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Published on: July 25, 2017
Bifidobacterium longum subsp. infantis YLGB-1496-Toxicological evaluation
Jian Zhao1, Yueyi Guo1, Qiuyue Jiang2
1Beijing Key Laboratory of Bioactive Substances and Functional Foods, Beijing Union University, Beijing, China.
Abstract:
Bifidobacterium infantis YLGB-1496, originally isolated from breast milk from a Taiwanese mother, is under study for use as a probiotic. As part of safety assessment, an Ames, in vivo mouse micronucleus, and in vivo mouse spermatocyte chromosome aberration assay were conducted along with a 13-week oral rat toxicity study. B. infantis YLGB-1496 had no activity in any of the genotoxicity assays. Administration of the bacteria to Sprague-Dawley rats at doses ranging from 0 to 1.5 g/kg bw/day had no treatment-related effects on any of the endpoints measured. There appear to be no concerns for translocation or pathogenicity of B. infantis YLGB-1496 based on extensive experience with the species in general. The results of the current investigations support potential use of B. infantis YLGB-1496 as a probiotic in infant formula.
Insights
Bifidobacterium infantis YLGB-1496, a potential probiotic, demonstrated safety in genotoxicity and rat toxicity studies. These findings support its use in infant formula.
Area of Science:
- Microbiology
- Toxicology
- Probiotic research
Background:
- Bifidobacterium infantis YLGB-1496 is a bacterial strain isolated from human breast milk.
- Extensive research is needed to assess the safety of potential probiotic strains.
Purpose of the Study:
- To evaluate the safety of Bifidobacterium infantis YLGB-1496 for use as a probiotic.
- To conduct genotoxicity assays and a 13-week oral rat toxicity study.
Main Methods:
- Ames test, in vivo mouse micronucleus assay, and in vivo mouse spermatocyte chromosome aberration assay were performed.
- Sprague-Dawley rats were administered B. infantis YLGB-1496 orally at doses up to 1.5 g/kg bw/day for 13 weeks.
Main Results:
- B. infantis YLGB-1496 showed no genotoxic activity in any assay.
- No treatment-related adverse effects were observed in rats during the 13-week toxicity study.
- No concerns regarding translocation or pathogenicity were identified.
Conclusions:
- The safety assessments indicate no adverse effects associated with B. infantis YLGB-1496.
- Results support the potential use of B. infantis YLGB-1496 as a probiotic in infant formula.
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