Genetic diversity and evolution of the virulence plasmids encoding aerobactin and salmochelin in Klebsiella pneumoniae

Virulence. 2021 Dec;12(1):1323-1333. doi: 10.1080/21505594.2021.1924019.

Abstract

Virulence plasmids of hypervirulent Klebsiella pneumoniae (hvKp) have the potential to transfer to drug-resistant strains or integrate with other plasmids, facilitating the genome evolution of threatening pathogens. We conducted an in-depth analysis of the publicly available 156 complete genome sequences of hvKp together with a multi-region clinical cohort of 171 hvKp strains from China to provide evidence for the virulence plasmid evolution. Virulence plasmids were frequently detected in the ST23 and ST11 K. pneumoniae strains. Multidrug-resistant hvKp (MDR-hvKp) occupied a large proportion of hvKp, and the coexistence of virulence and resistance plasmids may be the major cause. Virulence plasmids commonly possessed multiple replicons, of which IncFIBK was the most prevalent (84.6%). We identified 49 IncFIBK alleles among 583 IncFIBK plasmids, and they could be divided into Clades I, II, and III. We further observed that conjugative and non-conjugative virulence plasmids could be distinguished by IncFIBK genetic diversity, and IncFIBK subtyping could also indirectly indicate a chimeric preference of conjugative virulence plasmids. On this basis, we developed an open-access web tool called KpVR for IncFIBK subtyping. In conclusion, the genetic diversity of IncFIBK virulence plasmids could be used for tracking the evolution of virulence plasmids, and further preventing the emergence of MDR-hvKp strains.

Keywords: Hypervirulent Klebsiella pneumoniae; conjugative transfer; epidemiology; genome evolution; virulence plasmid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enterobactin / analogs & derivatives*
  • Enterobactin / genetics
  • Genetic Variation
  • Humans
  • Hydroxamic Acids*
  • Klebsiella Infections / microbiology
  • Klebsiella pneumoniae* / genetics
  • Klebsiella pneumoniae* / pathogenicity
  • Plasmids* / genetics
  • Virulence / genetics

Substances

  • Hydroxamic Acids
  • salmochelin
  • aerobactin
  • Enterobactin

Grants and funding

This work was supported by National Natural Science Foundation of China under Grant 81871692 and 81572031; and Science and Technology Commission of Shanghai Municipality under Grant 19JC1413000 and 19430750600.