijie Dan
Ruilan Wang
Hong-Yu Ou
Jian Lu
Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
Journal of Global Antimicrobial Resistance
Carbapenem resistance
ST15
Klebsiella pneumoniae
Plasmid transfer
Conjugative plasmid
Antibiotic resistance
title Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
title_full Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
title_fullStr Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
title_full_unstemmed Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
title_short Molecular characterization of ST15 carbapenem-resistant Klebsiella pneumoniae isolated in a single patient
title_sort molecular characterization of st15 carbapenem resistant klebsiella pneumoniae isolated in a single patient
topic Carbapenem resistance
ST15
Klebsiella pneumoniae
Plasmid transfer
Conjugative plasmid
Antibiotic resistance
url http://www.sciencedirect.com/science/article/pii/S2213716524004442
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