Whelan Fiona J, Heirali Alya A, Rossi Laura, Rabin Harvey R, Parkins Michael D, Surette Michael G
Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.
Department of Microbiology, Immunology and Infectious Diseases, The University of Calgary, Calgary, Canada.
PLoS One. 2017 Mar 2;12(3):e0172811. doi: 10.1371/journal.pone.0172811. eCollection 2017.
Cystic fibrosis (CF) manifests in the lungs resulting in chronic microbial infection. Most morbidity and mortality in CF is due to cycles of pulmonary exacerbations-episodes of acute inflammation in response to the lung microbiome-which are difficult to prevent and treat because their cause is not well understood. We hypothesized that longitudinal analyses of the bacterial component of the CF lung microbiome may elucidate causative agents within this community for pulmonary exacerbations. In this study, 6 participants were sampled thrice-weekly for up to one year. During sampling, sputum, and data (antibiotic usage, spirometry, and symptom scores) were collected. Time points were categorized based on relation to exacerbation as Stable, Intermediate, and Treatment. Retrospectively, a subset of were interrogated via 16S rRNA gene sequencing. When samples were examined categorically, a significant difference between the lung microbiota in Stable, Intermediate, and Treatment samples was observed in a subset of participants. However, when samples were examined longitudinally, no correlations between microbial composition and collected data (antibiotic usage, spirometry, and symptom scores) were observed upon exacerbation onset. In this study, we identified no universal indicator within the lung microbiome of exacerbation onset but instead showed that changes to the CF lung microbiome occur outside of acute pulmonary episodes and are patient-specific.
囊性纤维化(CF)在肺部表现出来,导致慢性微生物感染。CF患者的大多数发病和死亡是由于肺部病情加重的循环——即对肺部微生物群作出反应的急性炎症发作——由于其病因尚未完全了解,所以难以预防和治疗。我们假设,对CF肺部微生物群的细菌成分进行纵向分析,可能会阐明该群落中导致肺部病情加重的病原体。在这项研究中,6名参与者每周接受三次采样,持续长达一年。在采样期间,收集痰液和数据(抗生素使用情况、肺活量测定和症状评分)。根据与病情加重的关系,将时间点分为稳定期、中间期和治疗期。回顾性地,通过16S rRNA基因测序对一部分样本进行分析。当对样本进行分类检查时,在一部分参与者中观察到稳定期、中间期和治疗期样本的肺部微生物群之间存在显著差异。然而,当对样本进行纵向检查时,在病情加重发作时,未观察到微生物组成与收集的数据(抗生素使用情况、肺活量测定和症状评分)之间存在相关性。在这项研究中,我们在肺部微生物群中未发现病情加重发作的通用指标,而是表明CF肺部微生物群的变化发生在急性肺部发作之外,且具有个体特异性。