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. 2020 Nov 5;56(1):1–11. doi: 10.1007/s00535-020-01740-5

Table 1.

Gut mycobiome or fungal-derived products in chronic liver diseases

Disease Species Mycobiome alterations in diseased individuals References
Alcoholic hepatitis Human

Decreased fungal diversity

Increased Candida (genus) and C. albicans

Decreased Penicillium (genus)

Decreased Saccharomyces (genus)

Increased serum ASCA

Increased fecal ECE1 gene

[43, 44, 81]
Ethanol-induced liver disease Mouse

Increased total number of fecal fungi

Increased plasma 1,3-β-D-glucan

Disease exacerbation by candidalysin

[44]
Obesity Human

Decreased fungal diversity (family level)

Decreased Zygomycota (phylum), Decreased Agaricomycetes (class) and Mucor (genus)

Increased Tremellomycetes (class)

[45]
PSC Human

Increased fungal diversity in PSC

(compared with IBD)

Decreased Saccharomycetales (order), Saccharomycetes (class), Saccharomycetaceae (family), and

S. cerevisiae (species)

[92]
Cirrhosis Human

Decreased fungal diversity in cirrhosis

Increased Candida in inpatients

Decreased Basidiomycota/Ascomycota in inpatients vs. outpatients and controls

[46]

C. albicans, Candida albicans, ASCA, anti-Saccharomyces cerevisiae antibodies, ECE1, extent of cell elongation 1, PSC, primary sclerosing cholangitis, IBD, inflammatory bowel disease, S. cerevisiae, Saccharomyces cerevisiae