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The Microbiome in Bronchial Biopsies from Smokers and Ex-Smokers with Stable COPD - A Metatranscriptomic Approach
B Ditz1,2, J Boekhoudt2,3, N Couto4,5
1Department of Pulmonary Diseases, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Metatranscriptomics in COPD lung biopsies reveals ultra-low microbial mass. While no differences were found between smokers and ex-smokers, host-microbiome interactions were identified, highlighting potential for airway research.
Area of Science:
- Respiratory medicine
- Microbiome research
- Genomics
Background:
- Current respiratory microbiome studies primarily use 16S rRNA sequencing.
- Metatranscriptomics offers deeper insights into viable microbiome and host interactions but its feasibility in lung biopsies is under-explored.
Purpose of the Study:
- To assess the feasibility of metatranscriptomic analysis in bronchial biopsies from COPD patients.
- To investigate differences in the respiratory microbiome between stable COPD smokers and ex-smokers.
- To explore host-microbiome interactions using transcriptomic data.
Main Methods:
- RNA sequencing was performed on bronchial biopsies from 5 stable COPD smokers and 6 ex-smokers.
- The Trinity assembler was used for unbiased microbial transcriptional analysis.
- Host-microbiome interactions were analyzed by correlating host and microbial transcriptomic data.
Main Results:
- Ultra-low microbial mass (0.009%) was detected in RNA-seq data from bronchial biopsies.
- No significant differences in microbiome diversity or microbial transcriptional profiles were observed between COPD smokers and ex-smokers.
- An upregulated host gene set associated with specific bacteria (Bradyrhizobium, Roseomonas, Brevibacterium spp.) and the PERK-mediated unfolded protein response was identified.
Conclusions:
- Metatranscriptomic profiling of bronchial biopsies from stable COPD patients yields minimal microbial RNA.
- The study demonstrates the potential of transcriptional profiling for understanding host-microbiome interactions in the airways.
- Further research is needed to optimize methods for detecting and analyzing the respiratory microbiome in lung tissue.
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