Exacerbation induces a microbiota shift in sputa of COPD patients

PLoS One. 2018 Mar 26;13(3):e0194355. doi: 10.1371/journal.pone.0194355. eCollection 2018.

Abstract

Little is known about the microbiota shift induced by exacerbation in chronic obstructive pulmonary disease (COPD) patients. The sputa microbiota of COPD patients was evaluated when clinically stable and during acute exacerbations of the disease. Sputa microbiota was analyzed using 16S ribosomal RNA gene pyrosequencing and quantitative polymerase chain reaction-based pathogen detection. Nine COPD patients were enrolled. Pyrosequencing of 16S rRNA genes identified 2,267 unique bacterial operational taxonomic units. Principal microbiota shifts during exacerbation were in either Proteobacteria, Firmicutes or Bacteroidetes. Streptococcus and Moraxella levels were detected during exacerbation in severe (Global Initiative for Chronic Obstructive Lung Disease 3) COPD patients. Most of the clinically-important genera found in the sputum with the pyrosequencing of 16S rRNA gene correlated with specific quantitative polymerase chain reactions for bacteria while respiratory viruses were nearly absent. Sputum microbiotas of exacerbated COPD patients are complex. This pilot study shows a clear shift in the microbiota of patients during exacerbation. The nature of this shift varies from patient to patient in such a way that the treatment should be patient-specific. Further studies are needed to establish the impact of microbial exacerbations on the pulmonary microbiota.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Bacteria / classification*
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • DNA, Bacterial / genetics
  • DNA, Ribosomal / genetics
  • DNA, Viral / genetics
  • Female
  • High-Throughput Nucleotide Sequencing / methods*
  • Humans
  • Male
  • Microbiota
  • Middle Aged
  • Pilot Projects
  • Pulmonary Disease, Chronic Obstructive / metabolism*
  • RNA, Ribosomal, 16S / genetics*
  • RNA, Viral / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA / methods*
  • Sputum / microbiology
  • Viruses / classification*
  • Viruses / genetics
  • Viruses / isolation & purification

Substances

  • DNA, Bacterial
  • DNA, Ribosomal
  • DNA, Viral
  • RNA, Ribosomal, 16S
  • RNA, Viral

Grants and funding

This work was supported by the Natural Sciences and Engineering Research Council of Canada (CA) - Discovery Grant (Grant no. 5900) to CD (http://www.nserc-crsng.gc.ca/Professors-Professeurs/Grants-Subs/DGIGP-PSIGP_eng.asp) and the Fondation de l’IUCPQ en parteneriat avec la chaire de pneumologie de la fondation J-D Bégin de l’Université Laval. FM reports research support from Boehringer Ingelheim, GlaxoSmithKline, AstraZeneca, Grifols and Novartis. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.