Bifidobacterium longum Subspecies infantis (B. infantis) in Pediatric Nutrition: Current State of Knowledge
- 2020-05-28
- Nutrients 12(6)
- M. Chichlowski
- N. Shah
- J. Wampler
- Steven S. Wu
- J. Vanderhoof
- PubMed: 32481558
- DOI: 10.3390/nu12061581
Abstract
Abstract: Since originally isolated in 1899, the genus Bifidobacterium has been demonstrated to predominate in the gut microbiota of breastfed infants and to benefit the host by accelerating maturation of the immune response, balancing the immune system to suppress inflammation, improving intestinal barrier function, and increasing acetate production. In particular, Bifidobacterium longum subspecies infantis (B. infantis) is well adapted to the infant gut and has co-evolved with the mother-infant dyad and gut microbiome, in part due to its ability to consume complex carbohydrates found in human milk. B. infantis and its human host have a symbiotic relationship that protects the preterm or term neonate and nourishes a healthy gut microbiota prior to weaning. To provide benefits associated with B. infantis to all infants, a number of commercialized strains have been developed over the past decades. As new ingredients become available, safety and suitability must be assessed in preclinical and clinical studies. Consideration of the full clinical evidence for B. infantis use in pediatric nutrition is critical to better understand its potential impacts on infant health and development. Herein we summarize the recent clinical studies utilizing select strains of commercialized B. infantis.
Keywords: B. infantis; Bifidobacterium longum subspecies infantis; acetate; gut health; human milk oligosaccharides; inflammation; microbiome; pediatric nutrition; probiotics; short chain fatty acids.
Research Insights
Supplement | Health Outcome | Effect Type | Effect Size |
---|---|---|---|
Bifidobacterium infantis | Accelerated Immune Response Maturation | Beneficial | Moderate |
Bifidobacterium infantis | Improved Intestinal Barrier Function | Beneficial | Moderate |
Bifidobacterium infantis | Increased Production of Acetate | Beneficial | Moderate |
Bifidobacterium infantis | Reduced Inflammation | Beneficial | Moderate |
Bifidobacterium infantis BI02 | Accelerated Immune Response Maturation | Beneficial | Moderate |
Bifidobacterium infantis BI02 | Improved Intestinal Barrier Function | Beneficial | Moderate |
Bifidobacterium infantis BI02 | Increased Production of Acetate | Beneficial | Moderate |
Bifidobacterium infantis BI02 | Reduced Inflammatory Response | Beneficial | Moderate |
Bifidobacterium infantis SD-6720 | Accelerated Immune Response Maturation | Beneficial | Moderate |
Bifidobacterium infantis SD-6720 | Improved Intestinal Barrier Function | Beneficial | Moderate |
Bifidobacterium infantis SD-6720 | Increased Production of Acetate | Beneficial | Moderate |
Bifidobacterium infantis SD-6720 | Reduced Inflammation | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis | Accelerated Immune Response Maturation | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis | Improved Intestinal Barrier Function | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis | Increased Production of Acetate | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis | Reduced Inflammation | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis M-63 | Accelerated Immune Response Maturation | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis M-63 | Improved Intestinal Barrier Function | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis M-63 | Increased Production of Acetate | Beneficial | Moderate |
Bifidobacterium longum subsp. infantis M-63 | Reduced Inflammatory Response | Beneficial | Moderate |