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Please use this identifier to cite or link to this item: http://hdl.handle.net/11019/1261

Title: The altered gut microbiota in adults with cystic fibrosis
Authors: Burke, D.G.
Fouhy, Fiona
Harrison, M. J
Rea, Mary C
Cotter, Paul D
O’Sullivan, Orla
Stanton, Catherine
Hill, C.
Shanahan, F.
Plant, B. J
Ross, R. Paul
Keywords: Cystic fibrosis
Gut microbiota
454-pyrosequencing
Microbial diversity
Antibiotic therapy
Issue Date: 9-Mar-2017
Publisher: Biomed Central
Citation: Burke DG, Fouhy F, Harrison MJ, Rea MC, Cotter PD, O’Sullivan O, Stanton C, Hill C, Shanahan F, Plant BJ and others. The altered gut microbiota in adults with cystic fibrosis. BMC Microbiology 2017;17(1):58; doi 10.1186/s12866-017-0968-8.
Series/Report no.: BMC Microbiology;vol 17
Abstract: Background Cystic Fibrosis (CF) is an autosomal recessive disease that affects the function of a number of organs, principally the lungs, but also the gastrointestinal tract. The manifestations of cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction in the gastrointestinal tract, as well as frequent antibiotic exposure, undoubtedly disrupts the gut microbiota. To analyse the effects of CF and its management on the microbiome, we compared the gut microbiota of 43 individuals with CF during a period of stability, to that of 69 non-CF controls using 454-pyrosequencing of the 16S rRNA gene. The impact of clinical parameters, including antibiotic therapy, on the results was also assessed. Results The CF-associated microbiome had reduced microbial diversity, an increase in Firmicutes and a reduction in Bacteroidetes compared to the non-CF controls. While the greatest number of differences in taxonomic abundances of the intestinal microbiota was observed between individuals with CF and the healthy controls, gut microbiota differences were also reported between people with CF when grouped by clinical parameters including % predicted FEV1 (measure of lung dysfunction) and the number of intravenous (IV) antibiotic courses in the previous 12 months. Notably, CF individuals presenting with severe lung dysfunction (% predicted FEV1 ≤ 40%) had significantly (p < 0.05) reduced gut microbiota diversity relative to those presenting with mild or moderate dysfunction. A significant negative correlation (−0.383, Simpson’s Diversity Index) was also observed between the number of IV antibiotic courses and gut microbiota diversity. Conclusions This is one of the largest single-centre studies on gut microbiota in stable adults with CF and demonstrates the significantly altered gut microbiota, including reduced microbial diversity seen in CF patients compared to healthy controls. The data show the impact that CF and it's management have on gut microbiota, presenting the opportunity to develop CF specific probiotics to minimise microbiota alterations.
Description: peer-reviewed
URI: http://hdl.handle.net/11019/1261
http://dx.doi.org/10.1186/s12866-017-0968-8
ISSN: 1471-2180
Appears in Collections:Teagasc publications in Biomed Central
Food Biosciences

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