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

被引:36
作者
Bruchmann, Sebastian [1 ,2 ]
Feltwell, Theresa [2 ,3 ]
Parkhill, Julian [1 ]
Short, Francesca L. [2 ,3 ,4 ,5 ]
机构
[1] Univ Cambridge, Dept Vet Med, Madingley Rd, Cambridge CB3 0ES, England
[2] Wellcome Sanger Inst, Pathogen Genom, Wellcome Genome Campus, Hinxton CB10 1SA, England
[3] Univ Cambridge, Old Sch, Dept Med, Cambridge CB2 3PU, England
[4] Macquarie Univ, Dept Mol Sci, N Ryde, NSW 2113, Australia
[5] Monash Univ, Biomed Discovery Inst, Dept Microbiol, Clayton, Vic 3800, Australia
基金
英国惠康基金;
关键词
Klebsiella pneumoniae; Galleria mellonella; TraDIS; Tn-seq; ST258; ESCHERICHIA-COLI; SALMONELLA-TYPHIMURIUM; NOSOCOMIAL PATHOGENS; BACTERIA; GENES; SYSTEM; REGULATOR; ESKAPE; FAMILY; IRON;
D O I
10.1093/femspd/ftab009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:15
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