TY - JOUR
T1 - A prevalent and culturable microbiota links ecological balance to clinical stability of the human lung after transplantation
AU - Das, Sudip
AU - Bernasconi, Eric
AU - Koutsokera, Angela
AU - Wurlod, Daniel Adrien
AU - Tripathi, Vishwachi
AU - Bonilla-Rosso, Germán
AU - Aubert, John David
AU - Derkenne, Marie France
AU - Mercier, Louis
AU - Pattaroni, Céline
AU - Rapin, Alexis
AU - von Garnier, Christophe
AU - Marsland, Benjamin J.
AU - Engel, Philipp
AU - Nicod, Laurent P.
N1 - Funding Information:
The project was funded by a Marie Sklodowska-Curie Individual Fellowship (awarded to SD, “HUMANITY”, Grant no. 800301), an Interdisciplinary grant from the Faculty of Biology and Medicine of the University of Lausanne (awarded to P.E. and B.M., Grant no. 26075716), an ERC StG (awarded to P.E., “MicroBeeOme”, Grant No. 714804), two Swiss National Science Foundation grants (awarded to P.E., Grant no. 31003A_160345 and 31003A_179487), a HFSP Young Investigator grant (awarded to P.E., Grant no. RGY0077/2016), a grant from the Swiss Lung Association (awarded to A.K., Grant no. 2018-16), a “Pépinière” grant from the Faculty of Biology and Medicine of the University of Lausanne (awarded to A.K.), and a GlaxoSmithKline educational grant (awarded to A. K.). E.B. was supported by “Fondation Professeur Placide Nicod”. B.J.M. is a VESKI innovation fellow and an NHMRC Senior Research Fellow.
Publisher Copyright:
© 2021, The Author(s).
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/12
Y1 - 2021/12
N2 - There is accumulating evidence that the lower airway microbiota impacts lung health. However, the link between microbial community composition and lung homeostasis remains elusive. We combine amplicon sequencing and bacterial culturing to characterize the viable bacterial community in 234 longitudinal bronchoalveolar lavage samples from 64 lung transplant recipients and establish links to viral loads, host gene expression, lung function, and transplant health. We find that the lung microbiota post-transplant can be categorized into four distinct compositional states, ‘pneumotypes’. The predominant ‘balanced’ pneumotype is characterized by a diverse bacterial community with moderate viral loads, and host gene expression profiles suggesting immune tolerance. The other three pneumotypes are characterized by being either microbiota-depleted, or dominated by potential pathogens, and are linked to increased immune activity, lower respiratory function, and increased risks of infection and rejection. Collectively, our findings establish a link between the lung microbial ecosystem, human lung function, and clinical stability post-transplant.
AB - There is accumulating evidence that the lower airway microbiota impacts lung health. However, the link between microbial community composition and lung homeostasis remains elusive. We combine amplicon sequencing and bacterial culturing to characterize the viable bacterial community in 234 longitudinal bronchoalveolar lavage samples from 64 lung transplant recipients and establish links to viral loads, host gene expression, lung function, and transplant health. We find that the lung microbiota post-transplant can be categorized into four distinct compositional states, ‘pneumotypes’. The predominant ‘balanced’ pneumotype is characterized by a diverse bacterial community with moderate viral loads, and host gene expression profiles suggesting immune tolerance. The other three pneumotypes are characterized by being either microbiota-depleted, or dominated by potential pathogens, and are linked to increased immune activity, lower respiratory function, and increased risks of infection and rejection. Collectively, our findings establish a link between the lung microbial ecosystem, human lung function, and clinical stability post-transplant.
UR - http://www.scopus.com/inward/record.url?scp=85104108418&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-22344-4
DO - 10.1038/s41467-021-22344-4
M3 - Article
C2 - 33837203
AN - SCOPUS:85104108418
SN - 2041-1723
VL - 12
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 2126
ER -