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Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Study on the correlation between respiratory microbiome alterations and disease location/severity in children with
Guangqi Gao1,2,3, Ziqing Wei1,2,3, Qian Zhang1,2,3
1Key Laboratory of Dairy Biotechnology and Engineering, Ministry of Education, Inner Mongolia Agricultural University, Hohhot, 010000, China.
Abstract:
Mycoplasma pneumoniae pneumonia (MPP) is a common form of community-acquired pneumonia in children, potentially involving multiple organ systems. Accumulating evidence suggests that dysbiosis of the respiratory microbiota is associated with various respiratory diseases. Nevertheless, it remains unclear how the respiratory microbiota varies across anatomical sites, interacts with other microbes, and correlates with host immunity in children with MPP compared to non‑MPP respiratory diseases. In this study, we collected and analyzed pharyngeal swabs, sputum, and bronchoalveolar lavage fluid samples from 401 pediatric MPP patients and 287 control subjects (MPP-negative children with other respiratory conditions).Comparative analysis revealed significant respiratory microbiome dysbiosis in MPP patients, with Mycoplasmoides constituting 30.33% of the total microbial community. A discriminative model based on Mycoplasmoides abundance demonstrated excellent performance (AUC = 0.983, sensitivity = 95.3%, specificity = 98.3%). Notably, Mycoplasmoides abundance showed significant negative correlations with Prevotella, Veillonella_A, Staphylococcus, and Rothia, suggesting potential inhibitory effects.Anatomical distribution analysis indicated distinct microbial distributions: Prevotella and Veillonella_A were predominantly enriched in the upper respiratory tract, while Mycoplasmoides showed greater abundance in the lower respiratory tract. Consistency analysis supported the hypothesis of microbial translocation from upper to lower respiratory tract in affected children.Severe MPP cases exhibited significantly higher Mycoplasmoides abundance. For correlations with clinical indicators, both Mycoplasmoides and Streptococcus showed nominal associations. Our findings elucidate the complex interplay between respiratory microbiota in pediatric MPP patients and its association with disease severity and clinical outcomes. This study highlights the need for further research to explore and validate the prognostic relevance of value of these microbial markers.
Insights
Pediatric Mycoplasma pneumoniae pneumonia (MPP) shows distinct respiratory microbiome dysbiosis, with Mycoplasmoides dominating. This finding aids in diagnosing MPP and understanding its impact on children's respiratory health.
Area of Science:
- Microbiology
- Pediatric Pulmonology
- Immunology
Background:
- Mycoplasma pneumoniae pneumonia (MPP) is a common pediatric respiratory illness.
- Respiratory microbiome dysbiosis is linked to respiratory diseases, but its role in pediatric MPP is unclear.
- Understanding microbial variations across anatomical sites and host interactions in MPP is crucial.
Purpose of the Study:
- To investigate respiratory microbiota composition, inter-microbial interactions, and host immune correlations in pediatric MPP.
- To compare the respiratory microbiome of MPP patients with non-MPP respiratory conditions.
- To identify potential microbial biomarkers for MPP diagnosis and severity.
Main Methods:
- Analysis of pharyngeal swabs, sputum, and bronchoalveolar lavage fluid from 401 pediatric MPP patients and 287 controls.
- Comparative microbiome analysis using 16S rRNA sequencing.
- Correlation analysis between microbial abundance, disease severity, and clinical indicators.
Main Results:
- Significant respiratory microbiome dysbiosis in MPP patients, with Mycoplasmoides as a dominant species (30.33%).
- A Mycoplasmoides-based model showed high diagnostic accuracy (AUC=0.983).
- Mycoplasmoides abundance negatively correlated with Prevotella, Veillonella_A, Staphylococcus, and Rothia, suggesting inhibition. Distinct anatomical distributions were observed, with Mycoplasmoides enriched in the lower respiratory tract.
Conclusions:
- Pediatric MPP is characterized by significant respiratory microbiome dysbiosis, with Mycoplasmoides being a key player.
- The abundance and distribution of specific microbes, particularly Mycoplasmoides, can serve as potential diagnostic markers for MPP.
- Further research is needed to validate the prognostic value of these microbial markers in pediatric respiratory infections.
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