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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorCrua Asensio, Nuria
dc.contributor.authorMacho Rendón, Javier
dc.contributor.authorTorrent, Marc
dc.contributor.authorGonzález-López, Juan José
dc.contributor.authorGartner, Silvia
dc.contributor.authorMartin Gomez, M. Teresa
dc.date.accessioned2025-10-07T10:24:57Z
dc.date.available2025-10-07T10:24:57Z
dc.date.issued2025-12
dc.identifier.citationCrua Asensio N, Macho Rendón J, González López JJ, Gartner Tizzano S, Martín Gómez MT, Torrent Burgas M. Time-resolved dual transcriptomics of Pseudomonas aeruginosa biofilm formation in cystic fibrosis. Biofilm. 2025 Dec;10:100301.
dc.identifier.issn2590-2075
dc.identifier.urihttp://hdl.handle.net/11351/13803
dc.descriptionDual transcriptomics; Pseudomonas aeruginosa; Cystic fibrosis
dc.description.abstractPseudomonas aeruginosa biofilms cause severe infections in the airways of patients suffering from cystic fibrosis (CF) that are difficult to eradicate, even with intensive antibiotic therapy. The main goal of this study was to define the dual transcriptional response associated with the formation of P. aeruginosa biofilms in a polarized lung epithelium monolayer. We analyzed the dual response of healthy and CF epithelium after infection with P. aeruginosa isolates from acute and chronic infections. Our results show that strains of P. aeruginosa isolated from chronic infections specifically increase the expression of secretion systems of type I, III and VI to hijack the host response. Conversely, strains associated with acute illness use ABC transporters to counteract the antimicrobial response. In return, a distinctive expression pattern in the CF epithelium, including a high degree of cytokine secretion and keratinization, is largely observed in acute infections. Our results show that both host and pathogen genomic backgrounds contribute to the outcome of infection and specific transcriptional signatures could be used in the diagnosis, particularly in CF patients.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesBiofilm;10
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectFibrosi quística
dc.subjectBiofilms
dc.subjectPseudomones aeruginosa
dc.subjectTranscriptomes
dc.subject.meshBiofilms
dc.subject.meshPseudomonas aeruginosa
dc.subject.meshCystic Fibrosis
dc.subject.meshTranscriptome
dc.titleTime-resolved dual transcriptomics of Pseudomonas aeruginosa biofilm formation in cystic fibrosis
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.bioflm.2025.100301
dc.subject.decsbiopelículas
dc.subject.decsPseudomonas aeruginosa
dc.subject.decsfibrosis quística
dc.subject.decstranscriptoma
dc.relation.publishversionhttps://doi.org/10.1016/j.bioflm.2025.100301
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Crua Asensio N, Macho Rendón J, Torrent Burgas M] The Systems Biology of Infection Laboratory, Department of Biochemistry and Molecular Biology, Universitat Autònoma de Barcelona, Bellaterra, Spain. [González López JJ] Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Genètica i Microbiologia, Universitat Autònoma de Barcelona, Bellaterra, Spain. CIBER de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain. [Gartner Tizzano S] Unitat de Pneumologia Pediàtrica i Fibrosi Quística, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Martín Gómez MT] Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid40697188
dc.identifier.wos001539155700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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