4.6 Article

The Genomic Characterization of KPC-Producing Klebsiella pneumoniae from the ICU of a Teaching Hospital in Shanghai, China

期刊

INFECTION AND DRUG RESISTANCE
卷 15, 期 -, 页码 69-81

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S343673

关键词

Klebsiella pneumoniae; blaKPC-2; whole-genome sequencing; single nucleotide; polymorphism; drug-resistant plasmids

资金

  1. National Natural Science Foundation of China [81871540]
  2. Clinical Research Plan of SHDC [SHDC2020CR6030-003]
  3. three-year action plan for constructing the Shanghai public health system [GWV-3.1]
  4. Construction Plan of Important and Weak Disciplines of Shanghai Health Commission [2016ZB0204-01]
  5. Shanghai Science and Technology Innovation Action Plan [18ZR1429500]

向作者/读者索取更多资源

This study retrospectively analyzed the genome characteristics of blaKPC-2 in multidrug-resistant Klebsiella pneumoniae collected from a teaching hospital in Shanghai, China. The results showed that blaKPC-2 gene is relatively conservative in evolution, and there are significant differences in the plasmid-encoded region. The coexistence of blaKPC-2 with fosA6 or blaCTX-M variants is associated with increased resistance.
Purpose: This study retrospectively analyzed the genome characteristics of blaKPC-2 in multidrug-resistant Klebsiella pneumoniae collected from the ICU of a teaching hospital in Shanghai, China. Methods: From February 2018 to December 2019, 36 strains of multidrug-resistant Klebsiella pneumoniae were collected from the bronchoalveolar lavage fluid of critically ill patients. The genome of all isolates was obtained through the Illumina sequence, and single nucleotide polymorphisms of the blaKPC-2 gene were analyzed to explore blaKPC2's evolutionary characteristics. Different strains' genetic relationships and homology were studied by constructing an evolutionary tree on a single copy orthologue. Pacbio combined Illumina sequence was conducted to evaluate the structure and potential mobility of drug resistant plasmids of the strain KP-s26. Results: The distribution of resistance and virulence genes had little difference, but most strains had significant differences in the plasmid-encoded region. Most strains (31/36) carried the carbapenemase gene blaKPC-2, with no single nucleotide polymorphism in different strains. Extended-spectrum beta-lactamase resistance genes, such as blaCTX-M and blaSHV, were found in the isolates, but no metallo-beta-lactamases were detected. All strains with blaKPC-2 coexisted with chromosomal-associated fosfomycin resistance genes fosA6, and the coexistence of blaKPC-2 and blaCTX variants (blaCTX-M-15, blaCTX-M-65, and blaCTX-M-27) was also detected in 29/31 strains. The isolate KP-s26 carried five circular plasmids. pA and pB were conjugate plasmids, as they carried drug resistance genes and contained a complete IV secretion system. Conclusion: The blaKPC-2 carbapenemase gene is relatively conservative in the process of evolution; drug-resistant plasmids containing conjugated transfer elements contribute to the spreading of drug resistance. The coexistence of blaKPC-2 with fosA6 or blaCTX-M variants was associated with increased fosfomycin resistance and broad-spectrum beta-lactam resistance, respectively.

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