Garlic-Derived Metabolites Exert Antioxidant Activity, Modulate Gut Microbiota Composition and Limit Citrobacter rodentium Infection in Mice

• Published in: Antioxidants Vol. 11; no. 10; p. 2033
• Main Authors: Zhu, Ling, Andersen-Civil, Audrey I S, Castro-Meija, Josue L, Nielsen, Dennis S, Blanchard, Alexandra, Olsen, John E, Thamsborg, Stig M, Williams, Andrew R
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 15.10.2022; MDPI
• Subjects: Antibiotics; antioxidant activity; Antioxidants; Citrobacter rodentium; Dietary supplements; Digestive system; Drinking water; E coli; Experiments; Garlic; Gastrointestinal tract; Inflammation; Intestinal microflora; Lipopolysaccharides; Macrophages; Metabolism; Metabolites; Microbiota; Nitric oxide; nuclear factor erythroid factor 2-related factor 2; Oxidative stress; Pathogens; Propane; propyl propane thiosulfinate; propyl propane thiosulfonate; Proteins; Reactive oxygen species; Staphylococcus infections; United Kingdom > UK; United States > US; Germany; nuclear factor erythroid factor 2-related factor 2; Citrobacter rodentium; propyl propane thiosulfonate; antioxidant activity; propyl propane thiosulfinate
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox11102033

The garlic-derived compounds propyl propane thiosulfinate (PTS) and propyl propane thiosulfonate (PTSO) are metabolites with putative health benefits against intestinal inflammation that may be related to their antioxidant activity. However, the underlying mechanisms remain unclear, and whether PTS-PTSO can promote gut health by altering the microbiota and exert protection against enteric pathogens needs further investigation. Here, we explored the antioxidant activity of PTS-PTSO in murine macrophages in vitro, and in an in vivo model of bacterial infection with the bacterial pathogen . PTS-PTSO attenuated reactive oxygen species in lipopolysaccharide-stimulated macrophages in a nuclear factor erythroid factor 2-related factor 2 (Nrf2)-dependent manner, decreased nitric oxide levels both in macrophages in vitro and in the sera of mice fed PTS-PTSO, and had putatively beneficial effects on the commensal gut microbiota. Importantly, PTS-PTSO decreased faecal counts, concomitant with upregulation of Nrf2-related genes in colon tissue. Thus, PTS-PTSO mediates Nrf2-mediated antioxidant activity and modulates gut microbiota, which may protect the host against colonization. Our results provide further insight into how PTS-PTSO and related bioactive dietary compounds may reduce enteric infections.