Identifying virulence determinants of multidrug-resistant Klebsiella pneumoniae in Galleria mellonella

Pathog Dis. 2021 Mar 20;79(3):ftab009. doi: 10.1093/femspd/ftab009.

Abstract

Infections caused by Klebsiella pneumoniae are a major public health threat. Extensively drug-resistant and even pan-resistant strains have been reported. Understanding K. pneumoniae pathogenesis is hampered by the fact that murine models of infection offer limited resolution for non-hypervirulent strains which cause the majority of infections. The insect Galleria mellonella larva is a widely used alternative model organism for bacterial pathogens. We have performed genome-scale fitness profiling of a multidrug-resistant K. pneumoniae ST258 strain during infection of G. mellonella, to determine if this model is suitable for large-scale virulence factor discovery in this pathogen. Our results demonstrated a dominant role for surface polysaccharides in infection, with contributions from siderophores, cell envelope proteins, purine biosynthesis genes and additional genes of unknown function. Comparison with a hypervirulent strain, ATCC 43816, revealed substantial overlap in important infection-related genes, as well as additional putative virulence factors specific to ST258, reflecting strain-dependent fitness effects. Our analysis also identified a role for the metalloregulatory protein NfeR (YqjI) in virulence. Overall, this study offers new insight into the infection fitness landscape of K. pneumoniae, and provides a framework for using the highly flexible and easily scalable G. mellonella infection model to dissect molecular virulence mechanisms of bacterial pathogens.

Keywords: Galleria mellonella; Klebsiella pneumoniae; ST258; Tn-seq; TraDIS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • DNA, Bacterial
  • Disease Models, Animal
  • Drug Resistance, Multiple, Bacterial
  • Genetic Complementation Test
  • Genome, Bacterial
  • Humans
  • Klebsiella Infections / microbiology*
  • Klebsiella pneumoniae / drug effects
  • Klebsiella pneumoniae / genetics*
  • Klebsiella pneumoniae / pathogenicity*
  • Larva / microbiology*
  • Membrane Proteins / genetics
  • Moths / microbiology*
  • Mutagenesis
  • Polysaccharides / genetics
  • Purines
  • Siderophores / genetics
  • Siderophores / metabolism
  • Virulence Factors / genetics*
  • Virulence*

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Membrane Proteins
  • Polysaccharides
  • Purines
  • Siderophores
  • Virulence Factors
  • purine