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Published on: January 27, 2019
Pulse probiotic administration induces repeated small intestinal Muc3 expression in rats
Natalie S Dykstra1, Lucie Hyde, Diya Adawi
1Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Abstract:
Upon ingestion, probiotics may act to protect the host through a number of protective mechanisms including modulation of genes involved in intestinal innate mucosal defense such as epithelial cell-derived mucin glycoproteins and inhibitor of apoptosis proteins. To determine the specificity of effect and sustainability of response in vivo, Lactobacillus plantarum 299v (Lp299v), Lactobacillus rhamnosus R0011 (LrR0011), and Bifidobacterium bifidum R0071 (BbR0071) were added repeatedly or intermittently to the drinking water of Sprague-Dawley rats. After killing the rats via CO2 suffocation, Muc2, Muc3, neuronal apoptosis inhibitor protein (NAIP), human inhibitor of apoptosis protein 1/cellular inhibitor of apoptosis 2 (HIAP1/cIAP2), and human inhibitor of apoptosis protein 2/cellular inhibitor of apoptosis 1 (HIAP2/cIAP1) mRNA and protein levels were analyzed via RT-PCR and immunohistochemistry. Live Lp299v, BbR0071, and LrR0011 increased Muc3 protein and mRNA expression in jejunum and ileum. Heat-killed and a nonadherent derivative of Lp299v failed to induce Muc3 expression. Lp299v did induce expression of HIAP2/cIAP1 and NAIP expression. Muc3 mucin expression was elevated for 5 d after oral administration of Lp299v; however, this effect was not sustained despite ongoing daily ingestion of a probiotic. Intermittent pulse ingestion of probiotics, however, was found to repeatedly increase Muc3 expression. We conclude that selected probiotics can induce protective genes of mucosal intestinal epithelial cells, an effect that is reproducible with pulse probiotic administration.
Insights
Selected probiotics, including Lactobacillus plantarum 299v, enhance intestinal defense genes like Muc3. Intermittent probiotic dosing, not continuous, effectively boosts these protective mechanisms in the gut.
Area of Science:
- Microbiology
- Immunology
- Gastroenterology
Background:
- Probiotics offer host protection via innate mucosal defense gene modulation.
- Key genes include mucin glycoproteins and apoptosis inhibitors.
Purpose of the Study:
- To investigate the specificity and sustainability of probiotic effects on host defense genes in vivo.
- To compare continuous versus intermittent administration of specific probiotic strains.
Main Methods:
- Rats were administered Lactobacillus plantarum 299v, Lactobacillus rhamnosus R0011, or Bifidobacterium bifidum R0071.
- Gene and protein expression of Muc3, NAIP, HIAP1/cIAP2, and HIAP2/cIAP1 were analyzed.
- RT-PCR and immunohistochemistry were employed for analysis.
Main Results:
- Live probiotics (Lp299v, BbR0071, LrR0011) upregulated Muc3 mRNA and protein in the jejunum and ileum.
- Heat-killed or nonadherent Lp299v did not induce Muc3 expression.
- Lp299v also induced HIAP2/cIAP1 and NAIP expression, with Muc3 elevation lasting 5 days.
- Continuous daily probiotic intake did not sustain Muc3 expression, but intermittent dosing did.
Conclusions:
- Specific live probiotics can induce protective genes in intestinal epithelial cells.
- Probiotic-induced mucosal defense gene expression is reproducible with intermittent administration.
- The findings highlight the importance of administration strategy for probiotic efficacy.
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