4.5 Article

Bacteria and sputum inflammatory cell counts; a COPD cohort analysis

Journal

RESPIRATORY RESEARCH
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12931-020-01552-4

Keywords

Microbiome; COPD; Haemophilus influenzae; Sputum; Eosinophil

Funding

  1. Medical Research Council (MRC)
  2. COPD MAP consortium
  3. National Institute for Health Research Respiratory and Allergy Clinical Research Facility at Manchester University NHS Foundation Trust
  4. National Institute for Health Research (NIHR) Leicester Respiratory Biomedical Research Unit
  5. National Institute for Health Research (NIHR) Respiratory Biomedical Research Unit at the Royal Brompton and Harefield NHS Foundation Trust
  6. Imperial College, London UK
  7. MRC [G0800570, G1001365] Funding Source: UKRI

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Background There is evidence that bacterial colonisation in chronic obstructive pulmonary disease (COPD) is associated with increased neutrophilic airway inflammation. This study tested the hypothesis that different bacterial phyla and species cause different inflammatory profiles in COPD patients. Methods Sputum was analysed by quantitative polymerase chain reaction (qPCR) to quantify bacterial load and 16S rRNA gene sequencing to identify taxonomic composition. Sputum differential cell counts (DCC) and blood DCC were obtained at baseline and 6 months. Patients were categorised into five groups based on bacterial load defined by genome copies/ml of >= 1 x 10(4), no colonisation and colonisation by Haemophilus influenzae (H. influenzae), Moraxella catarrhalis (M. catarrhalis), Streptococcus pneumoniae (S. pneumoniae), or > 1 potentially pathogenic microorganism (PPM). Results We observed an increase in sputum neutrophil (%), blood neutrophil (%) and neutrophil-lymphocyte ratio (NLR) in patients colonised with H. influenzae (82.6, 67.1, and 3.29 respectively) compared to those without PPM colonisation at baseline (69.5, 63.51 and 2.56 respectively) (p < 0.05 for all analyses), with similar findings at 6 months. The bacterial load of H. influenzae and Haemophilus determined by qPCR and 16s rRNA gene sequencing respectively, and sputum neutrophil % were positively correlated between baseline and 6 months visits (p < 0.0001, 0.0150 and 0.0002 with r = 0.53, 0.33 and 0.44 respectively). Conclusions These results demonstrate a subgroup of COPD patients with persistent H. influenzae colonisation that is associated with increased airway and systemic neutrophilic airway inflammation, and less eosinophilic airway inflammation.

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