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Published on: March 17, 2014
Pneumocystis jirovecii and cystic fibrosis
Enrique J Calderón1, Vicente Friaza, Francisco J Dapena
1Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, CIBER de Epidemiología y Salud Pública, Seville, Spain. ecalderon@ibis-sevilla.es
Abstract:
Pneumocystis jirovecii is an atypical opportunistic fungus with lung tropism and worldwide distribution that causes pneumonia in immunosuppressed individuals. The development of sensitive molecular techniques has led to the recognition of a colonization or carrier state of P. jirovecii, in which low levels of the organism are detected in persons who do not have pneumonia. Pneumocystis colonization has been described in individuals with various lung diseases, and accumulating evidence suggests that it may be a relevant issue with potential clinical impact. Only a few published studies carried out in Europe have evaluated the prevalence of Pneumocystis colonization in patients with cystic fibrosis, reporting ranges from 1.3-21.6%. The evolution of P. jirovecii colonization in cystic fibrosis patients is largely unknown. In a longitudinal study, none of the colonized patients developed pneumonia during a 1-year follow-up. Since patients with cystic fibrosis could act as major reservoirs and sources of infection for susceptible individuals further research is thus warranted to assess the true scope of the problem and to design rational preventive strategies if necessary. Moreover, it's necessary to elucidate the role of P. jirovecii infection in the natural history of cystic fibrosis in order to improve the clinical management of this disease.
Insights
Pneumocystis jirovecii colonization is common in cystic fibrosis patients but does not typically lead to pneumonia. Further research is needed to understand its role in cystic fibrosis progression and transmission.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Pulmonology
Background:
- Pneumocystis jirovecii is an opportunistic fungus causing pneumonia in immunocompromised individuals.
- Pneumocystis colonization, detected via molecular methods, occurs in individuals without pneumonia.
- Colonization prevalence in cystic fibrosis patients varies (1.3-21.6%), with limited longitudinal data.
Purpose of the Study:
- To investigate the prevalence and clinical significance of Pneumocystis jirovecii colonization in cystic fibrosis patients.
- To understand the evolution of P. jirovecii colonization in this patient group.
- To assess the potential role of cystic fibrosis patients as reservoirs for P. jirovecii.
Main Methods:
- Longitudinal study design.
- Molecular detection techniques for P. jirovecii.
- Clinical monitoring of patients for pneumonia development.
Main Results:
- Pneumocystis jirovecii colonization was observed in cystic fibrosis patients.
- None of the colonized patients developed P. jirovecii pneumonia during a 1-year follow-up.
- The long-term evolution and clinical impact of colonization remain largely uncharacterized.
Conclusions:
- Pneumocystis jirovecii colonization may be prevalent in cystic fibrosis patients without causing immediate pneumonia.
- Further research is essential to determine the scope of P. jirovecii colonization and its impact on cystic fibrosis.
- Understanding this role is crucial for developing preventive strategies and improving clinical management.
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