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Composition of airway bacterial community correlates with chest HRCT in adults with bronchiectasis
Author(s) -
O'Neill Katherine,
Einarsson Gisli G.,
Rowan Stephen,
McIlreavey Leanne,
Lee Andrew J.,
Lawson John,
Lynch Tom,
Horsley Alex,
Bradley Judy M.,
Elborn J. Stuart,
Tunney Michael M.
Publication year - 2020
Publication title -
respirology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 85
eISSN - 1440-1843
pISSN - 1323-7799
DOI - 10.1111/resp.13653
Subject(s) - medicine , bronchiectasis , spirometry , sputum , pulmonary function testing , gastroenterology , pathology , lung , asthma , tuberculosis
ABSTRACT Background and objective In bronchiectasis (BE) not caused by cystic fibrosis, chronic, polymicrobial airway infection contributes to the underlying pathogenesis of disease. There is little information on whether bacterial community composition relates to clinical status. We determined the relationship between bacterial community composition, chest high‐resolution computed tomography (HRCT) scores and clinical markers in BE. Methods A subgroup of BE patients from a previous cross‐sectional study were analysed. Spontaneously expectorated sputum was analysed using culture‐independent sequencing on the Roche 454‐FLX platform covering the V1–V3 region of the 16S rRNA marker gene. Chest HRCT scans, multiple breath washout, spirometry and blood inflammatory markers were collected. Spearman's rank (r) correlation coefficient was used to assess relationships. Results Data from 21 patients were analysed (mean (SD) age: 64.0 (7.7); female : male 14:7; mean (SD) forced expiratory volume in 1 s (FEV 1 ): 76.5 (17.2)). All bacterial community composition metrics (bacterial richness, diversity, evenness and dominance) correlated with percentage BE score, with more severe HRCT abnormality relating to lower bacterial richness, evenness and diversity (range r = −0.47 to −0.66; P < 0.05). Inflammation (C‐reactive protein and white cell count) was greater in patients with lower diversity and richness (range r = −0.44 to −0.47; P < 0.05). Bacterial community characteristics did not correlate with lung function. Conclusion This is the first study to indicate a relationship between bacterial community characteristics by 16S rRNA marker gene sequencing, structural damage as determined by chest HRCT and clinical measures in BE. The association between loss of diversity and chest HRCT severity suggests that bacterial dominance with pathogenic bacteria may contribute to disease pathology.