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Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation

Ivacaftor has been shown to restore the functionality of the S1251N (also known as c.3752G>A) mutated CFTR, which may cause alterations in both airway and gut physiology and micro-environment, resulting in a change of microbiota in these organs. The aim of the present study was to analyze the eff...

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Autores principales: Kristensen, Maartje I., de Winter-de Groot, Karin M., Berkers, Gitte, Chu, Mei Ling J. N., Arp, Kayleigh, Ghijsen, Sophie, Heijerman, Harry G. M., Arets, Hubertus G. M., Majoor, Christof J., Janssens, Hettie M., van der Meer, Renske, Bogaert, Debby, van der Ent, Cornelis K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146888/
https://www.ncbi.nlm.nih.gov/pubmed/33925519
http://dx.doi.org/10.3390/jpm11050350
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author Kristensen, Maartje I.
de Winter-de Groot, Karin M.
Berkers, Gitte
Chu, Mei Ling J. N.
Arp, Kayleigh
Ghijsen, Sophie
Heijerman, Harry G. M.
Arets, Hubertus G. M.
Majoor, Christof J.
Janssens, Hettie M.
van der Meer, Renske
Bogaert, Debby
van der Ent, Cornelis K.
author_facet Kristensen, Maartje I.
de Winter-de Groot, Karin M.
Berkers, Gitte
Chu, Mei Ling J. N.
Arp, Kayleigh
Ghijsen, Sophie
Heijerman, Harry G. M.
Arets, Hubertus G. M.
Majoor, Christof J.
Janssens, Hettie M.
van der Meer, Renske
Bogaert, Debby
van der Ent, Cornelis K.
author_sort Kristensen, Maartje I.
collection PubMed
description Ivacaftor has been shown to restore the functionality of the S1251N (also known as c.3752G>A) mutated CFTR, which may cause alterations in both airway and gut physiology and micro-environment, resulting in a change of microbiota in these organs. The aim of the present study was to analyze the effects of ivacaftor on the microbial community composition of both airway and gut in subjects with CF carrying one S1251N mutation, using a 16S rRNA gene-based sequencing approach. In 16 subjects with CF, repetitive samples from airways and gut were collected just before, and 2 months after, and, for 8 patients, also 9 and 12 months after, start of ivacaftor. 16S rRNA based sequencing identified 344 operational taxonomical units (OTUs) in a total of 139 samples (35 nasopharyngeal, 39 oropharyngeal, 29 sputum, and 36 fecal samples). Ivacaftor significantly enhanced bacterial diversity and overall microbiota composition in the gut (p < 0.01). There were no significant changes in the overall microbial composition and alpha diversity in upper and lower airways of these patients after ivacaftor treatment. Treatment with ivacaftor induces changes in gut microbiota whereas airway microbiota do not change significantly over time.
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spelling pubmed-81468882021-05-26 Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation Kristensen, Maartje I. de Winter-de Groot, Karin M. Berkers, Gitte Chu, Mei Ling J. N. Arp, Kayleigh Ghijsen, Sophie Heijerman, Harry G. M. Arets, Hubertus G. M. Majoor, Christof J. Janssens, Hettie M. van der Meer, Renske Bogaert, Debby van der Ent, Cornelis K. J Pers Med Article Ivacaftor has been shown to restore the functionality of the S1251N (also known as c.3752G>A) mutated CFTR, which may cause alterations in both airway and gut physiology and micro-environment, resulting in a change of microbiota in these organs. The aim of the present study was to analyze the effects of ivacaftor on the microbial community composition of both airway and gut in subjects with CF carrying one S1251N mutation, using a 16S rRNA gene-based sequencing approach. In 16 subjects with CF, repetitive samples from airways and gut were collected just before, and 2 months after, and, for 8 patients, also 9 and 12 months after, start of ivacaftor. 16S rRNA based sequencing identified 344 operational taxonomical units (OTUs) in a total of 139 samples (35 nasopharyngeal, 39 oropharyngeal, 29 sputum, and 36 fecal samples). Ivacaftor significantly enhanced bacterial diversity and overall microbiota composition in the gut (p < 0.01). There were no significant changes in the overall microbial composition and alpha diversity in upper and lower airways of these patients after ivacaftor treatment. Treatment with ivacaftor induces changes in gut microbiota whereas airway microbiota do not change significantly over time. MDPI 2021-04-27 /pmc/articles/PMC8146888/ /pubmed/33925519 http://dx.doi.org/10.3390/jpm11050350 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kristensen, Maartje I.
de Winter-de Groot, Karin M.
Berkers, Gitte
Chu, Mei Ling J. N.
Arp, Kayleigh
Ghijsen, Sophie
Heijerman, Harry G. M.
Arets, Hubertus G. M.
Majoor, Christof J.
Janssens, Hettie M.
van der Meer, Renske
Bogaert, Debby
van der Ent, Cornelis K.
Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title_full Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title_fullStr Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title_full_unstemmed Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title_short Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N Mutation
title_sort individual and group response of treatment with ivacaftor on airway and gut microbiota in people with cf and a s1251n mutation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146888/
https://www.ncbi.nlm.nih.gov/pubmed/33925519
http://dx.doi.org/10.3390/jpm11050350
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