Literature DB >> 34824018

A restructuring of microbiome niche space is associated with Elexacaftor-Tezacaftor-Ivacaftor therapy in the cystic fibrosis lung.

Lo M Sosinski1, Christian Martin H1, Kerri A Neugebauer1, Lydia-Ann J Ghuneim1, Douglas V Guzior2, Alicia Castillo-Bahena3, Jenna Mielke4, Ryan Thomas5, Marc McClelland3, Doug Conrad4, Robert A Quinn6.   

Abstract

BACKGROUND: Elexacaftor-Tezacaftor-Ivacaftor (ETI) therapy is showing promising efficacy for treatment of cystic fibrosis (CF) and is becoming more widely available since recent FDA approval. However, little is known about how these drugs will affect lung infections, which are the leading cause of morbidity and mortality among people with CF (pwCF).
METHODS: We analyzed sputum microbiome and metabolome data from pwCF (n=24) before and after ETI therapy using 16S rRNA gene sequencing and untargeted metabolomics.
RESULTS: The sputum microbiome diversity, particularly its evenness, was increased (p=0.036) and the microbiome profiles were different between individuals before and after therapy (PERMANOVA F=1.92, p=0.044). Despite these changes, the microbiomes remained more similar within an individual than across the sampled population. No specific microbial taxa differed in relative abundance before and after therapy, but the collective log-ratio of classic CF pathogens to anaerobes significantly decreased (p=0.013). The sputum metabolome also showed changes associated with ETI (PERMANOVA F=4.22, p=0.002) and was characterized by greater variation across subjects while on treatment. Changes in the metabolome were driven by a decrease in peptides, amino acids, and metabolites from the kynurenine pathway, which were associated with a decrease in CF pathogens. Metabolism of the three small molecules that make up ETI was extensive, including previously uncharacterized structural modifications.
CONCLUSIONS: ETI therapy is associated with a changing microbiome and metabolome in airway mucus. This effect was stronger on sputum biochemistry, which may reflect changing niche space for microbial residency in lung mucus as the drug's effects take hold. FUNDING: This project was funded by a National Institute of Allergy and Infectious Disease Grant R01AI145925.
Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic Fibrosis; Metabolome; Microbiome; Sputum; Trikafta

Year:  2021        PMID: 34824018      PMCID: PMC9124239          DOI: 10.1016/j.jcf.2021.11.003

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.527


  46 in total

1.  Oxidative stress and lipid-derived inflammatory mediators during acute exacerbations of cystic fibrosis.

Authors:  David W Reid; Neil Misso; Shashi Aggarwal; Philip J Thompson; E Haydn Walters
Journal:  Respirology       Date:  2007-01       Impact factor: 6.424

2.  SIRIUS 4: a rapid tool for turning tandem mass spectra into metabolite structure information.

Authors:  Kai Dührkop; Markus Fleischauer; Marcus Ludwig; Alexander A Aksenov; Alexey V Melnik; Marvin Meusel; Pieter C Dorrestein; Juho Rousu; Sebastian Böcker
Journal:  Nat Methods       Date:  2019-03-18       Impact factor: 28.547

3.  Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation.

Authors:  J Kirk Harris; Brandie D Wagner; Edith T Zemanick; Charles E Robertson; Mark J Stevens; Sonya L Heltshe; Steven M Rowe; Scott D Sagel
Journal:  Ann Am Thorac Soc       Date:  2020-02

4.  CORK Study in Cystic Fibrosis: Sustained Improvements in Ultra-Low-Dose Chest CT Scores After CFTR Modulation With Ivacaftor.

