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Updated: Jan 12, 2026

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Maternal-to-neonatal microbial transmission and impact of prenatal probiotics on neonatal gut development
Lulu Meng1,2, Ge Fan2, Haishan Xie3
1High-Risk Perinatal Medicine Center, Third Affiliated Hospital of Sun Yat- sen University, Guangzhou, 510632, China.
Insights
Prenatal probiotic supplementation transiently altered neonatal gut microbiota by increasing placental microbial contribution. Maternal gut and placenta are key sources for infant gut colonization, with minimal vaginal influence.
Area of Science:
- Microbiome research
- Maternal-fetal medicine
- Pediatric health
Background:
- Maternal microbiota is critical for establishing the neonatal gut microbiome.
- Early infant gut colonization is essential for overall health.
- Understanding maternal microbial sources is key to infant health.
Purpose of the Study:
- To trace maternal microbial sources contributing to neonatal gut colonization.
- To assess the impact of prenatal probiotic supplementation on maternal-to-neonatal microbial transmission.
Main Methods:
- 26 mother-neonate pairs undergoing vaginal delivery.
- Intervention group received probiotics (Bifidobacterium longum, Lactobacillus delbrueckii bulgaricus, Streptococcus thermophilus) from week 32 until delivery.
- Maternal (fecal, vaginal, placental) and neonatal fecal samples analyzed using 16S rRNA sequencing and FEAST algorithm.
Main Results:
- Prenatal probiotics transiently altered neonatal meconium microbiota diversity.
- Maternal gut and placenta were primary sources of neonatal meconium microbiota.
- Probiotic supplementation increased placental contribution to meconium microbiota (P=0.02).
Conclusions:
- Maternal-to-neonatal microbial transmission is dynamic.
- Prenatal probiotics can transiently modify early infant gut colonization patterns.
- Modulation of microbial source contributions is a key mechanism of probiotic effects.
Background:
Maternal microbiota during pregnancy plays a crucial role in establishing the neonatal gut microbiota, which is essential for infant health. This study aimed to trace maternal microbial sources contributing to early neonatal gut colonization and assess the effect of prenatal probiotic supplementation on maternal-to-neonatal microbial transmission.
Methods:
A total of 26 mother-neonate pairs undergoing full-term vaginal delivery were enrolled. From gestational week 32 until delivery, the intervention group received a probiotic supplement containing Bifidobacterium longum, Lactobacillus delbrueckii bulgaricus, and Streptococcus thermophilus twice daily, while the control group received no supplementation. Maternal fecal, vaginal, and placental samples were collected at full term, and neonatal fecal samples were collected longitudinally at Days 1, 3, 14, and 6 months postpartum. Microbial community profiling was performed using 16 S rRNA gene sequencing. Microbial source attribution was conducted using the FEAST algorithm.
Results:
Alpha and beta diversity analyses showed that prenatal probiotics transiently altered the composition of neonatal meconium microbiota, with no significant differences observed at later time points. Volatility analysis revealed enhanced microbial stability in the probiotic group during Days 1 to 3 (P < 0.001). FEAST source-tracking indicated that maternal gut and placenta were the major contributors to neonatal meconium colonization, with gut-derived input increasing over time and vaginal contributions remaining minimal throughout. Probiotic supplementation significantly increased the placental contribution to meconium microbiota (P = 0.02), with a sustained but non-significant elevation observed through later stages. Meanwhile, gut-derived and vaginal-derived inputs were consistently reduced in the probiotic group, though these differences did not reach statistical significance.
Conclusion:
This study highlights the dynamic nature of maternal-to-neonatal microbial transmission and demonstrates that prenatal probiotic supplementation can transiently reshape early colonization patterns by modulating source contributions.
Trial Registration:
ClinicalTrials.gov, NCT06241222 ( https://clinicaltrials.gov/study/NCT06241222 ); retrospectively registered on 2024-01-17 (study start 2018-01-01; completion 2021-12-31; first posted 2024-02-05).
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