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  4. Longitudinal development of the airway microbiota in infants with cystic fibrosis
 
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Longitudinal development of the airway microbiota in infants with cystic fibrosis
File(s)
supplementary material proof.pdf (275.65 KB)
Supporting information
s41598-019-41597-0.pdf (1.7 MB)
Published version
Author(s)
Ahmed, Bushra
Cox, Michael
Cuthbertson, Leah
James, Phillip
Cookson, William
more
Type
Journal Article
Abstract
The pathogenesis of airway infection in cystic fibrosis (CF) is poorly understood. We performed a longitudinal study coupling clinical information with frequent sampling of the microbiota to identify changes in the airway microbiota in infancy that could underpin deterioration and potentially be targeted therapeutically. Thirty infants with CF diagnosed on newborn screening (NBS) were followed for up to two years. Two hundred and forty one throat swabs were collected as a surrogate for lower airway microbiota (median 35 days between study visits) in the largest longitudinal study of the CF oropharyngeal microbiota. Quantitative PCR and Illumina sequencing of the 16S rRNA bacterial gene were performed. Data analyses were conducted in QIIME and Phyloseq in R. Streptococcus spp. and Haemophilus spp. were the most common genera (55% and 12.5% of reads respectively) and were inversely related. Only beta (between sample) diversity changed with age (Bray Curtis r2 = 0.15, P = 0.03). Staphylococcus and Pseudomonas were rarely detected. These results suggest that Streptococcus spp. and Haemophilus spp., may play an important role in early CF. Whether they are protective against infection with more typical CF micro-organisms, or pathogenic and thus meriting treatment needs to be determined.
Date Issued
2019-03-26
Date Acceptance
2019-03-08
Citation
Scientific Reports, 2019, 9
URI
http://hdl.handle.net/10044/1/68582
DOI
https://www.dx.doi.org/10.1038/s41598-019-41597-0
ISSN
2045-2322
Publisher
Nature Publishing Group
Journal / Book Title
Scientific Reports
Volume
9
Copyright Statement
© The Author(s) 2019. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Cre-ative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not per-mitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Sponsor
National Institute for Health Research
Grant Number
BRU 6279
Publication Status
Published
Article Number
ARTN 5143
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