Publication:
Developing collaborative works for faster progress on fungal respiratory infections in cystic fibrosis.

dc.contributor.authorSchwarz, Carsten
dc.contributor.authorVandeputte, Patrick
dc.contributor.authorRougeron, Amandine
dc.contributor.authorGiraud, Sandrine
dc.contributor.authorDugé de Bernonville, Thomas
dc.contributor.authorDuvaux, Ludovic
dc.contributor.authorGastebois, Amandine
dc.contributor.authorAlastruey-Izquierdo, Ana
dc.contributor.authorMartín-Gomez, Maria Teresa
dc.contributor.authorMazuelos, Estrella Martin
dc.contributor.authorSole, Amparo
dc.contributor.authorCano, Josep
dc.contributor.authorPemán, Javier
dc.contributor.authorQuindos, Guillermo
dc.contributor.authorBotterel, Françoise
dc.contributor.authorBougnoux, Marie-Elisabeth
dc.contributor.authorChen, Sharon
dc.contributor.authorDelhaès, Laurence
dc.contributor.authorFavennec, Loïc
dc.contributor.authorRanque, Stéphane
dc.contributor.authorSedlacek, Ludwig
dc.contributor.authorSteinmann, Joerg
dc.contributor.authorVazquez, Jose
dc.contributor.authorWilliams, Craig
dc.contributor.authorMeyer, Wieland
dc.contributor.authorLe Gal, Solène
dc.contributor.authorNevez, Gilles
dc.contributor.authorFleury, Maxime
dc.contributor.authorPapon, Nicolas
dc.contributor.authorSymoens, Françoise
dc.contributor.authorBouchara, Jean-Philippe
dc.contributor.authorECMM/ISHAM working group Fungal respiratory infections in Cystic Fibrosis (Fri-CF)
dc.date.accessioned2023-01-25T10:05:07Z
dc.date.available2023-01-25T10:05:07Z
dc.date.issued2018
dc.description.abstractCystic 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.
dc.identifier.doi10.1093/mmy/myx106
dc.identifier.essn1460-2709
dc.identifier.pmid29538733
dc.identifier.unpaywallURLhttps://academic.oup.com/mmy/article-pdf/56/suppl_1/S42/26573073/myx106.pdf
dc.identifier.urihttp://hdl.handle.net/10668/12239
dc.issue.numbersuppl_1
dc.journal.titleMedical mycology
dc.journal.titleabbreviationMed Mycol
dc.language.isoen
dc.organizationÁrea de Gestión Sanitaria Sur de Sevilla
dc.organizationAGS - Sur de Sevilla
dc.page.number42-59
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rights.accessRightsopen access
dc.subject.meshAntifungal Agents
dc.subject.meshCystic Fibrosis
dc.subject.meshDrug Resistance, Multiple, Fungal
dc.subject.meshFungi
dc.subject.meshGenomics
dc.subject.meshHumans
dc.subject.meshMicrobiological Techniques
dc.subject.meshMycoses
dc.subject.meshRespiratory Tract Infections
dc.subject.meshScedosporium
dc.titleDeveloping collaborative works for faster progress on fungal respiratory infections in cystic fibrosis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number56
dspace.entity.typePublication

Files