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Published on: August 7, 2017
Distinct patterns of neonatal gut microflora in infants in whom atopy was and was not developing
M Kalliomäki1, P Kirjavainen, E Eerola
1Department of Pediatrics, University of Turku, Turku.
Insights
Early gut bacteria differences in infants precede atopic sensitization. A lower ratio of bifidobacteria to clostridia in newborns is linked to developing atopy, highlighting the importance of gut microbiome balance for immune development.
Area of Science:
- Microbiome research
- Immunology
- Pediatric allergy
Background:
- Improved hygiene reduces early microbial exposure, potentially increasing atopic disease prevalence.
- Commensal microflora exposure may modulate immunity against atopy.
Purpose of the Study:
- Investigate if early gut microflora differences predict atopic sensitization in infants.
- Examine the relationship between neonatal gut microbiota composition and the development of atopy.
Main Methods:
- Analyzed intestinal microflora in 76 high-risk infants at 3 weeks and 3 months.
- Utilized bacterial cultivation, fatty acid profiling (GC-FAME), and fluorescence in situ hybridization (FISH).
- Classified infants as atopic or non-atopic based on skin prick tests at 12 months.
Main Results:
- Atopic sensitization occurred in 29% of infants.
- Significant differences in fecal fatty acid profiles were found at 3 weeks (P=.005).
- Atopic infants showed higher Clostridia and lower Bifidobacteria counts (FISH, P=.04 and P=.11 respectively), with a reduced Bifidobacteria/Clostridia ratio (P=.03).
- Bacterial cultivation did not detect these differences.
Conclusions:
- Neonatal gut microflora composition precedes atopy development.
- The balance of intestinal bacteria plays a critical role in guiding human immunity towards a non-atopic phenotype.
- Culture-independent methods are crucial for detecting early microbial differences linked to atopy.
Background:
Improved hygiene has altered early microbial exposure by reducing childhood infections, which has been suggested as a cause for the continuously rising prevalence of atopic diseases. On the basis of both intensity and timing of stimulus, it has been hypothesized that exposure to commensal microflora may represent another key protective modulator of immunity against atopy and subsequent atopic diseases.
Objective:
We sought to investigate whether differences in early gut microflora precede the later development of atopic sensitization.
Methods:
Intestinal microflora from 76 infants at high risk of atopic diseases were analyzed at 3 weeks and 3 months of age by using conventional bacterial cultivation and 2 culture-independent methods, gas-liquid chromatography of bacterial cellular fatty acids and quantitative fluorescence in situ hybridization of bacterial cells. Infants evincing at least one positive skin prick reaction at 12 months were grouped as atopic subjects, and those without positive reactions were grouped as nonatopic subjects.
Results:
Atopic sensitization was observed in 22 (29%) of 76 children. At 3 weeks, the bacterial cellular fatty acid profile in fecal samples differed significantly between infants in whom atopy was and was not developing (P =.005). By using fluorescence in situ hydridization, atopic subjects had more clostridia (geometric mean [95% confidence interval]: 9.3 x 10(7) [3.8-22.9 x 10(7)] vs 3.3 x 10(7) [1.8-6.1 x 10(7)], P =.04) and tended to have fewer bifidobacteria (1.8 x 10(9) [0.4-7.6 x 10(9)] vs 6.1 x 10(9) [2.5-14.6 x 10(9)], P =.11) in their stools than nonatopic subjects, resulting in a reduced ratio of bifidobacteria to clostridia (P =.03). The differences were not detected by bacterial cultivation.
Conclusion:
Differences in the neonatal gut microflora precede the development of atopy, suggesting a crucial role of the balance of indigenous intestinal bacteria for the maturation of human immunity to a nonatopic mode.
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