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

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 sequ...

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Bibliographic Details
Published in:Virulence 2021-12, Vol.12 (1), p.1323-1333
Main Authors: Tian, Dongxing, Wang, Meng, Zhou, Ying, Hu, Dakang, Ou, Hong-Yu, Jiang, Xiaofei
Format: Article
Language:English
Subjects:
conjugative transfer
Enterobactin - analogs & derivatives
Enterobactin - genetics
epidemiology
Genetic Variation
genome evolution
Humans
Hydroxamic Acids
Hypervirulent Klebsiella pneumoniae
Klebsiella Infections - microbiology
Klebsiella pneumoniae - genetics
Klebsiella pneumoniae - pathogenicity
Plasmids - genetics
Research Paper
Virulence - genetics
virulence plasmid
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Summary: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 IncFIB K was the most prevalent (84.6%). We identified 49 IncFIB K alleles among 583 IncFIB K 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 IncFIB K genetic diversity, and IncFIB K 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 IncFIB K subtyping. In conclusion, the genetic diversity of IncFIB K virulence plasmids could be used for tracking the evolution of virulence plasmids, and further preventing the emergence of MDR-hvKp strains.
ISSN:2150-5594
2150-5608
DOI:10.1080/21505594.2021.1924019