Authors:  Nicola J Ronan; Gisli G Einarsson; Maria Twomey; Denver Mooney; David Mullane; Muireann NiChroinin; Grace O'Callaghan; Fergus Shanahan; Desmond M Murphy; Owen J O'Connor; Cathy A Shortt; Michael M Tunney; Joseph A Eustace; Michael M Maher; J Stuart Elborn; Barry J Plant
Journal:  Chest       Date:  2017-10-14       Impact factor: 9.410

5.  Decade-long bacterial community dynamics in cystic fibrosis airways.

Authors:  Jiangchao Zhao; Patrick D Schloss; Linda M Kalikin; Lisa A Carmody; Bridget K Foster; Joseph F Petrosino; James D Cavalcoli; Donald R VanDevanter; Susan Murray; Jun Z Li; Vincent B Young; John J LiPuma
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-26       Impact factor: 11.205

Review 6.  The cystic fibrosis airway microbiome.

Authors:  Susan V Lynch; Kenneth D Bruce
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915

7.  Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial.

Authors:  Harry G M Heijerman; Edward F McKone; Damian G Downey; Eva Van Braeckel; Steven M Rowe; Elizabeth Tullis; Marcus A Mall; John J Welter; Bonnie W Ramsey; Charlotte M McKee; Gautham Marigowda; Samuel M Moskowitz; David Waltz; Patrick R Sosnay; Christopher Simard; Neil Ahluwalia; Fengjuan Xuan; Yaohua Zhang; Jennifer L Taylor-Cousar; Karen S McCoy
Journal:  Lancet       Date:  2019-10-31       Impact factor: 79.321

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

Authors:  Maartje I Kristensen; Karin M de Winter-de Groot; Gitte Berkers; Mei Ling J N Chu; Kayleigh Arp; Sophie Ghijsen; Harry G M Heijerman; Hubertus G M Arets; Christof J Majoor; Hettie M Janssens; Renske van der Meer; Debby Bogaert; Cornelis K van der Ent
Journal:  J Pers Med       Date:  2021-04-27

9.  Lumacaftor/ivacaftor changes the lung microbiome and metabolome in cystic fibrosis patients.

Authors:  Anne H Neerincx; Katrine Whiteson; Joann L Phan; Paul Brinkman; Mahmoud I Abdel-Aziz; Els J M Weersink; Josje Altenburg; Christof J Majoor; Anke H Maitland-van der Zee; Lieuwe D J Bos
Journal:  ERJ Open Res       Date:  2021-04-19
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  4 in total

1.  Elexacaftor-Tezacaftor-Ivacaftor as a Final Frontier in the Treatment of Cystic Fibrosis: Definition of the Clinical and Microbiological Implications in a Case-Control Study.

Authors:  Giuseppe Migliorisi; Mirella Collura; Francesca Ficili; Tiziana Pensabene; Dafne Bongiorno; Antonina Collura; Francesca Di Bernardo; Stefania Stefani
Journal:  Pharmaceuticals (Basel)       Date:  2022-05-14

Review 2.  CFTR Modulator Therapies: Potential Impact on Airway Infections in Cystic Fibrosis.

Authors:  Francesca Saluzzo; Luca Riberi; Barbara Messore; Nicola Ivan Loré; Irene Esposito; Elisabetta Bignamini; Virginia De Rose
Journal:  Cells       Date:  2022-04-06       Impact factor: 6.600

3.  Complex and unexpected outcomes of antibiotic therapy against a polymicrobial infection.

Authors:  Lydia-Ann J Ghuneim; Ruma Raghuvanshi; Kerri A Neugebauer; Douglas V Guzior; Martin H Christian; Bella Schena; Jeremiah M Feiner; Alicia Castillo-Bahena; Jenna Mielke; Marc McClelland; Douglas Conrad; Isaac Klapper; Tianyu Zhang; Robert A Quinn
Journal:  ISME J       Date:  2022-05-21       Impact factor: 11.217

Review 4.  Exploring the Cystic Fibrosis Lung Microbiome: Making the Most of a Sticky Situation.

Authors:  Christina S Thornton; Nicole Acosta; Michael G Surette; Michael D Parkins
Journal:  J Pediatric Infect Dis Soc       Date:  2022-09-07       Impact factor: 5.235

  4 in total

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