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Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples
Published on: December 22, 2014
Functional and Resistome Profiling of Paediatric Airway Microbiota in Asthma Using Shotgun Metagenomics
Aisha Alamri1, Abdullah K Almutairi2,3, Fatimah AlSinan4
1Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Imam Abdulrahamn Bin Faisal University, Dammam 34212, Saudi Arabia.
Insights
The airway microbiome in children with asthma shows an enrichment of antibiotic resistance genes (ARGs), particularly against common antibiotics. This study highlights differences in microbial function across anatomical sites in pediatric asthma.
Area of Science:
- Microbiome research
- Pediatric respiratory diseases
- Genomic analysis
Background:
- Asthma significantly impacts children's quality of life globally.
- Airway microbiota and antibiotic resistance genes (ARGs) are implicated in asthma pathogenesis.
- Limited research exists on the association between airway microbiota and ARGs in pediatric asthma.
Purpose of the Study:
- To characterize ARGs, virulence factors, and active pathways in the airway microbiota of children with asthma.
- To compare functional profiles between pediatric asthma patients and healthy controls.
- To investigate the influence of anatomical location on airway microbiome function.
Main Methods:
- Shotgun sequencing of DNA from nasal and oropharyngeal swabs of 29 children with asthma and 20 controls.
- Bioinformatic analysis to identify microbial patterns, ARGs, virulence factors, and metabolic pathways.
- Evaluation of functional capacity across different anatomical niches.
Main Results:
- Microbiome functional capacity varied significantly by anatomical location (oropharyngeal vs. nasal).
- Asthma-related functional differences in the microbiome were modest and not statistically significant after correction.
- Enrichment of ARGs, especially those conferring resistance to beta-lactams, macrolides, and tetracyclines, was observed in the asthma cohort.
Conclusions:
- Anatomical location is a dominant factor shaping airway microbiome gene content and function.
- While functional differences were modest, ARGs were enriched in pediatric asthma patients.
- Further research into differential activities across anatomical niches may yield biomarkers for asthma diagnosis and therapy.
Abstract:
Background/Objectives: Asthma affects millions of patients worldwide and impacts their quality of life, particularly among children. Colonisation or an imbalance within natural resident microbiota may drive inflammatory responses in asthma; antibiotic resistance genes (ARGs) have also been investigated in asthma microbiome studies. However, research on the association between airway microbiota and ARGs remains limited. Therefore, we elucidated functional-level characterisation at the level of ARGs, virulence factors, and active pathways among a paediatric asthma cohort relative to a healthy control. Methods: Overall, 29 children with asthma and 20 control subjects were enrolled, and 3 swabs (2 nasal and 1 oropharyngeal) were obtained from each participant. Genomic DNA was extracted and sent for shotgun sequencing, after which bioinformatic analysis was conducted to remove human reads and analyse the microbiota pattern in the samples. The abundance of antibiotic resistance genes was evaluated along with the distribution of virulence genetic markers. Functional investigation of the most prevalent metabolic pathways was also performed. Results: Upper airway microbiome functional capacity varied by anatomical location, with oropharyngeal communities exhibiting greater metabolic breadth than nasal communities, suggesting the sample source to be the dominant factor shaping gene content, pathway profiles, and community structure. Asthma-related functional differences were modest, and no biological pathways remained significant following false discovery rate correction. Enrichment of antimicrobial resistance genes was observed, particularly those conferring resistance to β-lactams, macrolides, and tetracyclines. Conclusions: Different anatomical niches exhibit differential activities, and further exploration in this direction could aid in the development of diagnostic and therapeutic biomarkers for asthma.
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