Table 1.
Diseases | Reference | Findings |
---|---|---|
Gastrointestinal Infections | Singer et al., 2019 [222] | Provide resistance against colonization and invasion by pathobiont. |
Tovaglieri et al., 2019 [223] | Human gut microbiome metabolites induce expression of flagellin (a bacterial protein) increases EHEC motility and epithelial injury. | |
IBD | Lee and chang, 2021 [224] | Gut microbiota dysbiosis of IBD patients is consistently marked by an overgrowth in Proteobacteria. |
Furusawa et al., 2013 [110] | SCFA confers protection against IBD by maintaining gut barrier integrity, promoting Treg cell differentiation, and inhibiting histone deacetylases. | |
Colorectal carcinoma |
Sepich-Poore et al., 2021 [225] | Generation of genotoxin such as Bacteroides fragilis toxin (Bft), cytolethal distending toxin (CDT), and colibactin. |
Hale et al., 2017 [226] | Bacterial-derived secondary bile acids and hydrogen sulfide promote proinflammatory milieu that increases CRC risk. | |
Yeoh et al., 2020 [227] | Bacteria such as F. nucleatum can adhere to colon tumors and aggravate tumorigenesis. | |
Hepatocellular carcinoma | Lin et al., 1995 [228] | Systemic translocation of LPS promotes chronic liver injury and predisposes to HCC. |
Singh et al., 2018 [229] | Excess butyrate production promotes HCC progression. | |
Yoshimoto et al., 2013 [230] | Secondary bile acids promote carcinogenesis and impede anti-tumor immunosurveillance in the liver. | |
Cardiometabolic disease | Cani et al., 2007 [231] Guasch-Ferré et al., 2017 [232] Millard et al., 2018 [233] |
LPS and other microbial ligands drive low-grade chronic inflammation and predispose to CVD. |
Bacterial trimethylamine and its conversion to trimethylamine-N-oxide in the liver increases the risk of coronary artery disease, metabolic syndrome, stroke, and vascular inflammation. | ||
Rheumatoid Arthritis |
Scher et al., 2013 [234] | Prevotella spp. Abundance is positively associated with new-onset rheumatoid arthritis. |
Allergic Diseases |
Fazlollahi et al., 2018 [235] Bunyavanich et al., 2016 [236] |
Gut microbiota dysbiosis increases risk for allergic disease, e.g., food allergy and asthma. |