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Published on: April 28, 2014
Lung microbiome on admission in critically ill patients with acute bacterial and viral pneumonia
Jose María Marimón1,2, Ane Sorarrain3, Maria Ercibengoa3
1Biodonostia, Infectious Diseases Area, Respiratory Infection and Antimicrobial Resistance Group, Microbiology Department, Osakidetza Basque Health Service, Donostialdea Integrated Health Organization, 20014, Donostia-San Sebastian, Spain. josemaria.marimonortizdez@osakidetza.eus.
Abstract:
Composition of pulmonary microbiome of patients with severe pneumonia is poorly known. The aim of this work was to analyse the lung microbiome of patients admitted to the intensive care unit (ICU) with severe community acquired pneumonia (CAP) between 2019 and 2021 in comparison with a control group of 6 patients undergoing digestive surgery. As a second objective, the diagnostic capabilities of metagenomics was also studied in a small group of selected patients. The lung microbiome of patients with viral (5 with Influenza A and 8 with SARS-CoV-2) pneumonia at admission showed a similar diversity as the control group (p = 0.140 and p = 0.213 respectively). Contrarily, the group of 12 patients with pneumococcal pneumonia showed a significant lower Simpson´s index (p = 0.002). In the control group (n = 6) Proteobacteria (36.6%), Firmicutes (24.2%) and Actinobacteria (23.0%) were the predominant phyla. In SARS-CoV-2 patients (n = 8), there was a predominance of Proteobacteria (mean 41.6%) (Moraxella and Pelomonas at the genus level), Actinobacteria (24.6%) (Microbacterium) and Firmicutes (22.8%) mainly Streptococcus, Staphylococcus and Veillonella. In patients with Influenza A pneumonia (n = 5) there was a predominance of Firmicutes (35.1%) mainly Streptococcus followed by Proteobacteria (29.2%) (Moraxella, Acinetobacter and Pelomonas). In the group of pneumococcal pneumonia (n = 12) two phyla predominated: Firmicutes (53.1%) (Streptococcus) and Proteobacteria (36.5%) (Haemophilus). In the 7 patients with non-pneumococcal bacterial pneumonia Haemophilus influenzae (n = 2), Legionella pneumophila (n = 2), Klebsiella pneumoniae, Streptococcus pyogenes and Leptospira were detected by metagenomics, confirming the diagnosis done using conventional microbiological techniques. The diversity of the respiratory microbiome in patients with severe viral pneumonia at ICU admission was similar to that of the control group. Contrarily, patients with pneumococcal pneumonia showed a lower grade of diversity. At initial stages of SARS-CoV-2 infection, no important alterations in the pulmonary microbiome were observed. The analysis of bacterial microbiome showed promising results as a diagnostic tool.
Insights
The pulmonary microbiome in severe pneumonia varies by cause. Viral pneumonia shows similar lung microbiome diversity to controls, while pneumococcal pneumonia has significantly lower diversity. Metagenomics shows promise for diagnosing bacterial pneumonia.
Area of Science:
- Pulmonary microbiology
- Intensive care medicine
- Infectious diseases
Background:
- The lung microbiome's composition in severe community-acquired pneumonia (CAP) is not well understood.
- Understanding these microbial communities is crucial for diagnosis and treatment.
Purpose of the Study:
- To analyze the lung microbiome in intensive care unit (ICU) patients with severe CAP.
- To compare the lung microbiome of viral pneumonia, pneumococcal pneumonia, and bacterial pneumonia patients with a control group.
- To evaluate metagenomics as a diagnostic tool for pulmonary infections.
Main Methods:
- Lung microbiome analysis of severe CAP patients (Influenza A, SARS-CoV-2, pneumococcal, and other bacterial pneumonia) and a control group.
- Comparison of microbial diversity using the Simpson's index.
- Metagenomic analysis to identify specific bacterial pathogens.
Main Results:
- Viral pneumonia (Influenza A, SARS-CoV-2) showed lung microbiome diversity similar to the control group.
- Pneumococcal pneumonia patients exhibited significantly lower lung microbiome diversity.
- Metagenomics successfully identified pathogens like Haemophilus influenzae and Legionella pneumophila, confirming conventional diagnoses.
Conclusions:
- Severe viral pneumonia does not significantly alter respiratory microbiome diversity upon ICU admission.
- Pneumococcal pneumonia is associated with a reduced lung microbiome diversity.
- Metagenomics holds potential as a diagnostic method for bacterial pulmonary infections.
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