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Updated: Mar 15, 2026

Oral Biofilm Sampling for Microbiome Analysis in Healthy Children
Published on: December 31, 2017
Household siblings and nasal and fecal microbiota in infants
Kohei Hasegawa1, Rachel W Linnemann2, Jonathan M Mansbach3
1Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Infants with siblings show distinct nasal and gut bacteria. Having siblings is linked to a higher likelihood of Moraxella nasal microbes and Bifidobacterium gut microbes in babies.
Area of Science:
- Microbiology
- Pediatrics
- Immunology
Background:
- Early-life exposure to siblings is linked to reduced asthma risk.
- No prior studies have investigated sibling impact on infant airway and gut microbiota.
- This study addresses the gap in understanding sibling influence on infant microbiome development.
Purpose of the Study:
- To profile nasal airway and fecal microbiota in infants.
- To investigate the association between having siblings and infant microbiota composition.
Main Methods:
- Cross-sectional study of 105 healthy infants (<1 year).
- 16S rRNA gene sequencing used for microbiota analysis.
- Unbiased clustering identified nasal and fecal microbiota profiles.
Main Results:
- Infants with siblings were more likely to have Moraxella-dominant nasal microbiota (76% vs 18%).
- Infants without siblings showed a higher prevalence of Corynebacterium/Dolosigranulum nasal profiles (50% vs 18%).
- Sibling presence correlated with Bifidobacterium-dominant fecal microbiota (49% vs 24%) compared to Escherichia-dominant profiles.
Conclusions:
- Infants with siblings exhibit distinct nasal and fecal microbiota profiles.
- A higher prevalence of Moraxella (nasal) and Bifidobacterium (fecal) was observed in infants with siblings.
- Findings suggest a link between early-life environment, microbiome, and childhood asthma.
Background:
Early-life exposure to older siblings is associated with a lower risk of asthma. To date, no study has addressed the impact of having siblings on both the airway and fecal microbiota during infancy. The aim of this study was therefore to profile the nasal airway and fecal microbiota in infants, and to examine the association between having siblings and microbiota profile.
Methods:
We conducted a cross-sectional study of 105 healthy infants (aged <1 year). Using 16S rRNA gene sequencing and an unbiased clustering approach to the nasal airway and fecal samples, we identified microbiota profiles and then determined the association between having siblings and microbiome profile.
Results:
Overall, the median age was 3.4 months (IQR, 2.0-4.7 months); 43% had siblings in the household. Unbiased clustering of nasal airway microbiota identified three profiles: Moraxella dominant (43%), Corynebacterium/Dolosigranulum dominant (36%), and mixed (21%). Infants with siblings were more likely to have a Moraxella-dominant profile than Corynebacterium/Dolosigranulum-dominant profile (76% vs 18%), while those without siblings had the opposite pattern (18% vs 50%; P < 0.001, multivariable-adjusted). Fecal microbiota consisted of three profiles: Bifidobacterium dominant (39%), Escherichia dominant (31%), and Enterobacter dominant (30%). Infants with siblings were more likely to have a Bifidobacterium-dominant profile than Escherichia-dominant profile (49% vs 24%) while those without siblings had the opposite pattern (32% vs 37%; P = 0.04, multivariable-adjusted).
Conclusions:
In this cross-sectional study, infants with siblings were more likely to have a Moraxella-dominant nasal microbiota profile and Bifidobacterium-dominant fecal microbiota profile. These findings should facilitate further investigation of the interplay between early-life environmental exposure, the microbiome, and childhood asthma.
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