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Published on: March 21, 2019
Neonatal intestinal immune regulation by the commensal bacterium, P. UF1
Yong Ge1,2, Minghao Gong1,2, Natacha Colliou1,2
1Department of Infectious Diseases & Immunology, University of Florida, Gainesville, FL, USA.
Insights
Propionibacterium strain P. UF1 enhances neonatal immunity by boosting protective Th17 cells and regulatory T cells (Tregs). This gut microbe protects newborn mice against intestinal Listeria monocytogenes infection.
Area of Science:
- Immunology
- Microbiology
- Neonatal Health
Background:
- Newborns possess immature immune systems, increasing susceptibility to infections.
- Gut microbiota plays a crucial role in developing neonatal immunity.
- Previous studies identified Propionibacterium strain P. UF1 as a Th17 cell inducer.
Purpose of the Study:
- To investigate the immunomodulatory effects of P. UF1 in neonatal mice.
- To evaluate P. UF1's protective capacity against intestinal pathogen infection.
- To elucidate the mechanisms underlying P. UF1-mediated immune enhancement.
Main Methods:
- Administration of P. UF1 to newborn mice.
- Assessment of Th17 cell populations and regulatory T cells (Tregs).
- Challenging mice with Listeria monocytogenes (L. m) infection.
- Analysis of gut microbiota composition and B vitamin metabolites.
- Transcriptomic analysis of P. UF1-induced Th17 cells.
Main Results:
- P. UF1 significantly increased protective Th17 cells and IL-10+ Tregs in newborn mice.
- P. UF1 conferred protection against intestinal L. m infection.
- P. UF1 maintained gut microbiota homeostasis and induced beneficial B vitamin metabolites.
- Transcriptomic data revealed key genes involved in Th17 cell differentiation and regulation.
Conclusions:
- P. UF1 enhances neonatal host defense against intestinal pathogens.
- P. UF1 modulates T cell immunity through microbiota and metabolite interactions.
- P. UF1 shows potential as a probiotic for improving neonatal immunity.
Abstract:
Newborns are highly susceptible to pathogenic infections with significant worldwide morbidity possibly due to an immature immune system. Recently, we reported that Propionibacterium strain, P. UF1, isolated from the gut microbiota of preterm infants, induced the differentiation of bacteria-specific Th17 cells. Here, we demonstrate that P. UF1 significantly increased the number of protective Th17 cells and maintained IL-10+ regulatory T cells (Tregs) in newborn mice. In addition, P. UF1 protected mice from intestinal Listeria monocytogenes (L. m) infection. P. UF1 also functionally sustained the gut microbiota and induced critical B vitamin metabolites implicated in the regulation of T cell immunity during L. m intestinal infection. Transcriptomic analysis of P. UF1-induced Th17 cells revealed genes involved in the differentiation and regulation of these cells. These results illustrate the potency of P. UF1 in the enhancement of neonatal host defense against intestinal pathogen infection.
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