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Microbial Communities of Conducting and Respiratory Zones of Lung-Transplanted Patients

Authors :
Juliane Rick
Yves Chalandon
Dominik Heim
Jörg Halter
Michel A. Duchosal
Nicolas J. Mueller
Christoph Berger
Olivier de Rougemont
Guido Toso
Jacques Schrenzel
Dimitri Tsinalis
Frank Ruschitzka
David Nadal
Chantal Piot Ziegler
John-David Aubert
Günther F.L. Hofbauer
Madeleine Wick
Jürg Steiger
Guido Beldi
Luca Martinolli
Patrick Yerly
Christian Benden
Thierry Carell
Patrizia Amico
Antonia M.S. Müller
Nadia Gaïa
Jakob Passweg
Sabina De Geest
Michael T. Koller
Eddy Roosnek
Urs Schanz
Paola Gasche
Rita Achermann
Emiliano Giostra
Daniel Good
Philippe Morel
Richard Klaghofer
Pierre Y. Martin
Jean Villard
Beat Müllhaupt
Jean-Pierre Venetz
Isabelle Binet
Susanne Stampf
Philippe Baumann
Leo Buhler
Heiner C. Bucher
Thomas Fehr
Anne Rosselet
Bettina Laesser
Ulrike Mueller
Elsa Boely
Michael Dickenmann
Stefan Schaub
Oriol Manuel
Vladimir Lazarevic
Paul Mohacsi
Pascal Meylan
Christian Lovis
Markus J. Wilhelm
Sven Hillinger
Christian Garzoni
Roger Lehmann
Isabelle Morard
Emmanuelle Catana
Thomas Müller
Christian van Delden
Pierre-Yves Bochud
Thilo Köhler
Christian Seiler
Paola Gasche Soccal
Helen Mueller-McKenna
Manuel Pascual
Silvia Rothlin
Karine Hadaya
Franz Immer
Laurent Farinelli
Marie Beaume
Christoph Hess
Hans-Peter Marti
Cédric Hirzel
Dela Golshayan
Guido Stirnimann
Uyen Huynh-Do
Sylvie Ferrari-Lacraz
Loïc Baerlocher
Hans H. Hirsch
Swiss Transplant Cohort Study
Source :
Frontiers in Microbiology, Vol. 7 (2016) P. 1749, Frontiers in Microbiology, Vol 7 (2016), Frontiers in Microbiology, Frontiers in microbiology, vol. 7, pp. 1749
Publication Year :
2016

Abstract

Background: Lung transplantation (LT) is a recognized treatment for end-stage pulmonary disease. Bacteria from the recipient nasopharynx seed the new lungs leading to infections and allograft damage. Understanding the characteristics and topological variations of the microbiota may be important to apprehend the pathophysiology of allograft dysfunction. Objectives: To examine the characteristics and relationship of bacterial compositions between conducting and respiratory zones of the allograft. Methods: We performed 16S rRNA gene sequencing on bronchial aspirates (BAs) and bronchoalveolar lavages (BALs) collected in pairs in 19 patients at several time-points post-LT. Results: The respiratory zone was characterized independently of the time post-LT by a higher bacterial richness than the conducting zone (p = 0.041). The phyla Firmicutes and Proteobacteria dominated both sampling zones, with an inverse correlation between these two phyla (Spearman r = -0.830). Samples of the same pair, as well as pairs from the same individual clustered together (Pseudo-F = 3.8652, p < 0.01). Microbiota of BA and BAL were more closely related in samples from the same patient than each sample type across different patients, with variation in community structure being mainly inter-individual (p < 0.01). Both number of antibiotics administered (p < 0.01) and time interval post-LT (p < 0.01) contributed to the variation in global microbiota structure. Longitudinal analysis of BA-BAL pairs of two patients showed dynamic wave like fluctuations of the microbiota. Conclusions: Our results show that post-transplant respiratory zones harbor higher bacterial richness, but overall similar bacterial profiles as compared to conductive zones. They further support an individual microbial signature following LT.

Details

Language :
English
ISSN :
1664302X
Database :
OpenAIRE
Journal :
Frontiers in Microbiology, Vol. 7 (2016) P. 1749, Frontiers in Microbiology, Vol 7 (2016), Frontiers in Microbiology, Frontiers in microbiology, vol. 7, pp. 1749
Accession number :
edsair.doi.dedup.....4ed9911a83b54f27c240a9aeb0405b4d