The characterization of an IncN-IncR fusion plasmid co-harboring blaTEM−40, blaKPC−2, and blaIMP−4 derived from ST1393 Klebsiella pneumoniae

• Published in: Scientific reports 2024-11, Vol.14 (1), p.26723, Article 26723
• Main Authors: Fang, Lei, Shen, Yanhao, Chen, Ruyan, Li, Chenyu, Liu, Ruishan, Jia, Yuanyuan, Qi, Saiqi, Guo, Xiaobing
• Format: Article
• Language: English
• Subjects: 631/326; 692/308; Bacteria; Carbapenems; Chromosomes; Conjugation; E coli; Genetic analysis; Humanities and Social Sciences; Insertion sequences; Ionization; Klebsiella pneumoniae; Mass spectrometry; Mass spectroscopy; Molecular structure; multidisciplinary; Multidrug resistance; Phenotypes; Plasmids; Polymerase chain reaction; Pulsed-field gel electrophoresis; Recombination; Science; Science (multidisciplinary); Southern blotting; Strains (organisms); Whole genome sequencing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-78205-9

Plasmids, as important genetic elements apart from chromosomes, often carry multiple resistance genes and various mobile genetic elements, enabling them to acquire more exogenous genes and confer additional resistance phenotypes to bacteria. Various carbapenem resistance genes are often located on IncN plasmids, and several reports have linked fusion plasmids to IncN plasmids. Therefore, this study aims to explore the emergence, molecular structure characteristics, and resistance features mediated by IncN fusion plasmids carrying multiple carbapenem resistance genes. In this study, species identification was performed using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS). Polymerase chain reaction (PCR) was employed to detect the presence of carbapenem resistance genes in the strains. PCR-based replicon typing (PBRT) was used to identify IncN plasmids. Plasmids were analyzed through S1-nuclease pulsed-field gel electrophoresis (S1-PFGE), Southern blotting, conjugation experiments, and stability tests. Whole-genome sequencing (WGS) and antimicrobial susceptibility testing (AST) were conducted to characterize the target strains. Four strains containing IncN plasmids were identified: two Klebsiella pneumoniae, one Escherichia coli, and one Enterobacter cloacae, all harboring carbapenem resistance genes. Among them, two IncN plasmids (pFAHZZU7605-KPC-IMP and pFAHZZU7865-IMP) contained blaIMP−4 and exhibited similar molecular structure characteristics. Notably, the pFAHZZU7605-KPC-IMP plasmid harbored both IncN and IncR replicons. We hypothesize that the pFAHZZU7605-KPC-IMP fusion plasmid resulted from the recombination of a pFAHZZU7865-IMP-like plasmid and an IncR-like plasmid. Further analysis of the plasmid’s genetic elements revealed that insertion sequences ISKpn19 and ISKpn27 played crucial roles in the plasmid recombination and fusion process. In clinical settings, plasmids carrying different resistance genes can undergo fusion, mediated by genetic elements, thereby expanding the resistance spectrum of host bacteria. Hence, it is essential to enhance the monitoring and research of transposable elements to control the spread of multidrug-resistant bacteria.