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Extended-culture and culture-independent molecular analysis of the airway microbiota in cystic fibrosis following CFTR modulation with ivacaftor.
Einarsson, Gisli G; Ronan, Nicola J; Mooney, Denver; McGettigan, Clodagh; Mullane, David; NiChroinin, Muireann; Shanahan, Fergus; Murphy, Desmond M; McCarthy, Mairead; McCarthy, Yvonne; Eustace, Joseph A; Gilpin, Deirdre F; Elborn, J Stuart; Plant, Barry J; Tunney, Michael M.
  • Einarsson GG; Halo Research Group, Queen's University Belfast, Belfast, UK; Wellcome-Wolfson Institute for Experimental Medicine. School of Medicine, Dentistry and Biomedical Sciences Queen's University Belfast, Belfast, UK. Electronic address: g.einarsson@qub.ac.uk.
  • Ronan NJ; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland; HRB Clinical Research Facility, University College Cork, Cork, Ireland.
  • Mooney D; Halo Research Group, Queen's University Belfast, Belfast, UK; Wellcome-Wolfson Institute for Experimental Medicine. School of Medicine, Dentistry and Biomedical Sciences Queen's University Belfast, Belfast, UK.
  • McGettigan C; Halo Research Group, Queen's University Belfast, Belfast, UK; School of Pharmacy, Queen's University Belfast, Belfast, UK.
  • Mullane D; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland.
  • NiChroinin M; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland.
  • Shanahan F; Department of Medicine, Cork University Hospital, Wilton, Cork, Ireland.
  • Murphy DM; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland; HRB Clinical Research Facility, University College Cork, Cork, Ireland.
  • McCarthy M; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland.
  • McCarthy Y; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland.
  • Eustace JA; HRB Clinical Research Facility, University College Cork, Cork, Ireland.
  • Gilpin DF; Halo Research Group, Queen's University Belfast, Belfast, UK; School of Pharmacy, Queen's University Belfast, Belfast, UK.
  • Elborn JS; Halo Research Group, Queen's University Belfast, Belfast, UK; Wellcome-Wolfson Institute for Experimental Medicine. School of Medicine, Dentistry and Biomedical Sciences Queen's University Belfast, Belfast, UK.
  • Plant BJ; Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland; HRB Clinical Research Facility, University College Cork, Cork, Ireland; Department of Medicine, Cork University Hospital, Wilton, Cork, Ireland.
  • Tunney MM; Halo Research Group, Queen's University Belfast, Belfast, UK; School of Pharmacy, Queen's University Belfast, Belfast, UK.
J Cyst Fibros ; 20(5): 747-753, 2021 09.
Article en En | MEDLINE | ID: mdl-33549519
BACKGROUND: Treatment with Ivacaftor provides a significant clinical benefit in people with cystic fibrosis (PWCF) with the class III G551D-CFTR mutation. This study determined the effect of CFTR modulation with ivacaftor on the lung microbiota in PWCF. METHODS: Using both extended-culture and culture-independent molecular methods, we analysed the lower airway microbiota of 14 PWCF, prior to commencing ivacaftor treatment and at the last available visit within the following year. We determined total bacterial and Pseudomonas aeruginosa densities by both culture and qPCR, assessed ecological parameters and community structure and compared these with biomarkers of inflammation and clinical outcomes. RESULTS: Significant improvement in FEV1, BMI, sweat chloride and levels of circulating inflammatory biomarkers were observed POST-ivacaftor treatment. Extended-culture demonstrated a higher density of strict anaerobic bacteria (p = 0.024), richness (p = 1.59*10-4) and diversity (p = 0.003) POST-treatment. No significant difference in fold change was observed by qPCR for either total bacterial 16S rRNA copy number or P. aeruginosa density for oprL copy number with treatment. Culture-independent (MiSeq) analysis revealed a significant increase in richness (p = 0.03) and a trend towards increased diversity (p = 0.07). Moreover, improvement in lung function, richness and diversity displayed an inverse correlation with the main markers of inflammation (p < 0.05). CONCLUSIONS: Following treatment with ivacaftor, significant improvements in clinical parameters were seen. Despite modest changes in overall microbial community composition, there was a shift towards a bacterial ecology associated with less severe CF lung disease. Furthermore, a significant correlation was observed between richness and diversity and levels of circulating inflammatory markers.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quinolonas / Fibrosis Quística / Microbiota / Aminofenoles Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quinolonas / Fibrosis Quística / Microbiota / Aminofenoles Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article