Halo Research Group, Queen's University Belfast, Belfast, UK; Wellcome-Wolfson Institute for Experimental Medicine. School of Medicine, Dentistry and Biomedical Sciences Queen's University Belfast, Belfast, UK.
Cork Centre for Cystic Fibrosis, Cork University Hospital, University College Cork, Ireland; HRB Clinical Research Facility, University College Cork, Cork, Ireland.
J Cyst Fibros. 2021 Sep;20(5):747-753. doi: 10.1016/j.jcf.2020.12.023. Epub 2021 Feb 4.
Treatment with Ivacaftor provides a significant clinical benefit in people with cystic fibrosis (PWCF) with the class III G551D-CFTR mutation. This study determined the effect of CFTR modulation with ivacaftor on the lung microbiota in PWCF.
Using both extended-culture and culture-independent molecular methods, we analysed the lower airway microbiota of 14 PWCF, prior to commencing ivacaftor treatment and at the last available visit within the following year. We determined total bacterial and Pseudomonas aeruginosa densities by both culture and qPCR, assessed ecological parameters and community structure and compared these with biomarkers of inflammation and clinical outcomes.
Significant improvement in FEV, BMI, sweat chloride and levels of circulating inflammatory biomarkers were observed POST-ivacaftor treatment. Extended-culture demonstrated a higher density of strict anaerobic bacteria (p = 0.024), richness (p = 1.59*10) and diversity (p = 0.003) POST-treatment. No significant difference in fold change was observed by qPCR for either total bacterial 16S rRNA copy number or P. aeruginosa density for oprL copy number with treatment. Culture-independent (MiSeq) analysis revealed a significant increase in richness (p = 0.03) and a trend towards increased diversity (p = 0.07). Moreover, improvement in lung function, richness and diversity displayed an inverse correlation with the main markers of inflammation (p < 0.05).
Following treatment with ivacaftor, significant improvements in clinical parameters were seen. Despite modest changes in overall microbial community composition, there was a shift towards a bacterial ecology associated with less severe CF lung disease. Furthermore, a significant correlation was observed between richness and diversity and levels of circulating inflammatory markers.
依伐卡托治疗囊性纤维化(CF)患者的 III 类 G551D-CFTR 突变,能显著改善患者的临床获益。本研究旨在确定依伐卡托对 CF 患者肺部微生物群的调节作用。
采用扩展培养和非培养分子方法,分析了 14 例 CF 患者在开始依伐卡托治疗前和治疗后 1 年内的最后一次可随访时间点的下呼吸道微生物群。通过培养和 qPCR 测定总细菌和铜绿假单胞菌密度,评估生态参数和群落结构,并将其与炎症标志物和临床结果进行比较。
依伐卡托治疗后,FEV1、BMI、汗液氯化物和循环炎症生物标志物水平显著改善。扩展培养显示治疗后严格厌氧菌的密度(p = 0.024)、丰富度(p = 1.59*10)和多样性(p = 0.003)增加。qPCR 检测的总细菌 16S rRNA 拷贝数或 oprL 拷贝数的细菌密度,治疗前后无明显变化。MiSeq 分析显示,丰富度显著增加(p = 0.03),多样性呈增加趋势(p = 0.07)。此外,肺功能、丰富度和多样性的改善与主要炎症标志物呈负相关(p < 0.05)。
依伐卡托治疗后,临床参数明显改善。尽管整体微生物群落组成变化不大,但细菌生态向与 CF 肺部疾病严重程度较低相关的方向转变。此外,还观察到丰富度和多样性与循环炎症标志物水平之间存在显著相关性。