Gram‐negative microbiota is related to acute exacerbation in children with asthma

• Published in: Clinical and translational allergy 2021-10, Vol.11 (8), p.e12069-n/a
• Main Authors: Kim, Yoon Hee, Jang, Haerin, Kim, Soo Yeon, Jung, Jae Hwa, Kim, Ga Eun, Park, Mi Reu, Hong, Jung Yeon, Kim, Mi Na, Kim, Eun Gyul, Kim, Min Jung, Kim, Kyung Won, Sohn, Myung Hyun
• Format: Article
• Language: English
• Subjects: Allergens; Allergies; Asthma; Bioinformatics; Biomarkers; children; Cytokines; Discriminant analysis; Immunotherapy; induced sputum; induzierter auswurf; Influenza; kinder; lipopolysaccharid; lipopolysaccharide; microbiome; Microbiota; mikrobiom; Spirometry; Steroids; Viruses
• ISSN: 2045-7022; 2045-7022
• DOI: 10.1002/clt2.12069

Background The upper‐airway microbiota may be associated with the pathogenesis of asthma and useful for predicting acute exacerbation. However, the relationship between the lower‐airway microbiota and acute exacerbation in children with asthma is not well understood. We evaluated the characteristics of the airway microbiome using induced sputum from children with asthma exacerbation and compared the microbiota‐related differences of inflammatory cytokines with those in children with asthma. Methods We analysed the microbiome using induced sputum during acute exacerbation of asthma in children. We identified microbial candidates that were prominent in children with asthma exacerbation and compared them with those in children with stable asthma using various analytical methods. The microbial candidates were analysed to determine their association with inflammatory cytokines. We also developed a predictive functional profile using PICRUSt. Results A total of 95 children with allergic sensitisation including 22 with asthma exacerbation, 67 with stable asthma, and 6 controls were evaluated. We selected 26 microbial candidates whose abundances were significantly increased, decreased, or correlated during acute exacerbation in children with asthma. Among the microbial candidates, Campylobacter, Capnocytophaga, Haemophilus, and Porphyromonas were associated with inflammatory cytokines including macrophage inflammatory protein (MIP)‐1β, programmed death‐ligand 1, and granzyme B. Both Campylobacter and MIP‐1β levels were correlated with sputum eosinophils. Increased lipopolysaccharide biosynthesis and decreased glycan degradation were observed in children with asthma exacerbation. Conclusion Gram‐negative microbes in the lower airway were related to acute exacerbation in children with asthma. These microbes and associated cytokines may play a role in exacerbating asthma in children.