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Sputum microbiome temporal variability and dysbiosis in chronic obstructive pulmonary disease exacerbations: an analysis of the COPDMAP study

机译:慢性阻塞性肺疾病急性加重期痰微生物组时间变异性和生态失调:COpDmap研究分析

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摘要

Background Recent studies suggest that lung microbiome dysbiosis, the disease associated disruption of the lung microbial community, might play a key role in chronic obstructive pulmonary disease (COPD) exacerbations. However, characterising temporal variability of the microbiome from large longitudinal COPD cohorts is needed to better understand this phenomenon.Methods We performed a 16S ribosomal RNA survey of microbiome on 716 sputum samples collected longitudinally at baseline and exacerbations from 281 subjects with COPD at three UK clinical centres as part of the COPDMAP consortium.Results The microbiome composition was similar among centres and between stable and exacerbations except for a small significant decrease of Veillonella at exacerbations. The abundance of Moraxella was negatively associated with bacterial alpha diversity. Microbiomes were distinct between exacerbations associated with bacteria versus eosinophilic airway inflammation. Dysbiosis at exacerbations, measured as significant within subject deviation of microbial composition relative to baseline, was present in 41% of exacerbations. Dysbiosis was associated with increased exacerbation severity indicated by a greater fall in forced expiratory volume in one second, forced vital capacity and a greater increase in CAT score, particularly in exacerbations with concurrent eosinophilic inflammation. There was a significant difference of temporal variability of microbial alpha and beta diversity among centres. The variation of beta diversity significantly decreased in those subjects with frequent historical exacerbations.Conclusions Microbial dysbiosis is a feature of some exacerbations and its presence, especially in concert with eosinophilic inflammation, is associated with more severe exacerbations indicated by a greater fall in lung function.
机译:背景技术最近的研究表明,与肺微生物群落破坏相关的疾病-肺微生物组功能失调可能在慢性阻塞性肺疾病(COPD)恶化中起关键作用。然而,为了更好地了解这一现象,需要表征大型纵向COPD人群中微生物组的时间变异性。方法我们对基线时纵向收集的716份痰样本进行了16S核糖体RNA微生物学调查,并在三项英国临床研究中对281名COPD受试者的病情加重了结果中心之间以及稳定期和恶化期之间的微生物组组成相似,除了在恶化时Veillonella的少量显着减少。莫拉氏菌的丰度与细菌的α多样性呈负相关。在与细菌相关的病情加重与嗜酸性气道炎症之间,微生物组是不同的。病情加重时发生的病情恶化,在微生物成分相对于基线的受试者偏离范围内测得为显着,占病情加重的比例为41%。代谢异常与病情加重的严重程度增加有关,表现为一秒钟的呼气量下降幅度更大,被迫的肺活量和CAT评分的升高幅度更大,特别是在并发嗜酸性粒细胞炎症的情况下。各中心之间微生物α和β多样性的时间变异性存在显着差异。在那些具有历史性发作频繁的受试者中,β多样性的变化显着降低。结论微生物营养不良是某些发作的一个特征,尤其是与嗜酸性粒细胞炎症相伴的微生物病,与肺功能下降更大的更严重的发作有关。

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