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Published on: February 23, 2014
Genetic Mouse Models of Pneumocystis Pneumonia
J Claire Hoving1,2,3, Ferris T Munyonho4, Jay K Kolls5
1AFRICA CMM Medical Mycology Research Unit, Institute of Infectious Disease and Molecular Medicine (IDM), Cape Town, South Africa. Jennifer.hoving@uct.ac.za.
Abstract:
Pneumocystis jirovecii causes pneumonia in immunocompromised patients. A major challenge in drug susceptibility testing and in understanding host/pathogen interactions is that Pneumocystis spp. are not viable in vitro. Continuous culture of the organism is not currently available, and therefore, developing new drug targets is very limited. Due to this limitation, mouse models of Pneumocystis pneumonia have proven to be an invaluable resource to researchers. In this chapter, we provide an overview of selected methods used in mouse models of infection including, in vivo Pneumocystis murina propagation, routes of transmission, genetic mouse models available, a P. murina life form-specific model, a mouse model of PCP immune reconstitution inflammatory syndrome (IRIS), and the experimental parameters associated with these models.
Insights
Mouse models are crucial for studying Pneumocystis pneumonia (PCP) when in vitro culture is not possible. This chapter details methods for using these models to research PCP and host-pathogen interactions.
Area of Science:
- * Infectious Diseases
- * Immunology
- * Microbiology
Background:
- * *Pneumocystis jirovecii* causes severe pneumonia in immunocompromised individuals.
- * The inability to culture *Pneumocystis* species *in vitro* hinders drug development and host-pathogen interaction studies.
- * Mouse models are essential for overcoming these research limitations.
Purpose of the Study:
- * To provide an overview of established methods for using mouse models of *Pneumocystis* pneumonia (PCP).
- * To highlight the utility of these models in the absence of *in vitro* culture systems.
- * To guide researchers in selecting appropriate models for studying PCP and related immune responses.
Main Methods:
- * In vivo propagation of *Pneumocystis murina* (a related species).
- * Description of transmission routes within mouse models.
- * Overview of available genetic mouse models and life form-specific models.
- * Details on a mouse model for *Pneumocystis* pneumonia immune reconstitution inflammatory syndrome (IRIS).
Main Results:
- * Mouse models enable the study of *Pneumocystis* infection dynamics and host responses.
- * Various models allow for life form-specific investigations and the study of immune reconstitution.
- * Experimental parameters for effective model utilization are outlined.
Conclusions:
- * Mouse models are indispensable tools for advancing the understanding of *Pneumocystis* pneumonia.
- * These models facilitate the development of novel therapeutic strategies and drug targets.
- * The described methods provide a foundation for reproducible and impactful research in PCP.
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