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Identification of Biomarkers for Differentiation of Hypervirulent Klebsiella pneumoniae from Classical K. pneumoniae

Journal of Clinical Microbiology · 2018 · Vol. 56(9)
Thomas A. RussoRuth OlsonChi‐Tai FangNicole StoesserMark A. MillerUlrike MacDonaldAlan D. HutsonJason BarkerRicardo M. La HozJames R. JohnsonMartín BäckerRajinder BajwaAndrew CatanzaroDerrick W. CrookKleper de AlmedaJoshua FiererDavid E. GreenbergMichael KlevayPayal PatelAdam J. RatnerJann‐Tay WangJaroslaw Zola

Abstract

A hypervirulent <i>Klebsiella pneumoniae</i> (hvKp) pathotype is undergoing global dissemination. In contrast to the usual health care-associated epidemiology of classical <i>K. pneumoniae</i> (cKp) infections, hvKp causes tissue-invasive infections in otherwise healthy individuals from the community, often involving multiple sites. An accurate test to identify hvKp strains is needed for improved patient care and epidemiologic studies. To fill this knowledge gap, clinical criteria or random blood isolates from North American and United Kingdom strain collections were used to assemble hvKp-rich (<i>n</i> = 85) and cKp-rich (<i>n</i> = 90) strain cohorts, respectively. The isolates were then assessed for multiple candidate biomarkers hypothesized to accurately differentiate the two cohorts. The genes <i>peg-344</i>, <i>iroB</i>, <i>iucA</i>, plasmid-borne <i>rmpA</i> gene ( <sub><i>p</i></sub><i>rmpA</i>), and <sub>p</sub><i>rmpA2</i> all demonstrated >0.95 diagnostic accuracy for identifying strains in the hvKp-rich cohort. Next, to validate this epidemiological analysis, all strains were assessed experimentally in a murine sepsis model. <i>peg-344</i>, <i>iroB</i>, <i>iucA</i>, <sub><i>p</i></sub><i>rmpA</i>, and <sub><i>p</i></sub><i>rmpA2</i> were all associated with a hazard ratio of >25 for severe illness or death, additionally supporting their utility for identifying hvKp strains. Quantitative siderophore production of ≥30 μg/ml also strongly predicted strains as members of the hvKp-rich cohort (accuracy, 0.96) and exhibited a hazard ratio of 31.7 for severe illness or death. The string test, a widely used marker for hvKp strains, performed less well, achieving an accuracy of only 0.90. Last, using the most accurate biomarkers to define hvKp, prevalence studies were performed on two Western strain collections. These data strongly support the utility of several laboratory markers for identifying hvKp strains with a high degree of accuracy.

Antibiotic Resistance in BacteriaBacterial Infections and VaccinesPneumonia and Respiratory InfectionsKlebsiella pneumoniaeMicrobiologyKlebsiella infectionsBiologyKlebsiellaIdentification (biology)VirologyEscherichia coliGeneticsGene

MeSH terms

AnimalsCanadaDisease Models, AnimalGenes, BacterialUnited KingdomHumansKlebsiella InfectionsKlebsiella pneumoniaeMaleBiomarkersSurvival AnalysisSiderophoresMolecular EpidemiologySepsisMolecular Diagnostic Techniques

Funding

  • National Institutes of Health
  • Centers for Disease Control and Prevention
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Cited by
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References
Regression Models and Life-Tables
Journal of the Royal Statistical Society Series B (Statistical Methodology) · 1972 · 38,926 citations
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