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Beta-glucan, extracted from oat, enhances disease resistance against bacterial and parasitic infections
Cheol-Heui Yun1, Alberto Estrada, Andrew Van Kessel
1Animal Biotechnology Centre, Department of Animal and Poultry Science, 51 Campus Drive, University of Saskatchewan, Saskatoon, SK, Canada S7N 5A8.
Abstract:
The effect of beta-glucan, extracted from oats, on the enhancement of resistance to infections caused by Staphylococcus aureus and Eimeria vermiformis was studied in mice. In vitro study using macrophages isolated from the peritoneal cavity showed that beta-glucan treatment significantly enhanced phagocytic activity. In vivo study further demonstrated that beta-glucan treatment induced a significant (P<0.05) protection against the challenge with 5 x 10(8) of S. aureus in mice. Fecal oocyst shedding in the C57BL/6 mice infected with E. vermiformis was diminished by beta-glucan treatment by 39.6% in intraperitoneal and 28.5% in intragastric group compared to non-treated control. Patency period was shorter and antigen (sporozoites and merozoites) specific antibodies were significantly (P<0.05-0.01) higher in beta-glucan-treated group compared to non-treated control group. There were an increasing number of splenic IFN-gamma-secreting cells in glucan-treated group via intraperitoneal route, which might be responsible for the enhancement of the disease resistance. Glucan treatment was able to effectively change the lymphocytes population (Thy 1.2(+), CD4(+) and CD8(+) cells) in the mesenteric lymph nodes and Peyer's patches in mice infected with E. vermiformis. In conclusion, the oral or parenteral oat beta-glucan treatment enhanced the resistance to S. aureus or E. vermiformis infection in the mice.
Insights
Oat beta-glucan boosts mice's immune defense against Staphylococcus aureus and Eimeria vermiformis infections. This dietary supplement enhances macrophage activity and specific antibody production, improving disease resistance.
Area of Science:
- Immunology
- Microbiology
- Nutritional Science
Background:
- Bacterial and parasitic infections pose significant health challenges.
- Immune-modulating compounds like beta-glucans are explored for their therapeutic potential.
- Staphylococcus aureus and Eimeria vermiformis are common pathogens with varying infection mechanisms.
Purpose of the Study:
- To investigate the immunomodulatory effects of oat beta-glucan.
- To assess the efficacy of beta-glucan in enhancing resistance to Staphylococcus aureus and Eimeria vermiformis infections in mice.
- To elucidate the mechanisms underlying beta-glucan-mediated immune enhancement.
Main Methods:
- In vitro studies with isolated macrophages to evaluate phagocytic activity.
- In vivo experiments in mice challenged with S. aureus and E. vermiformis.
- Measurement of fecal oocyst shedding, antibody levels, and cytokine production (IFN-gamma).
- Analysis of lymphocyte populations (Thy 1.2(+), CD4(+), CD8(+)) in lymphoid tissues.
Main Results:
- Beta-glucan significantly enhanced macrophage phagocytic activity in vitro.
- Mice treated with beta-glucan showed significant protection against S. aureus challenge.
- Beta-glucan treatment reduced E. vermiformis fecal oocyst shedding and shortened the patency period.
- Increased antigen-specific antibody levels and splenic IFN-gamma-secreting cells were observed in beta-glucan-treated mice.
- Alterations in lymphocyte populations within mesenteric lymph nodes and Peyer's patches were noted.
Conclusions:
- Oat beta-glucan administration, both orally and parenterally, enhances resistance to S. aureus and E. vermiformis infections in mice.
- Beta-glucan modulates innate and adaptive immune responses, including phagocytosis, antibody production, and cellular immunity.
- These findings suggest beta-glucan as a potential natural immunomodulator for preventing or treating infections.
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