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The microbiome in respiratory medicine: Current challenges and future perspectives

  • Rosa Faner
  • , Oriol Sibila
  • , Alvar Agustí
  • , Eric Bernasconi
  • , James D. Chalmers
  • , Gary B. Huffnagle
  • , Chaysavanh Manichanh
  • , Philip L. Molyneaux
  • , Roger Paredes
  • , Vicente Pérez Brocal
  • , Julia Ponomarenko
  • , Sanjay Sethi
  • , Jordi Dorca
  • , Eduard Monsó
  • University of Barcelona
  • Centro de Investigación Biomédica en Red Enfermedades Respiratorias (CIBERES)
  • Hospital de la Sant Pau
  • University of Lausanne
  • University of Dundee
  • University of Michigan, Ann Arbor
  • Vall d'Hebron Research Institute
  • Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas
  • Royal Brompton and Harefield NHS Foundation Trust
  • Generalitat de Catalunya
  • Centro de Investigación Biomédicaen Red de Epidemiología y Salud Pública (CIBERESP)
  • University of Valencia
  • Barcelona Biomedical Research Park
  • Pompeu Fabra University
  • L'Hospitalet Del Llobregat
  • Autonomous University of Barcelona

Research output: Contribution to journalArticlepeer-review

215 Scopus citations

Abstract

The healthy lung has previously been considered to be a sterile organ because standard microbiological culture techniques consistently yield negative results. However, culture-independent techniques report that large numbers of microorganisms coexist in the lung. There are many unknown aspects in the field, but available reports show that the lower respiratory tract microbiota: 1) is similar in healthy subjects to the oropharyngeal microbiota and dominated by members of the Firmicutes, Bacteroidetes and Proteobacteria phyla; 2) shows changes in smokers and well-defined differences in chronic respiratory diseases, although the temporal and spatial kinetics of these changes are only partially known; and 3) shows relatively abundant non-cultivable bacteria in chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, cystic fibrosis and bronchiectasis, with specific patterns for each disease. In all of these diseases, a loss of diversity, paralleled by an over-representation of Proteobacteria (dysbiosis), has been related to disease severity and exacerbations. However, it is unknown whether dysbiosis is a cause or a consequence of the damage to bronchoalveolar surfaces. Finally, little is known about bacterial functionality and the interactions between viruses, fungi and bacteria. It is expected that future research in bacterial gene expressions, metagenomics longitudinal analysis and host-microbiome animal models will help to move towards targeted microbiome interventions in respiratory diseases.

Original languageEnglish
Article number1602086
JournalEuropean Respiratory Journal
Volume49
Issue number4
DOIs
StatePublished - Apr 1 2017

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