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Updated: Mar 27, 2026

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Probiotic improves respiratory and gastrointestinal health, immune homeostasis, and gut microbiota composition in
Mageswaran Uma Mageswary1, Lan Hanglian2, Pin Li3
1School of Industrial Technology, Universiti Sains Malaysia, Gelugor, Pulau Pinang, Malaysia.
Insights
Supplementation with Bifidobacterium infantis YLGB-1496 improved infant gastrointestinal health and modulated gut microbiota. This probiotic intervention enhanced immune markers and reduced pathobionts, supporting gut barrier function and immune development in infants.
Area of Science:
- Microbiology
- Immunology
- Pediatrics
Background:
- The early infant gut microbiota is crucial for immune development and metabolic programming.
- Disruptions in infant gut microbiota are linked to infections and metabolic disorders.
- Limited strain-specific data exists for probiotics like Bifidobacterium infantis in infants.
Purpose of the Study:
- To assess the impact of Bifidobacterium infantis YLGB-1496 on infant clinical outcomes.
- To evaluate immune markers and gut microbiota composition following probiotic supplementation.
- To investigate the safety and efficacy of B. infantis YLGB-1496 in infants under one year.
Main Methods:
- A 12-week randomized, double-blind, placebo-controlled trial involving 119 healthy infants.
- Daily administration of Bifidobacterium infantis YLGB-1496 (1 × 10¹⁰ CFU) or placebo.
- Assessment of clinical outcomes, immune markers (sIgA, cytokines, cortisol), and gut microbiota via 16S rRNA sequencing.
Main Results:
- B. infantis YLGB-1496 significantly improved gastrointestinal outcomes, reducing stomach ache and diarrhea incidence.
- Supplementation increased fecal and oral sIgA, IL-10, and decreased IL-1β, indicating immune modulation.
- Microbiota analysis showed enrichment of beneficial bacteria and reduction of pathobionts, suggesting improved gut barrier function.
Conclusions:
- Bifidobacterium infantis YLGB-1496 demonstrates significant benefits for infant gastrointestinal health and immune development.
- The probiotic effectively modulated the gut microbiota, promoting a healthier microbial profile.
- These findings support the use of B. infantis YLGB-1496 for supporting infant gut health and immunity.
Introduction:
The early postnatal period is a critical window for shaping the gut microbiota, which plays a pivotal role in immune maturation, infection resistance, and metabolic programming. Disruptions to this process may predispose infants to infections and allergic or metabolic disorders. Probiotics such as Bifidobacterium infantis have shown promise in modulating gut microbial ecology and immune function, but strain-specific and mechanistic evidence in infants remains limited. This study aimed to evaluate the effects of B. infantis YLGB-1496 supplementation on clinical outcomes, immune markers, and gut microbiota composition in healthy infants below one year of age.
Methods:
In a 12-week, randomized, double-blind, placebo-controlled trial, 119 healthy infants were enrolled (B. infantis YLGB-1496 n=59, placebo n=60). Participants received one daily sachet of B. infantis YLGB-1496 (1 × 10¹⁰ CFU) or placebo. Clinical outcomes for respiratory health and gastrointestinal (GI) health were assessed via validated questionnaires. Oral and fecal samples were collected for analysis of sIgA, cortisol, and cytokines (TNF-α, IFN-γ, IL-1β, IL-10, calprotectin). Gut microbiota was profiled by 16S rRNA sequencing, and diversity indices and taxonomic shifts were analyzed.
Results:
Compared with placebo, B. infantis YLGB-1496 supplementation was associated with consistent numerical reductions in respiratory symptom days, although these did not remain statistically significant after false discovery rate (FDR) adjustment. In contrast, gastrointestinal outcomes showed robust improvements after FDR correction, including reduced stomach ache (q = 0.010), lower diarrhea incidence (q < 0.001), and fewer diarrhea-related clinical visits (q < 0.001). Fecal sIgA remained elevated in the B. infantis YLGB-1496 group (P = 0.138 vs P = 0.000 in placebo), accompanied by increased IL-10 (P < 0.001) and reduced IL-1β (P = 0.002). Oral sIgA was enhanced (P = 0.001), while cortisol declined similarly in both groups. Microbiota analysis revealed enrichment of beneficial taxa in the B. infantis YLGB-1496 group with concurrent reductions in pathobionts. In contrast, the placebo group exhibited increases in Campylobacter, Staphylococcus, and Desulfovibrio desulfuricans, and decreases in Faecalibacterium prausnitzii and Anaerostipes caccae, indicative of dysbiosis. These compositional changes support improved gut barrier function and immune development.
Clinical Trial Registration:
https://clinicaltrials.gov/study/NCT05794815?term=NCT05794815&rank=1, Identifier: NCT05794815.
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