Animal models of Klebsiella pneumoniae mucosal infections

Lucas Assoni1, Ana Julia Melo Couto1, Brenda Vieira1

  • 1Laboratório de Microbiologia Molecular e Clínica, Universidade São Francisco, Bragança Paulista, Brazil.

PubMed

Insights

Choosing the right animal model is crucial for studying Klebsiella pneumoniae infections. This review compares models, highlighting limitations in reproducing human mucosal infections, especially with mice.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Immunology

Background:

  • Klebsiella pneumoniae is a significant global pathogen associated with high morbidity, mortality, and increasing antibiotic resistance.
  • Understanding K. pneumoniae pathogenesis and developing effective treatments necessitate reliable animal models that mimic human infections.
  • Current research relies on animal models to identify therapeutic targets and evaluate vaccines, but model limitations can impact data validity.

Purpose of the Study:

  • To review and compare animal models used for investigating Klebsiella pneumoniae infections, focusing on mucosal sites.
  • To discuss the advantages and limitations of various models in reproducing human disease hallmarks.
  • To explore applications, human extrapolations, and potential improvements for K. pneumoniae infection models.

Main Methods:

  • Comprehensive literature review of animal models for K. pneumoniae research.
  • Comparative analysis of model systems including mice, Drosophila melanogaster, Caenorhabditis elegans, Galleria mellonella, and Danio rerio.
  • Evaluation of model suitability for studying mucosal infections and immune responses.

Main Results:

  • Mice are widely used but exhibit limitations in mimicking human K. pneumoniae mucosal infections due to natural resistance.
  • Invertebrate models like fruit flies, C. elegans, waxworms, and zebrafish offer insights into bacterial lethality, colonization, and innate immunity but lack mammalian immunological complexity.
  • No single model perfectly replicates all aspects of human K. pneumoniae infections.

Conclusions:

  • The selection of an appropriate animal model for K. pneumoniae research depends on the specific research question.
  • Further understanding of host-pathogen interactions is vital for developing effective preventive and therapeutic strategies.
  • Future research should focus on refining existing models or developing novel ones to better recapitulate human K. pneumoniae disease.