Modulatory Effects of Heat-Inactivated Streptococcus Thermophilus Strain 7 on the Inflammatory Response: A Study on an Animal Model with TLR3-Induced Intestinal Injury

Author:

Lee Gilbert Aaron1234,Chang Yu-Wei1,Lin Wan-Li1,Yang Yu-Chen S. H.5ORCID,Chen Wei-Jen6,Huang Fu-Huan7ORCID,Liu Yun-Ru5

Affiliation:

1. Department of Medical Research, Taipei Medical University Hospital, Taipei City 110, Taiwan

2. Department of Microbiology and Immunology, School of Medicine, College of Medicine, Taipei Medical University, Taipei City 110, Taiwan

3. Child Development Research Center, Taipei Medical University Hospital, Taipei City 110, Taiwan

4. TMU Research Center for Digestive Medicine, Taipei Medical University, Taipei City 110, Taiwan

5. Joint Biobank, Office of Human Research, Taipei Medical University, Taipei City 110, Taiwan

6. Syngen Biotech International, Shah Alam 40460, Malaysia

7. Division of Pediatric Surgery, Department of Surgery, Taipei Medical University Hospital, Taipei City 110, Taiwan

Abstract

Rotavirus infections result in severe gastroenteritis with a detrimental inflammatory response in the intestine. Because probiotics have an anti-inflammatory effect and can modulate the gut microbiota profile, they can be used as a biotherapy for inflammatory intestinal diseases. In this study, we isolated Streptococcus thermophilus strain 7 (ST7) from cow milk and examined the effect of heat-inactivated ST7 on the intestinal histopathological score, inflammatory cytokine levels, T-cell activation and effector function, and microbiome profile in a mouse model with intestinal injury induced by polyinosinic-polycytidylic acid (poly I:C), a Toll-like receptor 3 agonist. The results indicated that ST7 treatment prevented weight loss and intestinal injury and prevented the upregulation of serum interleukin-6 (IL-6), tumor necrosis factor-α, and IL-15 levels in intestinal epithelial cells; prevented the upregulation of inflammation-associated Gammaproteobacteria and Alistipes; and increased the levels of Firmicutes in fecal microbiota after poly I:C stimulation. ST7 treatment also increased the serum interferon-γ (IFN-γ) level and promoted the expression of IFN-γ in both CD8 and CD4 T cells. In summary, ST7 prevented the inflammatory response, promoted the T-cell effector function, and modulated the microbiota profile of mice with poly I:C-induced small intestine injury.

Funder

Taipei Medical University

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

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