Abstract

Over 90% of cystic fibrosis (CF) patients die due to chronic lung infections leading to respiratory failure. The decline in CF lung function is greatly accelerated by intermittent and progressively severe acute pulmonary exacerbations (PEs). Despite their clinical impact, surprisingly few microbiological signals associated with PEs have been identified. Here we introduce an unsupervised, systems-oriented approach to identify key members of the microbiota. We used two CF sputum microbiome data sets that were longitudinally collected through periods spanning baseline health and PEs. Key taxa were defined based on three strategies: overall relative abundance, prevalence, and co-occurrence network interconnectedness. We measured the association between changes in the abundance of the key taxa and changes in patient clinical status over time via change-point detection, and found that taxa with the highest level of network interconnectedness tracked changes in patient health significantly better than taxa with the highest abundance or prevalence. We also cross-sectionally stratified all samples into the clinical states and identified key taxa associated with each state. We found that network interconnectedness most strongly delineated the taxa among clinical states, and that anaerobic bacteria were over-represented during PEs. Many of these anaerobes are oropharyngeal bacteria that have been previously isolated from the respiratory tract, and/or have been studied for their role in CF. The observed shift in community structure, and the association of anaerobic taxa and PEs lends further support to the growing consensus that anoxic conditions and the subsequent growth of anaerobic microbes are important predictors of PEs.

Highlights

  • Cystic fibrosis (CF) is a systemic, genetic disease accompanied by chronic airway infections largely caused by defective mucociliary clearance.[1]

  • We examined CF lung microbiome dynamics on a longitudinal collection of 266 expectorated sputum samples obtained from 18 CF patients and show that changes in the abundances of highly interconnected taxa track clinical changes more closely than the taxa with either the highest relative abundance or prevalence

  • We have focused on identifying which measure of variation in the CF lung microbiome most closely tracks changes in patient health

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Summary

Introduction

Cystic fibrosis (CF) is a systemic, genetic disease accompanied by chronic airway infections largely caused by defective mucociliary clearance.[1]. One of the most intriguing associations between the CF lung microbiome and PEs identified to date comes from Quinn and colleagues[13] who used network analysis on both taxonomic and inferred metabolic data obtained from 126 CF sputum samples to identify distinct microbial clusters. This cross-sectional study found that taxa clustered into three distinct groups. On the other hand, are more transient communities associated with early lung colonization and PEs.[13]

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