# Microbial community organization designates distinct pulmonary exacerbation types and predicts treatment outcome in cystic fibrosis

**Authors:** Stefanie Widder, Lisa Carmody, Kristopher Opron, Linda Kalikin, Lindsay Caverly, John LiPuma

PMC · DOI: 10.21203/rs.3.rs-4128740/v1 · Research Square · 2024-03-21

## TL;DR

This study shows that different types of lung infections in cystic fibrosis patients can be identified by their microbial communities, which helps predict how well treatments will work.

## Contribution

The study identifies two distinct microbial dysbiosis regimes in pulmonary exacerbations and links them to treatment outcomes.

## Key findings

- Pathogen-governed PEx is characterized by hierarchical community reorganization and reduced diversity.
- Anaerobic bloom PEx shows stochasticity and increased diversity.
- Antimicrobial treatment simulations suggest better efficacy for hierarchically organized communities.

## Abstract

Polymicrobial infection of the airways is a hallmark of obstructive lung diseases such as cystic fibrosis (CF), non-CF bronchiectasis, and chronic obstructive pulmonary disease. Pulmonary exacerbations (PEx) in these conditions are associated with accelerated lung function decline and higher mortality rates. An understanding of the microbial underpinnings of PEx is challenged by high inter-patient variability in airway microbial community profiles. We analyzed bacterial communities in 880 CF sputum samples and developed microbiome descriptors to model community reorganization prior to and during 18 PEx. We identified two microbial dysbiosis regimes with opposing ecology and dynamics. Pathogen-governed PEx showed hierarchical community reorganization and reduced diversity, whereas anaerobic bloom PEx displayed stochasticity and increased diversity. A simulation of antimicrobial treatment predicted better efficacy for hierarchically organized communities. This link between PEx type, microbiome organization, and treatment success advances the development of personalized clinical management in CF and, potentially, other obstructive lung diseases.

## Linked entities

- **Diseases:** cystic fibrosis (MONDO:0009061), chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Diseases:** infection (MESH:D007239), CF (MESH:D003550), PEx (MESH:D018450), obstructive lung diseases (MESH:D008173), bronchiectasis (MESH:D001987), function (MESH:D003291), chronic obstructive pulmonary disease (MESH:D029424)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10984025/full.md

## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC10984025/full.md

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Source: https://tomesphere.com/paper/PMC10984025