Burkholderia pseudomallei: animal models of infection

Richard W Titball1, Paul Russell, Jon Cuccui

  • 1School of Biosciences, Geoffrey Pope Building, University of Exeter, Exeter EX4 4QD, UK. r.w.titball@exeter.ac.uk

Insights

Animal models for Burkholderia pseudomallei infection vary in disease presentation. Findings suggest diabetic rats and specific mouse models mimic distinct aspects of human melioidosis.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Animal Models

Background:

  • Burkholderia pseudomallei causes melioidosis, a disease with varied presentations in humans.
  • Numerous animal models exist for studying B. pseudomallei infection, but host susceptibility and disease pathogenesis differ significantly.
  • The optimal animal model that accurately reflects human melioidosis remains unclear.

Purpose of the Study:

  • To review and compare existing animal models for Burkholderia pseudomallei infection.
  • To assess how different host species and experimental conditions influence disease outcomes.
  • To identify which models may best represent specific facets of human melioidosis.

Main Methods:

  • Review of reported animal models of Burkholderia pseudomallei infection.
  • Analysis of host species susceptibility and disease pathogenesis in various models.
  • Comparison of disease manifestations across different animal models (mice, rats, hamsters).

Main Results:

  • Mouse models exhibit a spectrum of disease, from chronic/latent to acute fulminant, dependent on strain, dose, and route.
  • Diabetic rats and hamsters serve as alternative small animal models.
  • Larger animal models are underdeveloped.
  • Inhalation exposure in mice often leads to more acute disease.
  • Diabetic rats show susceptibility, and some mouse strains develop persistent, reactivatable infections.

Conclusions:

  • Existing small animal models (mice, diabetic rats) capture different aspects of human melioidosis.
  • Diabetic rats and specific mouse models showing persistent infections or acute responses may offer valuable insights into human disease.
  • Further development of larger animal models is needed for comprehensive study.

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