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Updated: Jun 25, 2025

Methodology for Sputum Induction and Laboratory Processing
Published on: December 17, 2017
Highly diverse sputum microbiota correlates with the disease severity in patients with community-acquired pneumonia:
Jing Yang1,2,3, Jinman Li4, Linfeng Zhang1,2
1Beijing Institute of Genomics, Chinese Academy of Sciences, China National Center for Bioinformation, Beijing, 100101, China.
Background:
Community-acquired pneumonia (CAP) is a common and serious condition that can be caused by a variety of pathogens. However, much remains unknown about how these pathogens interact with the lower respiratory commensals, and whether any correlation exists between the dysbiosis of the lower respiratory microbiota and disease severity and prognosis.
Methods:
We conducted a retrospective cohort study to investigate the composition and dynamics of sputum microbiota in patients diagnosed with CAP. In total, 917 sputum specimens were collected consecutively from 350 CAP inpatients enrolled in six hospitals following admission. The V3-V4 region of the 16 S rRNA gene was then sequenced.
Results:
The sputum microbiota in 71% of the samples were predominately composed of respiratory commensals. Conversely, 15% of the samples demonstrated dominance by five opportunistic pathogens. Additionally, 5% of the samples exhibited sterility, resembling the composition of negative controls. Compared to non-severe CAP patients, severe cases exhibited a more disrupted sputum microbiota, characterized by the highly dominant presence of potential pathogens, greater deviation from a healthy state, more significant alterations during hospitalization, and sparser bacterial interactions. The sputum microbiota on admission demonstrated a moderate prediction of disease severity (AUC = 0.74). Furthermore, different pathogenic infections were associated with specific microbiota alterations. Acinetobacter and Pseudomonas were more abundant in influenza A infections, with Acinetobacter was also enriched in Klebsiella pneumoniae infections.
Conclusion:
Collectively, our study demonstrated that pneumonia may not consistently correlate with severe dysbiosis of the respiratory microbiota. Instead, the degree of microbiota dysbiosis was correlated with disease severity in CAP patients.
Insights
The severity of community-acquired pneumonia (CAP) correlates with disruptions in the respiratory tract's microbial community (dysbiosis). Specific pathogens are linked to distinct microbiota changes in CAP patients.
Area of Science:
- Microbiology
- Pulmonary Medicine
- Genomics
Background:
- Community-acquired pneumonia (CAP) is a significant global health concern.
- The interplay between respiratory pathogens and the lower airway microbiome in CAP remains poorly understood.
- The relationship between respiratory microbiota dysbiosis and CAP severity/prognosis requires further investigation.
Purpose of the Study:
- To investigate the composition and dynamics of sputum microbiota in patients with CAP.
- To explore the correlation between respiratory microbiota dysbiosis and CAP disease severity.
- To identify specific microbiota alterations associated with different CAP pathogens.
Main Methods:
- Retrospective cohort study involving 917 sputum specimens from 350 CAP inpatients.
- 16S rRNA gene sequencing (V3-V4 region) to analyze sputum microbiota composition.
- Comparison of microbiota profiles between severe and non-severe CAP cases.
Main Results:
- Commensal bacteria predominated in most samples (71%); opportunistic pathogens were dominant in 15%.
- Severe CAP cases showed more disrupted sputum microbiota, with increased pathogen dominance and deviation from healthy states.
- Sputum microbiota on admission moderately predicted disease severity (AUC=0.74), with specific pathogens linked to distinct microbial alterations.
Conclusions:
- Pneumonia does not always correlate with severe respiratory microbiota dysbiosis.
- The extent of microbiota dysbiosis is linked to disease severity in community-acquired pneumonia patients.
- Specific microbial shifts are associated with particular infectious agents in CAP.
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