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  • Extended-culture and cultur...
    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.

    Journal of cystic fibrosis, September 2021, 2021-09-00, 20210901, Letnik: 20, Številka: 5
    Journal Article

    •CFTR modulation with ivacaftor significantly improves clinical outcomes for PWCF.•Only modest changes in overall microbial community composition are observed following one year of ivacaftor treatment.•However, there was a shift towards a bacterial ecology associated with less severe CF lung disease with an increased microbial richness and diversity.•Furthermore, a significant correlation was observed between richness and diversity and lower levels of circulating markers of inflammation. 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. 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. 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). 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.