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Developing collaborative works for faster progress on fungal respiratory infections in cystic fibrosis
Carsten Schwarz1, Patrick Vandeputte2,3, Amandine Rougeron4
1Department of Pediatric Pneumology and Immunology, Cystic Fibrosis Center Berlin/Charité -Universitätsmedizin Berlin, Berlin, Germany.
Abstract:
Cystic fibrosis (CF) is the major genetic inherited disease in Caucasian populations. The respiratory tract of CF patients displays a sticky viscous mucus, which allows for the entrapment of airborne bacteria and fungal spores and provides a suitable environment for growth of microorganisms, including numerous yeast and filamentous fungal species. As a consequence, respiratory infections are the major cause of morbidity and mortality in this clinical context. Although bacteria remain the most common agents of these infections, fungal respiratory infections have emerged as an important cause of disease. Therefore, the International Society for Human and Animal Mycology (ISHAM) has launched a working group on Fungal respiratory infections in Cystic Fibrosis (Fri-CF) in October 2006, which was subsequently approved by the European Confederation of Medical Mycology (ECMM). Meetings of this working group, comprising both clinicians and mycologists involved in the follow-up of CF patients, as well as basic scientists interested in the fungal species involved, provided the opportunity to initiate collaborative works aimed to improve our knowledge on these infections to assist clinicians in patient management. The current review highlights the outcomes of some of these collaborative works in clinical surveillance, pathogenesis and treatment, giving special emphasis to standardization of culture procedures, improvement of species identification methods including the development of nonculture-based diagnostic methods, microbiome studies and identification of new biological markers, and the description of genotyping studies aiming to differentiate transient carriage and chronic colonization of the airways. The review also reports on the breakthrough in sequencing the genomes of the main Scedosporium species as basis for a better understanding of the pathogenic mechanisms of these fungi, and discusses treatment options of infections caused by multidrug resistant microorganisms, such as Scedosporium and Lomentospora species and members of the Rasamsonia argillacea species complex.
Insights
Fungal respiratory infections are a growing concern in cystic fibrosis (CF) patients. Research is advancing diagnostics, understanding pathogenesis, and treatment for these challenging infections.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Pulmonology
Background:
- Cystic fibrosis (CF) patients are susceptible to respiratory infections due to viscous mucus.
- Fungal infections are an emerging cause of morbidity and mortality in CF, alongside bacterial infections.
Purpose of the Study:
- To review collaborative research outcomes on fungal respiratory infections in CF.
- To improve clinical management through enhanced knowledge of fungal pathogenesis and treatment.
Main Methods:
- Standardization of culture procedures and species identification.
- Development of non-culture-based diagnostic methods and microbiome studies.
- Genotyping for differentiating fungal carriage and colonization, and genome sequencing of pathogenic fungi.
Main Results:
- Progress in diagnostic methods, including molecular approaches.
- Insights into the pathogenesis of fungal infections in CF airways.
- Identification of treatment strategies for multidrug-resistant fungal pathogens.
Conclusions:
- Collaborative efforts are crucial for advancing the understanding and management of fungal respiratory infections in CF.
- Further research is needed to combat emerging multidrug-resistant fungal threats in CF patients.
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