Animal models of hospital-acquired pneumonia: current practices and future perspectives
Kenny Bielen1,2, Bart 's Jongers1,2, Surbhi Malhotra-Kumar2
1Molecular Pathology Group, Faculty of Medicine and Health Sciences, Laboratory of Cell Biology and Histology, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium.
Abstract:
Lower respiratory tract infections are amongst the leading causes of mortality and morbidity worldwide. Especially in hospital settings and more particularly in critically ill ventilated patients, nosocomial pneumonia is one of the most serious infectious complications frequently caused by opportunistic pathogens. Pseudomonas aeruginosa is one of the most important causes of ventilator-associated pneumonia as well as the major cause of chronic pneumonia in cystic fibrosis patients. Animal models of pneumonia allow us to investigate distinct types of pneumonia at various disease stages, studies that are not possible in patients. Different animal models of pneumonia such as one-hit acute pneumonia models, ventilator-associated pneumonia models and biofilm pneumonia models associated with cystic fibrosis have been extensively studied and have considerably aided our understanding of disease pathogenesis and testing and developing new treatment strategies. The present review aims to guide investigators in choosing appropriate animal pneumonia models by describing and comparing the relevant characteristics of each model using P. aeruginosa as a model etiology for hospital-acquired pneumonia. Key to establishing and studying these animal models of infection are well-defined end-points that allow precise monitoring and characterization of disease development that could ultimately aid in translating these findings to patient populations in order to guide therapy. In this respect, and discussed here, is the development of humanized animal models of bacterial pneumonia that could offer unique advantages to study bacterial virulence factor expression and host cytokine production for translational purposes.
Insights
This review guides researchers in selecting animal models for studying pneumonia, particularly infections caused by Pseudomonas aeruginosa. It details various models to advance understanding and treatment of hospital-acquired pneumonia.
Area of Science:
- Infectious Diseases
- Microbiology
- Translational Medicine
Background:
- Lower respiratory tract infections cause significant global mortality and morbidity.
- Nosocomial pneumonia, especially ventilator-associated pneumonia (VAP), is a severe complication in hospital settings.
- Pseudomonas aeruginosa is a key pathogen in VAP and chronic cystic fibrosis lung infections.
Purpose of the Study:
- To guide investigators in selecting appropriate animal models for pneumonia research.
- To compare characteristics of different animal pneumonia models using P. aeruginosa.
- To highlight the importance of well-defined endpoints for translational research.
Main Methods:
- Review of existing literature on animal models of pneumonia.
- Description and comparison of acute, VAP, and biofilm pneumonia models.
- Discussion of humanized animal models for studying bacterial virulence and host response.
Main Results:
- Various animal models (acute, VAP, biofilm) have advanced understanding of pneumonia pathogenesis.
- P. aeruginosa serves as a relevant model organism for hospital-acquired pneumonia studies.
- Humanized models offer potential for studying virulence factors and cytokine production.
Conclusions:
- Appropriate animal models are crucial for understanding pneumonia and developing new therapies.
- Well-defined endpoints are essential for translating animal model findings to clinical practice.
- Future research may benefit from humanized models for studying host-pathogen interactions in bacterial pneumonia.
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