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Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Antibiotics in pregnancy influence nasal microbiome and respiratory morbidity in infancy
Céline Rüttimann1,2, Annika Nissen-Kratzert1,2, Nadja Mostacci3
1University Children's Hospital Basel (UKBB), University of Basel, Basel, Switzerland.
Insights
Prenatal antibiotic exposure in the third trimester impacts infant nasal microbiome diversity and increases respiratory illness risk. These effects on respiratory health occur independently of microbiome changes and do not persist into childhood.
Area of Science:
- Microbiology
- Pediatrics
- Epidemiology
Background:
- Prenatal antibiotic exposure's effects on infant respiratory health and underlying mechanisms remain unclear.
- Investigating the link between third-trimester antibiotic use, infant nasal microbiome, and respiratory outcomes is crucial.
Purpose of the Study:
- To determine if prenatal antibiotic exposure is associated with nasal microbiome composition and respiratory morbidity in infancy and school age.
- To assess if the nasal microbiome mediates the relationship between prenatal antibiotic exposure and respiratory morbidity.
Main Methods:
- 16S rRNA gene sequencing of nasal swabs from 296 infants.
- Assessment of respiratory symptoms via weekly interviews and a 6-year clinical visit.
- Structural equation modeling to analyze direct and indirect associations.
Main Results:
- Infants exposed to antibiotics prenatally showed reduced nasal microbiome diversity (Shannon index p=0.006).
- Prenatal antibiotic exposure correlated with increased risk of respiratory symptoms in infancy (RR 1.38, p=0.032).
- No mediating effect of the nasal microbiome on respiratory symptoms was observed.
Conclusions:
- Prenatal antibiotic exposure is linked to reduced nasal microbiome diversity in infancy.
- Respiratory morbidity in infancy associated with prenatal antibiotic exposure appears independent of microbiome alterations.
- No long-term respiratory symptoms were observed in childhood related to prenatal antibiotic exposure.
Background:
The effects of prenatal antibiotic exposure on respiratory morbidity in infancy and the involved mechanisms are still poorly understood. We aimed to examine whether prenatal antibiotic exposure in the third trimester is associated with nasal microbiome and respiratory morbidity in infancy and at school age, and whether this association with respiratory morbidity is mediated by the nasal microbiome.
Methods:
We performed 16S ribosomal RNA gene sequencing (regions V3-V4) on nasal swabs obtained from 296 healthy term infants from the prospective Basel-Bern birth cohort (BILD) at age 4-6 weeks. Information about antibiotic exposure was derived from birth records and standardised interviews. Respiratory symptoms were assessed by weekly telephone interviews in the first year of life and a clinical visit at age 6 years. Structural equation modelling was used to test direct and indirect associations accounting for known risk factors.
Results:
α-Diversity indices were lower in infants with antibiotic exposure compared to nonexposed infants (e.g. Shannon index p-value 0.006). Prenatal antibiotic exposure was also associated with a higher risk of any, as well as severe, respiratory symptoms in the first year of life (risk ratio 1.38, 95% CI 1.03-1.84; adjusted p-value (padj)=0.032 and risk ratio 1.75, 95% CI 1.02-2.97; padj=0.041, respectively), but not with wheeze or atopy in childhood. However, we found no indirect mediating effect of nasal microbiome explaining these clinical symptoms.
Conclusion:
Prenatal antibiotic exposure was associated with lower diversity of nasal microbiome in infancy and, independently of microbiome, with respiratory morbidity in infancy, but not with symptoms later in life.
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